Rainier S - Search Results

1

Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM.

Rainier S, Hedera P, Alvarado D, Zhao X, Kleopa KA, Heiman-Patterson T, Fink JK. Rainier S, et al. J Med Genet. 2001 Nov;38(11):E39. doi: 10.1136/jmg.38.11.e39. J Med Genet. 2001. PMID: 11694553 Free PMC article. No abstract available.

2

NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK. Rainier S, et al. Am J Hum Genet. 2003 Oct;73(4):967-71. doi: 10.1086/378817. Epub 2003 Sep 23. Am J Hum Genet. 2003. PMID: 14508710 Free PMC article.

3

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

Hedera P, Rainier S, Alvarado D, Zhao X, Williamson J, Otterud B, Leppert M, Fink JK. Hedera P, et al. Among authors: rainier s. Am J Hum Genet. 1999 Feb;64(2):563-9. doi: 10.1086/302258. Am J Hum Genet. 1999. PMID: 9973294 Free PMC article.

4

Prenatal diagnosis of hereditary spastic paraplegia.

Hedera P, Williamson JA, Rainier S, Alvarado D, Tukel T, Apak M, Fink JK. Hedera P, et al. Among authors: rainier s. Prenat Diagn. 2001 Mar;21(3):202-6. doi: 10.1002/1097-0223(200103)21:3<202::aid-pd4>3.0.co;2-u. Prenat Diagn. 2001. PMID: 11260609 Free article.

5

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.

Zhao X, Alvarado D, Rainier S, Lemons R, Hedera P, Weber CH, Tukel T, Apak M, Heiman-Patterson T, Ming L, Bui M, Fink JK. Zhao X, et al. Among authors: rainier s. Nat Genet. 2001 Nov;29(3):326-31. doi: 10.1038/ng758. Nat Genet. 2001. PMID: 11685207

6

Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia.

Hedera P, Eldevik OP, Maly P, Rainier S, Fink JK. Hedera P, et al. Among authors: rainier s. Neuroradiology. 2005 Oct;47(10):730-4. doi: 10.1007/s00234-005-1415-3. Epub 2005 Sep 6. Neuroradiology. 2005. PMID: 16143870 Free article.

7

Hereditary spastic paraplegia: spastin phenotype and function.

Fink JK, Rainier S. Fink JK, et al. Among authors: rainier s. Arch Neurol. 2004 Jun;61(6):830-3. doi: 10.1001/archneur.61.6.830. Arch Neurol. 2004. PMID: 15210518 Review. No abstract available.

8

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

Rainier S, Thomas D, Tokarz D, Ming L, Bui M, Plein E, Zhao X, Lemons R, Albin R, Delaney C, Alvarado D, Fink JK. Rainier S, et al. Arch Neurol. 2004 Jul;61(7):1025-9. doi: 10.1001/archneur.61.7.1025. Arch Neurol. 2004. PMID: 15262732

9

De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsy.

Rainier S, Sher C, Reish O, Thomas D, Fink JK. Rainier S, et al. Arch Neurol. 2006 Mar;63(3):445-7. doi: 10.1001/archneur.63.3.445. Arch Neurol. 2006. PMID: 16533974

10

Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegia.

Albin RL, Koeppe RA, Rainier S, Fink JK. Albin RL, et al. Among authors: rainier s. J Neurogenet. 2008;22(4):289-94. doi: 10.1080/01677060802337307. J Neurogenet. 2008. PMID: 19085270 Free PMC article.

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