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Neurology|January 1, 1983
Lipomembranous polycystic osteodysplasia (brain, bone, and fat disease): a genetic cause of presenile dementiaT D Bird, R M Koerker, B J Leaird, et al.
Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.
Urological Research|January 1, 1987
Urothelial carcinogenesis and portocaval anastomosis in the ratD M Wallace, D Ackermann, B Davis, et al.
Biological Psychiatry|January 15, 1997
The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tanglesD Tsuang, M A Raskind, J Leverenz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1990
Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxiaS R Hamilton, G E Chatrian, R P Mills, et al.
American Journal of Human Genetics|December 1, 1990
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)P F Chance, T D Bird, P O'Connell, et al.
Neurology|March 27, 2002
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS Zareparsi, D M James, J A Kaye, et al.
Annals of Neurology|January 1, 1997
Amyloid (Abeta) deposition in chromosome 1-linked Alzheimer's disease: the Volga German familiesD M Mann, T Iwatsubo, D Nochlin, et al.
The Journal of Laboratory and Clinical Medicine|March 1, 1976
Extracorporeal treatment with cyanate in sickle cell disease: preliminary observations in four patientsE E Langer, G Stamatoyannopoulos, M P Hlastala, et al.
British Journal of Urology|November 1, 1992
Urologists' attitudes to the management of bladder cancerT H Lynch, B Waymont, J A Dunn, et al.
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