Schapira AH - Search Results

1

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.

Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, Brice A, Aasly J, Zabetian CP, Goldwurm S, Ferreira JJ, Tolosa E, Kay DM, Klein C, Williams DR, Marras C, Lang AE, Wszolek ZK, Berciano J, Schapira AH, Lynch T, Bhatia KP, Gasser T, Lees AJ, Wood NW; International LRRK2 Consortium. Healy DG, et al. Among authors: schapira ah. Lancet Neurol. 2008 Jul;7(7):583-90. doi: 10.1016/S1474-4422(08)70117-0. Epub 2008 Jun 6. Lancet Neurol. 2008. PMID: 18539534 Free PMC article.

2

Mitochondrial function and parental sex effect in Huntington's disease.

Mann VM, Cooper JM, Javoy-Agid F, Agid Y, Jenner P, Schapira AH. Mann VM, et al. Among authors: schapira ah. Lancet. 1990 Sep 22;336(8717):749. doi: 10.1016/0140-6736(90)92242-a. Lancet. 1990. PMID: 1975918 No abstract available.

3

Mitochondrial respiratory chain function in multiple system atrophy.

Gu M, Gash MT, Cooper JM, Wenning GK, Daniel SE, Quinn NP, Marsden CD, Schapira AH. Gu M, et al. Among authors: schapira ah. Mov Disord. 1997 May;12(3):418-22. doi: 10.1002/mds.870120323. Mov Disord. 1997. PMID: 9159739

4

Genetic counselling in mitochondrial diseases.

Warner TT, Schapira AH. Warner TT, et al. Among authors: schapira ah. Curr Opin Neurol. 1997 Oct;10(5):408-12. doi: 10.1097/00019052-199710000-00009. Curr Opin Neurol. 1997. PMID: 9330887 Review.

5

Pathogenesis of Parkinson's disease.

Schapira AH. Schapira AH. Baillieres Clin Neurol. 1997 Apr;6(1):15-36. Baillieres Clin Neurol. 1997. PMID: 9426866 Review.

6

Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A).

Hanna MG, Stewart J, Schapira AH, Wood NW, Morgan-Hughes JA, Murray NM. Hanna MG, et al. Among authors: schapira ah. J Neurol Neurosurg Psychiatry. 1998 Aug;65(2):248-50. doi: 10.1136/jnnp.65.2.248. J Neurol Neurosurg Psychiatry. 1998. PMID: 9703181 Free PMC article.

7

The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom.

Warner TT, Schapira AH. Warner TT, et al. Among authors: schapira ah. J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):378-9. doi: 10.1136/jnnp.65.3.378. J Neurol Neurosurg Psychiatry. 1998. PMID: 9728955 Free PMC article.

8

Guidelines for the management of Parkinson's disease. The Parkinson's Disease Consensus Working Group.

Bhatia K, Brooks DJ, Burn DJ, Clarke CE, Playfer J, Sawle GV, Schapira AH, Stewart D, Williams AC. Bhatia K, et al. Among authors: schapira ah. Hosp Med. 1998 Jun;59(6):469-80. Hosp Med. 1998. PMID: 9775275

9

Mitochondrial DNA in Parkinson's disease.

Schapira AH. Schapira AH. Adv Neurol. 1999;80:233-7. Adv Neurol. 1999. PMID: 10410727 Review. No abstract available.

10

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP. Münchau A, et al. Among authors: schapira ah. J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766892 Free PMC article.

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