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Why I joined the research laboratory of Prof. D. Carleton Gajdusek in 1968

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2008-11, Vol.363 (1510), p.3631

Cathala, Françoise

2008

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Natural and Experimental Oral Infection of Nonhuman Primates by Bovine Spongiform Encephalopathy Agents

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (7), p.4046-4051

1999

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Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases

Annals of neurology, 1986-11, Vol.20 (5), p.597-602

1986

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Creutzfeldt-Jakob disease of long duration: Clinicopathological characteristics, transmissibility, and differential diagnosis

Annals of neurology, 1984-09, Vol.16 (3), p.295-304

1984

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High incidence of Creutzfeldt-Jakob disease in North African immigrants to France

Neurology, 1985-06, Vol.35 (6), p.894

1985

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Epidemiologic comparisons between Creutzfeldt-Jakob disease and scrapie in France during the 12-year period 1968–1979

Journal of the neurological sciences, 1981-09, Vol.51 (3), p.329-337

1981

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Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

Annals of neurology, 1992-03, Vol.31 (3), p.274-281

1992

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Cluster of Creutzfeldt-Jakob disease in France associated with the codon 200 mutation (E200K) in the prion protein gene

European journal of neurology, 1998-07, Vol.5 (4), p.375-379

1998

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An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

Journal of the neurological sciences, 1992-09, Vol.111 (2), p.189-194

1992

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The molecular genetics of familial Creutzfeldt-Jakob disease in France

Journal of the neurological sciences, 1991-10, Vol.105 (2), p.240-246

1991

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Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977

Annals of neurology, 1979-11, Vol.6 (5), p.430-437

1979

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Phenotypic characteristics of familial Creutzfeldt‐Jakob disease assoicated with the codon 178 Asn PRNP mutation

Annals of neurology, 1992-03, Vol.31 (3), p.282-285

1992

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Mycobacterial and fungal skin sensitivity patterns among remote population groups in Papua New Guinea, and in the New Hebrides, Solomon, and Caroline Islands

The American journal of tropical medicine and hygiene, 1981-09, Vol.30 (5), p.1085

1981

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THE QUESTION OF CLUSTERING OF CREUTZFELDT-JAKOB DISEASE

American journal of epidemiology, 1989-01, Vol.129 (1), p.146-154

1989

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Creutzfeldt-Jakob disease in France: I. Retrospective study of the Paris area during the ten-year period 1968-1977

Annals of neurology, 1979-02, Vol.5 (2), p.189-192

1979

Volltextzugriff (PDF)

Phenotypic characteristics of familial Creutzfeldt-Jakob disease assoicated with the codon 178Asn PRNP mutation

Annals of neurology, 1992-03, Vol.31 (3), p.282-285

1992

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Transmission of Creutzfeldt-Jakob disease from formalin-fixed, paraffin-embedded human brain tissue

The New England journal of medicine, 1986-12, Vol.315 (25), p.1614

1986

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Biologic distinction between sporadic and familial Alzheimer disease by an in vitro cell fusion test

Neurology, 1981-03, Vol.31 (3), p.323

1981

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Serum antibodies to neurofilament antigens in patients with neurological and other diseases and in healthy controls

Journal of neuroimmunology, 1983-10, Vol.5 (2), p.191-196

1983

Volltextzugriff (PDF)

Creutzfeldt‐Jakob disease cosegregates with the codon 178 Asn PRNP mutation in families of European origin

Annals of neurology, 1992-03, Vol.31 (3), p.274-281

1992

Volltextzugriff (PDF)

Correlation between population density and the frequency of Creutzfeldt-Jakob disease in France

Journal of the neurological sciences, 1983-01, Vol.60 (1), p.169-176

1983

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Spread of scrapie agent to the central nervous system: study of a rat model

Brain research, 1986-09, Vol.383 (1), p.397-401

1986

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Scrapie in France

Journal of the American Veterinary Medical Association, 1990-05, Vol.196 (10), p.1680

Cathala, F

1990

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Scrapie in France: Some possible predisposing factors in the naturally-acquired disease of sheep

Veterinary microbiology, 1983-01, Vol.8 (5), p.511-515

1983

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Familial Creutzfeldt-Jakob disease

Journal of the neurological sciences, 1980-09, Vol.47 (3), p.343-351

1980

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Why I joined the research laboratory of Prof. D. Carleton Gajdusek in 1968

Natural and Experimental Oral Infection of Nonhuman Primates by Bovine Spongiform Encephalopathy Agents

Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases

Creutzfeldt-Jakob disease of long duration: Clinicopathological characteristics, transmissibility, and differential diagnosis

High incidence of Creutzfeldt-Jakob disease in North African immigrants to France

Epidemiologic comparisons between Creutzfeldt-Jakob disease and scrapie in France during the 12-year period 1968–1979

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

Cluster of Creutzfeldt-Jakob disease in France associated with the codon 200 mutation (E200K) in the prion protein gene

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

The molecular genetics of familial Creutzfeldt-Jakob disease in France

Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977

Phenotypic characteristics of familial Creutzfeldt‐Jakob disease assoicated with the codon 178 Asn PRNP mutation

Mycobacterial and fungal skin sensitivity patterns among remote population groups in Papua New Guinea, and in the New Hebrides, Solomon, and Caroline Islands

THE QUESTION OF CLUSTERING OF CREUTZFELDT-JAKOB DISEASE

Creutzfeldt-Jakob disease in France: I. Retrospective study of the Paris area during the ten-year period 1968-1977

Phenotypic characteristics of familial Creutzfeldt-Jakob disease assoicated with the codon 178Asn PRNP mutation

Transmission of Creutzfeldt-Jakob disease from formalin-fixed, paraffin-embedded human brain tissue

Biologic distinction between sporadic and familial Alzheimer disease by an in vitro cell fusion test

Serum antibodies to neurofilament antigens in patients with neurological and other diseases and in healthy controls

Creutzfeldt‐Jakob disease cosegregates with the codon 178 Asn PRNP mutation in families of European origin

Correlation between population density and the frequency of Creutzfeldt-Jakob disease in France

Spread of scrapie agent to the central nervous system: study of a rat model

Scrapie in France

Scrapie in France: Some possible predisposing factors in the naturally-acquired disease of sheep

Familial Creutzfeldt-Jakob disease

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