Anselm IA - Search Results

1

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.

Anselm IA, Sweadner KJ, Gollamudi S, Ozelius LJ, Darras BT. Anselm IA, et al. Neurology. 2009 Aug 4;73(5):400-1. doi: 10.1212/WNL.0b013e3181b04acd. Neurology. 2009. PMID: 19652145 Free PMC article. No abstract available.

2

Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8.

Anselm IA, Coulter DL, Darras BT. Anselm IA, et al. Neurology. 2008 Apr 29;70(18):1642-4. doi: 10.1212/01.wnl.0000310987.04106.45. Neurology. 2008. PMID: 18443316 No abstract available.

3

Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiency.

Anselm IA, Darras BT. Anselm IA, et al. Pediatr Neurol. 2006 Aug;35(2):142-4. doi: 10.1016/j.pediatrneurol.2006.01.008. Pediatr Neurol. 2006. PMID: 16876014

4

Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial.

Anselm IA, Darras BT. Anselm IA, et al. Neurology. 2006 Oct 10;67(7):1313; author reply 1313. doi: 10.1212/01.wnl.0000243807.14293.07. Neurology. 2006. PMID: 17030784 No abstract available.

5

De Novo TUBB2A Variant Presenting With Anterior Temporal Pachygyria.

Rodan LH, El Achkar CM, Berry GT, Poduri A, Prabhu SP, Yang E, Anselm I. Rodan LH, et al. J Child Neurol. 2017 Jan;32(1):127-131. doi: 10.1177/0883073816672998. Epub 2016 Oct 23. J Child Neurol. 2017. PMID: 27770045

6

Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.

Dy ME, Chang FC, Jesus SD, Anselm I, Mahant N, Zeilman P, Rodan LH, Foote KD, Tan WH, Eskandar E, Sharma N, Okun MS, Fung VS, Waugh JL. Dy ME, et al. J Child Neurol. 2016 Jul;31(8):1027-35. doi: 10.1177/0883073816635749. Epub 2016 Apr 6. J Child Neurol. 2016. PMID: 27052971

7

Adrenal Insufficiency in Mitochondrial Disease: A Rare Case of GFER-Related Mitochondrial Encephalomyopathy and Review of the Literature.

Calderwood L, Holm IA, Teot LA, Anselm I. Calderwood L, et al. Among authors: anselm i. J Child Neurol. 2016 Feb;31(2):190-4. doi: 10.1177/0883073815587327. Epub 2015 May 26. J Child Neurol. 2016. PMID: 26018198 Review.

8

Brain involvement in Charcot-Marie-Tooth disease due to ganglioside-induced differentiation associated-protein 1 mutation.

Al-Ghamdi F, Anselm I, Yang E, Ghosh PS. Al-Ghamdi F, et al. Neuromuscul Disord. 2017 Sep;27(9):848-851. doi: 10.1016/j.nmd.2017.06.003. Epub 2017 Jun 7. Neuromuscul Disord. 2017. PMID: 28673555

9

Rhabdomyolysis, acute renal failure, and cardiac arrest secondary to status dystonicus in a child with glutaric aciduria type I.

Jamuar SS, Newton SA, Prabhu SP, Hecht L, Costas KC, Wessel AE, Harris DJ, Anselm I, Berry GT. Jamuar SS, et al. Mol Genet Metab. 2012 Aug;106(4):488-90. doi: 10.1016/j.ymgme.2012.05.018. Epub 2012 May 30. Mol Genet Metab. 2012. PMID: 22771013

10

Progressive intracranial vascular disease with strokes and seizures in a boy with progeria.

Rosman NP, Anselm I, Bhadelia RA. Rosman NP, et al. J Child Neurol. 2001 Mar;16(3):212-5. doi: 10.1177/088307380101600309. J Child Neurol. 2001. PMID: 11305689

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