Thrombosis in inherited factor VII deficiency
Mariani, G., Herrmann, F. H., Schulman, S., Batorova, A., Wulff, K., Etro, D., Dolce, A., Auerswald, G., Astermark, J., Schved, J.‐F., Ingerslev, J., Bernardi, F.
Published in Journal of thrombosis and haemostasis (01.10.2003)
Published in Journal of thrombosis and haemostasis (01.10.2003)
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Journal Article
Prevalence of factor V Leiden mutation in various populations
Herrmann, F.H., Koesling, M., Schröder, W., Altman, R., Bonilla, R. Jiménez, Lopaciuk, S., Perez-Requejo, J.L., Singh, J.R.
Published in Genetic epidemiology (1997)
Published in Genetic epidemiology (1997)
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Journal Article
High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL
Herrmann, F H, Salazar-Sanchez, L, Jimenez-Arce, G, Grimm, R, Schröder, W
Published in Thrombosis and haemostasis (01.06.2001)
Published in Thrombosis and haemostasis (01.06.2001)
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Journal Article
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene
HERRMANN, F. H., AUERSWALD, G., RUIZ-SAEZ, A., NAVARRETE, M., POLLMANN, H., LOPACIUK, S., BATOROVA, A., WULFF, K.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2006)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2006)
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Journal Article
LONG-TERM FVII SUBSTITUTION IN A PRETERM INFANT WITH SEVERE GASTROINTESTINAL BLEEDING AND FVII DEFICIENCY DUE TO A HOMOZYGOUS DONOR SPLICE MUTATION IVS4+1G→A
Hennewig, U., Eisert, S., Wulff, K., Herrmann, F. H., Schneider, D. T., Göbel, U.
Published in Pediatric hematology and oncology (01.03.2006)
Published in Pediatric hematology and oncology (01.03.2006)
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Journal Article
A de novo translocation 46,X,t(X;15) causing haemophilia B in a girl: a case report
SCHÖDER, W, POETSCH, M, GAZDA, H, WERNER, W, REICHELT, T, KNOLL, W, ROKICKA-MILEWSKA, R, ZIELENIEWSKA, B, HERRMANN, F. H
Published in British journal of haematology (01.03.1998)
Published in British journal of haematology (01.03.1998)
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Journal Article
Factor VIII gene polymorphisms in the Asian Indian population
Chowdhury, M. R., Herrmann, F. H., Schroder, W., Lambert, C. T., Lalloz, M. R. A., Layton, M., Kumbnani, H. K., Kabra, M., Menon, P. S. N., Verma, I. C.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2000)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2000)
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Journal Article
Relationships between homocysteine, folate and vitamin B12 levels with the methylenetetrahydrofolate reductase polymorphism, in Indians from Western Venezuela
Vizcaíno, G, Diez-Ewald, M, Herrmann, F H, Schuster, G, Pérez-Requejo, J L
Published in Thrombosis and haemostasis (01.01.2001)
Published in Thrombosis and haemostasis (01.01.2001)
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Journal Article
Molecular biology and clinical manifestation of hereditary factor VII deficiency
Herrmann, F H, Wulff, K, Auberger, K, Aumann, V, Bergmann, F, Bergmann, K, Bratanoff, E, Franke, D, Grundeis, M, Kreuz, W, Lenk, H, Losonczy, H, Maak, B, Marx, G, Mauz-Körholz, C, Pollmann, H, Serban, M, Sutor, A, Syrbe, G, Vogel, G, Weinstock, N, Wenzel, E, Wolf, K
Published in Seminars in thrombosis and hemostasis (2000)
Published in Seminars in thrombosis and hemostasis (2000)
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Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma : FISH deletion screening with YAC DNA probes
POETSCH, M, WOENCKHAUS, C, DITTBERNER, T, PAMBOR, M, LORENZ, G, HERRMANN, F. H
Published in Virchows Archiv : an international journal of pathology (01.08.1999)
Published in Virchows Archiv : an international journal of pathology (01.08.1999)
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Journal Article
Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy
Hoeltzenbein, Maria, Karow, Thomas, Zeller, Joern A, Warzok, Rolf, Wulff, Karin, Zschiesche, Marlies, Herrmann, Falko H, Große-Heitmeyer, Wolfgang, Wehnert, Manfred S
Published in Neuromuscular disorders : NMD (01.05.1999)
Published in Neuromuscular disorders : NMD (01.05.1999)
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Journal Article
Segregation and sporadic cases in families with Hunter's syndrome
Machill, G, Barbujani, G, Danieli, G A, Herrmann, F H
Published in Journal of medical genetics (01.06.1991)
Published in Journal of medical genetics (01.06.1991)
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Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at risk
Schröder, W, Petruschka, L, Wehnert, M, Zschiesche, M, Seidlitz, G, Hopwood, J J, Herrmann, F H
Published in Journal of medical genetics (01.03.1993)
Published in Journal of medical genetics (01.03.1993)
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Journal Article
Molecular analysis of FVIII gene in severe HA patients of Costa Rica
Salazar-Sánchez, L, Jiménez-Cruz, G, Mendez, M, Chaverri, P, Alvarado, P, Schröder, W, Wulff, K, Sandoval, M, Herrmann, F H, Pavlova, A, Oldenburg, J
Published in Hämostaseologie (01.11.2010)
Published in Hämostaseologie (01.11.2010)
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