Brin MF - Search Results

1

Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism.

Leung JC, Klein C, Friedman J, Vieregge P, Jacobs H, Doheny D, Kamm C, DeLeon D, Pramstaller PP, Penney JB, Eisengart M, Jankovic J, Gasser T, Bressman SB, Corey DP, Kramer P, Brin MF, Ozelius LJ, Breakefield XO. Leung JC, et al. Among authors: brin mf. Neurogenetics. 2001 Jul;3(3):133-43. doi: 10.1007/s100480100111. Neurogenetics. 2001. PMID: 11523564

2

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF, et al. Ozelius LJ, et al. Among authors: brin mf. Am J Hum Genet. 1992 Mar;50(3):619-28. Am J Hum Genet. 1992. PMID: 1347197 Free PMC article.

3

Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.

Schuback D, Kramer P, Ozelius L, Holmgren G, Forsgren L, Kyllerman M, Wahlström J, Craft CM, Nygaard T, Brin M, et al. Schuback D, et al. Hum Genet. 1991 Jul;87(3):311-6. doi: 10.1007/BF00200910. Hum Genet. 1991. PMID: 1677923

4

Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.

Kwiatkowski DJ, Nygaard TG, Schuback DE, Perman S, Trugman JM, Bressman SB, Burke RE, Brin MF, Ozelius L, Breakefield XO, et al. Kwiatkowski DJ, et al. Among authors: brin mf. Am J Hum Genet. 1991 Jan;48(1):121-8. Am J Hum Genet. 1991. PMID: 1985454 Free PMC article.

5

Delayed-onset dystonia due to perinatal or early childhood asphyxia.

Saint Hilaire MH, Burke RE, Bressman SB, Brin MF, Fahn S. Saint Hilaire MH, et al. Among authors: brin mf. Neurology. 1991 Feb;41(2 ( Pt 1)):216-22. doi: 10.1212/wnl.41.2_part_1.216. Neurology. 1991. PMID: 1992364

6

Therapeutic uses of botulinum toxin.

Jankovic J, Brin MF. Jankovic J, et al. Among authors: brin mf. N Engl J Med. 1991 Apr 25;324(17):1186-94. doi: 10.1056/NEJM199104253241707. N Engl J Med. 1991. PMID: 2011163 Review. No abstract available.

7

Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.

Risch NJ, Bressman SB, deLeon D, Brin MF, Burke RE, Greene PE, Shale H, Claus EB, Cupples LA, Fahn S. Risch NJ, et al. Among authors: brin mf. Am J Hum Genet. 1990 Mar;46(3):533-8. Am J Hum Genet. 1990. PMID: 2309703 Free PMC article.

8

Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.

Kramer PL, de Leon D, Ozelius L, Risch N, Bressman SB, Brin MF, Schuback DE, Burke RE, Kwiatkowski DJ, Shale H, et al. Kramer PL, et al. Among authors: brin mf. Ann Neurol. 1990 Feb;27(2):114-20. doi: 10.1002/ana.410270203. Ann Neurol. 1990. PMID: 2317008

9

Human gene for torsion dystonia located on chromosome 9q32-q34.

Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D, et al. Ozelius L, et al. Among authors: brin mf. Neuron. 1989 May;2(5):1427-34. doi: 10.1016/0896-6273(89)90188-8. Neuron. 1989. PMID: 2576373

10

Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance.

Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. Bressman SB, et al. Among authors: brin mf. Ann Neurol. 1989 Nov;26(5):612-20. doi: 10.1002/ana.410260505. Ann Neurol. 1989. PMID: 2817837

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