Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Muscle & Nerve|April 1, 2024
Feasibility of virtual reality and comparison of its effectiveness to biofeedback in children with Duchenne and Becker muscular dystrophiesMerve Kurt-Aydin, Dilan Savaş-Kalender, Tülay Tarsuslu, et al.
Biomed Research International|April 29, 2016
Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular DystrophiesUluç Yis, Figen Baydan, Mert Karakaya, et al.
Journal of Child Neurology|July 11, 2007
Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutationOrkide Hüdaoglu, Semra Kurul, Uluç Yis, et al.
International Urology and Nephrology|September 12, 2007
Serum and urine cystatin C levels in children with post-pyelonephritic renal scarring: a pilot studyHüray Islekel, Alper Soylu, Zekiye Altun, et al.
Journal of Child Neurology|March 18, 2009
Temporary diazepam responsive apneic attacks and congenital myasthenic syndromeUluç Yis, Semra Hiz Kurul, Ibrahim Oztura, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutationUluç Yis, Gökhan Uyanik, Semra Kurul, et al.
Journal of Neurovirology|September 14, 2019
Herpes simplex virus-1 as a rare etiology of isolated acute cerebellitis: case report and literature reviewCem Paketci, Pinar Edem, Canan Okumus, et al.
Journal of Child Neurology|February 13, 2013
Severe neurologic involvement of Degos disease in a pediatric patientPakize Karaoğlu, Yasemin Topçu, Erhan Bayram, et al.
Brain & Development|November 24, 2016
Dropped head congenital muscular dystrophy caused by de novo mutations in LMNAPakize Karaoglu, Nicolas Quizon, Matthias Pergande, et al.
Movement Disorders Clinical Practice|February 10, 2022
Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic AtrophyFrancesca Magrinelli, Elisa Cali, Vinícius Lopes Braga, et al.
Pageof 1