Showing results (101-110 of 112) with videos related to
Sort By:
Pageof 12
Archives of Neurology|December 1, 1995
Absence of mutations in superoxide dismutase and catalase genes in patients with Parkinson's diseaseJ S Parboosingh, M Rousseau, F Rogan, et al.American Journal of Medical Genetics|June 5, 1998
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonismJ Hardy, J Pérez-Tur, M Baker, et al.American Journal of Medical Genetics|October 21, 1998
Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locusS L Kugler, E S Stenroos, D E Mandelbaum, et al.Journal of Medical Genetics|August 1, 1996
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifidaF A Hol, M P Geurds, S Chatkupt, et al.Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.Annals of Neurology|March 20, 1998
Low frequency of alpha-synuclein mutations in familial Parkinson's diseaseM Farrer, F Wavrant-De Vrieze, R Crook, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 26, 1999
Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigreesA Lazzarini, A S Walters, K Hickey, et al.Transplantation|July 29, 2003
Long-term improvement in renal function with sirolimus after early cyclosporine withdrawal in renal transplant recipients: 2-year results of the Rapamune Maintenance Regimen StudyRainer Oberbauer, Henri Kreis, Robert W G Johnson, et al.Annals of Neurology|February 5, 1998
Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosisK E Wisniewski, N Zhong, W Kaczmarski, et al.Science (New York, N.Y.)|November 15, 1996
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23M H Polymeropoulos, J J Higgins, L I Golbe, et al.Pageof 12