Shaibani A - Search Results

1

Clinical and biochemical improvement of very long-chain acyl-CoA dehydrogenase deficiency in pregnancy.

Mendez-Figueroa H, Shchelochkov OA, Shaibani A, Aagaard-Tillery K, Shinawi MS. Mendez-Figueroa H, et al. Among authors: shaibani a. J Perinatol. 2010 Aug;30(8):558-62. doi: 10.1038/jp.2009.198. J Perinatol. 2010. PMID: 20668464

2

Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation.

Shchelochkov O, Wong LJ, Shaibani A, Shinawi M. Shchelochkov O, et al. Among authors: shaibani a. Muscle Nerve. 2009 Mar;39(3):374-82. doi: 10.1002/mus.21157. Muscle Nerve. 2009. PMID: 19208414

3

Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.

Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Shaibani A, et al. Arch Neurol. 2009 Aug;66(8):1028-32. doi: 10.1001/archneurol.2009.139. Arch Neurol. 2009. PMID: 19667227 Free PMC article.

4

Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene.

Shaibani A, Wong LJ, Wei Zhang V, Lewis RA, Shinawi M. Shaibani A, et al. Int J Neurosci. 2015 Jan;125(1):43-9. doi: 10.3109/00207454.2014.904858. Epub 2014 May 16. Int J Neurosci. 2015. PMID: 24628582

5

Autosomal Dominant ANO5-Related Disorder Associated With Myopathy and Gnathodiaphyseal Dysplasia.

Shaibani A, Khan S, Shinawi M. Shaibani A, et al. Neurol Genet. 2021 Jul 16;7(4):e612. doi: 10.1212/NXG.0000000000000612. eCollection 2021 Aug. Neurol Genet. 2021. PMID: 34291158 Free PMC article.

6

Progressive myopathy with multiple symmetric lipomatosis.

Brunetti-Pierri N, Shaibani A, Zhang S, Wong LJ, Shinawi M. Brunetti-Pierri N, et al. Among authors: shaibani a. Arch Neurol. 2009 Dec;66(12):1576-7. doi: 10.1001/archneurol.2009.239. Arch Neurol. 2009. PMID: 20008669 No abstract available.

7

POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria.

Bekheirnia MR, Zhang W, Eble T, Willis A, Shaibani A, Wong LJ, Scaglia F, Dhar SU. Bekheirnia MR, et al. Among authors: shaibani a. Gene. 2012 May 10;499(1):209-12. doi: 10.1016/j.gene.2012.02.034. Epub 2012 Mar 3. Gene. 2012. PMID: 22405928

8

Transient hydrocephalus as a presenting sign associated with adrenoleukodystrophy.

Wong M, Shaibani A, Lee BC. Wong M, et al. Among authors: shaibani a. Neurology. 1999 Jan 15;52(2):424-5. doi: 10.1212/wnl.52.2.424. Neurology. 1999. PMID: 9932976 No abstract available.

9

Nonsarcoid granulomatous myopathy: two cases and a review of literature.

Jasim S, Shaibani A. Jasim S, et al. Among authors: shaibani a. Int J Neurosci. 2013 Jul;123(7):516-20. doi: 10.3109/00207454.2013.765871. Epub 2013 Feb 19. Int J Neurosci. 2013. PMID: 23311755 Review.

10

Placebo response in pain, fatigue, and performance: Possible implications for neuromuscular disorders.

Shaibani A, Frisaldi E, Benedetti F. Shaibani A, et al. Muscle Nerve. 2017 Sep;56(3):358-367. doi: 10.1002/mus.25635. Epub 2017 May 30. Muscle Nerve. 2017. PMID: 28249354 Review.

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