Huq AHMM - Search Results

1

Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations.

Cameron JM, Maljevic S, Nair U, Aung YH, Cogné B, Bézieau S, Blair E, Isidor B, Zweier C, Reis A, Koenig MK, Maarup T, Sarco D, Afenjar A, Huq AHMM, Kukolich M, Billette de Villemeur T, Nava C, Héron B, Petrou S, Berkovic SF. Cameron JM, et al. Among authors: huq ahmm. Ann Clin Transl Neurol. 2019 Jul;6(7):1263-1272. doi: 10.1002/acn3.50822. Epub 2019 Jul 1. Ann Clin Transl Neurol. 2019. PMID: 31353855 Free PMC article.

2

Evaluation of neuroinflammation in X-linked adrenoleukodystrophy.

Kumar A, Chugani HT, Chakraborty P, Huq AH. Kumar A, et al. Pediatr Neurol. 2011 Feb;44(2):143-6. doi: 10.1016/j.pediatrneurol.2010.10.006. Pediatr Neurol. 2011. PMID: 21215916

3

A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autism.

Asano E, Kuivaniemi H, Huq AH, Tromp G, Behen M, Rothermel R, Herron J, Chugani DC. Asano E, et al. J Child Neurol. 2001 May;16(5):357-63. doi: 10.1177/088307380101600509. J Child Neurol. 2001. PMID: 11392521

4

Evidence of somatic mosaicism in Sturge-Weber syndrome.

Huq AH, Chugani DC, Hukku B, Serajee FJ. Huq AH, et al. Neurology. 2002 Sep 10;59(5):780-2. doi: 10.1212/wnl.59.5.780. Neurology. 2002. PMID: 12221183 No abstract available.

5

Novel Presentation of Rosai-Dorfman Histiocytosis With a Prolonged Course of Cranial and Peripheral Neuropathies.

Tripathi R, Serajee F, Jiang H, Huq AHMM. Tripathi R, et al. Among authors: huq ahmm. Pediatr Neurol. 2017 Jun;71:70-72. doi: 10.1016/j.pediatrneurol.2017.02.013. Epub 2017 Mar 8. Pediatr Neurol. 2017. PMID: 28377039

6

No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.

Nabi R, Zhong H, Serajee FJ, Huq AH. Nabi R, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):98-101. doi: 10.1002/ajmg.b.10012. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707945

7

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism.

Nabi R, Serajee FJ, Chugani DC, Zhong H, Huq AH. Nabi R, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):63-8. doi: 10.1002/ajmg.b.20147. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755447

8

No association between the EN2 gene and autistic disorder.

Zhong H, Serajee FJ, Nabi R, Huq AH. Zhong H, et al. J Med Genet. 2003 Jan;40(1):e4. doi: 10.1136/jmg.40.1.e4. J Med Genet. 2003. PMID: 12525552 Free PMC article. No abstract available.

9

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.

Serajee FJ, Zhong H, Nabi R, Huq AH. Serajee FJ, et al. J Med Genet. 2003 Apr;40(4):e42. doi: 10.1136/jmg.40.4.e42. J Med Genet. 2003. PMID: 12676915 Free PMC article. No abstract available.

10

Isolation, mapping, and functional expression of the mouse X chromosome glycerol kinase gene.

Huq AH, Lovell RS, Sampson MJ, Decker WK, Dinulos MB, Disteche CM, Craigen WJ. Huq AH, et al. Genomics. 1996 Sep 15;36(3):530-4. doi: 10.1006/geno.1996.0500. Genomics. 1996. PMID: 8884278

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