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Plasma high-density lipoproteins and ischemic heart disease: studies in a large kindred with familial hypercholesterolemia.
Linkage between phosphoglycerate kinase and Xg in a large German kindred.
The AD1 locus in familial Alzheimer disease.
A large kindred with autosomal dominant Parkinson's disease.
Cognitive Decline in a Colombian Kindred With Autosomal Dominant Alzheimer Disease: A Retrospective Cohort Study.
Familial pheochromocytoma: a report of 2 cases in a kindred.
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindred.
Alzheimer's disease: a model from the quantitative study of a large kindred.
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia.
Ankylosing spondylitis in a large kindred: clinical and genetic studies.
Idiopathic cholestasis of pregnancy in a large kindred.
Misleading phenotype in kindred with familial adenomatous polyposis.
Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease.
Lipidemia--a multigeneration predictability study.
Alois Alzheimer--Alzheimer disease.
A novel presenilin 1 mutation (Ala275Val) as cause of early-onset familial Alzheimer disease.
Converging approaches to understanding early onset familial Alzheimer disease: A First Nation study.
Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree.
A clinical and neurophysiological investigation of a Danish kindred with heterozygous familial hypobetalipoproteinemia.
Familial IgA nephropathy: a study of HLA class II allogenotypes in a Chinese kindred.
A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.
Familial Alzheimer disease: a large, multigeneration German kindred.
A German family with 21 members affected by Alzheimer disease (AD) was studied clinically and genetically. The diagnosis was histologically verified i...
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Plasma high-density lipoproteins and ischemic heart disease: studies in a large kindred with familial hypercholesterolemia.
Linkage between phosphoglycerate kinase and Xg in a large German kindred.
The AD1 locus in familial Alzheimer disease.
A large kindred with autosomal dominant Parkinson's disease.
Cognitive Decline in a Colombian Kindred With Autosomal Dominant Alzheimer Disease: A Retrospective Cohort Study.
Familial pheochromocytoma: a report of 2 cases in a kindred.
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
A novel transthyretin variant p.H110D (H90D) as a cause of familial amyloid polyneuropathy in a large Irish kindred.
Alzheimer's disease: a model from the quantitative study of a large kindred.
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