Showing results (171-180 of 182) with videos related to

Sort By:
Pageof 19
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Archives of Neurology|November 1, 1986
Total and free serum concentrations of carbamazepine and carbamazepine-10,11-epoxide in children with epilepsyO A Agbato, A A Elyas, P N Patsalos, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.
Nature Genetics|February 1, 1995
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesP Rutland, L J Pulleyn, W Reardon, et al.
Clinical Dysmorphology|August 5, 1998
Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six casesM M Lees, P Hodgkins, W Reardon, et al.
Neuropediatrics|August 1, 1987
Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight casesV T Ramaekers, B D Lake, B Harding, et al.
American Journal of Human Genetics|January 1, 1991
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNAM A McShane, S R Hammans, M Sweeney, et al.
European Journal of Pediatrics|January 1, 1989
Neurodevelopmental delay and focal seizures as presenting symptoms of human immunodeficiency virus I infectionP Habibi, S Strobel, I Smith, et al.
Pageof 19