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Neuroscience Letters|November 25, 1991

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequenceF Crawford, J Hardy, M Mullan, et al.

Nature Genetics|December 1, 1992

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin geneM Mullan, H Houlden, M Windelspecht, et al.

American Journal of Medical Genetics|February 27, 1995

Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causativeC Bennett, F Crawford, A Osborne, et al.

Journal of the Neurological Sciences|February 1, 1993

Genetic characterization of a familial non-specific dementia originating in Jutland, DenmarkJ Brown, S Gydesen, S A Sorensen, et al.

Human Molecular Genetics|June 1, 1992

Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->IleL Fidani, K Rooke, M C Chartier-Harlin, et al.

Practical Neurology|December 13, 2016

Leprosy in a patient infected with HIVClare M Galtrey, Hamid Modarres, Zane Jaunmuktane, et al.

Neurology|December 1, 2017

Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.

American Journal of Medical Genetics|March 26, 1998

ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease familiesH Houlden, R Crook, H Backhovens, et al.

Nature|October 31, 1991

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein geneM C Chartier-Harlin, F Crawford, H Houlden, et al.

Journal of the Peripheral Nervous System : JPNS|October 5, 2019

Plasma neurofilament light chain concentration is increased and correlates with the severity of neuropathy in hereditary transthyretin amyloidosisMahima Kapoor, Martha Foiani, Amanda Heslegrave, et al.

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Showing results (71-80 of 149) with videos related to

Sort By:

Pageof 15

Neuroscience Letters|November 25, 1991

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequenceF Crawford, J Hardy, M Mullan, et al.

Nature Genetics|December 1, 1992

A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin geneM Mullan, H Houlden, M Windelspecht, et al.

American Journal of Medical Genetics|February 27, 1995

Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causativeC Bennett, F Crawford, A Osborne, et al.

Journal of the Neurological Sciences|February 1, 1993

Genetic characterization of a familial non-specific dementia originating in Jutland, DenmarkJ Brown, S Gydesen, S A Sorensen, et al.

Human Molecular Genetics|June 1, 1992

Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->IleL Fidani, K Rooke, M C Chartier-Harlin, et al.

Practical Neurology|December 13, 2016

Leprosy in a patient infected with HIVClare M Galtrey, Hamid Modarres, Zane Jaunmuktane, et al.

Neurology|December 1, 2017

Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.

American Journal of Medical Genetics|March 26, 1998

ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease familiesH Houlden, R Crook, H Backhovens, et al.

Nature|October 31, 1991

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein geneM C Chartier-Harlin, F Crawford, H Houlden, et al.

Journal of the Peripheral Nervous System : JPNS|October 5, 2019

Plasma neurofilament light chain concentration is increased and correlates with the severity of neuropathy in hereditary transthyretin amyloidosisMahima Kapoor, Martha Foiani, Amanda Heslegrave, et al.

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