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Jean-Claude Kaplan

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Jean-Claude Kaplan
The 2012 version of the gene table of monogenic neuromuscular disorders.
Amets Sáenz; Hiroyuki Sorimachi; Miguel Urtasun; Margarita Azpitarte; L Blázquez; Naoko Doi; Federico García-Bragado; Maria Goicoechea; Jean-Claude Kaplan; France Leturcq; Alberto Marina; Yasuko Ono; Juan José Poza; Adolfo López de Munain
Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?
Jean-Claude Kaplan
The 2011 version of the gene table of neuromuscular disorders.

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All Publications

2011: Jean-Claude Kaplan
The 2012 version of the gene table of monogenic neuromuscular disorders.
Neuromuscular disorders : NMD 2011;21(12):833-61.
2011: Amets Sáenz; Hiroyuki Sorimachi; Miguel Urtasun; Margarita Azpitarte; L Blázquez; Naoko Doi; Federico García-Bragado; Maria Goicoechea; Jean-Claude Kaplan; France Leturcq; Alberto Marina; Yasuko Ono; Juan José Poza; Adolfo López de Munain
Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?
Muscle & nerve 2011;44(5):710-4.
2010: Jean-Claude Kaplan
The 2011 version of the gene table of neuromuscular disorders.
Neuromuscular disorders : NMD 2010;20(12):852-73.
2010: Dominique Labie; Jean-Claude Kaplan
[Update on RNA splicing repair: applications to beta thalassemia and other perspectives].
Médecine sciences : M/S 2010;26(1):38-41.
2009: Fatma Daoud; Nathalie Angeard; Bénédicte Demerre; Itxaso Martie; Rabah Benyaou; France Leturcq; Mireille Cossée; Nathalie Deburgrave; Yoann Saillour; Sylvie Tuffery; Andoni Urtizberea; Annick Toutain; Bernard Echenne; Martine Frischman; Michèle Mayer; Isabelle Desguerre; Brigitte Estournet; Christian Réveillère; Jean Marie Cuisset; Jean-Claude Kaplan; Delphine Héron; François Rivier; Jamel Chelly
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression.
Human molecular genetics 2009;18(20):3779-94.
2009: Sylvie Tuffery-Giraud; Christophe Béroud; France Leturcq; Rabah Ben Yaou; dalil hamroun; Laurence Michel-Calemard; Marie-Pierre Moizard; Rafaëlle Bernard; Mireille Cossée; Pierre Boisseau; Martine Blayau; Isabelle Creveaux; Anne Guiochon-Mantel; Bérengère de Martinville; Christophe Philippe; Nicole Monnier; Eric Bieth; Philippe Khau Van Kien; François-Olivier Desmet; Véronique Humbertclaude; Jean-Claude Kaplan; Jamel Chelly; Mireille Claustres
Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.
Human mutation 2009;30(6):934-45.
2009: Jean-Claude Kaplan
Gene table of monogenic neuromuscular disorders (nuclear genome only) Vol 19. No 1 January 2009.
Neuromuscular disorders : NMD 2009;19(1):77-98.
2008: Jean-Claude Kaplan
[Lost after translation].
Médecine sciences : M/S 2008;24(11):912-5.
2008: Madiha Trabelsi; Niloufar Kavian; Fatma Daoud; Virginie Commere; Nathalie Deburgrave; Caroline Beugnet; Stephane Llense; Jean Claude Barbot; Aurélie Vasson; Jean-Claude Kaplan; France Leturcq; Jamel Chelly
Revised spectrum of mutations in sarcoglycanopathies.
European journal of human genetics : EJHG 2008;16(7):793-803.
2008: Jean-Claude Kaplan
[In mito veritas?].
Médecine sciences : M/S 2008;24(5):470-2.
2008: Jean-Claude Kaplan
[Ex vivo veritas].
Médecine sciences : M/S 2008;24(4):427.
2008: Jean-Claude Kaplan; Jamel Chelly; Luis Garcia
[Effective exon skipping in humans: a symbolic but promising jump into DMD therapy].
Médecine sciences : M/S 2008;24(2):215-7.
2007: Nathalie Deburgrave; Fatma Daoud; Stéphane Llense; Jean Claude Barbot; Dominique Récan; Cécile Peccate; Arthur H M Burghes; Christophe Béroud; Luis Garcia; Jean-Claude Kaplan; Jamel Chelly; France Leturcq
Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
Human mutation 2007;28(2):183-95.
2005: Jean-Claude Kaplan
[Neither genes, nor junk, but... TAR/TUF!].
Médecine sciences : M/S 2005;21(11):1005.
2005: Amets Sáenz; France Leturcq; Anna Maria Cobo; Juan José Poza; Xavier Ferrer; David Otaegui; Pilar Camaño; Miguel Urtasun; Juan J Vílchez; E Gutiérrez-Rivas; JI Emparanza; Luciano Merlini; C Paisán; Maria Goicoechea; L Blázquez; Bruno Eymard; H Lochmuller; M Walter; C Bonnemann; Dominique Figarella-Branger; Jean-Claude Kaplan; J Andoni Urtizberea; José Félix Martí-Massó; Adolfo López de Munain
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
Brain : a journal of neurology 2005;128(Pt 4):732-42.
2005: France Leturcq; Jean-Claude Kaplan
[Molecular bases of dystrophinopathies].
Journal de la Société de biologie 2005;199(1):5-11.
2005: dalil hamroun; Christophe Béroud; Bertrand Fontaine; Jean-Claude Kaplan
Introducing the online version of the gene table for neuromuscular disease (nuclear genes only).
Neuromuscular disorders : NMD 2005;15(1):88.
2004: Aurélie Goyenvalle; Adeline Vulin; Françoise Fougerousse; France Leturcq; Jean-Claude Kaplan; Luis Garcia; Olivier Danos
Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping.
Science (New York, N.Y.) 2004;306(5702):1796-9.
2004: Aurélie Goyenvalle; Adeline Vulin; Françoise Fougerousse; France Leturcq; Jean-Claude Kaplan; Luis Garcia; Olivier Danos
[An opening in Duchenne muscular dystrophy: persistent therapeutic rescue of dystrophin by vectorized antisense mediated exon skipping in mdx mice].
Médecine sciences : M/S 2004;20(12):1163-5.
2004: Norma B Romero; Serge Braun; Olivier Benveniste; France Leturcq; Jean-Yves Hogrel; Glenn E Morris; Annie Barois; Bruno Eymard; Christine Payan; Véronique Ortega; Anne-Laure Boch; Lise Lejean; Christine Thioudellet; Brigitte Mourot; Christophe Escot; Aurore Choquel; Dominique Recan; Jean-Claude Kaplan; George Dickson; David Klatzmann; Valérie Molinier-Frenckel; Jean-Gérard Guillet; Patrick Squiban; Serge Herson; Michel Fardeau
Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophy.
Human gene therapy 2004;15(11):1065-76.
2004: Nina Canki-Klain; Astrid Milic; Biserka Kovac; Anuska Trlaja; Damir Grgicevic; Niko Zurak; Michel Fardeau; France Leturcq; Jean-Claude Kaplan; J Andoni Urtizberea; Luisa Politano; Giulio Piluso; JOSUE FEINGOLD
Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia.
American journal of medical genetics. Part A 2004;125A(2):152-6.
2004: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2004;14(1):85-106.
2004: Christophe Béroud; Alain Carrié; Cherif Beldjord; Nathalie Deburgrave; Stéphane Llense; Nadège Carelle; Cécile Peccate; Jean-Marie Cuisset; Florence Pandit; Frédérique Carré-Pigeon; Michèle Mayer; Rémi Bellance; Dominique Récan; Jamel Chelly; Jean-Claude Kaplan; France Leturcq
Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene.
Neuromuscular disorders : NMD 2004;14(1):10-8.
2003: Jean-Claude Kaplan
Neuromuscular disorders:gene location.
Neuromuscular disorders : NMD 2003;13(10):837-47.
2003: J Andoni Urtizberea; Qi Shi Fan; Elizabeth Vroom; Dominique Récan; Jean-Claude Kaplan
Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicine.
Neuromuscular disorders : NMD 2003;13(9):705-7.
2003: Genoveva Keyeux; Clemencia Rodas; Thierry Bienvenu; Pilar Garavito; Dominique Vidaud; Dora Sanchez; Jean-Claude Kaplan; Gustavo Aristizábal
CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programs.
Human mutation 2003;22(3):259.
2002: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2002;12(5):513-23.
2002: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2002;12(3):324-33.
2002: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2002;12(2):214-23.
2002: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2002;12(1):82-100.
2001: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2001;11(8):764-73.
2001: Jean-Claude Kaplan
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2001;11(6-7):680-9.
2001: Norma B Romero; P De Lonlay; Stéphane Llense; France Leturcq; G Touati; J Andoni Urtizberea; Jean-Marie Saudubray; A Munnich; Jean-Claude Kaplan; Dominique Récan
Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin gene.
Neuromuscular disorders : NMD 2001;11(5):494-8.
2001: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2001;11(2):221-9.
2000: Jean-Claude Kaplan; C Junien
Genomics and medicine: an anticipation. From Boolean Mendelian genetics to multifactorial molecular medicine.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 2000;323(12):1167-74.
2000: Nina Canki-Klain; Dominique Récan; D Milicić; Stéphane Llense; France Leturcq; Nathalie Deburgrave; Jean-Claude Kaplan; M Debevec; Niko Zurak
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy.
Croatian medical journal 2000;41(4):389-95.
2000: Jean-Claude Kaplan
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2000;10(7):I-IX.
2000: Luciano Merlini; Jean-Claude Kaplan; C Navarro; Annie Barois; Dominique Bonneau; J Brasa; B Echenne; Pía Gallano; L Jarre; Marc Jeanpierre; Luba Kalaydjieva; France Leturcq; A Levi-Gomes; Annick Toutain; Ivailo Tournev; Andoni Urtizberea; J M Vallat; T Voit; J M Warter
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation.
Neurology 2000;54(5):1075-9.
2000: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.Vol. 10 No. 2, February 2000.
Neuromuscular disorders : NMD 2000;10(2):I-VIII.
2000: Jean-Claude Kaplan
[Presentation. The birth of molecular medicine].
Bulletin de l'Académie nationale de médecine 2000;184(7):1359-61.
2000: Jean-Claude Kaplan; Bertrand Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 2000;10(1):I-XV.
1999: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1999;9(8):I-VIII.
1999: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1999;9(6-7):I-VIII.
1999: Xavier Puéchal; Isabelle Fajac; Thierry Bienvenu; Nadine Desmazes-Dufeu; Dominique Hubert; Jean-Claude Kaplan; CJ Menkès; Daniel Dusser
Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritis.
The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology 1999;13(6):1281-7.
1999: O Loumi; M Baghriche; M Delpech; Jean-Claude Kaplan; T Bienvenu
Analysis of the complete coding region of the CFTR gene in ten Algerian cystic fibrosis families.
Human heredity 1999;49(2):81-4.
1998: Pervin Dinçer; Federica Piccolo; France Leturcq; Jean-Claude Kaplan; Marc Jeanpierre; H Topaloğlu
Prenatal diagnosis of limb-girdle muscular dystrophy type 2C.
Prenatal diagnosis 1998;18(12):1300-3.
1998: Isabelle Fajac; Dominique Hubert; Thierry Bienvenu; B Richaud-Thiriez; R Matran; Jean-Claude Kaplan; Josette Dall'Ava-Santucci; Daniel Dusser
Relationships between nasal potential difference and respiratory function in adults with cystic fibrosis.
The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology 1998;12(6):1295-300.
1998: Miguel Urtasun; Amets Sáenz; Carinne Roudaut; Juan José Poza; J Andoni Urtizberea; Anna Maria Cobo; Isabelle Richard; F García-Bragado; France Leturcq; Jean-Claude Kaplan; José Félix Martí-Massó; Jacques Beckmann; Adolfo López de Munain
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain).
Brain : a journal of neurology 1998;121 ( Pt 9)():1735-47.
1998: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1998;8(2):I-VII.
1998: F Duclos; O Broux; Nathalie Bourg; Volker Straub; Gerald L Feldman; Y Sunada; LE Lim; Federica Piccolo; S Cutshall; F Gary; F Quetier; Jean-Claude Kaplan; CE Jackson; Jacques Beckmann; Kevin P Campbell
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
Neuromuscular disorders : NMD 1998;8(1):30-8.
1998: Thierry Bienvenu; S Bousquet; Dominique Vidaud; Dominique Hubert; C Francoual; Cherif Beldjord; Jean-Claude Kaplan
A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. Online.
Human mutation 1998;12(3):213-4.
1998: J Steffann; Dominique Vidaud; S Bousquet; M Jullien; A Ninot; Jean-Claude Kaplan; Cherif Beldjord; Thierry Bienvenu
Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus.
Annales de génétique 1998;41(4):213-5.
1998: Thierry Bienvenu; Jacques Lepercq; J P Allard; Dominique Hubert; C Francoual; Cherif Beldjord; Jean-Claude Kaplan
Compound heterozygotes for a CF mutation and the 5T splice variant associated with variable presentations in a French family.
Annales de génétique 1998;41(1):63-4.
1997: Norma B Romero; Dominique Récan; Odile Rigal; France Leturcq; Stéphane Llense; Jean Claude Barbot; Nathalie Deburgrave; M A Cheval; F Deniau; Jean-Claude Kaplan
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci.
Neuromuscular disorders : NMD 1997;7(8):499-504.
1997: R M Quinlivan; S A Robb; Caroline Sewry; V Dubowitz; Federica Piccolo; Jean-Claude Kaplan
Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophy.
Developmental medicine and child neurology 1997;39(11):770-4.
1997: Pervin Dinçer; France Leturcq; Isabelle Richard; Federica Piccolo; Dilek Yalnizoglu; C de Toma; Zuhal Akçören; O Broux; Nathalie Deburgrave; L Brenguier; Carinne Roudaut; J Andoni Urtizberea; D Jung; Ersin Tan; Marc Jeanpierre; Kevin P Campbell; Jean-Claude Kaplan; Jacques Beckmann; Haluk Topaloglu
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
Annals of neurology 1997;42(2):222-9.
1997: Alain Carrié; Federica Piccolo; France Leturcq; C de Toma; K Azibi; Cherif Beldjord; J M Vallat; Luciano Merlini; T Voit; Caroline Sewry; J Andoni Urtizberea; Norma B Romero; Fernando M S Tomé; Michel Fardeau; Y Sunada; Kevin P Campbell; Jean-Claude Kaplan; Marc Jeanpierre
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
Journal of medical genetics 1997;34(6):470-5.
1997: Thierry Bienvenu; S Bousquet; Stanislas LYONNET; Jean-Claude Kaplan; Cherif Beldjord
1283 del A: a novel mutation in exon 8 of the cystic fibrosis gene.
Human heredity 1997;47(3):173-5.
1997: Bruno Eymard; Norma B Romero; France Leturcq; Federica Piccolo; Alain Carrié; Marc Jeanpierre; H Collin; Nathalie Deburgrave; K Azibi; M Chaouch; Luciano Merlini; C Thémar-Noël; I Penisson; Michèle Mayer; O Tanguy; Kevin P Campbell; Jean-Claude Kaplan; Fernando M S Tomé; Michel Fardeau
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.
Neurology 1997;48(5):1227-34.
1997: Sophie Valleix; K Nafa; Natalie Stieltjes; M Viemont; Y Sultan; Jean-Claude Kaplan; Marc Delpech
Prevalence, male germ-line origin and new patterns of inversions in haemophilia A.
Annales de génétique 1997;40(1):35-40.
1997: Thierry Bienvenu; M Adjiman; Nicolas Thiounn; Marc Jeanpierre; Dominique Hubert; J Lepercoq; C Francoual; J Wolf; Vincent Izard; Pierre Jouannet; Jean-Claude Kaplan; Cherif Beldjord
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.
Annales de génétique 1997;40(1):5-9.
1997: Lilien Chertkoff; A Visich; T Bienvenu; M Grenoville; E Segal; L Carniglia; Jean-Claude Kaplan; Cristina Barreiro
Spectrum of CFTR mutations in Argentine cystic fibrosis patients.
Clinical genetics 1997;51(1):43-7.
1996: Marc Jeanpierre; Alain Carrié; Federica Piccolo; France Leturcq; K Azibi; C de Toma; Cherif Beldjord; Luciano Merlini; T Voit; Norma B Romero; Y Sunada; Fernando M S Tomé; M Fardeau; Kevin P Campbell; Jean-Claude Kaplan
From adhalinopathies to alpha-sarcoglycanopathies: an overview.
Neuromuscular disorders : NMD 1996;6(6):463-5.
1996: Federica Piccolo; Marc Jeanpierre; France Leturcq; Catherine Dodé; K Azibi; A Toutain; Luciano Merlini; L Jarre; C Navarro; R Krishnamoorthy; Fernando M S Tomé; J Andoni Urtizberea; Jacques Beckmann; Kevin P Campbell; Jean-Claude Kaplan
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India.
Human molecular genetics 1996;5(12):2019-22.
1996: Dominique Hubert; Thierry Bienvenu; N Desmazes-Dufeu; Isabelle Fajac; Jacques Lacronique; R Matran; Jean-Claude Kaplan; Daniel Dusser
Genotype-phenotype relationships in a cohort of adult cystic fibrosis patients.
The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology 1996;9(11):2207-14.
1996: Thierry Bienvenu; François Cartault; F Lesure; Michel Renouil; Cherif Beldjord; Jean-Claude Kaplan
A splicing mutation in intron 16 of the cystic fibrosis transmembrane conductance regulator gene, associated with severe disease, is common on Reunion Island.
Human heredity 1996;46(3):168-71.
1996: D Jung; France Leturcq; Y Sunada; F Duclos; Fernando M S Tomé; Carolyn Moomaw; Luciano Merlini; K Azibi; M Chaouch; C Slaughter; M Fardeau; Jean-Claude Kaplan; Kevin P Campbell
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
FEBS letters 1996;381(1-2):15-20.
1996: K Oexle; R Herrmann; Catherine Dodé; France Leturcq; Christoph Hübner; Jean-Claude Kaplan; Y Mizuno; E Ozawa; Kevin P Campbell; T Voit
Neurosensory hearing loss in secondary adhalinopathy.
Neuropediatrics 1996;27(1):32-6.
1996: Thierry Bienvenu; Cherif Beldjord; Jamel Chelly; N Fonknechten; Dominique Hubert; Daniel Dusser; Jean-Claude Kaplan
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients.
European journal of human genetics : EJHG 1996;4(3):127-34.
1996: Thierry Bienvenu; Dominique Hubert; E Setbon; Daniel Dusser; Jean-Claude Kaplan; Cherif Beldjord
A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patients.
Human mutation 1996;7(2):182.
1996: Christophe Pêcheux; A L Gall; Jean-Claude Kaplan; Catherine Dodé
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian species.
Annales de génétique 1996;39(2):81-6.
1996: T Bienvenu; Lilien Chertkoff; C Beldjord; E Segal; L Carniglia; Cristina Barreiro; Jean-Claude Kaplan
Identification of three novel mutations in the cystic fibrosis transmembrane conductance regulator gene in Argentinian CF patients.
Human mutation 1996;7(4):376-7.
1995: Thierry Bienvenu; C Beldjord; Jean-Claude Kaplan; D Hubert; D Dusser
Severe cystic fibrosis phenotype in a delta F508/3272-26A-->G compound heterozygote.
Journal of medical genetics 1995;32(11):919.
1995: Thierry Bienvenu; V Lacronique; Michel Raymondjean; C Cazeneuve; Dominique Hubert; Jean-Claude Kaplan; Cherif Beldjord
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect.
Human genetics 1995;95(6):698-702.
1995: Christophe Pêcheux; J F Mouret; Alexandra Dürr; Yves Agid; J Feingold; Alexis Brice; Catherine Dodé; Jean-Claude Kaplan
Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes.
Journal of medical genetics 1995;32(5):399-400.
1995: Alexandra Dürr; Catherine Dodé; V Hahn; Christophe Pêcheux; Bernard Pillon; J Feingold; Jean-Claude Kaplan; Yves Agid; Alexis Brice
Diagnosis of "sporadic" Huntington's disease.
Journal of the neurological sciences 1995;129(1):51-5.
1995: C Cazeneuve; Cherif Beldjord; Jean-Claude Kaplan; Thierry Bienvenu
Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Annales de génétique 1995;38(4):202-5.
1995: Thierry Bienvenu; C Cazeneuve; Jean-Claude Kaplan; Cherif Beldjord
Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotide.
Human mutation 1995;6(1):23-9.
1995: Thierry Bienvenu; C Cazeneuve; Isabelle Fajac; Daniel Dusser; Dominique Hubert; Jean-Claude Kaplan; Cherif Beldjord
Identification of a novel missense mutation G239R in exon 6a of the CFTR gene.
Human heredity 1995;45(1):53-4.
1994: V Allamand; France Leturcq; Federica Piccolo; Marc Jeanpierre; K Azibi; S L Roberds; LE Lim; Kevin P Campbell; Jacques Beckmann; Jean-Claude Kaplan
Adhalin gene polymorphism.
Human molecular genetics 1994;3(12):2269.
1994: Thierry Bienvenu; Dominique Hubert; N Fonknechten; Daniel Dusser; Jean-Claude Kaplan; Cherif Beldjord
Unexpected inactivation of acceptor consensus splice sequence by a -3 C to T transition in intron 2 of the CFTR gene.
Human genetics 1994;94(1):65-8.
1994: Frédérique Tihy; Nicolas Vogt; Dominique Recan; Bernard Malfoy; France Leturcq; M Coquet; F Serville; D Fontan; Jean-Michel Guillard; Jean-Claude Kaplan
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter.
Human genetics 1994;93(5):563-7.
1994: K Matsumura; Fernando M S Tomé; H Collin; France Leturcq; Marc Jeanpierre; Jean-Claude Kaplan; M Fardeau; Kevin P Campbell
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1994;4(2):115-20.
1994: Thierry Bienvenu; C Cazeneuve; Cherif Beldjord; Daniel Dusser; Jean-Claude Kaplan; Dominique Hubert
A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patient.
Human molecular genetics 1994;3(2):365-6.
1994: Thierry Ragot; L D Stratford-Perricaudet; N Vincent; P Chafey; Emmanuelle Vigne; H Gilgenkrantz; D Couton; Pascale Briand; Jean-Claude Kaplan; Axel Kahn
Adenovirus-mediated transfer of a human dystrophin gene to skeletal muscle of mdx mouse.
Gene therapy 1994;1 Suppl 1():S53-4.
1994: K Matsumura; A H Burghes; M Mora; Fernando M S Tomé; L Morandi; F Cornello; France Leturcq; Marc Jeanpierre; Jean-Claude Kaplan; P Reinert
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.
The Journal of clinical investigation 1994;93(1):99-105.
1994: Thierry Bienvenu; P Petitpretz; Cherif Beldjord; Jean-Claude Kaplan
A missense mutation (F87L) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene.
Human mutation 1994;3(4):395-6.
1994: Thierry Bienvenu; G Lenoir; N Fonknechten; F Desclaux-Arramond; Jean-Claude Kaplan; Cherif Beldjord
Identification of a new frameshift mutation (3724 delG) in exon 19 of the CFTR gene.
Human mutation 1994;3(1):69-70.
1993: N Fonknechten; Thierry Bienvenu; C Moriscot; Cherif Beldjord; Axel Kahn; C Figarella; Jean-Claude Kaplan
Skipping of exon 9 in CFTR mRNA of human adult and fetal pancreas from non-CF individuals.
Human molecular genetics 1993;2(12):2141-2.
1993: Catherine Dodé; Alexandra Dürr; Christophe Pêcheux; J F Mouret; Samir Belal; L Bachner; Yves Agid; Jean-Claude Kaplan; Alexis Brice; J Feingold
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1993;316(11):1374-80.
1993: E Fernandez; Thierry Bienvenu; F Desclaux Arramond; K Beldjord; Jean-Claude Kaplan; Cherif Beldjord
Use of chemical clamps in denaturing gradient gel electrophoresis: application in the detection of the most frequent Mediterranean beta-thalassemic mutations.
PCR methods and applications 1993;3(2):122-4.
1993: N Vincent; Thierry Ragot; H Gilgenkrantz; D Couton; P Chafey; A Grégoire; Pascale Briand; Jean-Claude Kaplan; Axel Kahn; Michel Perricaudet
Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene.
Nature genetics 1993;5(2):130-4.
1993: K Matsumura; Kay Ohlendieck; V V Ionasescu; Fernando M S Tomé; I Nonaka; A H Burghes; M Mora; Jean-Claude Kaplan; M Fardeau; Kevin P Campbell
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies.
Neuromuscular disorders : NMD 1993;3(5-6):533-5.
1993: M Lambert; P Chafey; J P Hugnot; Annette Koulakoff; Y Berwald-Netter; C Billard; G E Morris; Axel Kahn; Jean-Claude Kaplan; H Gilgenkrantz
Expression of the transcripts initiated in the 62nd intron of the dystrophin gene.
Neuromuscular disorders : NMD 1993;3(5-6):519-24.
1993: K Matsumura; Fernando M S Tomé; V Ionasescu; James M Ervasti; R D Anderson; Norma B Romero; D Simon; D Récan; Jean-Claude Kaplan; M Fardeau
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.
The Journal of clinical investigation 1993;92(2):866-71.
1993: K Matsumura; I Nonaka; Fernando M S Tomé; K Arahata; H Collin; France Leturcq; D Récan; Jean-Claude Kaplan; M Fardeau; Kevin P Campbell
Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.
American journal of human genetics 1993;53(2):409-16.
1993: M Fardeau; K Matsumura; Fernando M S Tomé; H Collin; France Leturcq; Jean-Claude Kaplan; Kevin P Campbell
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1993;316(8):799-804.
1993: Thierry Bienvenu; Cherif Beldjord; N Fonknechten; Jean-Claude Kaplan; G Lenoir
Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene.
Journal of medical genetics 1993;30(7):621-2.
1993: J P Hugnot; H Gilgenkrantz; P Chafey; M Lambert; Eric Eveno; Jean-Claude Kaplan; Axel Kahn
Expression of the dystrophin gene in cultured fibroblasts.
Biochemical and biophysical research communications 1993;192(1):69-74.
1993: Thierry Ragot; N Vincent; P Chafey; Emmanuelle Vigne; H Gilgenkrantz; D Couton; J Cartaud; Pascale Briand; Jean-Claude Kaplan; Michel Perricaudet
Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice.
Nature 1993;361(6413):647-50.
1993: J P Hugnot; H Gilgenkrantz; Marc Jeanpierre; Jamel Chelly; Jean-Claude Kaplan; Axel Kahn
Striking conservation of the brain-specific region of the dystrophin gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(7):393-6.
1993: Thierry Bienvenu; S Bousquet; C Herbulot; François Cartault; Jean-Claude Kaplan; Cherif Beldjord
Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.
Human mutation 1993;2(4):306-8.
1992: F Chevalier-Porst; Jean-Claude Chomel; D Hillaire; Alain Kitzis; Jean-Claude Kaplan; R Goutaland; M Mathieu; Dominique Bozon
A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island.
Human molecular genetics 1992;1(8):647-8.
1992: K Matsumura; Fernando M S Tomé; H Collin; K Azibi; M Chaouch; Jean-Claude Kaplan; M Fardeau; Kevin P Campbell
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.
Nature 1992;359(6393):320-2.
1992: J P Hugnot; H Gilgenkrantz; N Vincent; P Chafey; G E Morris; Anthony P Monaco; Y Berwald-Netter; Annette Koulakoff; Jean-Claude Kaplan; Axel Kahn
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(16):7506-10.
1992: N Fonknechten; Jean-Claude Chomel; Alain Kitzis; Axel Kahn; Jean-Claude Kaplan
Skipping of exon 5 as a consequence of the 711 + 1 G-->T mutation in the CFTR gene.
Human molecular genetics 1992;1(4):281-2.
1992: H Gilgenkrantz; J P Hugnot; M Lambert; P Chafey; Jean-Claude Kaplan; Axel Kahn
Positive and negative regulatory DNA elements including a CCArGG box are involved in the cell type-specific expression of the human muscle dystrophin gene.
The Journal of biological chemistry 1992;267(15):10823-30.
1992: N Fonknechten; Jamel Chelly; J Lepercq; Axel Kahn; Jean-Claude Kaplan; Alain Kitzis; Jean-Claude Chomel
CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcripts.
Human genetics 1992;88(5):508-12.
1992: Thierry Bienvenu; P Sebillon; Dominique Labie; Jean-Claude Kaplan; Cherif Beldjord
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification.
Human biology 1992;64(1):107-13.
1992: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1992;2(4):289-92.
1992: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1992;2(3):227-30.
1992: Jean-Claude Kaplan; Axel Kahn; J Chelly
Illegitimate transcription: its use in the study of inherited disease.
Human mutation 1992;1(5):357-60.
1992: Jean-Claude Kaplan; Jamel Chelly; H Gilgenkrantz; N Fonknechten; Axel Kahn
[Illegitimate transcription: discovery and application to gene molecular pathology].
Comptes rendus des séances de la Société de biologie et de ses filiales 1992;186(4):371-6.
1992: H Gilgenkrantz; Jamel Chelly; D Récan; P Chafey; Jean-Claude Kaplan
[Molecular pathology of Duchenne and Becker muscular dystrophy].
Comptes rendus des séances de la Société de biologie et de ses filiales 1992;186(4):349-53.
1992: Khedoudja Nafa; M Baudis; N Deburgrave; J M Bardin; Y Sultan; Jean-Claude Kaplan; Marc Delpech
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A.
Human mutation 1992;1(1):77-8.
1992: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1992;2(5-6):431-4.
1991: Jamel Chelly; H Gilgenkrantz; J P Hugnot; G Hamard; M Lambert; D Récan; S Akli; M Cometto; Axel Kahn; Jean-Claude Kaplan
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.
The Journal of clinical investigation 1991;88(4):1161-6.
1991: Jamel Chelly; J P Hugnot; J P Concordet; Jean-Claude Kaplan; Axel Kahn
Illegitimate (or ectopic) transcription proceeds through the usual promoters.
Biochemical and biophysical research communications 1991;178(2):553-7.
1991: J P Hugnot; D Récan; Marc Jeanpierre; Jean-Claude Kaplan; A Tolun
A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD).
Nucleic acids research 1991;19(11):3159.
1991: Jean-Claude Kaplan; B S Emanuel
Chromosome 22 workshop proceedings.
Genomics 1991;9(1):214-8.
1991: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1991;1(3):221-3.
1991: T S Khurana; simon simon watkins; P Chafey; Jamel Chelly; Fernando M S Tomé; M Fardeau; Jean-Claude Kaplan; Louis Kunkel
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.
Neuromuscular disorders : NMD 1991;1(3):185-94.
1991: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1991;1(6):457-9.
1991: Jean-Claude Kaplan; B Fontaine
Neuromuscular disorders: gene location.
Neuromuscular disorders : NMD 1991;1(5):379-81.
1991: P Sebillon; Thierry Bienvenu; R Girot; Dominique Labie; Jean-Claude Kaplan; Cherif Beldjord
Detection of the most frequent beta-thalassemic defect in Southeast Asia by PCR.
Hemoglobin 1991;15(4):313-5.
1990: S Ben Jelloun-Dellagi; P Chaffey; Faycal Hentati; Christiane Ben Hamida; F Tome; H Colin; K Dellagi; Jean-Claude Kaplan; M Fardeau; M Ben Hamida
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy.
Neurology 1990;40(12):1903.
1990: Jean-Claude Chomel; A Haliassos; L Tesson; Jean-Claude Kaplan; Alain Kitzis
Frequency of the major CF mutation in French CF patients.
Human genetics 1990;85(4):397-8.
1990: L Bachner; Marie-Claude Vinet; R Lacave; M C Babron; E Rondeau; J D Sraer; D Chevet; Jean-Claude Kaplan
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locus.
Human genetics 1990;85(2):221-7.
1990: C Melani; A Haliassos; Jean-Claude Chomel; Maurizio Miglino; Alessandro Ferraris; Gian Franco Gaetani; Jean-Claude Kaplan; Alain Kitzis
Ras activation in myelodysplastic syndromes: clinical and molecular study of the chronic phase of the disease.
British journal of haematology 1990;74(4):408-13.
1990: Khedoudja Nafa; F Meriane; Abderrezak Reghis; M Benabadji; F Demenais; M Guilloud-Bataille; Y Sultan; Jean-Claude Kaplan; Marc Delpech
Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.
Human genetics 1990;84(5):401-5.
1990: Jamel Chelly; G Hamard; Annette Koulakoff; Jean-Claude Kaplan; Axel Kahn; Y Berwald-Netter
Dystrophin gene transcribed from different promoters in neuronal and glial cells.
Nature 1990;344(6261):64-5.
1990: Patrick Aubourg; Robert Feil; S Guidoux; Jean-Claude Kaplan; H Moser; A Kahn; Jean-Louis Mandel
The red-green visual pigment gene region in adrenoleukodystrophy.
American journal of human genetics 1990;46(3):459-69.
1990: Jamel Chelly; Didier Montarras; Christian Pinset; Y Berwald-Netter; Jean-Claude Kaplan; Axel Kahn
Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cells.
European journal of biochemistry / FEBS 1990;187(3):691-8.
1989: A Haliassos; Jean-Claude Chomel; Sophie Grandjouan; J Kruh; Jean-Claude Kaplan; Alain Kitzis
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.
Nucleic acids research 1989;17(20):8093-9.
1989: H Gilgenkrantz; Jamel Chelly; M Lambert; D Récan; J C Barbot; G J van Ommen; Jean-Claude Kaplan
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies.
Genomics 1989;5(3):574-80.
1989: J P Grünfeld; L Bachener; Jean-Claude Kaplan
[Contribution of molecular biology to the study of polycystic kidney disease].
Presse médicale (Paris, France : 1983) 1989;18(26):1279-80.
1989: A Haliassos; Jean-Claude Chomel; L Tesson; M Baudis; J Kruh; Jean-Claude Kaplan; Alain Kitzis
Modification of enzymatically amplified DNA for the detection of point mutations.
Nucleic acids research 1989;17(9):3606.
1989: Jean-Claude Chomel; A Haliassos; L Tesson; M Mathieu; Jean-Claude Kaplan; Alain Kitzis
Usefulness of linkage disequilibrium of KM-19 and XV-2c DNA probes for genetic counselling in a high-risk CF family.
Prenatal diagnosis 1989;9(4):297-300.
1989: Jamel Chelly; J P Concordet; Jean-Claude Kaplan; Axel Kahn
Illegitimate transcription: transcription of any gene in any cell type.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(8):2617-21.
1989: Khedoudja Nafa; Abderrezak Reghis; M Benabadji; Marc Delpech; Jean-Claude Kaplan
A new TaqI allele at DXS52 frequent in Algeria.
Nucleic acids research 1989;17(3):1276.
1989: Jean-Claude Kaplan; B S Emanuel
Report of the committee on the genetic constitution of chromosome 22.
Cytogenetics and cell genetics 1989;51(1-4):372-83.
1989: Raouf Hafsia; Balkis Meddeb; B Mtimet; Aïcha Hafsia; F Galactéros; Jean-Claude Kaplan; M Boussen
Congenital cyanosis due to methemoglobin reductase deficiency: first reported Tunisian case.
Nouvelle revue française d'hématologie 1989;31(5):371-3.
1989: L Bachner; Jean-Claude Kaplan
Molecular genetics and polycystic kidney diseases.
Advances in nephrology from the Necker Hospital 1989;18():3-18.
1988: Alain Kitzis; Jean-Claude Chomel; A Haliassos; L Tesson; Jean-Claude Kaplan; J Feingold; G Giraud; A Lable; B Dastugue; V Dumur
Unusual segregation of cystic fibrosis alleles.
Nature 1988;336(6197):316.
1988: J Chelly; Jean-Claude Kaplan; Pascal Maire; S Gautron; Axel Kahn
Transcription of the dystrophin gene in human muscle and non-muscle tissue.
Nature 1988;333(6176):858-60.
1988: Alain Kitzis; Jean-Claude Chomel; Jean-Claude Kaplan; G Giraud; A Labbe; B Dastugue; V Dumur; J P Farriaux; P Roussel; R Williamson
Unusual segregation of cystic fibrosis allele to males.
Nature 1988;333(6170):215.
1988: J J Pernelle; P Chafey; Jamel Chelly; J P Wahrmann; Jean-Claude Kaplan; Fernando M S Tomé; M Fardeau
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene.
Human genetics 1988;78(3):285.
1988: Jamel Chelly; F Marlhens; Bernard Dutrillaux; G J Van Ommen; M Lambert; B Haioun; G Boissinot; M Fardeau; Jean-Claude Kaplan
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia.
Human genetics 1988;78(3):222-7.
1988: C Julier; G M Lathrop; A Reghis; M F Szajnert; J M Lalouel; Jean-Claude Kaplan
A linkage and physical map of chromosome 22, and some applications to gene mapping.
American journal of human genetics 1988;42(2):297-308.
1988: Jean-Claude Kaplan; B Emanuel
Report of the committee on the genetic constitution of chromosome 22.
Cytogenetics and cell genetics 1988;49(1-3):104-6.
1987: F Marlhens; Jamel Chelly; Jean-Claude Kaplan; D Lefrancois; J P Harpey; Bernard Dutrillaux
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia.
Human genetics 1987;77(4):379-83.
1987: Jean-Claude Kaplan; M Delpech
[Prenatal diagnosis by DNA analysis].
La Revue du praticien 1987;37(43):2595-611.
1987: Jean-Claude Kaplan; D C Crawford; A G Durno; R T Schooley
Inactivation of human immunodeficiency virus by Betadine.
Infection control : IC 1987;8(10):412-4.
1987: M F Szajnert; S Saule; G W Bornkamm; H Wajcman; G M Lenoir; Jean-Claude Kaplan
Clustered somatic mutations in and around first exon of non-rearranged c-myc in Burkitt lymphoma with t(8;22) translocation.
Nucleic acids research 1987;15(11):4553-65.
1987: Jean-Claude Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Human chromosome 22.
Journal of medical genetics 1987;24(2):65-78.
1987: Jean-Claude Kaplan; B Carritt
Report of the committee on the genetic constitution of chromosomes 20, 21, and 22.
Cytogenetics and cell genetics 1987;46(1-4):257-76.
1987: J Kaplan; M L Briard; M Jeanpierre; Jean-Claude Kaplan; J Frézal
[Genetic counseling and prenatal diagnosis in Duchenne myopathy: yesterday, today and tomorrow].
Journal de génétique humaine 1987;35(1):3-18.
1986: Marc Delpech; N Deburgrave; M Baudis; P Maissonneuve; J M Bardin; Y Sultan; Jean-Claude Kaplan
De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis.
Human genetics 1986;74(3):316-7.
1986: Jamel Chelly; F Marlhens; B Le Marec; Marc Jeanpierre; M Lambert; G Hamard; Bernard Dutrillaux; Jean-Claude Kaplan
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.
Human genetics 1986;74(2):193-6.
1986: Louis Kunkel; J Fielding Hejtmancik; C T Caskey; Astrid Speer; Anthony P Monaco; W Middlesworth; C A Colletti; C Bertelson; U Müller; M Bresnan; F Shapiro; U Tantravahi; J Speer; S A Latt; R Bartlett; Margaret Pericak-Vance; Allen D Roses; M W Thompson; P N Ray; R G Worton; Kenneth H Fischbeck; Pía Gallano; M Coulon; C Duros; J Boue; Claudine Junien; Jamel Chelly; G Hamard; Marc Jeanpierre; M Lambert; Jean-Claude Kaplan; A Emery; H Dorkins; S McGlade; Kay E Davies; Corinne D Boehm; B Arveiler; C Lemaire; G J Morgan; M J Denton; J Amos; Martin Bobrow; F Benham; E Boswinkel; C Cole; Victor Dubowitz; K Hart; S Hodgson; L Johnson; A Walker; L Roncuzzi; Alessandra Ferlini; C Nobile; Giovanni Romeo; D E Wilcox; N A Affara; M A Ferguson-Smith; M Lindolf; H Kaariainen; A de la Chapelle; V Ionasescu; Charles C Searby; R Ionasescu; Egbert Bakker; Gert-Jan B van Ommen; P L Pearson; Cheryl R Greenberg; J L Hamerton; Klaus Wrogemann; R A Doherty; R Polakowska; C Hyser; S Quirk; N Thomas; Jeffrey F Harper; B T Darras; U Francke
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: M Delpech; P Maisonneuve; M Baudis; N Deburgrave; G Hamard; M Lambert; J M Bardin; Y Sultan; Jean-Claude Kaplan
[Prenatal diagnosis of hemophilia A by analysis of DNA].
Annales de médecine interne 1986;137(2):112-4.
1985: J Frézal; J Kaplan; A Munnich; P Katz; M Jeanpierre; Jean-Claude Kaplan
[DNA and Duchenne de Boulogne myopathy].
Archives françaises de pédiatrie 1985;42(8):739-42.
1985: P Tippett; Jean-Claude Kaplan
Report of the Committee on the Genetic Constitution of Chromosomes 20, 21, and 22.
Cytogenetics and cell genetics 1985;40(1-4):268-95.
1984: M L Anderson; M F Szajnert; Jean-Claude Kaplan; L McColl; B D Young
The isolation of a human Ig V lambda gene from a recombinant library of chromosome 22 and estimation of its copy number.
Nucleic acids research 1984;12(17):6647-61.
1984: I Henry; G Uzan; D Weil; H Nicolas; Jean-Claude Kaplan; C Marguerie; A Kahn; C Junien
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2.
American journal of human genetics 1984;36(4):760-8.
1984: Jean-Claude Kaplan
[Cloning of human genes].
Presse médicale (Paris, France : 1983) 1984;13(25):1565-70.
1984: C Julier; D Weil; P Couillin; J C Côté; V C Nguyen; C Foubert; A Boué; J P Thirion; Jean-Claude Kaplan; C Junien
The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19.
Human genetics 1984;67(2):174-7.
1983: C Junien; C Turleau; G M Lenoir; T Philip; R Said; S Despoisse; C Laurent; M O Rethoré; Jean-Claude Kaplan; J de Grouchy
Catalase determination in various etiologic forms of Wilms' tumor and gonadoblastoma.
Cancer genetics and cytogenetics 1983;10(1):51-7.
1983: D Choury; A Reghis; A L Pichard; Jean-Claude Kaplan
Endogenous proteolysis of membrane-bound red cell cytochrome-b5 reductase in adults and newborns: its possible relevance to the generation of the soluble "methemoglobin reductase".
Blood 1983;61(5):894-8.
1983: A de la Chapelle; G Lenoir; J Boué; A Boué; Pía Gallano; C Huerre; M F Szajnert; Marc Jeanpierre; J M Lalouel; Jean-Claude Kaplan
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22).
Nucleic acids research 1983;11(4):1133-42.
1983: A Reghis; C Troungos; D Lostanlen; R Krishnamoorthy; Jean-Claude Kaplan
Characterization of weak alleles at the DIA1 locus (Mustapha 1, Mustapha 2, and Mustapha 3) in the Algerian population.
Human genetics 1983;64(2):173-5.
1982: C Huerre; C Junien; D Weil; M L Chu; M Morabito; N Van Cong; J C Myers; C Foubert; M S Gross; D J Prockop; A Boué; Jean-Claude Kaplan; A de la Chapelle; F Ramirez
Human type I procollagen genes are located on different chromosomes.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(21):6627-30.
1982: C Junien; S Despoisse; C Turleau; H Nicolas; F Picard; B Le Marec; Jean-Claude Kaplan; J de Grouchy
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.
Cancer genetics and cytogenetics 1982;6(4):281-7.
1982: D Lostanlen; Jean-Claude Kaplan
Expression of NADH-cytochrome b5 reductase during dimethyl sulfoxide-induced differentiation of Friend erythroleukemia cells.
FEBS letters 1982;143(1):35-9.
1982: C Junien; D Weil; J C Myers; N Van Cong; M L Chu; C Foubert; M S Gross; D J Prockop; Jean-Claude Kaplan; F Ramirez
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization.
American journal of human genetics 1982;34(3):381-7.
1982: C Junien; A Chaventré; Y Fofana; C Lapouméroulie; B Floury; B Duflo; D Labie; Jean-Claude Kaplan
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.
Human heredity 1982;32(5):318-28.
1981: A L Pichard; D Choury; Jean-Claude Kaplan
3',5' Cyclic nucleotide phosphodiesterase from human platelets: effect of heat upon the multiple forms and their interconversion.
Biochimie 1981;63(7):603-9.
1981: D Lostanlen; G Lenoir; Jean-Claude Kaplan
NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia.
The Journal of clinical investigation 1981;68(1):279-85.
1981: D Choury; H Wajcman; J P Boissel; Jean-Claude Kaplan
Evidence for endogenous proteolytic solubilization of human red-cell membrane NADH-cytochrome b5 reductase.
FEBS letters 1981;126(2):172-4.
1981: D Choury; A Leroux; Jean-Claude Kaplan
Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.
The Journal of clinical investigation 1981;67(1):149-55.
1981: C Junien; A Leroux; D Lostanlen; A Reghis; J Boue; H Nicolas; A Boue; Jean-Claude Kaplan
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases.
Prenatal diagnosis 1981;1(1):17-24.
1981: Abderrezak Reghis; M Benabadji; P Tchen; Jean-Claude Kaplan
Quantitative variations of red-cell cytochrome b5 reductase (NADH-methemoglobin-reductase) in the Algerian population: evidence for defective alleles.
Human genetics 1981;59(2):148-55.
1980: D Lostanlen; G Gacon; Jean-Claude Kaplan
Direct enzyme titration curve of NADH: cytochrome b5 reductase by combined isoelectric focusing/electrophoresis. Interactions between enzyme and cytochrome b5.
European journal of biochemistry / FEBS 1980;112(1):179-83.
1980: G Gacon; D Lostanlen; D Labie; Jean-Claude Kaplan
Interaction between cytochrome b5 and hemoglobin: involvement of beta 66 (E10) and beta 95 (FG2) lysyl residues of hemoglobin.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(4):1917-21.
1980: Jean-Claude Kaplan; D Lostanlen; G Gacon; A Leroux
[Enzymatic reduction of methemoglobin].
Exposés annuels de biochimie médicale 1980;34():81-94.
1980: M O Rethoré; C Junien; A Aurias; J Couturier; B Dutrillaux; Jean-Claude Kaplan; J Lejeune
[Increase of LDH A and partial trisomy 11p (author's transl)].
Annales de génétique 1980;23(1):35-9.
1980: C Junien; H Rubinson-Skala; J C Dreyfus; N Ravise; J Boué; A Boué; Jean-Claude Kaplan
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance.
Human genetics 1980;54(2):191-6.
1980: C Junien; Jean-Claude Kaplan; O Raoul; M O Rethoré; C Rurleau; J de Grouchy
[Sesquialter dosage effect of erythrocytic and leucocytic nucleoside phosphorylase in two patients with proximal trisomy 14q (author's transl)].
Annales de génétique 1980;23(2):86-8.
1980: D Choury; Jean-Claude Kaplan
Diaphorase P: a new fetal isozyme identified in human placenta.
Biochimica et biophysica acta 1980;613(1):18-25.
1979: E Beutler; K G Blume; Jean-Claude Kaplan; G W Löhr; B Ramot; W N Valentine
International Committee for Standardization in Haematology: recommended screening test for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
British journal of haematology 1979;43(3):465-7.
1979: H A Buc; Jean-Claude Kaplan; A Najman
Study of a case with severe red-cell pyrimidine 5'-nucleotidase deficiency.
Clinica chimica acta; international journal of clinical chemistry 1979;95(1):83-8.
1979: C Junien; Jean-Claude Kaplan; F Serville; G Lenoir
Triplex gene dosage effect of TPI and G3PD in a human lymphoblastoid cell line with partial trisomy 12p13 and 18p.
Human genetics 1979;49(2):221-3.
1979: C Junien; Jean-Claude Kaplan; A Bernheim; R Berger
Regional assignment of red cell acid phosphatase locus to band 2p25.
Human genetics 1979;48(1):17-21.
1979: Jean-Claude Kaplan; A Leroux; P Beauvais
[Clinical and biological forms of cytochrome b5 reductase deficiency].
Comptes rendus des séances de la Société de biologie et de ses filiales 1979;173(2):368-79.
1979: A Kahn; Jean-Claude Kaplan; J C Dreyfus
Advances in hereditary red cell enzyme anomalies.
Human genetics 1979;50(1):1-27.
1978: P G Righetti; G Gacon; E Gianazza; D Lostanlen; Jean-Claude Kaplan
Titration curves of interacting cytochrome b5 and hemoglobin by isoelectric focusing-electrophoresis.
Biochemical and biophysical research communications 1978;85(4):1575-81.
1978: E Suerinck; A Suerinck; Jean-Claude Kaplan; J Meyer; C Junien; B Noël; M O Rethoré
[Trisomy 12p caused by malsegregation of a paternal translocation t(12;22) (p11;p11)].
Annales de génétique 1978;21(4):243-6.
1978: F Serville; C Junien; Jean-Claude Kaplan; M Gachet; J Cadoux; A Broustet
Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p.
Human genetics 1978;45(1):63-9.
1978: Jean-Claude Kaplan; M Chirouze
Therapy of recessive congenital methaemoglobinaemia by oral riboflavine.
Lancet 1978;2(8098):1043-4.
1978: D Lostanlen; A Vieira de Barros; A Leroux; Jean-Claude Kaplan
Soluble NADH-cytochrome b5 reductase from rabbit liver cytosol: partial purification and characterization.
Biochimica et biophysica acta 1978;526(1):42-51.
1978: D Sicard; Jean-Claude Kaplan; D Labie
Haemoglobinopathies and G.-6-P.D. deficiency in Laos.
Lancet 1978;2(8089):571-2.
1978: H A Buc; Jean-Claude Kaplan
Red-cell pyrimidine 5'-nucleotidase and lead poisoning.
Clinica chimica acta; international journal of clinical chemistry 1978;87(1):49-55.
1978: C Junien; M Vibert; D Weil; N Van-Cong; Jean-Claude Kaplan
Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22.
Human genetics 1978;42(3):233-9.
1978: H Buc; Jean-Claude Kaplan
A radioassay for pyrimidine-5'-nucleotidase activity.
Clinica chimica acta; international journal of clinical chemistry 1978;85(2):193-6.
1978: C Junien; Jean-Claude Kaplan
[Gene dosage and chromosome enzymatic markers].
Annales de génétique 1978;21(1):19-32.
1978: A V De Barros; Jean-Claude Kaplan; P Duvaldestin; P Berthelot
Phenobarbital-induced increase of NADH-cytochrome b5 reductase activity in rat liver microsomes.
Biochemical pharmacology 1978;27(3):367-8.
1978: M Benabadji; F Merad; M Benmoussa; G Trabuchet; C Junien; J C Dreyfus; Jean-Claude Kaplan
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants.
Human genetics 1978;40(2):177-84.
1978: J L Vives-Corrons; A Pujades; E Vela; J M Corretger; A Leroux; Jean-Claude Kaplan
Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girl.
Acta haematologica 1978;59(6):348-53.
1977: F Nouailhat; Jean-Claude Kaplan; Y Giudicelli; J C Bourdain; C Junien; A Combes; A Giraud
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis].
Annales de médecine interne 1977;128(11):827-36.
1977: M O Rethoré; Jean-Claude Kaplan; C Junien; J Lejeune
12pter to 12p12.2: possible assignment of human triose phosphate isomerase.
Human genetics 1977;36(2):235-7.
1977: A Leroux; L Torlinski; Jean-Claude Kaplan
Soluble and microsomal forms of NADH-cytochrome beta 5 reductase from human placenta. Similarity with NADH-methemoglobin reductase from human erythrocytes.
Biochimica et biophysica acta 1977;481(1):50-62.
1977: A Leroux; P Beauvais; Jean-Claude Kaplan
[Congenital recessive methemoglobinemia: a unique disease and variations (proceedings)].
Nouvelle revue française d'hématologie; blood cells 1977;18(1):217.
1976: P Beauvais; A Leroux; Jean-Claude Kaplan
[Hereditary methemoglobinemia with mental retardation and neurologic disorders. Clinical and biochemical study of a case].
La Nouvelle presse médicale 1976;5(41):2793-5.
1976: J P Coulaud; M Payet; Jean-Claude Kaplan; M Ba
[Hemolytic effect of niridazole in G6PD deficiency].
La Nouvelle presse médicale 1976;5(40):2720-1.
1976: C Hermabessiere; C Poisson; B Leveque; A Leroux; Jean-Claude Kaplan
[Recessive congenital methemoglobinemia. Clinical and laboratory study of one case].
Annales de pédiatrie 1976;23(8-9):509-13.
1976: M O Rethoré; C Junien; G Malpuech; C Baccichetti; R Tenconi; Jean-Claude Kaplan; J de Romeuf; J Lejeune
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].
Annales de génétique 1976;19(2):140-2.
1976: M Ba; J P Coulaud; Jean-Claude Kaplan; M Payet
[Hemolytic effect of niridazole in G6PD deficient persons].
Bulletin de la Société de pathologie exotique et de ses filiales 1976;69(3):288-90.
1976: A Mast; R Milo; C Junien; A Leroux; R Krishnamoorthy; H Wajcman; D Labie; Jean-Claude Kaplan
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes.
Acta haematologica 1976;56(3):174-82.
1975: A Leroux; C Junien; Jean-Claude Kaplan; J Bamberger
Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation.
Nature 1975;258(5536):619-20.
1975: M O Rethoré; Jean-Claude Kaplan; C Junien; J Cruveiller; B Dutrillaux; A Aurias; S Carpentier; J Lafourcade
[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].
Annales de génétique 1975;18(2):81-7.
1975: A L Pichard; Jean-Claude Kaplan
Effect of N-2, 2'-O-dibutyryl cyclic AMP upon the interconvertible forms of cyclic AMP phosphodiesterase from human platelets.
Biochemical and biophysical research communications 1975;64(1):342-6.
1975: A L Pichard; Jean-Claude Kaplan
[Interconvertibility of molecular forms of 3'5' cyclic AMP phosphodiesterase of human platelets].
Comptes rendus hebdomadaires des séances de l'Académie des sciences. Série D: Sciences naturelles 1975;280(5):673-6.
1974: Jean-Claude Kaplan; A Leroux; S Bakouri; J P Grangaud; M Benabadji
[The enzyme defect in recessive congenital methemoglobinemia with encephalopathy. A new defective variant of NADH-diaphorase (Beni-Messous variant)].
Nouvelle revue française d'hématologie 1974;14(6):755-70.
1974: Jean-Claude Kaplan; D Choury; A Leroux
[Identification of specific NADH-diaphorase of placenta].
Comptes rendus hebdomadaires des séances de l'Académie des sciences. Série D: Sciences naturelles 1974;278(3):393-5.
1974: C Junien; Jean-Claude Kaplan; M C Meienhofer; P Maigret; A Sender
G6PD Baudelocque: a new unstable variant characterized in cultured fibroblasts.
Enzyme 1974;18(1):45-59.
1974: Jean-Claude Kaplan
Defective molecular variants of glucose-6-phosphate dehydrogenase and methaemoglobin reductase.
Journal of clinical pathology. Supplement (Royal College of Pathologists) 1974;8():134-41.
1973: Jean-Claude Kaplan; A L Pichard; M H Laudat; P Laudat
Kinetic and electrophoretic abnormality of cyclic AMP phosphodiesterase in genetically obese mouse adipocytes.
Biochemical and biophysical research communications 1973;51(4):1008-14.
1972: A Leroux; Jean-Claude Kaplan
Presence of red cell type NADH-methemoglobin reductase (NADH-diaphorase) in human non erythroid cells.
Biochemical and biophysical research communications 1972;49(4):945-50.
1972: A L Pichard; J Hanoune; Jean-Claude Kaplan
Human brain and platelet cyclic adenosine 3',5'-monophosphate phosphodiesterases: different response to drugs.
Biochimica et biophysica acta 1972;279(1):217-20.
1972: J Pagnier; D Labie; Jean-Claude Kaplan; C Junien; A Najman; J P Leroux
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes].
Nouvelle revue française d'hématologie 1972;12(3):317-32.
1972: Jean-Claude Kaplan
[Remarks on genetic enzyme defects of the erythrocyte].
Biochimie 1972;54(5):765-73.
1971: Jean-Claude Kaplan
[Erythrocyte metabolism and oxygen transport].
Schweizerische medizinische Wochenschrift 1971;101(49):1751-4.
1971: S Haidas; D Labie; Jean-Claude Kaplan
2,3-diphosphoglycerate content and oxygen affinity as a function of red cell age in normal individuals.
Blood 1971;38(4):463-7.
1971: Jean-Claude Kaplan
Defects of gluthathione reducing and synthetizing reactions in the red cells.
Revue européenne d'études cliniques et biologiques. European journal of clinical and biological research 1971;16(6):523-8.
1971: Jean-Claude Kaplan; A Hanzlickova-Leroux; A M Nicolas; R Rosa; C Weiler; G Lepercq
A new glucose-6-phosphate dehydrogenase variant (G6PD Port-Royal).
Enzyme 1971;12(1):25-32.
1970: H Léric; Jean-Claude Kaplan; G Broun
[A colorimetric micromethod for the enzymatic assay of ethanol in blood].
Clinica chimica acta; international journal of clinical chemistry 1970;29(3):523-8.
1970: Jean-Claude Kaplan; A M Nicolas; A Hanzlickova-Leroux; E Beutler
A simple spot screening test for fast detection of red cell NADH-diaphorase deficiency.
Blood 1970;36(3):330-3.
1970: R Rosa; Y Alexandre; Jean-Claude Kaplan; J C Dreyfus
[Immunological study of erythrocyte glucose-6-phosphate dehydrogenase in deficient mutants].
Clinica chimica acta; international journal of clinical chemistry 1970;29(2):209-14.
1970: J C Dreyfus; F Schapira; Jean-Claude Kaplan; Y Nordmann; D Allard
[New data on pathologic enzymology].
Annales de médecine interne 1970;121(6):625-8.
1970: Jean-Claude Kaplan; A Hanzlickova-Leroux; J C Dreyfus
[Study of NADH-diaphorase activity of leukocytes in congenital recessive methemoglobinemia].
Comptes rendus hebdomadaires des séances de l'Académie des sciences. Série D: Sciences naturelles 1970;18():2223-4.
1970: Jean-Claude Kaplan; Y Alexandre; J C Dreyfus
[Selective deficiency of 1 of the genetic loci of phosphoglucomutase in erythrocytes].
Comptes rendus hebdomadaires des séances de l'Académie des sciences. Série D: Sciences naturelles 1970;270(7):1061-3.
1970: Jean-Claude Kaplan; A Leroux
[Diaphorasic NADPH and NADH systems in human blood cells].
Bulletin de la Société de chimie biologique 1970;52(11):1243-9.
1969: J Boguslawska-Jaworska; Jean-Claude Kaplan
A simple screening test for glutathione peroxidase activity in red cells.
Clinica chimica acta; international journal of clinical chemistry 1969;26(3):459-63.
1969: F Schapira; Jean-Claude Kaplan
Electrophoretic abnormality of galactose-1-phosphate uridyl transferase in galactosemia.
Biochemical and biophysical research communications 1969;35(4):451-5.
1969: Jean-Claude Kaplan; E Beutler
Hexokinase isoenzymes.
The New England journal of medicine 1969;280(20):1129.
1969: Jean-Claude Kaplan
[Rare variants of erythrocyte glucose-6-phosphate dehydrogenase].
Annales des sociétés belges de médecine tropicale, de parasitologie, et de mycologie 1969;49(3):305-20.
1969: Jean-Claude Kaplan
[Erythrocyte diaphorases and glutathione reductase].
Exposés annuels de biochimie médicale 1969;29():77-99.
1968: P Seringe; Jean-Claude Kaplan; J Rosa; J C Hoeffel; C Bertrand
[Importance of the study of glucose-6-phosphate dehydrogenase in clinical medicine].
Recenti progressi in medicina 1968;45(4):363-86.
1968: Jean-Claude Kaplan; N Shore; E Beutler
The rapid detection of triose phosphate isomerase deficiency.
Technical bulletin of the Registry of Medical Technologists 1968;38(10):274-6.
1968: Jean-Claude Kaplan; L Teeple; N Shore; E Beutler
Electrophoretic abnormality in triosephosphate isomerase deficiency.
Biochemical and biophysical research communications 1968;31(5):768-73.
1968: P Seringe; J C Hoeffel; Jean-Claude Kaplan
[Glucose-6-phosphate dehydrogenase in the clinic: enzymatic deficit and qualitative variations].
La semaine des hôpitaux : organe fondé par l'Association d'enseignement médical des hôpitaux de Paris 1968;44(19):1269-77.
1968: Jean-Claude Kaplan; E Beutler
Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.
Nature 1968;217(5125):256-8.
1968: Jean-Claude Kaplan; E Beutler
Hexokinase isoenzymes in human erythrocytes.
Science (New York, N.Y.) 1968;159(3811):215-6.
1967: Jean-Claude Kaplan; E Beutler
Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.
Biochemical and biophysical research communications 1967;29(4):605-10.
1967: Jean-Claude Kaplan; R Rosa; P Seringe; J C Hoeffel
[The genetic polymorphism of erythrocyte glucose-6-phosphate dehydrogenase in man. II. Study of a new varient with diminished activity: th "Kabyle" type].
Enzymologia biologica et clinica 1967;8(5):332-40.
1967: Jean-Claude Kaplan; R Rosa; P Seringe; J C Hoeffel
[The genetic polymorphism of erythrocyte glucose-6-phosphate dehydrogenase in man. 1. Study of a slow variant with normal activity].
Enzymologia biologica et clinica 1967;8(5):321-31.
1965: Jean-Claude Kaplan; J C Dreyfus
[Determination of erythrocyte glucose-6-phosphate dehydrogenase].
Revue française d'études cliniques et biologiques 1965;10(5):552-4.
1964: J C DREYFUS; N MALEKNIA; Jean-Claude Kaplan
[RESEARCH ON GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN FRANCE. APROPOS OF 200 DETERMINATIONS].
Nouvelle revue française d'hématologie 1964;4():791-802.
1964: J C DREYFUS; M RESSIS; Jean-Claude Kaplan
[THE EXISTENCE OF 2 POPULATIONS OF ERYTHROCYTES IN WOMEN HETEROZYGOTIC FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. DEMONSTRATION BY SPECTROPHOTOMETRY ON INDIVIDUALLY EXAMINED ERYTHROCYTES].
Comptes rendus hebdomadaires des séances de l'Académie des sciences 1964;258():3791-3.
1961: P MILLIEZ; G LAGRUE; P SAMARCQ; Jean-Claude Kaplan
[The kidney in collagenoses].
La Revue du praticien 1961;11():941-4.
1960: M KAPLAN; R GRUMBACH; Jean-Claude Kaplan
[Infectious jaundice during infections with gram-negative bacilli in newborn and other infants].
Annales de pédiatrie 1960;36():151-6.