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Neurology. Genetics|April 12, 2016
Is PARKIN parkinsonism a cancer predisposition syndrome?Birgitt Schüle, Christie Byrne, Linda Rees, et al.Neurology. Genetics|April 12, 2016
Milder forms of muscular dystrophy associated with POMGNT2 mutationsYukari Endo, Mingrui Dong, Satoru Noguchi, et al.Neurology. Genetics|April 12, 2016
Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblingsPatrick Ferreira, Stephanie M Luco, Sarah L Sawyer, et al.Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.Neurology. Genetics|April 12, 2016
Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndromeLance H Rodan, Maria Zak, James Stavropoulos, et al.Neurology. Genetics|April 12, 2016
Dysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsyMikko Muona, Yuko Fukata, Anna-Kaisa Anttonen, et al.Neurology. Genetics|April 12, 2016
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.Neurology. Genetics|April 12, 2016
Tubular aggregate myopathy caused by a novel mutation in the cytoplasmic domain of STIM1Hidehiko Okuma, Fumiaki Saito, Jun Mitsui, et al.Neurology. Genetics|April 12, 2016
Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosisRyan S Dhindsa, Shelton S Bradrick, Xiaodi Yao, et al.Neurology. Genetics|April 12, 2016
Epilepsy with auditory features: A heterogeneous clinico-molecular diseaseTommaso Pippucci, Laura Licchetta, Sara Baldassari, et al.Pageof 86