Pericak-Vance MA - Search Results

1

Apolipoprotein E controls the risk and age at onset of Parkinson disease.

Li YJ, Hauser MA, Scott WK, Martin ER, Booze MW, Qin XJ, Walter JW, Nance MA, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Goetz CG, Small GW, Mastaglia F, Haines JL, Pericak-Vance MA, Vance JM. Li YJ, et al. Neurology. 2004 Jun 8;62(11):2005-9. doi: 10.1212/01.wnl.0000128089.53030.ac. Neurology. 2004. PMID: 15184605

2

Genetic linkage studies in Huntington disease.

Pericak-Vance MA, Conneally PM, Merritt AD, Roos R, Norton JA Jr, Vance JM. Pericak-Vance MA, et al. Cytogenet Cell Genet. 1978;22(1-6):640-5. doi: 10.1159/000131042. Cytogenet Cell Genet. 1978. PMID: 156628 No abstract available.

3

Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

Pritchard C, Zhu N, Zuo J, Bull L, Pericak-Vance MA, Vance JM, Roses AD, Milatovich A, Francke U, Cox DR, et al. Pritchard C, et al. Am J Hum Genet. 1992 Jun;50(6):1218-30. Am J Hum Genet. 1992. PMID: 1350884 Free PMC article.

4

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

5

North Carolina macular dystrophy is assigned to chromosome 6.

Small KW, Weber JL, Roses A, Lennon F, Vance JM, Pericak-Vance MA. Small KW, et al. Genomics. 1992 Jul;13(3):681-5. doi: 10.1016/0888-7543(92)90141-e. Genomics. 1992. PMID: 1639395

6

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

7

Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.

Alberts MJ, Pericak-Vance MA, Royal V, Bebout J, Gaskell P, Thomas J, Hung WY, Clark C, Earl N, Roses AD. Alberts MJ, et al. Ann Neurol. 1991 Aug;30(2):216-9. doi: 10.1002/ana.410300217. Ann Neurol. 1991. PMID: 1680304

8

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

9

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

10

Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.

Yamaoka LH, Pericak-Vance MA, Speer MC, Gaskell PC Jr, Stajich J, Haynes C, Hung WY, Laberge C, Thibault MC, Mathieu J, et al. Yamaoka LH, et al. Neurology. 1990 Feb;40(2):222-6. doi: 10.1212/wnl.40.2.222. Neurology. 1990. PMID: 2300239

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