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Results:
1-8
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Results: 8
Authors:
Schara, U
Gencik, M
Mortier, J
Langen, M
Gencikova, A
Epplen, JT
Mortier, W
Citation: U. Schara et al., Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient care, EUR J PED, 160(7), 2001, pp. 452-453
Authors:
Vorgerd, M
Gencik, M
Mortier, J
Epplen, JT
Malin, JP
Mortier, W
Citation: M. Vorgerd et al., Isolated loss of gamma-sarcoglycan: Diagnostic implications in autosomal recessive limb-girdle muscular dystrophies, MUSCLE NERV, 24(3), 2001, pp. 421-424
Authors:
Gencik, M
Dahmen, N
Wieczorek, S
Kasten, M
Bierbrauer, J
Anghelescu, I
Szegedi, A
Saecker, AMM
Epplen, JT
Citation: M. Gencik et al., A prepro-orexin gene polymorphism is associated with narcolepsy, NEUROLOGY, 56(1), 2001, pp. 115-117
Authors:
Gencik, M
Meller, S
Borgmann, S
Sitter, T
Saecker, AMM
Fricke, H
Epplen, JT
Citation: M. Gencik et al., The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitides, CLIN IMMUNO, 94(1), 2000, pp. 9-12
Authors:
Epplen, JT
Gencik, M
Epplen, A
Andrich, J
Saft, C
Przuntek, H
Citation: Jt. Epplen et al., Morbus Huntington - a human genetic model disease, CYTOG C GEN, 91(1-4), 2000, pp. 90-96
Authors:
Gencik, M
Meller, S
Borgmann, S
Fricke, H
Citation: M. Gencik et al., Proteinase 3 gene polymorphisms and Wegener's granulomatosis, KIDNEY INT, 58(6), 2000, pp. 2473-2477
Authors:
Gencik, M
Epplen, JT
Mortier, W
Citation: M. Gencik et al., Diagnosis of neuromuscular diseases: advances through molecular genetic techniques, DEUT MED WO, 124(4), 1999, pp. 85-87
Authors:
Gencik, M
Borgmann, S
Zahn, R
Albert, E
Sitter, T
Epplen, JT
Fricke, H
Citation: M. Gencik et al., Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis, CLIN EXP IM, 117(2), 1999, pp. 412-417
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