Suchergebnisse - "Goldfarb, L.G."

1

Genetic analysis of Creutzfeldt-Jakob disease and related disorders

von: Goldfarb, L.G.

1994, in: Philosophical transactions / B

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2

Genetic identification, clinical features and prevalence of Spinocerebellar ataxia type 1 in Sakha Republic (Yakutia)

von: Goldfarb L.G.

2020, in: Сибирские исследования

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3

SIX LECTURES ON THE PREVENTION OF ENCEPHALITIS EPIDEMICS IN SIBERIA

von: Goldfarb L.G.

2020, in: Сибирские исследования

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4

A.P.6

von: Guglieri, M.

2014transfer abstract, in: Sperm competition in golden cuttlefish

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5

Support of linkage of Gerstmann-Straussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter

von: Speer, M.C.

1991, in: Genomics

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6

Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy

von: Cervenáková, L.

1994, in: Proceedings of the National Academy of Sciences of the United States of America

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7

Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy (Correction)

von: Cervenáková, L.

1995, in: Proceedings of the National Academy of Sciences of the United States of America

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8

Global distribution of Fatal familial insomnia: founder or recurrent mutations

von: Lee, H.-S.

2008, in: Neurogenetics

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9

The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease

von: Brown, P.

1991, in: European journal of epidemiology

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10

Familial Creutzfeldt-Jakob disease in Finland: Epidemiological, clinical, pathological and molecular genetic studies

von: Haltia, M.

1991, in: European journal of epidemiology

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11

Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy

von: Maerkens, A.

2013transfer abstract, in: A second-order

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12

Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 families

von: Goldfarb, L. G.

1991, in: European journal of epidemiology

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13

New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses

von: Maerkens, A.

2016, in: Acta Neuropathologica Communications

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