Johnson WG - Search Results

1

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Farrer M, et al. Among authors: johnson wg. Ann Neurol. 1998 Mar;43(3):394-7. doi: 10.1002/ana.410430320. Ann Neurol. 1998. PMID: 9506559

2

Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.

Hardy J, Pérez-Tur J, Baker M, Farrer M, Crook R, Hutton M, Johnson WG, Gwinn K, Muenter M, Rocca WA, Maraganore D. Hardy J, et al. Among authors: johnson wg. Am J Med Genet. 1998 Mar 28;81(2):166-71. Am J Med Genet. 1998. PMID: 9613857

3

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

Vaughan J, Durr A, Tassin J, Bereznai B, Gasser T, Bonifati V, De Michele G, Fabrizio E, Volpe G, Bandmann O, Johnson WG, Golbe LI, Breteler M, Meco G, Agid Y, Brice A, Marsden CD, Wood NW. Vaughan J, et al. Among authors: johnson wg. Ann Neurol. 1998 Aug;44(2):270-3. doi: 10.1002/ana.410440221. Ann Neurol. 1998. PMID: 9708553

4

A clinical genetic study of Parkinson's disease: evidence for dominant transmission.

Lazzarini AM, Myers RH, Zimmerman TR Jr, Mark MH, Golbe LI, Sage JI, Johnson WG, Duvoisin RC. Lazzarini AM, et al. Among authors: johnson wg. Neurology. 1994 Mar;44(3 Pt 1):499-506. doi: 10.1212/wnl.44.3_part_1.499. Neurology. 1994. PMID: 8145922

5

No evidence for association of familial Parkinson's disease with CAG repeat expansion.

Carĕro-Valenzuela R, Lindblad K, Payami H, Johnson W, Schalling M, Stenroos ES, Shattuc S, Nutt J, Brice A, Litt M. Carĕro-Valenzuela R, et al. Neurology. 1995 Sep;45(9):1760-3. doi: 10.1212/wnl.45.9.1760. Neurology. 1995. PMID: 7675242

6

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

Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL. Polymeropoulos MH, et al. Among authors: johnson wg. Science. 1997 Jun 27;276(5321):2045-7. doi: 10.1126/science.276.5321.2045. Science. 1997. PMID: 9197268

7

Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility.

Majoor-Krakauer D, Ottman R, Johnson WG, Rowland LP. Majoor-Krakauer D, et al. Among authors: johnson wg. Neurology. 1994 Oct;44(10):1872-7. doi: 10.1212/wnl.44.10.1872. Neurology. 1994. PMID: 7936240

8

Genetic susceptibility to Parkinson's disease.

Johnson WG. Johnson WG. Neurology. 1991 May;41(5 Suppl 2):82-7; discussion 88. doi: 10.1212/wnl.41.5_suppl_2.82. Neurology. 1991. PMID: 2041600 Review.

9

Glutathione S-transferase polymorphisms and onset age in alpha-synuclein A53T mutant Parkinson's disease.

Golbe LI, Di Iorio G, Markopoulou K, Athanassiadou A, Papapetropoulos S, Watts RL, Vance JM, Bonifati V, Williams TA, Spychala JR, Stenroos ES, Johnson WG. Golbe LI, et al. Among authors: johnson wg. Am J Med Genet B Neuropsychiatr Genet. 2007 Mar 5;144B(2):254-8. doi: 10.1002/ajmg.b.30450. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17034008

10

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.

Lazzarini A, Zimmerman TR Jr, Johnson WG, Duvoisin RC. Lazzarini A, et al. Among authors: johnson wg. Neurology. 1992 Nov;42(11):2118-24. doi: 10.1212/wnl.42.11.2118. Neurology. 1992. PMID: 1436521

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