Stajich JM - Search Results

1

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. Damji KF, et al. Among authors: stajich jm. Arch Neurol. 1996 Apr;53(4):338-44. doi: 10.1001/archneur.1996.00550040074016. Arch Neurol. 1996. PMID: 8929156 Review.

2

Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.

Speer MC, Pericak-Vance MA, Yamaoka L, Hung WY, Ashley A, Stajich JM, Roses AD. Speer MC, et al. Among authors: stajich jm. Neurology. 1990 Apr;40(4):671-6. doi: 10.1212/wnl.40.4.671. Neurology. 1990. PMID: 2320244

3

Ocular motility in North Carolina autosomal dominant ataxia.

Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M. Small KW, et al. Among authors: stajich jm. J Neuroophthalmol. 1996 Jun;16(2):91-5. doi: 10.3109/01658109609009667. J Neuroophthalmol. 1996. PMID: 8797163

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. Among authors: stajich j. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

5

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

6

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.

Oliveira SA, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons KE, Pahwa R, Stern MB, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Scott BL, Goetz CG, Small GW, Mastaglia FL, Stajich JM, Zhang F, Booze MW, Reaves JA, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM, Martin ER. Oliveira SA, et al. Among authors: stajich jm. Arch Neurol. 2003 Jul;60(7):975-80. doi: 10.1001/archneur.60.7.975. Arch Neurol. 2003. PMID: 12873854

7

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS, et al. Speer MC, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Jun;50(6):1211-7. Am J Hum Genet. 1992. PMID: 1598902 Free PMC article.

8

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Among authors: stajich jm. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

9

Confirmation of linkage in von Hippel-Lindau disease.

Vance JM, Small KW, Jones MA, Stajich JM, Yamaoka LH, Roses AD, Hung WY, Pericak-Vance MA. Vance JM, et al. Among authors: stajich jm. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994

10

Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.

Yamaoka LH, Westbrook CA, Speer MC, Gilchrist JM, Jabs EW, Schweins EG, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA. Yamaoka LH, et al. Among authors: stajich jm. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):471-5. doi: 10.1016/0960-8966(94)90086-8. Neuromuscul Disord. 1994. PMID: 7881291

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