Items where Author is "Cirak, Sebahattin"

Article

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

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

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 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

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