Nitin D. Mehta

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

Robert Clark, M. Hutton, M. Fuldner et al. · Nature Genetics · 1995 · 470 citations

Allelic Variant, Genetic Disorder, Genetics +7

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Richard Crook, Auli Verkkoniemi, Jordi Pérez‐Tur et al. · Nature Medicine · 1998 · 346 citations

Unusual Plaques, Alzheimer's Disease, Creutzfeldt-jakob Disease +10

Widespread Alterations of α-Synuclein in Multiple System Atrophy

Dennis W. Dickson, W.-K. Liu, John Hardy et al. · American Journal Of Pathology · 1999 · 304 citations · Full text

Neurodegenerative Diseases, Degenerative Diseases, Multiple System Atrophy +7

A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A 42(43)

Chris Eckman, Nitin D. Mehta, Richard Crook et al. · Human Molecular Genetics · 1997 · 227 citations · Full text

Distinctive neuropathology revealed by α-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p

Katrina Gwinn, Nitin D. Mehta, Matthew J. Farrer et al. · Acta Neuropathologica · 2000 · 174 citations

Neurodegenerative Diseases, Distinctive Neuropathology, Hereditary Parkinsonism +13