P01 NS 26630/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1990	1
1991	3
1992	1
1993	2
1995	1
2002	2
2005	1
2025	0

1

Hereditary motor and sensory neuropathies.

Vance JM. Vance JM. J Med Genet. 1991 Jan;28(1):1-5. doi: 10.1136/jmg.28.1.1. J Med Genet. 1991. PMID: 1999826 Free PMC article. Review. No abstract available.

2

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. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

3

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Pericak-Vance MA, Bebout JL, Gaskell PC Jr, Yamaoka LH, Hung WY, Alberts MJ, Walker AP, Bartlett RJ, Haynes CA, Welsh KA, et al. Pericak-Vance MA, et al. Am J Hum Genet. 1991 Jun;48(6):1034-50. Am J Hum Genet. 1991. PMID: 2035524 Free PMC article.

4

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).

Reid E, Kloos M, Ashley-Koch A, Hughes L, Bevan S, Svenson IK, Graham FL, Gaskell PC, Dearlove A, Pericak-Vance MA, Rubinsztein DC, Marchuk DA. Reid E, et al. Am J Hum Genet. 2002 Nov;71(5):1189-94. doi: 10.1086/344210. Epub 2002 Sep 24. Am J Hum Genet. 2002. PMID: 12355402 Free PMC article.

5

Nicotinic neuronal acetylcholine receptor alpha-3 subunit transcription in normal and myasthenic thymus.

Mihovilovic M, Hulette C, Mittelstaedt J, Austin C, Roses AD. Mihovilovic M, et al. Ann N Y Acad Sci. 1993 Jun 21;681:83-96. doi: 10.1111/j.1749-6632.1993.tb22872.x. Ann N Y Acad Sci. 1993. PMID: 8357212

6

Age at onset in two common neurodegenerative diseases is genetically controlled.

Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA Jr, Goetz CG, Mastaglia F, Stajich JM, Gibson RA, Middleton LT, Saunders AM, Scott BL, Small GW, Nicodemus KK, Reed AD, Schmechel DE, Welsh-Bohmer KA, Conneally PM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Li YJ, et al. Am J Hum Genet. 2002 Apr;70(4):985-93. doi: 10.1086/339815. Epub 2002 Mar 1. Am J Hum Genet. 2002. PMID: 11875758 Free PMC article.

7

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

8

Expression of mRNAs in human thymus coding for the alpha 3 subunit of a neuronal acetylcholine receptor.

Mihovilovic M, Roses AD. Mihovilovic M, et al. Exp Neurol. 1991 Feb;111(2):175-80. doi: 10.1016/0014-4886(91)90004-v. Exp Neurol. 1991. PMID: 1989896

9

Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val-->Ile mutation in the amyloid precursor protein gene.

Mullan M, Tsuji S, Miki T, Katsuya T, Naruse S, Kaneko K, Shimizu T, Kojima T, Nakano I, Ogihara T, et al. Mullan M, et al. Neurobiol Aging. 1993 Sep-Oct;14(5):407-19. doi: 10.1016/0197-4580(93)90099-w. Neurobiol Aging. 1993. PMID: 8247223

10

Accelerated head growth in early development of individuals with autism.

Dementieva YA, Vance DD, Donnelly SL, Elston LA, Wolpert CM, Ravan SA, DeLong GR, Abramson RK, Wright HH, Cuccaro ML. Dementieva YA, et al. Pediatr Neurol. 2005 Feb;32(2):102-8. doi: 10.1016/j.pediatrneurol.2004.08.005. Pediatr Neurol. 2005. PMID: 15664769

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