Familial Alzheimer disease: a large, multigeneration German kindred.

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.

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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.

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