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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

Bogdahn, U. and Zaaroor, M. and Parfenov, V. and Kunst, M. and Mahapatra, A. K. and Sastry, K. V. R. and Jachimczak, P. and Stockhammer, G. and Rappaport, Z. H. and Schlingensiepen, K. H. (2006) A phase IIb study in patients with recurrent malignant glioma with the TGF-beta2 inhibitor AP 12009. EJC SUPPLEMENTS, 4 (12). p. 103. ISSN 1359-6349

C

Cirak, Sebahattin and Uyanik, Goekhan and Herrmann, Ralf and Gross, Claudia and Hehr, Ute and Voit, Thomas (2006) Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K). NEUROMUSCULAR DISORDERS, 16 (Suppl1). S77. ISSN 0960-8966

G

Gryksa, Katharina and Schmidtner, Anna K. and Masis-Calvo, Marianella and Rodriguez-Villagra, Odir A. and Havasi, Andrea and Wirobski, Gwendolyn and Maloumby, Rodrigue and Jaegle, Herbert and Bosch, Oliver J. and Slattery, David A. and Neumann, Inga D. (2023) Selective breeding of rats for high (HAB) and low (LAB) anxiety-related behaviour: A unique model for comorbid depression and social dysfunctions. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

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.

M

Marschallinger, Julia and Krampert, Monika and Couillard-Despres, Sebastien and Heuchel, Rainer and Bogdahn, Ulrich and Aigner, Ludwig (2014) Age-dependent and differential effects of Smad7 Delta Ex1 on neural progenitor cell proliferation and on neurogenesis. EXPERIMENTAL GERONTOLOGY, 57. pp. 149-154. ISSN 0531-5565, 1873-6815

Mueller, Juergen L. and Roeder, Christian H. and Schuierer, Gerhardt and Klein, Helmfried E. (2002) Motor-induced brain activation in cortical, subcortical and cerebellar regions in schizophrenic inpatients. A whole brain fMRI fingertapping study. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 26 (3): PII S0278. pp. 421-426. ISSN 0278-5846

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

S

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

Schulte-Mattler, W. and Wegner, F. and Bogdahn, U. and Wohlfarth, K. (2013) Diffusion properties of two botulinum toxin type A complexes-post-hoc analysis of data from a double-blind, randomized, dose-ranging study. PERGAMON-ELSEVIER SCIENCE LTD, OXFORD.

Sellner, Johann and Cepok, Sabine and Kalluri, Sudhakar Reddy and Nestle, Axel and Kleiter, Ingo and Kuempfel, Tania and Linker, Ralf and Melms, Arthur and Menge, Til and Tumani, Hayrettin and Paul, Friedemann and Hemmer, Bernhard and Berthele, Achim (2010) Aquaporin 4 antibody positive central nervous system autoimmunity and multiple sclerosis are characterized by a distinct profile of antibodies to herpes viruses. NEUROCHEMISTRY INTERNATIONAL, 57 (6). pp. 662-667. ISSN 0197-0186

U

Uyanik, G. and Kortuem, F. and Das, S. and Flindt, M. and Rosendahl, D. J. Morris and Horn, D. (2010) Further delineation of FOXG1-associated encephalopathy. INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 28 (8). p. 715. ISSN 0736-5748

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

W

Wohlfarth, Kai and Schwandt, Imke and Florian, Wegner and Juergens, Tim and Gelbrich, Goetz and Wagner, Armin and Bogdahn, Ulrich and Schulte-Mattler, Wilhelm (2008) Biological activity of Dysport (R) and Botox (R) in the human EDB muscle: A double-blind, randomized, dose-ranging study. TOXICON, 51 (Suppl). p. 22. ISSN 0041-0101

Y

Yis, Uluc and Kurul, Semra and Uyanik, Goekhan and Dirik, Eray (2006) Walker-Warburg syndrome: case report. NEUROMUSCULAR DISORDERS, 16 (Suppl1). S77. ISSN 0960-8966

Z

Ziemus, B. and Baumann, O. and Luerding, R. and Schlosser, R. and Schuierer, G. and Bogdahn, U. and Greenlee, Mark W. (2007) Impaired working-memory after cerebellar infarcts paralleled by changes in BOLD signal of a cortico-cerebellar circuit. NEUROPSYCHOLOGIA, 45 (9). pp. 2016-2024. ISSN 0028-3932, 1873-3514

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.