Hedera P - Search Results

1

Reappraisal of the role of the DRD3 gene in essential tremor.

Blair MA, Ma S, Phibbs F, Fang JY, Cooper MK, Davis TL, Hedera P. Blair MA, et al. Among authors: hedera p. Parkinsonism Relat Disord. 2008 Aug;14(6):471-5. doi: 10.1016/j.parkreldis.2007.11.002. Epub 2008 Mar 3. Parkinsonism Relat Disord. 2008. PMID: 18316228 Free PMC article.

2

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.

Hedera P, Fenichel GM, Blair M, Haines JL. Hedera P, et al. Arch Neurol. 2004 Oct;61(10):1600-3. doi: 10.1001/archneur.61.10.1600. Arch Neurol. 2004. PMID: 15477516

3

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures.

Ma S, Abou-Khalil B, Sutcliffe JS, Haines JL, Hedera P. Ma S, et al. Among authors: hedera p. BMC Med Genet. 2005 Mar 30;6:13. doi: 10.1186/1471-2350-6-13. BMC Med Genet. 2005. PMID: 15799783 Free PMC article.

4

Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.

Ma S, Abou-Khalil B, Blair MA, Sutcliffe JS, Haines JL, Hedera P. Ma S, et al. Among authors: hedera p. Neurosci Lett. 2006 Feb 6;394(1):74-8. doi: 10.1016/j.neulet.2005.10.006. Epub 2005 Oct 25. Neurosci Lett. 2006. PMID: 16256272

5

Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia.

Blair MA, Ma S, Hedera P. Blair MA, et al. Among authors: hedera p. Neurogenetics. 2006 Mar;7(1):47-50. doi: 10.1007/s10048-005-0027-8. Epub 2006 Feb 18. Neurogenetics. 2006. PMID: 16489470

6

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?

Ma S, Davis TL, Blair MA, Fang JY, Bradford Y, Haines JL, Hedera P. Ma S, et al. Among authors: hedera p. Mov Disord. 2006 Sep;21(9):1368-74. doi: 10.1002/mds.20950. Mov Disord. 2006. PMID: 16721753

7

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.

Ma S, Blair MA, Abou-Khalil B, Lagrange AH, Gurnett CA, Hedera P. Ma S, et al. Among authors: hedera p. Epilepsy Res. 2006 Oct;71(2-3):129-34. doi: 10.1016/j.eplepsyres.2006.06.001. Epub 2006 Jul 12. Epilepsy Res. 2006. PMID: 16839746

8

Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.

Hedera P, Ma S, Blair MA, Taylor KA, Hamati A, Bradford Y, Abou-Khalil B, Haines JL. Hedera P, et al. Epilepsia. 2006 Oct;47(10):1622-8. doi: 10.1111/j.1528-1167.2006.00637.x. Epilepsia. 2006. PMID: 17054683 Free article.

9

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.

Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B. Hedera P, et al. Neurology. 2007 Jun 12;68(24):2107-12. doi: 10.1212/01.wnl.0000261246.75977.89. Epub 2007 Mar 21. Neurology. 2007. PMID: 17377072

10

Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients.

Blair MA, Ma S, Abou-Khalil B, Hedera P. Blair MA, et al. Among authors: hedera p. Eur J Neurol. 2007 Apr;14(4):424-7. doi: 10.1111/j.1468-1331.2007.01702.x. Eur J Neurol. 2007. PMID: 17388992

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