Boustany RM - Search Results

1

Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.

Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL, et al. Speer MC, et al. Among authors: boustany rm. Am J Med Genet. 1995 Aug 14;60(4):307-11. doi: 10.1002/ajmg.1320600409. Am J Med Genet. 1995. PMID: 7485266

2

Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.

Svenson IK, Ashley-Koch AE, Gaskell PC, Riney TJ, Cumming WJ, Kingston HM, Hogan EL, Boustany RM, Vance JM, Nance MA, Pericak-Vance MA, Marchuk DA. Svenson IK, et al. Among authors: boustany rm. Am J Hum Genet. 2001 May;68(5):1077-85. doi: 10.1086/320111. Epub 2001 Apr 16. Am J Hum Genet. 2001. PMID: 11309678 Free PMC article.

3

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.

Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA. Ashley-Koch A, et al. Among authors: boustany rm. Neurogenetics. 2001 Mar;3(2):91-7. doi: 10.1007/s100480000098. Neurogenetics. 2001. PMID: 11354831

4

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.

Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S, et al. Hentati A, et al. Among authors: boustany rm. Hum Mol Genet. 1994 Oct;3(10):1867-71. doi: 10.1093/hmg/3.10.1867. Hum Mol Genet. 1994. PMID: 7849714

5

Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.

Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA. Scott WK, et al. Among authors: boustany rm. Neurogenetics. 1997 Sep;1(2):95-102. doi: 10.1007/s100480050014. Neurogenetics. 1997. PMID: 10732810

6

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Hentati A, et al. Among authors: boustany rm. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

7

Role of subunit-9 of mitochondrial ATP synthase in Batten disease.

Johnson DW, Speier S, Qian WH, Lane S, Cook A, Suzuki K, Daniel P, Boustany RM. Johnson DW, et al. Among authors: boustany rm. Am J Med Genet. 1995 Jun 5;57(2):350-60. doi: 10.1002/ajmg.1320570250. Am J Med Genet. 1995. PMID: 7668362

8

Neurology of the neuronal ceroid-lipofuscinoses: late infantile and juvenile types.

Boustany RM. Boustany RM. Am J Med Genet. 1992 Feb 15;42(4):533-5. doi: 10.1002/ajmg.1320420421. Am J Med Genet. 1992. PMID: 1609833 Review.

9

Linkage analysis in juvenile neuronal ceroid lipofuscinosis.

Haines JL, Yan WL, Boustany RM, Jewell A, Julier C, Breakefield XO, Gusella JF. Haines JL, et al. Among authors: boustany rm. Am J Med Genet. 1992 Feb 15;42(4):542-5. doi: 10.1002/ajmg.1320420424. Am J Med Genet. 1992. PMID: 1609835

10

Genome-wide search for CLN2, the gene causing late-infantile neuronal ceroid-lipofuscinosis (LNCL).

Haines JL, Boustany RM, Worster T, Ter-Minassian M, Jondro P, Lerner TJ. Haines JL, et al. Among authors: boustany rm. Am J Med Genet. 1995 Jun 5;57(2):344-7. doi: 10.1002/ajmg.1320570248. Am J Med Genet. 1995. PMID: 7668360

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