Wilhelmsen KC - Search Results

1

Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32.

Morse JH, Jones AC, Barst RJ, Hodge SE, Wilhelmsen KC, Nygaard TG. Morse JH, et al. Among authors: wilhelmsen kc. Circulation. 1997 Jun 17;95(12):2603-6. doi: 10.1161/01.cir.95.12.2603. Circulation. 1997. PMID: 9193425

2

Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.

Nygaard TG, Wilhelmsen KC, Risch NJ, Brown DL, Trugman JM, Gilliam TC, Fahn S, Weeks DE. Nygaard TG, et al. Among authors: wilhelmsen kc. Nat Genet. 1993 Dec;5(4):386-91. doi: 10.1038/ng1293-386. Nat Genet. 1993. PMID: 8298648

3

Familial primary pulmonary hypertension locus mapped to chromosome 2q31-q32.

Morse JH, Jones AC, Barst RJ, Hodge SE, Wilhelmsen KC, Nygaard TG. Morse JH, et al. Among authors: wilhelmsen kc. Chest. 1998 Jul;114(1 Suppl):57S-58S. doi: 10.1378/chest.114.1_supplement.57s. Chest. 1998. PMID: 9676630 Free article. No abstract available.

4

Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome.

Wilhelmsen KC, Weeks DE, Nygaard TG, Moskowitz CB, Rosales RL, dela Paz DC, Sobrevega EE, Fahn S, Gilliam TC. Wilhelmsen KC, et al. Ann Neurol. 1991 Feb;29(2):124-31. doi: 10.1002/ana.410290203. Ann Neurol. 1991. PMID: 1672807

5

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG. Wilhelmsen KC, et al. Am J Hum Genet. 1994 Dec;55(6):1159-65. Am J Hum Genet. 1994. PMID: 7977375 Free PMC article.

6

Characterization of microsatellite polymorphisms DXS691 and DXS692: genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2.

Lasser DM, Wilhelmsen KC, Nygaard TG, Tantravahi U. Lasser DM, et al. Among authors: wilhelmsen kc. Genomics. 1993 Jun;16(3):785-6. doi: 10.1006/geno.1993.1269. Genomics. 1993. PMID: 8325656 Free article. No abstract available.

7

A high-resolution genetic linkage map of the pericentromeric region of the human X chromosome.

Weeks DE, Nygaard TG, Neystat M, Harby LD, Wilhelmsen KC. Weeks DE, et al. Among authors: wilhelmsen kc. Genomics. 1995 Mar 1;26(1):39-46. doi: 10.1016/0888-7543(95)80080-6. Genomics. 1995. PMID: 7782084 Free article.

8

Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women.

Waters CH, Takahashi H, Wilhelmsen KC, Shubin R, Snow BJ, Nygaard TG, Moskowitz CB, Fahn S, Calne DB. Waters CH, et al. Among authors: wilhelmsen kc. Neurology. 1993 Aug;43(8):1555-8. doi: 10.1212/wnl.43.8.1555. Neurology. 1993. PMID: 8351010

9

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.

Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC. Lynch T, et al. Among authors: wilhelmsen kc. Neurology. 2001 Nov;57(10 Suppl 3):S39-45. Neurology. 2001. PMID: 11775599 No abstract available.

10

Molecular genetic analysis of Lubag.

Wilhelmsen KC, Moskowitz CB, Weeks DE, Neystat M, Nygaard TG, Clark L, Dancoup M, Sobrevega EE, Rosales R, Gamez GL, Pacioles O, Perez M, Fahn S. Wilhelmsen KC, et al. Adv Neurol. 1998;78:341-8. Adv Neurol. 1998. PMID: 9750931 No abstract available.

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