A. Lazzarini

发表

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

M. Polymeropoulos, R. Nussbaum, J. Higgins, 1996, Science.

Trinucleotide repeat length instability and age of onset in Huntington's disease

J. Penney, S. Folstein, A. Falek, 1993, Nature Genetics.

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Robert L. Nussbaum, Giuseppe Di Iorio, William G. Johnson, 1997 .

A psychometric study of children at‐risk for Huntington disease

A. Lazzarini, M. C. Catona, M. McCormack, 1985, Clinical genetics.

Studies of penetrance and anticipation in five autosomal‐dominant restless legs syndrome pedigrees

M. Brin, A. Walters, B. Ehrenberg, 1999, Movement disorders : official journal of the Movement Disorder Society.

Gerstmann‐Sträussler‐Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

D. Dickson, B. Ghetti, S. Perlman, 1995, Neurology.

Fighting dragons: The construction of explanatory systems in genetic disease.

A. Lazzarini, E. Phipps, 1987 .

PATTERNS OF REPRODUCTION FOR PEOPLE AT RISK FOR HUNTINGTON'S DISEASE

A. Lazzarini, M. McCormack, 1982, The Lancet.

Attitudes of those at risk for Huntington's disease toward presymptomatic provocative testing.

A. Lazzarini, M. McCormack, 1982, The New England journal of medicine.

Variable expressivity in familial restless legs syndrome.

A. Walters, W. Hening, A. Lazzarini, 1990, Archives of neurology.

Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis

Kobert S. Schwartz, W. Brown, W. Johnson, 1998, Annals of neurology.

The Contursi kindred, a large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies.

P. Vieregge, L. Golbe, A. Lazzarini, 1999, Advances in neurology.

Gerstmann-Sträussler-Scheinker Disease (PRNP P102L): Amyloid Deposits Are Best Recognized by Antibodies Directed to Epitopes in PrP Region 90-165

P. S. St George-Hyslop, D. Dickson, B. Ghetti, 1995, Journal of neuropathology and experimental neurology.

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

S E Ide, A. Dehejia, M. Polymeropoulos, 1997, Science.

A genetic study of red cell osmotic fragility in Huntington's disease.

D. Toke, A. Lazzarini, M. McCormack, 1984, American journal of medical genetics.

Pelizaeus-Merzbacher-like disease: Exclusion of the proteolipid protein locus and documentation of a new locus on Xq

T. Lehner, W. Johnson, E. Stenroos, 1997, Neurology.

A haplotype at the PARK3 locus influences onset age for Parkinson’s disease

J. Growdon, C. Singer, M. Stacy, 2003, Neurology.

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

J. Gusella, W. Koroshetz, J. Vonsattel, 1993, Nature genetics.

A clinical genetic study of Parkinson's disease

L. Golbe, W. Johnson, A. Lazzarini, 1994, Neurology.

Autosomal dominant parkinsonism with benign course and typical Lewy-body pathology.

D. Dickson, L. Golbe, A. Lazzarini, 1993, Neurology.

Attitudes regarding utilization of artificial insemination by donor in Huntington disease.

A. Lazzarini, S. Leiblum, M. McCormack, 1983, American journal of medical genetics.

A low frequency mosaicism for monosomy 21 in a live born female

A. Lazzarini, L. Sciorra, B. Rajendra, 1979, Human Genetics.

Clinical genetic analysis of Parkinson's disease in the contursi kindred

L. Golbe, G. Iorio, G. Sanges, 1996, Annals of neurology.

Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study

Jane S. Paulsen, T. Gillis, J. Mysore, 2006, BMC Medical Genetics.

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.

A. Desautels, A. Walters, B. Ehrenberg, 2005, Archives of neurology.

Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).

J. Ott, T. Lehner, B. Gold, 1995, American journal of medical genetics.

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.

M. MacDonald, J. Growdon, J. Gusella, 2002, American journal of human genetics.

Segregation analysis of Parkinson disease revealing evidence for a major causative gene.

J. Wilk, G. Wooten, L. Golbe, 2002, American journal of medical genetics.

Genome-wide scan for Parkinson's disease: the GenePD Study.

J. Growdon, J. Hubble, C. Singer, 2001, Neurology.

The tau A0 allele in Parkinson's disease

L. Golbe, W. Johnson, E. Stenroos, 2001, Movement disorders : official journal of the Movement Disorder Society.

Altered red cell osmotic fragility in Huntington disease (HD).

A. Lazzarini, M. McCormack, J. Ullman, 1982, American journal of medical genetics.

Reduced fecundity in male ALS gene-carriers.

W. Johnson, A. Lazzarini, S. Chatkupt, 1995, American journal of medical genetics.

Epidemiologic study of 203 sibling pairs with Parkinson’s disease

J. Growdon, J. Hubble, C. Singer, 2002, Neurology.

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ‐1 (T497C) genes in familial Parkinson's disease from the GenePD study

Mark Guttman, R H Myers, P P Pramstaller, 2005, Movement disorders : official journal of the Movement Disorder Society.

A 17th-century founder gives rise to a large North American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6

W. Johnson, A. Lazzarini, R. Duvoisin, 1992, Neurology.

Genome-wide scan for Parkinson's disease

M. MacDonald, J. Growdon, J. Hubble, 2001, Neurology.