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AHM Huq

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Disorders

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TOP 3
Mohsin Maqbool; Deanna A Oleske; Bassel A Salman; AHM M Huq; Kevin Khodabakhsh; Harry T Chugani
Novel FDG-PET findings in anti-NMDA receptor encephalitis: a case based report.
Senthil Sundaram; AHM M Huq; Zhen Sun; Wu Yu; Lindsey Bennett; Benjamin J Wilson; Michael E Behen; Harry T Chugani
Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.
Benjamin J Wilson; Senthil Sundaram; AHM M Huq; Jeong-Won Jeong; Stacey R Halverson; Michael E Behen; Duy Q Bui; Harry T Chugani
Abnormal language pathway in children with Angelman syndrome.

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All Publications

2011: Mohsin Maqbool; Deanna A Oleske; Bassel A Salman; AHM M Huq; Kevin Khodabakhsh; Harry T Chugani
Novel FDG-PET findings in anti-NMDA receptor encephalitis: a case based report.
Journal of child neurology 2011;26(10):1325-8.
2011: Senthil Sundaram; AHM M Huq; Zhen Sun; Wu Yu; Lindsey Bennett; Benjamin J Wilson; Michael E Behen; Harry T Chugani
Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.
Annals of neurology 2011;69(5):901-4.
2011: Benjamin J Wilson; Senthil Sundaram; AHM M Huq; Jeong-Won Jeong; Stacey R Halverson; Michael E Behen; Duy Q Bui; Harry T Chugani
Abnormal language pathway in children with Angelman syndrome.
Pediatric neurology 2011;44(5):350-6.
2011: Ajay Kumar; Harry T Chugani; Pulak Chakraborty; AHM M Huq
Evaluation of neuroinflammation in X-linked adrenoleukodystrophy.
Pediatric neurology 2011;44(2):143-6.
2010: Senthil Sundaram; AHM M Huq; Benjamin J Wilson; Harry T Chugani
Tourette syndrome is associated with recurrent exonic copy number variants.
Neurology 2010;74(20):1583-90.
2008: A M Katramados; Raja Rabah; M D Adams; AHM M Huq; Panayiotis Mitsias
Longitudinal myelitis, aseptic meningitis, and conus medullaris infarction as presenting manifestations of pediatric systemic lupus erythematosus.
Lupus 2008;17(4):332-6.
2004: Rafiqun Nabi; Fatema J Serajee; Diane C Chugani; Hailang Zhong; AHM M Huq
Association of tryptophan 2,3 dioxygenase gene polymorphism with autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;125B(1):63-8.
2003: Rafiqun Nabi; Hailang Zhong; Fatema J Serajee; AHM M Huq
No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;119B(1):98-101.
2003: Fatema J Serajee; Hailang Zhong; Rafiqun Nabi; AHM M Huq
The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.
Journal of medical genetics 2003;40(4):e42.
2003: Hailang Zhong; Fatema J Serajee; Rafiqun Nabi; AHM M Huq
No association between the EN2 gene and autistic disorder.
Journal of medical genetics 2003;40(1):e4.
2002: AHM M Huq; Diane C Chugani; Bharati Hukku; Fatema J Serajee
Evidence of somatic mosaicism in Sturge-Weber syndrome.
Neurology 2002;59(5):780-2.
2001: Eishi Asano; Helena Kuivaniemi; AHM M Huq; Gerard Tromp; Michael E Behen; Robert D Rothermel; J Herron; Diane C Chugani
A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autism.
Journal of child neurology 2001;16(5):357-63.
1999: Y Pan; William Decker; AHM M Huq; William J Craigen
Retrotransposition of glycerol kinase-related genes from the X chromosome to autosomes: functional and evolutionary aspects.
Genomics 1999;59(3):282-90.
1997: AHM M Huq; R S Lovell; Ching-Nan Ou; Arthur L Beaudet; William J Craigen
X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death.
Human molecular genetics 1997;6(11):1803-9.
1997: AHM M Huq; James S Sutcliffe; M Nakao; Y Shen; R A Gibbs; Arthur L Beaudet
Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity.
Genome research 1997;7(6):642-8.
1997: AHM M Huq; Richard M Braverman; F Greenberg; Carlos A Bacino; David L Rimoin; R S Lachman; M L Levin
The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties.
American journal of medical genetics 1997;68(2):225-30.
1996: AHM M Huq; R S Lovell; Margaret J Sampson; William Decker; M B Dinulos; C M Disteche; William J Craigen
Isolation, mapping, and functional expression of the mouse X chromosome glycerol kinase gene.
Genomics 1996;36(3):530-4.
1992: M Ito; H Kobashi; Etsuo Naito; Takahiko Saijo; Eiji Takeda; AHM M Huq; Y Kuroda
Decrease of pyruvate dehydrogenase phosphatase activity in patients with congenital lactic acidemia.
Clinica chimica acta; international journal of clinical chemistry 1992;209(1-2):1-7.
1992: M Ito; AHM M Huq; Etsuo Naito; Takahiko Saijo; Eiji Takeda; Y Kuroda
Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein.
Journal of inherited metabolic disease 1992;15(6):848-56.
1991: Eiji Takeda; T Hashimoto; M Tayama; M Miyazaki; E Shirakawa; Y Shiino; Takahiko Saijo; M Ito; Etsuo Naito; AHM M Huq
Diagnosis of atlantoaxial subluxation in Morquio's syndrome and spondyloepiphyseal dysplasia congenita.
Acta paediatrica Japonica; Overseas edition 1991;33(5):633-8.
1991: Takahiko Saijo; M Ito; Eiji Takeda; AHM M Huq; Etsuo Naito; Ichiro Yokota; T Sone; J W Pike; Y Kuroda
A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detection.
American journal of human genetics 1991;49(3):668-73.
1991: AHM M Huq; M Ito; Etsuo Naito; Takahiko Saijo; Eiji Takeda; Y Kuroda
Demonstration of an unstable variant of pyruvate dehydrogenase protein (E1) in cultured fibroblasts from a patient with congenital lactic acidemia.
Pediatric research 1991;30(1):11-4.
1988: AHM M Huq; S Matsuoka; Yuko Kurahashi; Y Kuroda; S J Ma; T Ohuchi; M Oka
Dopamine 4-sulfate: effects on isolated perfused rat heart and role of atria.
Life sciences 1988;43(20):1599-606.