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Bratislavske Lekarske Listy|April 12, 2007
Systematic isolation and characterization of cDNAs encoding AAA proteins from human brainXinping Zhao, P Hedera, J K FinkSeminars in Neurology|August 27, 2002
Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlationJ K Fink, P HederaSeminars in Neurology|August 27, 2002
Diagnosis and treatment of Wilson's diseaseG J Brewer, J K Fink, P HederaNeurology|July 1, 1997
Paroxysmal dystonic choreoathetosis linked to chromosome 2q: clinical analysis and proposed pathophysiologyJ K Fink, P Hedera, J G Mathay, et al.Neuroradiology|September 7, 2005
Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegiaP Hedera, O P Eldevik, P Maly, et al.Neurology|July 17, 1999
Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8qP Hedera, S DiMauro, E Bonilla, et al.Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of hereditary spastic paraplegiaP Hedera, J A Williamson, S Rainier, et al.Hepatology (Baltimore, Md.)|February 3, 2000
Treatment of Wilson's disease with zinc. XVII: treatment during pregnancyG J Brewer, V D Johnson, R D Dick, et al.American Journal of Human Genetics|February 11, 1999
Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8qP Hedera, S Rainier, D Alvarado, et al.Journal of Geriatric Psychiatry and Neurology|January 17, 2002
Ethical principles and pitfalls of genetic testing for dementiaP HederaPageof 12