Margolis RL - Search Results

1

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Among authors: margolis rl. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

2

SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion.

O'Hearn E, Holmes SE, Calvert PC, Ross CA, Margolis RL. O'Hearn E, et al. Among authors: margolis rl. Neurology. 2001 Feb 13;56(3):299-303. doi: 10.1212/wnl.56.3.299. Neurology. 2001. PMID: 11171892

3

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Stevanin G, Camuzat A, Holmes SE, Julien C, Sahloul R, Dodé C, Hahn-Barma V, Ross CA, Margolis RL, Durr A, Brice A. Stevanin G, et al. Among authors: margolis rl. Neurology. 2002 Mar 26;58(6):965-7. doi: 10.1212/wnl.58.6.965. Neurology. 2002. PMID: 11914418

4

Huntington's disease--like 2 is associated with CUG repeat-containing RNA foci.

Rudnicki DD, Holmes SE, Lin MW, Thornton CA, Ross CA, Margolis RL. Rudnicki DD, et al. Among authors: margolis rl. Ann Neurol. 2007 Mar;61(3):272-82. doi: 10.1002/ana.21081. Ann Neurol. 2007. PMID: 17387722

5

Loss of junctophilin-3 contributes to Huntington disease-like 2 pathogenesis.

Seixas AI, Holmes SE, Takeshima H, Pavlovich A, Sachs N, Pruitt JL, Silveira I, Ross CA, Margolis RL, Rudnicki DD. Seixas AI, et al. Among authors: margolis rl. Ann Neurol. 2012 Feb;71(2):245-57. doi: 10.1002/ana.22598. Ann Neurol. 2012. PMID: 22367996

6

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.

Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA. Margolis RL, et al. Ann Neurol. 2001 Sep;50(3):373-80. Ann Neurol. 2001. Corrected and republished in: Ann Neurol. 2001 Dec;50(6):373-80. doi: 10.1002/ana.1312 PMID: 11558794 Corrected and republished.

7

SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia.

Holmes SE, Hearn EO, Ross CA, Margolis RL. Holmes SE, et al. Among authors: margolis rl. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):397-403. doi: 10.1016/s0361-9230(01)00596-2. Brain Res Bull. 2001. PMID: 11719278 Review.

8

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.

Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA. Margolis RL, et al. Ann Neurol. 2001 Dec;50(6):373-80. doi: 10.1002/ana.1312. Ann Neurol. 2001. PMID: 11761463

9

Why is SCA12 different from other SCAs?

Holmes SE, O'Hearn E, Margolis RL. Holmes SE, et al. Among authors: margolis rl. Cytogenet Genome Res. 2003;100(1-4):189-97. doi: 10.1159/000072854. Cytogenet Genome Res. 2003. PMID: 14526180 Review.

10

Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.

Bauer I, Gencik M, Laccone F, Peters H, Weber BH, Feder EH, Weirich H, Morris-Rosendahl DJ, Rolfs A, Gencikova A, Bauer P, Wenning GK, Epplen JT, Holmes SE, Margolis RL, Ross CA, Riess O. Bauer I, et al. Among authors: margolis rl. Ann Neurol. 2002 May;51(5):662. doi: 10.1002/ana.10184. Ann Neurol. 2002. PMID: 12112122 No abstract available.

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