O'Hearn E - Search Results

1

Phenotypic features of Huntington's disease-like 2.

Walker RH, Jankovic J, O'Hearn E, Margolis RL. Walker RH, et al. Mov Disord. 2003 Dec;18(12):1527-30. doi: 10.1002/mds.10587. Mov Disord. 2003. PMID: 14673892

2

Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutation.

Nicholas AP, O'Hearn E, Holmes SE, Chen DT, Margolis RL. Nicholas AP, et al. Mov Disord. 2004 Jun;19(6):641-8. doi: 10.1002/mds.20077. Mov Disord. 2004. PMID: 15197701

3

Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.

O'Hearn EE, Hwang HS, Holmes SE, Rudnicki DD, Chung DW, Seixas AI, Cohen RL, Ross CA, Trojanowski JQ, Pletnikova O, Troncoso JC, Margolis RL. O'Hearn EE, et al. Mov Disord. 2015 Nov;30(13):1813-1824. doi: 10.1002/mds.26348. Epub 2015 Sep 4. Mov Disord. 2015. PMID: 26340331 Free PMC article.

4

Psychopathology in patients with degenerative cerebellar diseases: a comparison to Huntington's disease.

Leroi I, O'Hearn E, Marsh L, Lyketsos CG, Rosenblatt A, Ross CA, Brandt J, Margolis RL. Leroi I, et al. Am J Psychiatry. 2002 Aug;159(8):1306-14. doi: 10.1176/appi.ajp.159.8.1306. Am J Psychiatry. 2002. PMID: 12153822

5

Cognitive impairments in cerebellar degeneration: a comparison with Huntington's disease.

Brandt J, Leroi I, O'Hearn E, Rosenblatt A, Margolis RL. Brandt J, et al. J Neuropsychiatry Clin Neurosci. 2004 Spring;16(2):176-84. doi: 10.1176/jnp.16.2.176. J Neuropsychiatry Clin Neurosci. 2004. PMID: 15260369

6

Huntington's Disease-like 2 (HDL2) in North America and Japan.

Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Margolis RL, et al. Ann Neurol. 2004 Nov;56(5):670-4. doi: 10.1002/ana.20248. Ann Neurol. 2004. PMID: 15468075

7

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. Neurology. 2001 Feb 13;56(3):299-303. doi: 10.1212/wnl.56.3.299. Neurology. 2001. PMID: 11171892

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 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.

9

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

10

Spinocerebellar ataxia type 12.

O'Hearn E, Holmes SE, Margolis RL. O'Hearn E, et al. Handb Clin Neurol. 2012;103:535-47. doi: 10.1016/B978-0-444-51892-7.00034-6. Handb Clin Neurol. 2012. PMID: 21827912 Review.

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