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B

Balci, B. and Uyanik, Goekhan and Dincer, Pervin and Gross, Claudia and Willer, Tobias and Talim, B. and Haliloglu, G. and Kale, G. and Hehr, Ute and Winkler, Juergen and Topaloglu, H. (2005) An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene. NEUROMUSCULAR DISORDERS, 15 (4). pp. 271-275. ISSN 0960-8966, 1873-2364

H

Haliloglu, G. and Gross, C. and Talim, B. and Hehr, U. and Uyanik, G. and Winkler, J. and Topaloglu, H. (2004) Severe autistic features in a child with muscle-eye-brain disease. In: 9th International Congress of the World Muscle Society, September 01-04, 2004, Göteborg, Sweden.

L

Lauer, Nadine and Fritsche, Lars G. and Weber, Bernhard H. F. and Hartmann, Andrea and Keilhauer, Claudia N. and Haelbich, Steffi and Oppermann, Martin and Pandey, Manoij and Koehl, Joerg and Zipfel, Peter F. and Skerka, Christine (2010) Imbalance of complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age related macular degeneration (AMD). MOLECULAR IMMUNOLOGY, 47 (13). p. 2211. ISSN 0161-5890

Lauer, Nadine and Mihlan, Michael and Hartmann, Andrea and Schloetzer-Schrehard, Ursula and Keilhauer, Claudia and Scholl, Hendrik P. N. and Charbel-Issa, Peter and Holz, Frank and Weber, Bernhard H. F. and Skerka, Christine and Zipfel, Peter F. (2010) Complement regulation at necrotic cell lesions is impaired by the AMD associated Factor H-H402 risk variant. MOLECULAR IMMUNOLOGY, 47 (13). p. 2211. ISSN 0161-5890

M

Mercedes Pujol-Lereis, Luciana and Fagali, Natalia Soledad and Rabossi, Alejandro and Catala, Angel and Alberto Quesada-Allue, Luis (2016) Chill-coma recovery time, age and sex determine lipid profiles in Ceratitis capitata tissues. JOURNAL OF INSECT PHYSIOLOGY, 87. pp. 53-62. ISSN 0022-1910, 1879-1611

Micklisch, Sven and Karlstetter, Marcus and Schmoelz, Lisa and Dahse, Hans-Martin and Weber, Bernhard H. and Lorkowski, Stefan and Langmann, Thomas and Zipfel, Peter F. and Skerka, Christine (2014) Age related maculopathy susceptibility protein 2 (ARMS2) mediates opsonization of apoptotic cells. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Molday, Robert S. and Kellner, Ulrich and Weber, Bernhard H. F. (2012) X-linked juvenile retinoschisis: Clinical diagnosis, genetic analysis, and molecular mechanisms. PROGRESS IN RETINAL AND EYE RESEARCH, 31 (3). pp. 195-212. ISSN 1350-9462, 1873-1635

O

Oelmez, Akguen and Cirak, Sebahattin and Uyanik, Goekhan and Gross, Claudia and Voit, Thomas and Hehr, Ute and Winkler, Juergen and Toplaoglu, Haluk (2006) Clinical and genetic features of five families with infantile-onset ascending Hereditary Spastic Paralysis. NEUROMUSCULAR DISORDERS, 16 (Suppl1). S63-S64. ISSN 0960-8966

Oelmez, Akguen and Uyanik, Goekhan and Gross, Claudia and Cirak, Sebahattin and Topcu, Meral and Elibol, Buelent and Anlar, Banu and Winner, Beate and Hehr, Ute and Winkler, Juergen and Topaloglu, Haluk (2006) Clinical and genetic features of 32 families with autosomal recessive Hereditary Spastic Paraplegias. NEUROMUSCULAR DISORDERS, 16 (Suppl1). S62-S63. ISSN 0960-8966

Oelmez, Akguen and Uyanik, Goekhan and Oezguel, R. Koeksal and Gross, Claudia and Cirak, Sebahattin and Elibol, Buelent and Anlar, Banu and Winner, Beate and Hehr, Ute and Topaloglu, Haluk and Winkler, Juergen (2006) Clinical and genetic characterization of SPG11: Hereditary Spastic Paraplegia with thin corpus callosum. NEUROMUSCULAR DISORDERS, 16 (Suppl1). S63. ISSN 0960-8966

P

Pauly, D. and Nagel, B. M. and Schaefer, N. and Weber, B. H. F. (2013) The role of Properdin in the development and progression of age-related macular degeneration. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Pauly, Diana and Schaefer, Nicole and Grosche, Antje (2017) Cell-type specific complement expression in aging, albino mice. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

R

Reinhard, Jens and Messias, Andre and Dietz, Klaus and MacKeben, Manfred and Lakmann, Raimund and Scholl, Hendrik P. N. and Apfelstedt-Sylla, Eckart and Weber, Bernhard H. F. and Seeliger, Mathias W. and Zrenner, Eberhart and Trauzettel-Klosinski, Susanne (2007) Quantifying fixation in patients with Stargardt disease. VISION RESEARCH, 47 (15). pp. 2076-2085. ISSN 0042-6989

S

Schaefer, Nicole and Brandl, Caroline and Skerka, Christine and Weber, Bernhard H. and Pauly, Diana (2014) Investigation of human anti-CFH autoantibodies and mouse anti-CFHR3 monoclonal antibodies in age-related macular degeneration. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Schaefer, Nicole and Foeckler, Renate and Eckert, Elfriede and Dannullis, Andrea and Reinders, Joerg and Weber, Bernhard and Skerka, Christine and Pauly, Diana (2015) Newly generated antibodies indicate CFHR3 function in the humane complement system. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Schara, U. and Kress, W. and Vorgerd, M. and Gross, C. and Winkler, J. and Hehr, U. and Mortier, W. and Uyanik, G. (2006) Phenotype and muscle biopsy findings in the first German patient with limb-girdle muscular dystrophy 2K - Important differential diagnosis of Becker muscular dystrophy. NEUROMUSCULAR DISORDERS, 16 (9-10). p. 680. ISSN 0960-8966

Seliger, G. and Kamin, G. and Rogenhofer, N. and Ebner, S. and Toth, B. and Schenk, M. and Henes, M. and Bohlmann, M. K. and Fischer, T. and Petroff, D. and Schleussner, E. (2017) Progesterone supplementation for preventing recurrent miscarriage - a secondary analysis of the ETHIG II trial. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Skerka, Christine and Lauer, Nadine and Hartmann, Andrea and Heinen, Stefan and Schlotzer-Schrehardt, Ursula and Weinberger, Andreas W. A. and Keilhauer, Claudia and Suehnel, Juergen and Weber, Bernhard H. F. and Zipfel, Peter F. (2007) Mutation in factor H (Y402H) associated with age related macular degeneration (AMD) results in reduced binding activities. MOLECULAR IMMUNOLOGY, 44 (1-3). pp. 241-242. ISSN 0161-5890

Skerka, Christine and Lauer, Nadine and Keilhauer, Claudia N. and Fritsche, Lars and Weber, Bernhard H. F. and Zipfel, Peter F. (2007) Defective complement control of factor H (Y402H) and FHL1 in age-related macular degeneration. MOLECULAR IMMUNOLOGY, 44 (16). p. 3914. ISSN 0161-5890

Skerka, Christine and Lauer, Nadine and Weinberger, Andreas A. W. A. and Keilhauer, Claudia N. and Suehnel, Juergen and Smith, Richard and Schloetzer-Schrehardt, Ursula and Fritsche, Lars and Heinen, Stefan and Hartmann, Andrea and Weber, Bernhard H. F. and Zipfel, Peter F. (2007) Defective complement control of Factor H (Y402H) and FHL-1 in age-related macular degeneration. MOLECULAR IMMUNOLOGY, 44 (13). pp. 3398-3406. ISSN 0161-5890

U

Uyanik, Goekhan and Kress, Wolfram and Mortier, Wilhelm and Gross, Claudia and Winkler, Juergen and Hehr, Ute and Schara, Ulrike (2006) A German patient with limb-girdle muscular dystrophy 2K caused by compound heterozygous POMT1 mutations. NEUROMUSCULAR DISORDERS, 16 (Suppl1). S77. ISSN 0960-8966

Y

Yis, Uluc and Uyanik, Goekhan and Heck, Pinar Bambul and Smitka, Martin and Nobel, Hannes and Ebinger, Friedrich and Dirik, Eray and Feng, Lucy and Kurul, Semra H. and Brocke, Katja and Unalp, Aycan and Oezer, Erdener and Cakmakci, Handan and Sewry, Caroline and Cirak, Sebahattin and Muntoni, Francesco and Hehr, Ute and Morris-Rosendahl, Deborah J. (2011) Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: Less severe mutations predominate in patients with a non-Walker-Warburg phenotype. NEUROMUSCULAR DISORDERS, 21 (1). pp. 20-30. ISSN 0960-8966, 1873-2364

Ö

Ölmez, A. and Uyanik, G. and Gross, C. and Winner, B. and Özgül, R. K. and Cirak, S. and Hehr, U. and Winkler, J. and Topaloglu, H. (2005) A cross section of autosomal recessive hereditary spastic paraplegias. In: 10th International Congress of the World Muscle Society, September 28-October 1, 2005, Iguassu Falls, Brazil.