UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 513

Sortiert nach

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

Nature genetics, 1994-06, Vol.7 (2), p.180-184

1994

Volltextzugriff (PDF)

Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5123), p.921-923

1993

Volltextzugriff (PDF)

Myotilin is mutated in limb girdle muscular dystrophy 1A

Human molecular genetics, 2000-09, Vol.9 (14), p.2141-2147

2000

Volltextzugriff (PDF)

Linkage studies in familial Alzheimer disease : evidence for chromosome 19 linkage

American journal of human genetics, 1991-06, Vol.48 (6), p.1034-1050

1991

Volltextzugriff (PDF)

Maternal lineages and Alzheimer disease risk in the Old Order Amish

Human genetics, 2005-11, Vol.118 (1), p.115-122

2005

Volltextzugriff (PDF)

An autosomal genomic screen for dementia in an extended Amish family

Neuroscience letters, 2005-05, Vol.379 (3), p.199-204

2005

Volltextzugriff (PDF)

Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease

Neurology, 1995-07, Vol.45 (7), p.1323

1995

Volltextzugriff (PDF)

Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus

Molecular psychiatry, 2006-03, Vol.11 (3), p.280-285

2006

Volltextzugriff (PDF)

Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation

Acta neuropathologica, 2000-08, Vol.100 (2), p.145-152

2000

Volltextzugriff (PDF)

Specificity, sensitivity, and predictive value of apolipoprotein-E genotyping for sporadic Alzheimer's disease

The Lancet (British edition), 1996-07, Vol.348 (9020), p.90-93

1996

Volltextzugriff (PDF)

Longitudinal follow-up of late-onset Alzheimer disease families

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-07, Vol.147B (5), p.571-578

2008

Volltextzugriff (PDF)

Linkage of frontotemporal dementia to chromosome 17 : Clinical and neuropathological characterization of phenotype

American journal of human genetics, 1996-12, Vol.59 (6), p.1306-1312

1996

Volltextzugriff (PDF)

Neuropathological Features of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17q21–22 (FTDP-17): Duke Family 1684

Journal of neuropathology and experimental neurology, 1999-08, Vol.58 (8), p.859-866

1999

Volltextzugriff (PDF)

Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease

Neurobiology of Aging, 1998, Vol.19 (1), p.S39-S42

1998

Volltextzugriff (PDF)

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.370-375

1993

Volltextzugriff (PDF)

Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugs

Neurobiology of aging, 1995, Vol.16 (4), p.523-530

1995

Volltextzugriff (PDF)

The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease

JAMA : the journal of the American Medical Association, 1995-02, Vol.273 (5), p.373

1995

Volltextzugriff (PDF)

Identification and Expression Analysis of Spastin Gene Mutations in Hereditary Spastic Paraplegia

American journal of human genetics, 2001-05, Vol.68 (5), p.1077-1085

2001

Volltextzugriff (PDF)

No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians

Neuroscience letters, 1996-05, Vol.209 (2), p.105-108

1996

Volltextzugriff (PDF)

Hereditary motor and sensory neuropathy, X-linked: a half century follow-up

Neurology, 1987-09, Vol.37 (9), p.1460

1987

Volltextzugriff (PDF)

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers

American journal of human genetics, 1991-03, Vol.48 (3), p.563-583

1991

Volltextzugriff (PDF)

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q

American journal of human genetics, 1992-06, Vol.50 (6), p.1211-1217

1992

Volltextzugriff (PDF)

Alzheimer's disease genes and genetic testing in clinical practice

JAAPA (Montvale, N.J.), 2004-03, Vol.17 (3), p.25

2004

Volltextzugriff (PDF)

Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

American journal of human genetics, 2006-08, Vol.79 (2), p.365-369

2006

Volltextzugriff (PDF)

1 – 25 von 513

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(445)
Mit Volltextzugriff
(473)

Publikationsform

Sprache

Englisch
(510)
Japanisch
(68)
Russisch
(2)

Erscheinungsjahr

n.n

Thema

Science & Technology
(300)
Life Sciences & Biomedicine
(129)
Physical Sciences
(125)
Humans
(103)
Physics
(97)
Female
(82)
Biological And Medical Sciences
(80)
Male
(77)
Medical Sciences
(64)
Exact Sciences And Technology
(61)
Technology
(59)
Animals
(50)
Neurology
(48)
Physics Of Elementary Particles And Fields
(47)
Astronomy & Astrophysics
(45)
Middle Aged
(36)
Nuclear Physics And Radiation Physics
(36)
Aged
(34)
Genetics & Heredity
(32)
Pedigree
(32)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families

Myotilin is mutated in limb girdle muscular dystrophy 1A

Linkage studies in familial Alzheimer disease : evidence for chromosome 19 linkage

Maternal lineages and Alzheimer disease risk in the Old Order Amish

An autosomal genomic screen for dementia in an extended Amish family

Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease

Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus

Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation

Specificity, sensitivity, and predictive value of apolipoprotein-E genotyping for sporadic Alzheimer's disease

Longitudinal follow-up of late-onset Alzheimer disease families

Linkage of frontotemporal dementia to chromosome 17 : Clinical and neuropathological characterization of phenotype

Neuropathological Features of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17q21–22 (FTDP-17): Duke Family 1684

Age at Onset in Two Common Neurodegenerative Diseases Is Genetically Controlled

Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugs

The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease

Identification and Expression Analysis of Spastin Gene Mutations in Hereditary Spastic Paraplegia

No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians

Hereditary motor and sensory neuropathy, X-linked: a half century follow-up

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q

Alzheimer's disease genes and genetic testing in clinical practice

Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

Suchergebnisse filtern