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Henri Wajcman

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Kamran Moradkhani; Jean Riou; Henri Wajcman
Pitfalls in the genetic diagnosis of Hb S.
Ikbel Benmansour; Abderraouf Ghanem; Raouf Hafsia; Kamran Moradkhani; Imen Moumni; Salem Abbès; Henri Wajcman; Claude Préhu
Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia.
Kamran Moradkhani; Serge Pissard; Claude Préhu; Christian Rose; Valerie Li Thiao Te; Henri Wajcman; Michel Bahuau; Muriel Holder; Chadia Mekki; Frédéric Galactéros
Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants.

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All Publications

2013: Kamran Moradkhani; Jean Riou; Henri Wajcman
Pitfalls in the genetic diagnosis of Hb S.
Clinical biochemistry 2013;46(4-5):291-9.
2013: Ikbel Benmansour; Abderraouf Ghanem; Raouf Hafsia; Kamran Moradkhani; Imen Moumni; Salem Abbès; Henri Wajcman; Claude Préhu
Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia.
Blood cells, molecules & diseases 2013;50(2):110-4.
2012: Kamran Moradkhani; Serge Pissard; Claude Préhu; Christian Rose; Valerie Li Thiao Te; Henri Wajcman; Michel Bahuau; Muriel Holder; Chadia Mekki; Frédéric Galactéros
Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants.
American journal of hematology 2012;87(2):208-10.
2011: Henri Wajcman; Kamran Moradkhani
Abnormal haemoglobins: detection & characterization.
The Indian journal of medical research 2011;134():538-46.
2011: Henri Wajcman; Serge Pissard; Corinne Vasseur; Véronique Baudin-Creuza
α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?
Hemoglobin 2011;35(5-6):463-8.
2010: Thomas Brillet; Véronique Baudin-Creuza; Corinne Vasseur; Elisa Domingues-Hamdi; Laurent Kiger; Henri Wajcman; Serge Pissard; Michael C Marden
Alpha-hemoglobin stabilizing protein (AHSP), a kinetic scheme of the action of a human mutant, AHSPV56G.
The Journal of biological chemistry 2010;285(23):17986-92.
2010: Laetitia Barbotte; Abdelhakim Ahmed-Belkacem; Stéphane Chevaliez; Alexandre Soulier; Christophe Hézode; Henri Wajcman; Doug J Bartels; Yi Zhou; Andrzej Ardzinski; Nagraj Mani; B Govinda Rao; Shelley George; Ann D Kwong; Jean-Michel Pawlotsky
Characterization of V36C, a novel amino acid substitution conferring hepatitis C virus (HCV) resistance to telaprevir, a potent peptidomimetic inhibitor of HCV protease.
Antimicrobial agents and chemotherapy 2010;54(6):2681-3.
2010: Philippe Joly; Henri Wajcman; Alain Francina
[Library of variants (LOV) v. 1.0: an help for the interpretation of the phenotypic haemoglobin data obtained with liquid chromatography Bio-Rad devices].
Annales de biologie clinique 2010;68(2):254-6.
2010: Philippe Joly; Anton Szymanowicz; Marie-Jeanne Neyron; Abdellah Zine; Henri Wajcman; Alain Francina
Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
Hemoglobin 2010;34(4):366-73.
2009: Henri Wajcman; Alain Francina
Special issue: hemoglobin disorders.
Clinical biochemistry 2009;42(18):1743-4.
2009: Henri Wajcman; Jean Riou
Globin chain analysis: an important tool in phenotype study of hemoglobin disorders.
Clinical biochemistry 2009;42(18):1802-6.
2009: Claude Préhu; Kamran Moradkhani; Jean Riou; Michel Bahuau; Pierre Launay; Natacha Martin; Henri Wajcman; Michel Goossens; Frédéric Galactéros
Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.
Haematologica 2009;94(11):1624-5.
2009: Kamran Moradkhani; Michel Bahuau; Claude Préhu; Natacha Martin; Catherine Bimet; Frederic Galactéros; Henri Wajcman
A rare G6PD variant (c.383T>G; p.128Leu>Arg) with a molecular pathophysiological mechanism similar to that of G6PD A- (68Val>Met, 126Asn>Asp).
Blood cells, molecules & diseases 2009;43(3):226-9.
2009: Kamran Moradkhani; Claude Préhu; John Old; Shirley Henderson; Vera Balamitsa; Hong-Yuan Luo; Man-Chiu Poon; David H K Chui; Henri Wajcman; George P Patrinos
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.
Annals of hematology 2009;88(6):535-43.
2009: Henri Wajcman; Laurent Kiger; Michael C Marden
Structure and function evolution in the superfamily of globins.
Comptes rendus biologies 2009;332(2-3):273-82.
2009: Isabelle Zanella-Cleon; Claude Préhu; Philippe Joly; Jean Riou; Michel Becchi; Henri Wajcman; Alain Francina
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
Hemoglobin 2009;33(3):177-87.
2009: Carsten W Lederer; A Nazli Basak; Yesim Aydinok; Soteroula Christou; Amal El-Beshlawy; Androulla Eleftheriou; Slaheddine Fattoum; Alex Felice; Eitan Fibach; Renzo Galanello; Roberto Gambari; Lucian Gavrila; Piero C Giordano; Frank Grosveld; Helen (or Eleni) Hassapopoulou; Eva Hladka; Emmanuel Kanavakis; Franco Locatelli; John M Old; George P Patrinos; Giovanni Romeo; Ali Taher; Joanne Traeger-Synodinos; Panayiotis Vassiliou; Ana Villegas; Ersi Voskaridou; Henri Wajcman; Anastasios Zafeiropoulos; Marina Kleanthous
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
Hemoglobin 2009;33(3):163-76.
2008: Maha Al-Sheikh; Elodie Mazurier; Betty Gardie; Nicole Casadevall; Frédéric Galactéros; Michel Goossens; Henri Wajcman; Claude Préhu; Valérie Ugo
A study of 36 unrelated cases with pure erythrocytosis revealed three new mutations in the erythropoietin receptor gene.
Haematologica 2008;93(7):1072-5.
2008: Isabelle Zanella-Cleon; Michel Becchi; Philippe Lacan; Piero C Giordano; Henri Wajcman; Alain Francina
Detection of a thalassemic alpha-chain variant (Hemoglobin Groene Hart) by reversed-phase liquid chromatography.
Clinical chemistry 2008;54(6):1053-9.
2008: Maha Al-Sheikh; Kamran Moradkhani; Marc Lopez; Henri Wajcman; Claude Préhu
Disturbance in the HIF-1alpha pathway associated with erythrocytosis: further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene.
Blood cells, molecules & diseases 2008;40(2):160-5.
2008: Kamran Moradkhani; Jean Riou; Alain Francina; Henri Wajcman; Claude Prehu
Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin gene.
Hemoglobin 2008;32(5):478-84.
2008: Kamran Moradkhani; Elodie Mazurier; Piero C Giordano; Henri Wajcman; Claude Préhu
An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.
Hemoglobin 2008;32(4):419-24.
2008: Henri Wajcman; Jan Traeger-Synodinos; Ioannis Papassotiriou; Piero C Giordano; Cornelis L Harteveld; Véronique Baudin-Creuza; John Old
Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
Hemoglobin 2008;32(4):327-49.
2007: Michael C Marden; Sylvia Dewilde; Laurent Kiger; Djemel Hamdane; Julien Uzan; Thorsten Burmester; Thomas Hankeln; Luc Moens; Véronique Baudin-Creuza; Chantal Celier; Henri Wajcman
Exploiting a list of protein sequences.
Gene 2007;398(1-2):35-41.
2007: Serge Pissard; Mariane de Montalembert; Dora Bachir; Isabelle Max-Audit; Michel Goossens; Henri Wajcman; Brigitte Bader-Meunier
Pyruvate kinase (PK) deficiency in newborns: the pitfalls of diagnosis.
The Journal of pediatrics 2007;150(4):443-5.
2007: Belinda Giardine; Sjozef van Baal; Polynikis Kaimakis; Cathy Riemer; Webb Miller; Maria Samara; Panagoula Kollia; Nicholas P Anagnou; David H K Chui; Henri Wajcman; Ross C Hardison; George P Patrinos
HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.
Human mutation 2007;28(2):206.
2007: Kamran Moradkhani; Joan S Henthorn; Jean Riou; Lorraine Phelan; Claude Préhu; Henri Wajcman
Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese.
Hemoglobin 2007;31(4):477-82.
2007: Cornelis L Harteveld; Willem C H van Helden; George L Boxma; Peter Van Delft; Margaretha Bakker-Verweij; Henri Wajcman; Isabelle Zanella-Cleon; Michel Becchi; Piero C Giordano
Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.
Hemoglobin 2007;31(3):325-32.
2007: Cornelis L Harteveld; F G A Versteegh; Eduard H G van Leer; Jaap S Starreveld; Peter J M J Kok; Irene H Van Rooijen-Nijdam; Peter Van Delft; Isabelle Zanella-Cleon; Michel Becchi; Henri Wajcman; Piero C Giordano
Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
Hemoglobin 2007;31(3):313-23.
2007: Piero C Giordano; Sonja Zweegman; Nicole Akkermans; Sandra Arkesteijn; Peter Van Delft; F G A Versteegh; Henri Wajcman; Cornelis L Harteveld
The first case of Hb Groene Hart [alpha119(H2)Pro-->Ser, CCT-->TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant.
Hemoglobin 2007;31(2):179-82.
2007: Claude Préhu; Jean Riou; Henri Wajcman
Hb Barika [alpha42(C7)Tyr-->His (alpha2)] leads to an alpha+ -Thalassemia-like syndrome.
Hemoglobin 2007;31(1):17-22.
2006: Corinne Vasseur-Godbillon; Michael C Marden; Piero Giordano; Henri Wajcman; Véronique Baudin-Creuza
Impaired binding of AHSP to alpha chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with alpha thalassemic like syndrome.
Blood cells, molecules & diseases 2006;37(3):173-9.
2006: Serge Pissard; Isabelle Max-Audit; Laurent Skopinski; Aurélie Vasson; Pascal Vivien; Catherine Bimet; Michel Goossens; Frédéric Galacteros; Henri Wajcman
Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations.
British journal of haematology 2006;133(6):683-9.
2006: Ioannis Papassotiriou; Alexandra Stamoulakatou; Henri Wajcman; Jean Kister; Gerasimos Dimisianos; Christina Lazaropoulou; Ino Kanavaki; Efstathios Vavourakis; Antonios Kattamis; Emmanuel Kanavakis; Joanne Traeger-Synodinos
Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family.
Hemoglobin 2006;30(4):409-18.
2006: Antonino Giambona; Margherita Vinciguerra; Filippo Cassarà; Rita Li Muli; Filippo Leto; Cristina Passarello; Henri Wajcman; Aurelio Maggio
Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.
Hemoglobin 2006;30(2):139-48.
2006: Valérie Bardet; Mircea Adam; Jeanine Yvart; Henri Wajcman; Frédéric Galacteros; Rémi Favier
Hb Calais [beta76(E20)Ala --> Pro]: a family study of a variant with decreased oxygen affinity.
Hemoglobin 2006;30(1):35-8.
2005: Ioannis Papassotiriou; Joanne Traeger-Synodinos; Michael C Marden; Jean Kister; Dimitra Liapi; Danielle Prome; Alexandra Stamoulakatou; Henri Wajcman; Emmanuel Kanavakis
The homozygous state for Hb Crete [beta129 (H7) Ala-->Pro] is associated with a complex phenotype including erythrocytosis and functional anemia.
Blood cells, molecules & diseases 2005;34(3):229-34.
2005: Jean Kister; Véronique Baudin-Creuza; Laurent Kiger; Claude Préhu; Ioannis Papassotiriou; Jean Riou; Frédéric Galactéros; Henri Wajcman
Hb Montfermeil [beta 130(H8) Tyr-->Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule.
Blood cells, molecules & diseases 2005;34(2):166-73.
2005: Claude Préhu; Serge Pissard; Maha Al-Sheikh; Catherine Le Niger; Dora Bachir; Frédéric Galactéros; Henri Wajcman
Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop]).
Hemoglobin 2005;29(3):229-33.
2005: Henri Wajcman; Frédéric Galactéros
Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts.
Hemoglobin 2005;29(2):91-106.
2005: Keren Borensztajn; Ouerdia Chafa; Bernard F Le Bonniec; Henri Wajcman; Abderrezak Reghis; Anne-Marie Fischer; Jacqueline Tapon-Bretaudière
Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.
Thrombosis research 2005;116(2):115-20.
2005: Jean Riou; Christian Godart; Mireille Mathis; Didier Hurtrel; Henri Wajcman; Claude Préhu; Josiane Bardakdjian
Evaluation of the Bio-Rad VARIANT II HbA2/HbA1C Dual Program for measurement of hemoglobin concentrations and detection of variants.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2005;43(2):237-43.
2005: Catherine Badens; Chantal Paolasso; Chantal Fossat; Henri Wajcman; Isabelle Thuret
Compound heterozygosity for unstable hemoglobin Genova and beta(o)-thalassemia associated with early onset of thalassemia major syndrome.
Haematologica 2005;90(1):ECR04.
2005: Marie-Catherine Giarratana; Ladan Kobari; Hélène Lapillonne; David Chalmers; Laurent Kiger; Thérèse Cynober; Michael C Marden; Henri Wajcman; Luc Douay
Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells.
Nature biotechnology 2005;23(1):69-74.
2004: Dimitri Tchernitchko; Michel Goossens; Henri Wajcman
In silico prediction of the deleterious effect of a mutation: proceed with caution in clinical genetics.
Clinical chemistry 2004;50(11):1974-8.
2004: Henri Wajcman
[Diagnosis and screening of sickle cell disease].
La Revue du praticien 2004;54(14):1543-7.
2004: Josiane Bardakdjian; Henri Wajcman
[Epidemiology of sickle cell anemia].
La Revue du praticien 2004;54(14):1531-3.
2004: Véronique Baudin-Creuza; Corinne Vasseur-Godbillon; Christine Pato; Claude Préhu; Henri Wajcman; Michael C Marden
Transfer of human alpha- to beta-hemoglobin via its chaperone protein: evidence for a new state.
The Journal of biological chemistry 2004;279(35):36530-3.
2004: Henri Wajcman; Frédéric Galactéros
[Glucose 6-phosphate dehydrogenase deficiency: a protection against malaria and a risk for hemolytic accidents].
Comptes rendus biologies 2004;327(8):711-20.
2004: George P Patrinos; Henri Wajcman
Recording human globin gene variation.
Hemoglobin 2004;28(2):v-vii.
2004: George P Patrinos; Belinda Giardine; Cathy Riemer; Webb Miller; David H K Chui; Nicholas P Anagnou; Henri Wajcman; Ross C Hardison
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.
Nucleic acids research 2004;32(Database issue):D537-41.
2003: Claude Préhu; P Groff; G Kalmes; B Golinska; Jean Riou; D Prome; Suzy Richelme-David; Laurent Kiger; Rolande Ducrocq; Henri Wajcman
Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68.
Blood cells, molecules & diseases 2003;31(2):234-9.
2003: Henri Wajcman; Josiane Bardakdjian-Michau; Jean Riou; Claude Préhu; Jean Kister; Véronique Baudin-Creuza; Danielle Promé; Suzy Richelme-David; Jean-Luc Harousseau; Frédéric Galactéros
Two new hemoglobin variants with increased oxygen affinity: Hb Nantes [beta34(B16)Val-->Leu] and Hb Vexin [beta116(G18)His-->Leu].
Hemoglobin 2003;27(3):191-9.
2003: Josiane Bardakdjian-Michau; J-L Dhondt; Rolande Ducrocq; Frédéric Galactéros; A Guyard; F-X Huchet; A Lahary; Danielle Lena-Russo; P Maboudou; M-L North; C Prehu; AM Soummer; M Verschelde; Henri Wajcman
[Good practices for the study of hemoglobin].
Annales de biologie clinique 2003;61(4):401-9.
2003: Claude Préhu; Elodie Mazurier; Jean Riou; Jean Kister; Danielle Promé; Suzy Richelme-David; Lina Al Jassem; Elisabeth Angellier; Henri Wajcman
A new unstable alpha2-globin gene variant: Hb Chartres [alpha33(B14)Phe --> Ser].
Hemoglobin 2003;27(2):111-5.
2003: Claude Préhu; Alain Francina; Lütje Jürgen Behnken; Danielle Promé; Frédéric Galactéros; Henri Wajcman
An identical mutation carried by different genes: Hb Frankfurt [alpha50(CE8)His->Gln].
Haematologica 2003;88(5):ECR19.
2003: Claude Préhu; Mohamed Rhabbour; Jean Claude Netter; Mathias Denier; Jean Riou; Frédéric Galactéros; Henri Wajcman
Hb F-M-Osaka [Ggamma63(E7)His --> tyr] in a newborn from southwest France.
Hemoglobin 2003;27(1):27-30.
2003: Henri Wajcman
Electrophoretic methods for study of hemoglobins.
Methods in molecular medicine 2003;82():93-100.
2003: Jean Kister; Henri Wajcman
Oxygen equilibrium measurements of human red blood cells.
Methods in molecular medicine 2003;82():49-64.
2003: Henri Wajcman
Analysis of hemoglobins and globin chains by high-performance liquid chromatography.
Methods in molecular medicine 2003;82():21-9.
2002: Henri Wajcman; Laurent Kiger
[Hemoglobin, from microorganisms to man: a single structural motif, multiple functions].
Comptes rendus biologies 2002;325(12):1159-74.
2002: Henri Wajcman; Jean Riou; Angoué P Yapo
Globin chain analysis by reversed phase high performance liquid chromatography: recent developments.
Hemoglobin 2002;26(3):271-84.
2002: Cornelis L Harteveld; Peter Van Delft; Rob Plug; F G A Versteegh; Balt Hagen; Irene van Rooijen; Peter J M J Kok; Henri Wajcman; Jean Kister; Piero C Giordano
Hb Groene Hart: a new Pro-->Ser amino acid substitution at position 119 of the alpha1-globin chain is associated with a mild alpha-thalassemia phenotype.
Hemoglobin 2002;26(3):255-60.
2002: Cornelis L Harteveld; Peter Van Delft; Rob Plug; Zoran Erjavec; Henri Wajcman; Piero C Giordano
Hb delfzicht [alpha9(A7)Asn-->Lys (alpha1)]: a new, clinically silent hemoglobin variant observed in a Dutch patient.
Hemoglobin 2002;26(2):181-4.
2002: Claude Préhu; Lütje J Behnken; Rüdiger Neumann; Jean Riou; Jean Kister; Laurent Kiger; Danielle Promé; Torsten Arndt; Britta Semmelroggen; Margot Schmidt; Frédéric Galactéros; Henri Wajcman
A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [beta41 (C7)Phe-->Cys].
Hemoglobin 2002;26(2):169-74.
2002: Thi My Anh Neildez-Nguyen; Henri Wajcman; Michael C Marden; Morad Bensidhoum; Vincent Moncollin; Marie-Catherine Giarratana; Ladan Kobari; Dominique Thierry; Luc Douay
Human erythroid cells produced ex vivo at large scale differentiate into red blood cells in vivo.
Nature biotechnology 2002;20(5):467-72.
2002: Philippe Lacan; G Souillet; Martine Aubry; Danielle Promé; Suzy Richelme-David; Jean Kister; Henri Wajcman; Alain Francina
New alpha 2 globin chain variant with low oxygen affinity affecting the N-terminal residue and leading to N-acetylation [Hb Lyon-Bron alpha 1(NA1)Val --> Ac-Ala].
American journal of hematology 2002;69(3):214-8.
2002: Ross C Hardison; David H K Chui; Belinda Giardine; Cathy Riemer; George P Patrinos; Nicholas P Anagnou; Webb Miller; Henri Wajcman
HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.
Human mutation 2002;19(3):225-33.
2002: Claude Préhu; Jean Riou; Isabelle Sartelet; Danielle Promé; Catherine Claparols; Mathias Denier; Jacques Motte; Frédéric Galactéros; Henri Wajcman
Hb O-Tibesti [beta121(GH4)Glu-->Lys; beta11(A8)Val-->Ile], a hemoglobin variant carrying in the same beta chain the substitutions of Hb O-Arab and Hb Hamilton, found in combination with Hb S [beta6(A3)Glu-->Val].
Hemoglobin 2002;26(1):13-20.
2002: Véronique Baudin-Creuza; Christophe Fablet; Franck Zal; Brian N Green; Danielle Promé; Michael C Marden; Josée Pagnier; Henri Wajcman
Hemoglobin Porto Alegre forms a tetramer of tetramers superstructure.
Protein science : a publication of the Protein Society 2002;11(1):129-36.
2001: Henri Wajcman; Angoué P Yapo; Jean Riou; Danielle Promé; Suzy Richelme-David; Didier Hurtrel; Josiane Bardakdjian-Michau
A new Ggamma chain variant: Hb F-Coignieres [gamma75(E19)Ile-->Val].
Hemoglobin 2001;25(4):425-8.
2001: Claude Préhu; A Hanichi; Angoué P Yapo; Catherine Claparols; Danielle Promé; Jean Riou; Henri Wajcman
Hb Douala [alpha3(A1)Ser --> Phe]: a new alpha1 gene mutation in a Cameroonian woman heterozygous for Hb S and a 3.7 kb deletional alpha-thalassemia.
Hemoglobin 2001;25(3):323-9.
2001: Ross C Hardison; David H K Chui; Cathy Riemer; Belinda Giardine; H Lehväslaiho; Henri Wajcman; Webb Miller
Databases of human hemoglobin variants and other resources at the globin gene server.
Hemoglobin 2001;25(2):183-93.
2001: Henri Wajcman; Claude Préhu; Josiane Bardakdjian-Michau; Danielle Promé; Jean Riou; Christian Godart; Mireille Mathis; Didier Hurtrel; Frédéric Galactéros
Abnormal hemoglobins: laboratory methods.
Hemoglobin 2001;25(2):169-81.
2001: Henri Wajcman; Frédéric Galacteros
[Sickle cell disease: laboratory and hemoglobin study].
Bulletin de la Société de pathologie exotique (1990) 2001;94(2):80-4.
2001: Angoué P Yapo; Danielle Promé; Catherine Claparols; Jean Riou; Frédéric Galactéros; Henri Wajcman
Hb Yaoundé [beta134(H12)Val-->Ala], a new neutral variant found in association with Hb Kenitra.
Hemoglobin 2001;25(1):97-101.
2001: Henri Wajcman; A Lahary; Danielle Promé; Jean Kister; Jean Riou; Christian Godart; Claude Préhu; Joanne Traeger-Synodinos; I Papassotiriou; Frédéric Galactéros
Hb Mont Saint Aignan [beta128(H6)Ala-->Pro]: a new unstable variant leading to chronic microcytic anemia.
Hemoglobin 2001;25(1):57-65.
2001: Ioannis Papassotiriou; Joanne Traeger-Synodinos; Danielle Promé; Jean Kister; Christina Vrettou; Athina Xaidara; Michael C Marden; Alexandra Stamoulakatou; Henri Wajcman; Emmanuel Kanavakis
Hb Sitia [beta128(H6)Ala-->Val]: an unstable variant with a substitution in the alpha1beta1 interface.
Hemoglobin 2001;25(1):45-56.
2001: M L North; I Duwig; Jean Riou; Danielle Promé; Angoué P Yapo; Jean Kister; Josiane Bardakdjian-Michau; J P Cazenave; Henri Wajcman
Hb Tsukumi [beta117(G19)His-->Tyr] found in a Moroccan woman.
Hemoglobin 2001;25(1):107-10.
2000: Claude Préhu; Christian Godart; Jean Riou; AM Soummer; Danielle Promé; Frédéric Galactéros; Henri Wajcman
Hb Nikaia [alpha20(B1)His-Asp]: a new variant of the alpha2 gene.
Hemoglobin 2000;24(4):305-9.
2000: P Groff; G Kalmes; B Golinska; A Miyazaki; Jean Riou; N Carte; Danielle Promé; Jean Kister; Frédéric Galactéros; Henri Wajcman
Hb Ernz [beta123(H1)Thr-->Asn] and Hb Renert [beta133(H11)Val-->Ala]: two new neutral variants revealed by reversed phase high performance liquid chromatography analysis.
Hemoglobin 2000;24(4):287-97.
2000: Henri Wajcman; Frédéric Galactéros; A Hanichi; Angoué P Yapo; Claude Préhu
HbF in the adult: could its composition discriminate normal from abnormal foetal globin gene expression?
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 2000;323(11):975-81.
2000: Claude Préhu; Jean Riou; Christian Godart; M Bost; C Barro; Danielle Promé; Jean Kister; Frédéric Galactéros; Henri Wajcman
Hb Diamant [alpha119(H2)Pro-->Leu]: a new variant with a modification at the alpha1beta1 interface.
Hemoglobin 2000;24(3):249-52.
2000: Henri Wajcman; F Drupt; Joan S Henthorn; Jean Kister; C Prehu; Jean Riou; Danielle Promé; Frédéric Galactéros
Two new variants with the same substitution at position beta122: Hb Bushey [beta122(GH5)Phe-->Leu] and Hb Casablanca [beta65(E9)lys-->Met; beta122(GH5)Phe-->Leu].
Hemoglobin 2000;24(2):125-32.
2000: Henri Wajcman; Keren Borensztajn; Jean Riou; Danielle Promé; Didier Hurtrel; Josiane Bardakdjian; D Léna-Russo; I Amouroux; Rolande Ducrocq
Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys].
Hemoglobin 2000;24(1):45-52.
1999: Catherine Badens; D Léna-Russo; Philippe Lacan; Alain Francina; Danielle Promé; Jean Riou; M Geoffroy; T Ayavou; Jean Kister; Frédéric Galactéros; Henri Wajcman
Hb Toulon [alpha77(EF6)Pro-->His]: a new variant due to a mutation in the alpha2 gene found during measurement of glycated hemoglobin.
Hemoglobin 1999;23(4):367-71.
1999: Claude Préhu; M Bost; C Barro; Danielle Promé; Jean Riou; Christian Godart; Jean Kister; Frédéric Galactéros; Henri Wajcman
Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene.
Hemoglobin 1999;23(4):361-5.
1999: Ioannis Papassotiriou; Joanne Traeger-Synodinos; Danielle Promé; Jean Kister; E Stamou; Theodota Liakopoulou; Alexandra Stamoulakatou; Emmanuel Kanavakis; Henri Wajcman
Association of unstable hemoglobin variants and heterozygous beta-thalassemia: example of a new variant Hb Acharnes or [beta53(D4) Ala --> Thr].
American journal of hematology 1999;62(3):186-92.
1999: Henri Wajcman; Jean Riou; Danielle Promé; Jean Kister; Frédéric Galactéros
Hb Brie Comte Robert [beta36(C2)Pro-->Ala]: a new hemoglobin variant with high oxygen affinity and marked hydrophobic properties.
Hemoglobin 1999;23(3):281-6.
1999: Joan S Henthorn; Henri Wajcman; Danielle Promé; Jean Riou; Jean Kister; Véronique Baudin-Creuza; Sally C Davies; Frédéric Galactéros
Hb Harrow [beta118(GH1)Phe-->Cys]: a new neutral hemoglobin variant.
Hemoglobin 1999;23(3):273-9.
1999: Joan S Henthorn; D Mantio; Sally C Davies; Jean Riou; Henri Wajcman; H Promé; Frédéric Galactéros
Hb Brent [beta117(G19)His-->Asn]: a new hemoglobin variant found during routine antenatal screening.
Hemoglobin 1999;23(1):89-93.
1999: Jean Kister; Claude Préhu; Jean Riou; Christian Godart; Josiane Bardakdjian; Danielle Promé; Frédéric Galactéros; Henri Wajcman
Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb Antananarivo [alpha1(NA1)Val-->Gly] and Hb Barbizon [beta144(HC1)Lys-->Met].
Hemoglobin 1999;23(1):21-32.
1999: Masako Nagai; Henri Wajcman; A Lahary; T Nakatsukasa; Shigenori Nagatomo; Teizo Kitagawa
Quaternary structure sensitive tyrosine residues in human hemoglobin: UV resonance raman studies of mutants at alpha140, beta35, and beta145 tyrosine.
Biochemistry 1999;38(4):1243-51.
1998: M Cohen-Solal; Claude Préhu; Henri Wajcman; Claude Poyart; Josiane Bardakdjian-Michau; Jean Kister; Danielle Promé; C Valentin; Dora Bachir; Frédéric Galactéros
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).
British journal of haematology 1998;103(4):950-6.
1998: AY Segbena; C Prehu; Henri Wajcman; Josiane Bardakdjian-Michau; K Messie; L Feteke; A Vovor; M David; JOSUE FEINGOLD; Frédéric Galacteros
Hemoglobins in Togolese newborns: Hb S, Hb C, Hb Bart's, and alpha-globin gene status.
American journal of hematology 1998;59(3):208-13.
1998: Henri Wajcman; Jean Kister; Claude Préhu; Jean Riou; Christian Godart; Josiane Bardakdjian; AM Soummer; Danielle Promé; Frédéric Galactéros
Hb Tende [beta124(H2)Pro-->Leu]: a new variant with a moderate increase in oxygen affinity.
Hemoglobin 1998;22(5-6):517-23.
1998: Ioannis Papassotiriou; Rolande Ducrocq; Claude Préhu; Josiane Bardakdjian-Michau; Henri Wajcman
Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatography.
Hemoglobin 1998;22(5-6):469-81.
1998: JC Bouanga; R Mouélé; Claude Préhu; Henri Wajcman; JOSUE FEINGOLD; Frédéric Galactéros
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo.
Human heredity 1998;48(4):192-7.
1998: Claude Préhu; Christian Godart; C Vigneron; Henri Wajcman
Hb Nancy and Hb Osler: two distinct genetic variants with identical clinical and hemoglobin phenotype.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1998;321(5):373-6.
1998: Henri Wajcman; Danielle Promé; Claude Préhu; C Déon; Jean Riou; JC Bouanga; I Papassotiriou; A Lahary; Frédéric Galactéros
HB Les Andelys [alpha83(F4)LEU-->PRO]: a new moderately unstable variant.
Hemoglobin 1998;22(2):129-40.
1998: Henri Wajcman; M Dahmane; Claude Préhu; Bruno Costes; Danielle Promé; Nicole Arous; Josiane Bardakdjian-Michau; Jean Riou; K C Ayache; Christian Godart; Frédéric Galactéros
Haemoglobin J-Biskra: a new mildly unstable alpha1 gene variant with a deletion of eight residues (alpha50-57, alpha51-58 or alpha52-59) including the distal histidine.
British journal of haematology 1998;100(2):401-6.
1998: Henri Wajcman; Jean Kister; Jean Riou; Frédéric Galactéros; Robert Girot; Micheline Maier-Redelsperger; N V Nayudu; P C Giordano
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobin.
Hemoglobin 1998;22(1):11-22.
1998: Henri Wajcman; MO Préhu; Claude Préhu; Y Blouquit; Danielle Promé; Frédéric Galactéros
Hemoglobin Phnom Penh [alpha117Phe(H1)-Ile-alpha118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the alpha1-globin gene.
Human mutation 1998;Suppl 1():S20-2.
1997: Jean Kister; Nathalie Griffon; Joan S Henthorn; Michael C Marden; Claude Poyart; Ioannis Papassotiriou; Danielle Promé; Frédéric Galactéros; Sally C Davies; Henri Wajcman
Alteration of an intersubunit contact in hemoglobin variants: comparative study of modifications at position alpha 126 Asp (H9).
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1997;320(11):849-55.
1997: C Déon; Jean-Claude Promé; Danielle Promé; Alain Francina; P Groff; G Kalmes; Frédéric Galactéros; Henri Wajcman
Combined mass spectrometric methods for the characterization of human hemoglobin variants localized within alpha T9 peptide: identification of Hb Villeurbanne alpha 89 (FG1) His-->Tyr.
Journal of mass spectrometry : JMS 1997;32(8):880-7.
1997: Jean Riou; Christian Godart; Didier Hurtrel; Mireille Mathis; Catherine Bimet; Josiane Bardakdjian-Michau; Claude Préhu; Henri Wajcman; Frédéric Galactéros
Cation-exchange HPLC evaluated for presumptive identification of hemoglobin variants.
Clinical chemistry 1997;43(1):34-9.
1996: Henri Wajcman; Danielle Promé; Jean Kister; Sally C Davies; Frédéric Galactéros; Joan S Henthorn
Hb Uxbridge [beta 20 (B2)Val-->Gly]: a new variant with mild increase in oxygen affinity found during a neonatal screening program.
Hemoglobin 1996;20(4):339-50.
1996: Nathalie Griffon; Catherine Badens; Danielle Lena-Russo; Jean Kister; Josiane Bardakdjian; Henri Wajcman; Michael C Marden; Claude Poyart
Hb Bruxelles, deletion of Phebeta42, shows a low oxygen affinity and low cooperativity of ligand binding.
The Journal of biological chemistry 1996;271(42):25916-20.
1996: Henri Wajcman; Jean Kister; Frédéric Galactéros; A Spielvogel; M J Lin; G J Vidugiris; Rhoda Elison Hirsch; Joel Mitchel Friedman; Ronald L Nagel
Hb Montefiore (126(H9)Asp-->Tyr). High oxygen affinity and loss of cooperativity secondary to C-terminal disruption.
The Journal of biological chemistry 1996;271(38):22990-8.
1996: Henri Wajcman; Frédéric Galactéros
Abnormal hemoglobins with high oxygen affinity and erythrocytosis.
Hematology and cell therapy 1996;38(4):305-12.
1996: Henri Wajcman; Rolande Ducrocq; Jean Riou; M Mathis; Christian Godart; C Prehu; F Galacteros
Perfusion chromatography on reversed-phase column allows fast analysis of human globin chains.
Analytical biochemistry 1996;237(1):80-7.
1996: Laurent Kiger; Jean Kister; P Groff; G Kalmes; Danielle Promé; Frédéric Galactéros; Henri Wajcman
Hb J-Europa [beta 62(E6)Ala-->Asp]: normal oxygen binding properties in a new variant involving a residue located distal to the heme.
Hemoglobin 1996;20(2):135-40.
1996: Philippe Lacan; Alain Francina; Danielle Promé; J Delaunay; Frédéric Galactéros; Henri Wajcman
Hb Aubenas [beta 62(B8)Glu-->Gly]: a new variant normally synthesized, affecting the same codon as in Hb E.
Hemoglobin 1996;20(2):113-24.
1996: Claude Poyart; Henri Wajcman
Hemolytic anemias due to hemoglobinopathies.
Molecular aspects of medicine 1996;17(2):129-42.
1996: Philippe Lacan; Jean Kister; Alain Francina; G Souillet; Frédéric Galactéros; J Delaunay; Henri Wajcman
Hemoglobin Debrousse (beta 96[FG3]Leu-->Pro): a new unstable hemoglobin with twofold increased oxygen affinity.
American journal of hematology 1996;51(4):276-81.
1996: Isabelle Thuret; Josiane Bardakdjian; Catherine Badens; Henri Wajcman; F Galacteros; D Vanuxem; H Perrimond; F Giraud; Danielle Lena-Russo
Priapism following splenectomy in an unstable hemoglobin: hemoglobin Olmsted beta 141 (H19) Leu-->Arg.
American journal of hematology 1996;51(2):133-6.
1995: Henri Wajcman; Emmanuelle Girodon; Danielle Promé; M L North; F Plassa; I Duwig; Jean Kister; J P Bergerat; F Oberling; E Lampert
Germline mosaicism for an alanine to valine substitution at residue beta 140 in hemoglobin Puttelange, a new variant with high oxygen affinity.
Human genetics 1995;96(6):711-6.
1995: François Morlé; Alain Francina; Rolande Ducrocq; Henri Wajcman; Colette Gonnet; Noël Philippe; G Souillet; Jacqueline Godet
A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient.
British journal of haematology 1995;91(3):608-11.
1995: G Vassilopoulos; Ioannis Papassotiriou; Ersi Voskaridou; Alexandra Stamoulakatou; E Premetis; Jean Kister; Michael C Marden; Nathalie Griffon; Claude Poyart; Henri Wajcman
Hb Arta [beta 45 (CD4) Phe-->Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with beta-thalassaemia.
British journal of haematology 1995;91(3):595-601.
1995: Henri Wajcman; Rolande Ducrocq; Danielle Promé; Frédéric Galactéros
Hb F-Mauritius [A gamma 23 (B5) Ala deleted]: evidence for an identical hotspot for deletions in the various beta-like genes.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1995;318(10):1065-71.
1995: Henri Wajcman; Y Blouquit; A Lahary; A M Soummer; P Groff; Josiane Bardakdjian; Claude Préhu; Jean Riou; C Godard; F Galactèros
Three new neutral alpha chain variants: Hb Bois Guillaume [alpha 65(E14(Ala-->Val], Hb Mantes-la-Jolie [alpha 79(EF8)Ala-Thr], and Hb Mosella [alpha 111(G18)Ala-->Thr].
Hemoglobin 1995;19(5):281-6.
1995: Henri Wajcman; Jean Kister; Danielle Promé; Y Blouquit; Claude Préhu; Claude Poyart; Frédéric Galactéros
Interaction of 2 amino acid substitutions within the same beta chain of human hemoglobin: the examples of Hb Corbeil and Hb Villeparisis.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1995;318(7):785-94.
1995: S Abbes; P A Fitzgerald; E Varady; R Girot; P Pic; Y Blouquit; R Ducrocq; F Drupt; Henri Wajcman
Two fetal hemoglobin variants affecting the same residue: Hb F-Emirates [G gamma 59(E3)Lys-->Glu] and Hb F-Sacromonte [G gamma 59(E3)Lys-->Gln].
Hemoglobin 1995;19(3-4):173-82.
1995: Jean Kister; Laurent Kiger; Alain Francina; P Hanny; A Szymanowicz; Y Blouquit; Danielle Promé; Frédéric Galactéros; J Delaunay; Henri Wajcman
Hemoglobin Roanne [alpha 94(G1) Asp-->Glu]: a variant of the alpha 1 beta 2 interface with an unexpected high oxygen affinity.
Biochimica et biophysica acta 1995;1246(1):34-8.
1995: Danielle Promé; Jean-Claude Promé; C Déon; P Groff; G Kalmes; F Galacteros; Henri Wajcman
Structural determination of a new electrophoreticaly silent variant: hemoglobin Alzette, beta 104(G6)Arg --> Lys.
Rapid communications in mass spectrometry : RCM 1995;Spec No():S165-8.
1995: B Chami; F Braconnier; Jean Riou; Josiane Bardakdjian-Michau; Claude Préhu; Y Blouquit; J Rosa; Henri Wajcman; Frédéric Galactéros
Geographic distribution of 119 alleles of the alpha and beta globin genes detected in 432 French Caucasian carriers of haemoglobin variant.
Annales de génétique 1995;38(4):206-16.
1994: Henri Wajcman; M Bost; Y Blouquiit; Claude Préhu; Jean Riou; F Galacteros
Two new alpha chain variants found during glycated hemoglobin screening: Hb Tatras [alpha 7(A5)Lys-->Asn] and HB Lisbon [alpha 23(B4)Glu-->Asp].
Hemoglobin 1994;18(6):427-32.
1994: Henri Wajcman; Mariane de Montalembert; Robert Girot; Jean Kister; Micheline Maier-Redelsperger; F Galacteros
The use of Staphylococcus V8 protease in the structural determination of human hemoglobin variants: HB Valparaiso [alpha 88(F9)Ala-->Gly] example.
Hemoglobin 1994;18(4-5):275-84.
1994: Henri Wajcman; Jean Kister; A M'Rad; A M Soummer; F Galacteros
Hb Cemenelum [alpha 92 (FG4) Arg-->Trp]: a hemoglobin variant of the alpha 1/beta 2 interface that displays a moderate increase in oxygen affinity.
Annals of hematology 1994;68(2):73-6.
1994: B Chami; Y Blouquit; Josiane Bardakdjian-Michau; Jean Riou; Henri Wajcman; J Rosa; Frédéric Galactéros
Hemoglobin variants in North Africa.
Hemoglobin 1994;18(1):39-51.
1994: Josiane Bardakdjian; Jean Kister; Henri Wajcman; P Boulard; B Bohn; Y Blouquit; F Galacteros
Hb Poitiers [alpha 45(CE3)His-->Asp]: a new hemoglobin variant with a two-fold increase in oxygen affinity.
Hemoglobin 1994;18(1):1-9.
1993: Henri Wajcman; Jean Kister; D Promé; F Galacteros; F Gilsanz
Hb Villaverde [beta 89 (F5) Ser-->Thr]: the structural modification of an intrasubunit contact is responsible for a high oxygen affinity.
Biochimica et biophysica acta 1993;1225(1):89-94.
1993: Henri Wajcman; Jean Kister; A M'Rad; Michael C Marden; Jean Riou; F Galacteros
Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant with moderate increase in oxygen affinity.
Hemoglobin 1993;17(5):407-17.
1993: Henri Wajcman; G Kalmès; P Groff; Danielle Promé; Jean Riou; F Galacteros
Hb Melusine [alpha 114(GH2)Pro-->Ser]: a new neutral hemoglobin variant.
Hemoglobin 1993;17(5):397-405.
1993: Henri Wajcman; Jean Kister; A M'Rad; Danielle Promé; N Milpied; M J Rapp; Jean-Luc Harousseau; Jean Riou; Josiane Bardakdjian; F Galacteros
Hb Saint Nazaire (beta 103[G5]Phe-->Ile): a new example of polycythemia due to a hemoglobin variant with increased oxygen affinity.
American journal of hematology 1993;44(1):16-21.
1993: Henri Wajcman; J Bardakdjian; Rolande Ducrocq
Structural characterization of abnormal hemoglobins from dried blood specimens in a neonatal screening program.
Annales de biologie clinique 1993;51(10-11):867-70.
1992: Henri Wajcman; Jean Kister; Michael C Marden; A Lahary; M Monconduit; F Galacteros
Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity.
Biochimica et biophysica acta 1992;1180(1):53-7.
1992: Henri Wajcman; Y Blouquit; C Vasseur; A Le Querrec; M Laniece; C Melevendi; A Rasore; F Galacteros
Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the alpha-chain and Hb Duino has two residues substituted in the beta-chain.
Human genetics 1992;89(6):676-80.
1992: Henri Wajcman; Jean Kister; C Vasseur; Y Blouquit; J C Trastour; D Cottenceau; F Galacteros
Structure of the EF corner favors deamidation of asparaginyl residues in hemoglobin: the example of Hb La Roche-sur-Yon [beta 81 (EF5) Leu----His].
Biochimica et biophysica acta 1992;1138(2):127-32.
1992: S Abbes; A M'Rad; P A Fitzgerald; P Dormer; Y Blouquit; Jean Kister; F Galacteros; Henri Wajcman
HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family.
Hemoglobin 1992;16(5):355-62.
1991: Henri Wajcman; C Vasseur; Y Blouquit; D E Santo; maria peres; M C Martins; Claude Poyart; F Galacteros
Hemoglobin Redondo [beta 92(F8) His----Asn]: an unstable hemoglobin variant associated with heme loss which occurs in two forms.
American journal of hematology 1991;38(3):194-200.
1991: D Yannoukakos; C Vasseur; C Driancourt; Y Blouquit; J Delaunay; Henri Wajcman; E Bursaux
Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods.
Blood 1991;78(4):1117-20.
1991: D Yannoukakos; H E Meyer; C Vasseur; C Driancourt; Henri Wajcman; E Bursaux
Three regions of erythrocyte band 3 protein are phosphorylated on tyrosines: characterization of the phosphorylation sites by solid phase sequencing combined with capillary electrophoresis.
Biochimica et biophysica acta 1991;1066(1):70-6.
1991: C Vasseur; F Galacteros; P Groff; Henri Wajcman
Cleavage by protease from Staphylococcus aureus V8: an improvement in the sequence analysis of human hemoglobin variants.
Journal of biochemical and biophysical methods 1991;22(3):195-205.
1991: D Yannoukakos; C Vasseur; J P Piau; Henri Wajcman; E Bursaux
Phosphorylation sites in human erythrocyte band 3 protein.
Biochimica et biophysica acta 1991;1061(2):253-66.
1990: Henri Wajcman; Jean Kister; Michael C Marden; B Bohn; Y Blouquit; J Descamps; M Goudemand; Claude Poyart; F Galacteros
Hemoglobin Calais [beta 76 (E20) Ala----Pro]: a hemoglobin variant with decreased intrinsic oxygen affinity.
Biochimica et biophysica acta 1990;1096(1):60-6.
1990: Claude Poyart; Henri Wajcman
[Mechanisms of adaptation of the oxyphoric function of hemoglobin in mammals].
Archives internationales de physiologie et de biochimie 1990;98(3):A81-105.
1990: Henri Wajcman; Y Blouquit; Jean Riou; Jean Kister; Claude Poyart; J Soria; F Galacteros
A new hemoglobin variant found during investigations of diabetes mellitus: Hb Pavie [alpha 135 (H18) Val----Glu].
Clinica chimica acta; international journal of clinical chemistry 1990;188(1):39-47.
1989: Henri Wajcman; A Mrad; Y Blouquit; C Parmentier; Jean Riou; F Galacteros
Hemoglobin Villejuif [beta 123(H1) Thr----Ile]: a new variant found in coincidence with polycythemia vera.
American journal of hematology 1989;32(4):294-7.
1989: A Mrad; J Kister; C Feo; C Poyart; R Kastally; R Blibech; F Galacteros; Henri Wajcman
Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in Tunisia.
American journal of hematology 1989;32(2):117-22.
1989: D Yannoukakos; C Vasseur; Y Blouquit; E Bursaux; Henri Wajcman
Primary structure of the cytoplasmic domain of human erythrocyte protein band 3. Comparison with its sequence in the mouse.
Biochimica et biophysica acta 1989;998(1):43-9.
1989: Henri Wajcman; J Delaunay; Alain Francina; J Rosa; F Galacteros
Hemoglobin Nouakchott [alpha 114(GH2)Pro----Leu]: a new hemoglobin variant displaying an unusual increase in hydrophobicity.
Biochimica et biophysica acta 1989;998(1):25-31.
1989: Henri Wajcman; G Gombaud-Saintonge; F Galacteros; M Martha; F Vertongen
Hb Belliard [alpha 56(E5)Lys----Asn] a new fast-moving alpha chain variant found in a subject of Spanish origin.
Hemoglobin 1989;13(2):157-62.
1989: P Groff; F Galacteros; G Kalmes; Y Blouquit; Henri Wajcman
Hb Luxembourg [alpha 24(B5) Tyr----His]: a new unstable variant.
Hemoglobin 1989;13(5):429-36.
1989: Henri Wajcman; Y Blouquit; G Gombaud-Saintonge; Jean Riou; F Galacteros
Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin.
Hemoglobin 1989;13(5):421-8.
1988: Faouzi Baklouti; V Baudin-Chich; Jean Kister; Michael C Marden; G Teyssier; Claude Poyart; Jean Delaunay; Henri Wajcman
Increased oxygen affinity with normal heterotropic effects in hemoglobin Loire [alpha 88(F9)Ala----Ser].
European journal of biochemistry / FEBS 1988;177(2):307-12.
1988: B Pautard; C Feo; D Dhermy; Henri Wajcman; V Baudin-Chich; J Delobel
Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: globin chain synthesis and visco diffractometric studies.
British journal of haematology 1988;70(2):239-45.
1988: Henri Wajcman; V Baudin-Chich; Jean Kister; C Feo; G Gombaud-Saintonge; B Bohn; Michael C Marden; Josée Pagnier; Claude Poyart; Catherine Dodé
Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from Benin.
American journal of hematology 1988;28(3):170-5.
1988: Faouzi Baklouti; Alain Francina; E Dorléac; V Baudin-Chich; G Gombaud-Saintonge; H Plauchu; Henri Wajcman; Jean Delaunay; Jacqueline Godet
Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan man.
American journal of hematology 1988;27(4):253-6.
1988: V Baudin-Chich; Michael C Marden; Henri Wajcman
Investigation of the tetramer-dimer equilibrium in haemoglobin solutions by high-performance size-exclusion chromatography on a diol column.
Journal of chromatography 1988;437(1):193-201.
1988: V Baudin-Chich; Henri Wajcman; G Gombaud-Saintonge; Nicole Arous; Jean Riou; J Brière; F Galacteros
Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior.
Hemoglobin 1988;12(2):179-88.
1986: Jacques Rochette; V Baudin; B Bohn; Claude Poyart; Henri Wajcman
Isolation of human haemoglobin variants with altered Bohr effect. Application to haemoglobin Rainier.
Journal of chromatography 1986;369(1):143-9.
1986: V Baudin; Josée Pagnier; D Labie; R Girot; Henri Wajcman
Heterogeneity of sickle cell disease as shown by density profiles: effects of fetal hemoglobin and alpha thalassemia.
Haematologia 1986;19(3):177-84.
1986: Josée Pagnier; V Baudin; D Labie; Henri Wajcman; G Jaeger; R Girot
Sickle cell anemia in Bantu speaking Africa.
Hemoglobin 1986;10(1):73-6.
1985: R L Nagel; Mary E Fabry; Josée Pagnier; I Zohoun; Henri Wajcman; V Baudin; D Labie
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type.
The New England journal of medicine 1985;312(14):880-4.
1985: Josée Pagnier; Henri Wajcman; V Baudin; D Labie
[Genetic polymorphism of drepanocytosis].
Annales de génétique 1985;28(1):5-12.
1984: Jacques Rochette; B Varet; J P Boissel; K Clough; D Labie; Henri Wajcman; B Bohn; P Magne; Claude Poyart
Structure and function of Hb Saint-Jacques (alpha 2 beta 2 140 (H18) Ala----Thr): a new high-oxygen-affinity variant with altered bisphosphoglycerate binding.
Biochimica et biophysica acta 1984;785(1-2):14-21.
1984: Jacques Rochette; J P Boissel; D Labie; Henri Wajcman; Claude Poyart; B Bohn; B Varet
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site].
Nouvelle revue française d'hématologie 1984;26(2):75-7.