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Wolfram Kress

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Germany

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Sarah Feldkirchner; Franz-Georg Hanisch; Sabine Krause; Wolfram Kress; Christiana Kubny; Stefan Müller; Benedikt Schoser; Maggie C Walter; Joachim Schessl
Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy.
Maggie C Walter; Marcus Deschauer; Ralf Kohnen; Wolfram Kress; Clemens Müller-Reible; Peter Reilich; Karlheinz Reiners; Joachim Schessl; Beate Schlotter-Weigel; Bertold Schrank; Herbert Schreiber; Simone Thiele; Peter Urban; Matthias Vorgerd; Hanns Lochmüller
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
Tiemo Grimm; Wolfram Kress; Gerhard Meng; Clemens R Müller
Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.

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2013: Sarah Feldkirchner; Franz-Georg Hanisch; Sabine Krause; Wolfram Kress; Christiana Kubny; Stefan Müller; Benedikt Schoser; Maggie C Walter; Joachim Schessl
Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy.
Neuromuscular disorders : NMD 2013;23(5):418-26.
2013: Maggie C Walter; Marcus Deschauer; Ralf Kohnen; Wolfram Kress; Clemens Müller-Reible; Peter Reilich; Karlheinz Reiners; Joachim Schessl; Beate Schlotter-Weigel; Bertold Schrank; Herbert Schreiber; Simone Thiele; Peter Urban; Matthias Vorgerd; Hanns Lochmüller
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
Orphanet journal of rare diseases 2013;8():26.
2012: Tiemo Grimm; Wolfram Kress; Gerhard Meng; Clemens R Müller
Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2012;31(3):179-83.
2012: Sabine Rudnik-Schöneborn; Jan Maarten Cobben; Thomas Eggermann; Wolfram Kress; Henny H Lemmink; Klaus Zerres
Clinical utility gene card for: proximal spinal muscular atrophy.
European journal of human genetics : EJHG 2012;20(6):.
2012: Joachim Schessl; Wolfram Kress; Benedikt Schoser
Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and Miyoshi type of muscular dystrophy.
Muscle & nerve 2012;45(5):740-2.
2010: Peter Reilich; Nicolai Schramm; Benedikt Schoser; Peter Schneiderat; Nicola Strigl-Pill; Josef Müller-Höcker; Wolfram Kress; Andreas Ferbert; Sabine Rudnik-Schöneborn; Johannes Noth; Hanns Lochmüller; Joachim Weis; Maggie C Walter
Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy.
Journal of neurology 2010;257(7):1108-18.
2010: L Kirzinger; A Schmidt; C Kornblum; Christiane Schneider-Gold; Wolfram Kress; Benedikt Schoser
Side effects of anesthesia in DM2 as compared to DM1: a comparative retrospective study.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2010;17(6):842-5.
2010: Peter Reilich; Benedikt Schoser; Nicolai Schramm; Sabine Krause; Joachim Schessl; Wolfram Kress; Josef Müller-Höcker; Maggie C Walter; Hanns Lochmuller
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy.
Neuromuscular disorders : NMD 2010;20(4):255-9.
2010: Angelika Stellzig-Eisenhauer; Eva Decker; Philipp Meyer-Marcotty; Christiane Rau; Britta S Fiebig; Wolfram Kress; Kathrin Saar; Franz Rüschendorf; Norbert Hubner; Tiemo Grimm; Emil Witt; Bernhard H F Weber
Primary failure of eruption (PFE)--clinical and molecular genetics analysis.
Journal of orofacial orthopedics = Fortschritte der Kieferorthopädie : Organ/official journal Deutsche Gesellschaft für Kieferorthopädie 2010;71(1):6-16.
2008: Sabine Rudnik-Schöneborn; Joachim Weis; Wolfram Kress; M Häusler; Klaus Zerres
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.
Neuromuscular disorders : NMD 2008;18(11):881-5.
2008: Ulrike Schara; Wolfram Kress; Carsten G Bönnemann; Nico Breitbach-Faller; Christoph G Korenke; Gudrun Schreiber; Mechthild Stoetter; Ana Ferreiro; Maja von der Hagen
The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2008;12(3):224-30.
2008: A L Schulz; Beate Albrecht; C Arici; Ineke van der Burgt; Annegret Buske; Gabriele Gillessen-Kaesbach; R Heller; Denise Horn; C A Hübner; Georg Christoph Korenke; Rainer König; Wolfram Kress; G Krüger; Peter Meinecke; J Mücke; Barbara Plecko; E Rossier; Albert Schinzel; A Schulze; Eva Seemanova; Heide Seidel; Stephanie Spranger; B Tuysuz; S Uhrig; Dagmar Wieczorek; Kerstin Kutsche; M Zenker
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
Clinical genetics 2008;73(1):62-70.
2007: Ilse Wieland; C Weidner; Roberto Ciccone; E Lapi; Donna McDonald-McGinn; Wolfram Kress; Sibylle Jakubiczka; Hartmut Collmann; Orsetta Zuffardi; Elaine Zackai; Peter Wieacker
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.
Clinical genetics 2007;72(6):506-16.
2007: Maggie C Walter; Peter Reilich; Angela Huebner; Dirk Fischer; Rolf Schröder; Matthias Vorgerd; Wolfram Kress; Christine Born; Benedikt Schoser; K H Krause; U Klutzny; S Bulst; J R Frey; Hanns Lochmüller
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.
Brain : a journal of neurology 2007;130(Pt 6):1485-96.
2007: Benedikt Schoser; J Michael Schröder; Timo Grimm; Damien Sternberg; Wolfram Kress
A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.
Muscle & nerve 2007;35(5):599-606.
2007: Anja Hiller; Johann Hagenah; Ana Djarmati; Katja Hedrich; Kathrin Reetz; Christiane Schneider-Gold; Wolfram Kress; Alexander Münchau; Christine Klein
Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.
Movement disorders : official journal of the Movement Disorder Society 2007;22(1):145-7.
2006: Sabine Hoffjan; Charlotte Thiels; Matthias Vorgerd; Eva Neuen-Jacob; Jörg T Epplen; Wolfram Kress
Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1.
Neuromuscular disorders : NMD 2006;16(11):749-53.
2006: Katja Hedrich; Johann Hagenah; Ana Djarmati; Anja Hiller; Thora Lohnau; Kathrin Lasek; Anne Grünewald; Rüdiger Hilker; Susanne Steinlechner; Heather Boston; Norman Kock; Christiane Schneider-Gold; Wolfram Kress; Hartwig R Siebner; Ferdinand Binkofski; Rebekka Lencer; Alexander Münchau; Christine Klein
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
Archives of neurology 2006;63(6):833-8.
2006: Sabine Rudnik-Schöneborn; Christiane Schneider-Gold; U Raabe; Wolfram Kress; Klaus Zerres; Benedikt Schoser
Outcome and effect of pregnancy in myotonic dystrophy type 2.
Neurology 2006;66(4):579-80.
2006: Maja von der Hagen; J Schallner; Angela M Kaindl; K Koehler; P Mitzscherling; Angela Abicht; U Grieben; R Korinthenberg; Wolfram Kress; Arpad von Moers; Juliane S Müller; Ulrike Schara; Matthias Vorgerd; Maggie C Walter; C Müller-Reible; Christoph Hübner; Hanns Lochmüller; Angela Huebner
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis.
Neuromuscular disorders : NMD 2006;16(1):4-13.
2006: Wolfram Kress; Christian Schropp; Gabriele Lieb; Birgit Petersen; Maria Büsse-Ratzka; Juergen Kunz; Edeltraut Reinhart; Wolf-Dieter Schäfer; Johanna Sold; Florian Hoppe; Jan Pahnke; Andreas Trusen; Niels Sörensen; Jürgen Krauss; Hartmut Collmann
Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
European journal of human genetics : EJHG 2006;14(1):39-48.
2005: Ilse Wieland; William Reardon; Sibylle Jakubiczka; Brunella Franco; Wolfram Kress; Catherine Vincent-Delorme; Patrick Thierry; Matt Edwards; Rainer König; Cristina Rusu; Susann Schweiger; Elizabeth Thompson; Sigrid Tinschert; Fiona Stewart; Peter Wieacker
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS).
Human mutation 2005;26(2):113-8.
2004: Benedikt Schoser; Kenneth Ricker; Christiane Schneider-Gold; C Hengstenberg; J Dürre; B Bültmann; Wolfram Kress; John W Day; Laura P W Ranum
Sudden cardiac death in myotonic dystrophy type 2.
Neurology 2004;63(12):2402-4.
2004: Benedikt Schoser; Wolfram Kress; Maggie C Walter; Birgit Halliger-Keller; Hanns Lochmüller; Kenneth Ricker
Homozygosity for CCTG mutation in myotonic dystrophy type 2.
Brain : a journal of neurology 2004;127(Pt 8):1868-77.
2004: Matthias Habeck; Christine Zühlke; Karl H P Bentele; Stephan Unkelbach; Wolfram Kress; Katrin Bürk; Eberhard Schwinger; Yorck Hellenbroich
Aprataxin mutations are a rare cause of early onset ataxia in Germany.
Journal of neurology 2004;251(5):591-4.
2004: Andreas Reif; Wolfram Kress; Karl Wurm; Jens Benninghoff; Bruno Pfuhlmann; Klaus-Peter Lesch
Duplication 15q14 --> pter: a rare chromosomal abnormality underlying bipolar affective disorder.
European psychiatry : the journal of the Association of European Psychiatrists 2004;19(3):179-81.
2004: Benedikt Schoser; Christiane Schneider-Gold; Wolfram Kress; Hans-Hilmar Goebel; Peter Reilich; Manuela C Koch; Dieter Pongratz; Klaus V Toyka; Hanns Lochmüller; Kenneth Ricker
Muscle pathology in 57 patients with myotonic dystrophy type 2.
Muscle & nerve 2004;29(2):275-81.
2004: Sibylle Jakubiczka; Stefan Vielhaber; Wolfram Kress; Peter Küpferling; Ulrike Reuner; Bernhard Kunath; Peter Wieacker
Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2.
Neurogenetics 2004;5(1):55-9.
2003: Ulrike Schara; Wolfram Kress; Jens Tücke; Wilhelm Mortier
X-linked myotubular myopathy in a female infant caused by a new MTM1 gene mutation.
Neurology 2003;60(8):1363-5.
2003: John W Day; Kenneth Ricker; J F Jacobsen; L J Rasmussen; Katherine A Dick; Wolfram Kress; C Schneider; Manuela C Koch; Gregory Beilman; A R Harrison; Joline C Dalton; Laura P W Ranum
Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.
Neurology 2003;60(4):657-64.
2002: Oliver Bartsch; K Locher; Peter Meinecke; Wolfram Kress; Eva Seemanová; A Wagner; Kai Ostermann; Gerhard Rödel
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP.
Journal of medical genetics 2002;39(7):496-501.
2002: Christiane Schneider; F Pedrosa Gil; M Schneider; Martin Anetseder; Wolfram Kress; Clemens R Müller
Intolerance to neuroleptics and susceptibility for malignant hyperthermia in a patient with proximal myotonic myopathy (PROMM) and schizophrenia.
Neuromuscular disorders : NMD 2002;12(1):31-5.
2001: Matthias Vorgerd; Kenneth Ricker; Focke Ziemssen; Wolfram Kress; Hans-Hilmar Goebel; W A Nix; Christian Kubisch; Benedikt Schoser; Wilhelm Mortier
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation.
Neurology 2001;57(12):2273-7.
2001: C L Liquori; Kenneth Ricker; Melinda L Moseley; J F Jacobsen; Wolfram Kress; Susan Naylor; John W Day; Laura P W Ranum
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
Science (New York, N.Y.) 2001;293(5531):864-7.
2000: Christiane Schneider; Tiemo Grimm; Wolfram Kress; Claudia Sommer; Clemens R Müller
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM).
Neuromuscular disorders : NMD 2000;10(7):481-3.
2000: Wolfram Kress; B Mueller-Myhsok; Kenneth Ricker; Christiane Schneider; Manuela C Koch; Klaus V Toyka; CR Mueller; Tiemo Grimm
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
Neuromuscular disorders : NMD 2000;10(7):478-80.
2000: Christiane Schneider; A Ziegler; Kenneth Ricker; Tiemo Grimm; Wolfram Kress; C D Reimers; Hans-Michael Meinck; Karlheinz Reiners; Klaus V Toyka
Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.
Neurology 2000;55(3):383-8.
2000: Wolfram Kress; B Petersen; Hartmut Collmann; Tiemo Grimm
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.
Cytogenetics and cell genetics 2000;91(1-4):138-40.
2000: Wolfram Kress; Hartmut Collmann; M Büsse; Birgit Halliger-Keller; CR Mueller
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
Cytogenetics and cell genetics 2000;91(1-4):134-7.
1999: Benjamin Ehmke; Wolfram Kress; Helge Karch; Tiemo Grimm; Bernd Klaiber; Thomas F Flemmig
Interleukin-1 haplotype and periodontal disease progression following therapy.
Journal of clinical periodontology 1999;26(12):810-3.
1999: Marie-Christine Dabauvalle; E Müller; Andrea Ewald; Wolfram Kress; Georg Krohne; Clemens R Müller
Distribution of emerin during the cell cycle.
European journal of cell biology 1999;78(10):749-56.
1999: Clemens R Müller; Andreas Fregin; Stefan Srsen; Klara Srsnova; Birgit Halliger-Keller; Ute Felbor; Eva Seemanova; Wolfram Kress
Allelic heterogeneity of alkaptonuria in Central Europe.
European journal of human genetics : EJHG 1999;7(6):645-51.
1999: Ute Felbor; YA Mutsch; Franz Grehn; Clemens R Müller; Wolfram Kress
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene.
The British journal of ophthalmology 1999;83(6):680-3.
1999: Franz X Weilbach; Wolfram Kress; Han-Michael Strassburg; Clemens R Müller; Ralf Gold
[Current diagnosis in muscular dystrophies. New developments, methods of examination and case examples].
Der Nervenarzt 1999;70(2):89-100.
1999: O Bartsch; Wolfram Kress; A Wagner; Eva Seemanova
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case.
Cytogenetics and cell genetics 1999;85(3-4):310-4.
1999: Kenneth Ricker; Tiemo Grimm; Manuela C Koch; Christiane Schneider; Wolfram Kress; C D Reimers; Wilhelm Schulte-Mattler; B Mueller-Myhsok; Klaus V Toyka; CR Mueller
Linkage of proximal myotonic myopathy to chromosome 3q.
Neurology 1999;52(1):170-1.
1999: Wolfram Kress; Stefan Schmidt; Birgit Halliger-Keller; X Montagutelli; Clemens R Müller
The genetic defect of the alkaptonuric mouse (aku).
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(1):68-70.
1998: Wolfram Kress; Birgit Halliger-Keller; T Grimm; H Porschke; Andreas Engelhardt; H H Goebel; B Müller-Mysok
No evidence for heterogeneity in oculopharyngeal muscular dystrophy.
Journal of medical genetics 1998;35(7):613-4.
1998: B Petersen; Han-Michael Strassburg; Wolfgang Feichtinger; Wolfram Kress; Michael Schmid
Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.
American journal of medical genetics 1998;77(1):60-2.
1997: Werner Wolz; Wolfram Kress; CR Mueller
Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M.
Genomics 1997;45(2):438-42.
1997: H Porschke; Wolfram Kress; Heinz Reichmann; H H Goebel; T Grimm
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency.
Neuromuscular disorders : NMD 1997;7 Suppl 1():S57-62.
1997: Johannes Oldenburg; E M Quenzel; Ursula Harbrecht; Andreas Fregin; Wolfram Kress; Clemens R Müller; Hans-Joerg Hertfelder; Rainer Schwaab; Hans H Brackmann; Peter Hanfland
Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy.
British journal of haematology 1997;98(1):240-4.
1997: Stefan Schmidt; Andrea Gehrig; MR Koehler; Michael Schmid; Clemens R Müller; Wolfram Kress
Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(3):168-71.
1997: Andrea Gehrig; Stefan Schmidt; Clemens R Müller; Stefan Srsen; Klara Srsnova; Wolfram Kress
Molecular defects in alkaptonuria.
Cytogenetics and cell genetics 1997;76(1-2):14-6.
1996: Wolfram Kress; Tiemo Grimm; Clemens R Müller; H Keller; R Bittner
Parental source effect on inherited mutations in the dystrophin gene of mice and humans.
Acta geneticae medicae et gemellologiae 1996;45(1-2):251-3.
1995: I Stec; Wolfram Kress; G Meng; B Müller; Clemens R Müller; Tiemo Grimm
Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.
Journal of medical genetics 1995;32(12):930-3.
1995: Reginald E Bittner; S Shorny; Berthold Streubel; C Hübner; T Voit; Wolfram Kress
Serum antibodies to the deleted dystrophin sequence after cardiac transplantation in a patient with Becker's muscular dystrophy.
The New England journal of medicine 1995;333(11):732-3.
1995: Volker Schuster; Tiemo Grimm; Wolfram Kress; Silvia Seidenspinner; B H Belohradsky; P Müller; Hans Wolfgang Kreth
[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies].
Klinische Pädiatrie 1995;207(5):271-6.
1995: Reginald E Bittner; S Shorny; R Ferlings; W Sperl; Wolfram Kress; Clemens R Müller; M Cremer; Jean J Léger; T Voit
Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin gene.
Neuromuscular disorders : NMD 1995;5(2):81-92.
1995: Stefan Schmidt; Clemens R Müller; Wolfram Kress
Murine liver homogentisate 1,2-dioxygenase. Purification to homogeneity and novel biochemical properties.
European journal of biochemistry / FEBS 1995;228(2):425-30.
1994: Volker Schuster; Silvia Seidenspinner; Tiemo Grimm; Wolfram Kress; S Zielen; M Bock; Hans Wolfgang Kreth
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease.
European journal of pediatrics 1994;153(6):432-7.
1994: Ralf Gold; Wolfram Kress; T Bettecken; Heinz Reichmann; Clemens R Müller
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.
Journal of neurology 1994;241(5):331-4.
1994: S Janocha; Werner Wolz; Stefan Srsen; Klara Srsnova; X Montagutelli; J L Guénet; Tiemo Grimm; Wolfram Kress; Clemens R Müller
The human gene for alkaptonuria (AKU) maps to chromosome 3q.
Genomics 1994;19(1):5-8.
1994: Volker Schuster; Wolfram Kress; K Kruse
Paternal and maternal transmission of pseudohypoparathyroidism type Ia in a family with Albright hereditary osteodystrophy: no evidence of genomic imprinting.
Journal of medical genetics 1994;31(1):84.
1993: Volker Schuster; Wolfram Kress; W Friedrich; Tiemo Grimm; Hans Wolfgang Kreth
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.
American journal of diseases of children (1960) 1993;147(12):1303-5.
1993: Ralf Gold; Wolfram Kress; Heinz Reichmann; Clemens R Müller
The use of monoclonal antibodies in diagnostic tests for Becker and Duchenne muscular dystrophy.
Journal of neurology 1993;240(1):21-4.
1992: Ralf Gold; Wolfram Kress; B Meurers; G Meng; Heinz Reichmann; Clemens R Müller
Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
Muscle & nerve 1992;15(2):214-8.
1992: Wolfram Kress; E Müller; K Kausch; Frank Kullmann; Maria Luisa Mostacciuolo; Marcella Rietschel; H W Rotthauwe; B Schmalenberger; Gabriele Siciliano; T Voit
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene.
Neuromuscular disorders : NMD 1992;2(2):111-5.
1991: Ralf Gold; Wolfram Kress; B Meurers; Clemens R Müller; Heinz Reichmann
[Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations].
Der Nervenarzt 1991;62(6):360-8.
1990: Ralf Gold; B Meurers; Heinz Reichmann; Wolfram Kress; Clemens R Müller
Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in man.
Journal of neurology 1990;237(8):494-5.