Minassian BA - Search Results

1

Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.

Boelman C, Lagman-Bartolome AM, MacGregor DL, McCabe J, Logan WJ, Minassian BA. Boelman C, et al. Among authors: minassian ba. Pediatr Neurol. 2014 Dec;51(6):850-3. doi: 10.1016/j.pediatrneurol.2014.08.015. Epub 2014 Aug 29. Pediatr Neurol. 2014. PMID: 25439493

2

Magnetoencephalographic localization in pediatric epilepsy surgery: comparison with invasive intracranial electroencephalography.

Minassian BA, Otsubo H, Weiss S, Elliott I, Rutka JT, Snead OC 3rd. Minassian BA, et al. Ann Neurol. 1999 Oct;46(4):627-33. doi: 10.1002/1531-8249(199910)46:4<627::aid-ana11>3.0.co;2-c. Ann Neurol. 1999. PMID: 10514100

3

Identification of new and common mutations in the EPM2A gene in Lafora disease.

Minassian BA, Ianzano L, Delgado-Escueta AV, Scherer SW. Minassian BA, et al. Neurology. 2000 Jan 25;54(2):488-90. doi: 10.1212/wnl.54.2.488. Neurology. 2000. PMID: 10668720

4

Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy.

Minassian BA, Ianzano L, Meloche M, Andermann E, Rouleau GA, Delgado-Escueta AV, Scherer SW. Minassian BA, et al. Neurology. 2000 Aug 8;55(3):341-6. doi: 10.1212/wnl.55.3.341. Neurology. 2000. PMID: 10932264

5

Cyclosporine A neurotoxicity in a patient with idiopathic renal magnesium wasting.

Al-Rasheed AK, Blaser SI, Minassian BA, Benson L, Weiss SK. Al-Rasheed AK, et al. Among authors: minassian ba. Pediatr Neurol. 2000 Oct;23(4):353-6. doi: 10.1016/s0887-8994(00)00198-3. Pediatr Neurol. 2000. PMID: 11068171

6

Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphatase.

Minassian BA, Andrade DM, Ianzano L, Young EJ, Chan E, Ackerley CA, Scherer SW. Minassian BA, et al. Ann Neurol. 2001 Feb;49(2):271-5. Ann Neurol. 2001. PMID: 11220751

7

Lafora's disease: towards a clinical, pathologic, and molecular synthesis.

Minassian BA. Minassian BA. Pediatr Neurol. 2001 Jul;25(1):21-9. doi: 10.1016/s0887-8994(00)00276-9. Pediatr Neurol. 2001. PMID: 11483392 Review.

8

Progressive myoclonus epilepsy with polyglucosan bodies: Lafora disease.

Minassian BA. Minassian BA. Adv Neurol. 2002;89:199-210. Adv Neurol. 2002. PMID: 11968446 Review. No abstract available.

9

Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy.

Minassian BA, Aiyar R, Alic S, Banwell B, Villanova M, Fardeau M, Mandell JW, Juel VC, Rafii M, Auranen M, Kalimo H. Minassian BA, et al. Neurology. 2002 Aug 27;59(4):596-601. doi: 10.1212/wnl.59.4.596. Neurology. 2002. PMID: 12196656

10

Unusual presentation of Lafora's disease.

Al Otaibi SF, Minassian BA, Ackerley CA, Logan WJ, Weiss S. Al Otaibi SF, et al. Among authors: minassian ba. J Child Neurol. 2003 Jul;18(7):499-501. doi: 10.1177/08830738030180070901. J Child Neurol. 2003. PMID: 12940657

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