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Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Variable phenotype of rapid-onset dystonia-parkinsonismA Brashear, M R Farlow, I J Butler, et al.Molecular Medicine Today|June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosisR J Leventer, D T Pilz, N Matsumoto, et al.American Journal of Medical Genetics|September 24, 1999
X-linked lissencephaly with absent corpus callosum and ambiguous genitaliaW B Dobyns, E Berry-Kravis, N J Havernick, et al.American Journal of Medical Genetics|December 14, 1999
Familial lissencephaly with cleft palate and severe cerebellar hypoplasiaB Kerner, J M Graham, J A Golden, et al.American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.Metabolism: Clinical and Experimental|November 1, 1986
Glucose intolerance in Friedreich's ataxia: association with insulin resistance and decreased insulin bindingR J Khan, E Andermann, I G FantusThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Electroencephalographic findings in Friedreich's ataxiaG Remillard, F Andermann, L Blitzer, et al.Annals of Neurology|September 1, 1980
An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremorB Zifkin, E Andermann, F Andermann, et al.The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Evidence for abnormal regulation of insulin receptors in Friedreich's ataxiaI G Fantus, M H Seni, E AndermannNeurology|April 1, 1992
Mechanisms of teratogenesis: folic acid and antiepileptic therapyL V Dansky, D S Rosenblatt, E AndermannPageof 64