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Huq, Ahm

M.D., Ph.D.

Clinical Professor
Professor

More about Ahm Huq

Cuccurullo C, Cerulli Irelli E, Ugga L, Riva A, D'Amico A, Cabet S, Lesca G, Bilo L, Zara F, Iliescu C, Barca D, Fung F, Helbig K, Ortiz-Gonzalez X, Schelhaas HJ, Willemsen MH, van der Linden I, Canafoglia L, Courage C, Gommaraschi S, Gonzalez-Alegre P, Bardakjian T, Syrbe S, Schuler E, Lemke JR, Vari S, Roende G, Bak M, Huq M, Powis Z, Johannesen KM, Hammer TB, Møller RS, Rabin R, Pappas J, Zupanc ML, Zadeh N, Cohen J, Naidu S, Krey I, Saneto R, Thies J, Licchetta L, Tinuper P, Bisulli F, Minardi R, Bayat A, Villeneuve N, Molinari F, Salimi Dafsari H, Moller B, Le Roux M, Houdayer C, Vecchi M, Mammi I, Fiorini E, Proietti J, Ferri S, Cantalupo G, Battaglia DI, Gambardella ML, Contaldo I, Brogna C, Trivisano M, De Dominicis A, Bova SM, Gardella E, Striano P, Coppola A (2024). Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants. Epilepsia.

Fatema J Serajee, Salman Rashid, Huq, AHM (2024). Carbamazepine responsive Episodic Dystonia and Hallucination due to Pyruvate Dehydrogenase E2 (DLAT) gene mutation Neurogenetics.

Li Y, Song J, Huq AM, Timilsina S, Gershwin ME (2023). Posterior reversible encephalopathy syndrome and autoimmunity. Autoimmunity reviews.

Set KK, Sen K, Huq AHM, Agarwal R (2019). Mitochondrial Disorders of the Nervous System: A Review. Clinical pediatrics.

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 (2019). Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations. Annals of clinical and translational neurology.

Sen K , Huq AHM, Agarwal R (2019). Mitochondrial Disorders of the Nervous System: A Review. Clin Pediatr.

Sen K, Hicks MA, Huq AHM, Agarwal R (2019). Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood-Expanding the Phenotype of a Recently Reported Condition. Neuropediatrics.

Liu Y, Schubert J, Sonnenberg L, Helbig KL, Hoei-Hansen CE, Koko M, Rannap M, Lauxmann S, Huq M, Schneider MC, Johannesen KM, Kurlemann G, Gardella E, Becker F, Weber YG, Benda J, Møller RS, Lerche H (2019). Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability. Brain : a journal of neurology.

Lee BH, Reijnders MRF, Abubakare O, Tuttle E, Lape B, Minks KQ, Stodgell C, Bennetto L, Kwon J, Fong CT, Gripp KW, Marsh ED, Smith WE, Huq AM, Coury SA, Tan WH, Solis O, Mehta RI, Leventer RJ, Baralle D, Hunt D, Paciorkowski AR (2018). Expanding the neurodevelopmental phenotype of PURA syndrome. American journal of medical genetics. Part A.

Ueda K, Serajee F, Huq AM (2018). Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation. Pediatrics.

Selvan N, George S, Serajee FJ, Shaw M, Hobson L, Kalscheuer V, Prasad N, Levy SE, Taylor J, Aftimos S, Schwartz CE, Huq AM, Gecz J, Wells L (2018). O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling. The Journal of biological chemistry.

Set KK, Weber ARB, Serajee FJ, Huq AM (2018). Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss. Neurology.

Fatema Serajee, AHM M Huq (2017). Exome Sequencing Identifying Dual Mutations in Calcium Signaling Genes GNAO1 and ATP2B3 in a Patient with Early Infantile Epileptic Encephalopathy. J of Pediatric Neurology.

Ueda K, Serajee F, Rajlich J, Taraman S, Steckling L, Huq AM (2017). Sibling response to initial antiepileptic medication predicts treatment success. Epilepsy research.

Tripathi R, Serajee F, Jiang H, Huq AHMM (2017). Novel Presentation of Rosai-Dorfman Histiocytosis With a Prolonged Course of Cranial and Peripheral Neuropathies. Pediatric neurology.

Ueda K, Serajee F, Huq AM (2017). A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions. Journal of clinical neurology (Seoul, Korea).

Set KK, Ghosh D, Huq AHM, Luat AF (2017). Episodic Ataxia Type 1 (K-channelopathy) Manifesting as Paroxysmal Nonkinesogenic Dyskinesia: Expanding the Phenotype. Movement disorders clinical practice.

59. Serajee F, Huq, AHHM (2015). Advances in Tourette syndrome: Diagnosis and Treatment Pediatr Clin North Am..

Serajee FJ, Huq AM (2015). Homozygous Mutation in Synaptic Vesicle Glycoprotein 2A Gene Results in Intractable Epilepsy, Involuntary Movements, Microcephaly, and Developmental and Growth Retardation. Pediatric neurology.

Sundaram S, Huq AH, Hsia T, Chugani H (2014). Exome sequencing and diffusion tensor imaging in developmental disabilities. Pediatric research.

Tiwari VN, Sundaram SK, Chugani HT, Huq AH (2013). Infantile spasms are associated with abnormal copy number variations. Journal of child neurology.

Sundaram SK, Chugani HT, Tiwari VN, Huq AH (2013). SCN2A mutation is associated with infantile spasms and bitemporal glucose hypometabolism. Pediatric neurology.

Sundaram SK, Huq AM, Sun Z, Yu W, Bennett L, Wilson BJ, Behen ME, Chugani HT (2011). Advances in Tourette syndrome: Diagnosis and Treatment in Pediatric Neurologic and Developmental Disorders in the Era of Genomics Annals of neurology.

Wilson BJ, Sundaram SK, Huq AH, Jeong JW, Halverson SR, Behen ME, Bui DQ, Chugani HT (2011). Abnormal language pathway in children with Angelman syndrome. Pediatric neurology.

Kumar A, Chugani HT, Chakraborty P, Huq AH (2011). Evaluation of neuroinflammation in X-linked adrenoleukodystrophy. Pediatric neurology.

Maqbool M, Oleske DA, Huq AH, Salman BA, Khodabakhsh K, Chugani HT (2011). Novel FDG-PET findings in anti-NMDA receptor encephalitis: a case based report. Journal of child neurology.

Sundaram SK, Huq AM, Sun Z, Yu W, Bennett L, Wilson BJ, Behen ME, Chugani HT (2011). Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder. Annals of neurology.

Sarnaik SA, Altinock D, Huq AHM M (2010). Stroke in sickle cell disease J Pediatric Neurology.

Sundaram SK, Huq AM, Wilson BJ, Chugani HT (2010). Tourette syndrome is associated with recurrent exonic copy number variants. Neurology.

Huq AHM M (2009). Association of Y chromosome haplotypes with autism J child Neurology.

Serajee FJ, Mahbubul Huq AH (2009). Association of Y chromosome haplotypes with autism. Journal of child neurology.

Tapos D, Serajee FJ, Huq AHM M (2008). Homozygous myotonic dystrophy with craniosynostosis. J Child Neurol.

Katramados AM, Rabah R, Adams MD, Huq AH, Mitsias PD (2008). Longitudinal myelitis, aseptic meningitis, and conus medullaris infarction as presenting manifestations of pediatric systemic lupus erythematosus. Lupus.

Cerghet M, Tapos D, Serajee FJ, Mahbubul Huq AH (2008). Homozygous myotonic dystrophy with craniosynostosis. Journal of child neurology.

Zhong H, Mahbubul Huq AH (2006). Association of Reelin gene polymorphisms in autism. Genomics.

Loeb JA, Sohrab SA, Huq M, Fuerst DR (2006). Brain calcifications induce neurological dysfunction that can be reversed by a bone drug. Journal of the neurological sciences.

Serajee FJ, Zhong H, Mahbubul Huq AH (2006). Association of Reelin gene polymorphisms with autism. Genomics.

Nabi R, Serajee FJ, Chugani DC, Zhong H, Huq AH (2004). 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.

Serajee FJ, Nabi R, Zhong H, Huq M (2004). Polymorphisms in xenobiotic metabolism genes and autism. Journal of child neurology.

Nabi R, Zhong H, Serajee FJ, Huq AH (2003). 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.

Zhong H, Serajee FJ, Nabi R, Huq AH (2003). No association between the EN2 gene and autistic disorder. Journal of medical genetics.

Serajee FJ, Zhong H, Nabi R, Huq AH (2003). The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism. Journal of medical genetics.

Serajee FJ, Nabi R, Zhong H, Mahbubul Huq AH (2003). Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism. Journal of medical genetics.

Huq AH, Chugani DC, Hukku B, Serajee FJ (2002). Evidence of somatic mosaicism in Sturge-Weber syndrome. Neurology.

Asano E, Kuivaniemi H, Huq AH, Tromp G, Behen M, Rothermel R, Herron J, Chugani DC (2001). A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autism. Journal of child neurology.

Nigro MA (2000). XY sex reversal and a nonprogressive neurologic disorder: a new syndrome? Pediatr Neurol.

Pan Y, Decker WK, Huq AH, Craigen WJ (1999). Retrotransposition of glycerol kinase-related genes from the X chromosome to autosomes: functional and evolutionary aspects. Genomics.

Almqvist E, Huq M, Lundin A, Hayden M, Edstrom L, Avret M, Zhiping Z (1998). A Hungtington disease-like neurodegenerrative disorder maps to chromosome 20p. Am J Hum Genet.

Huq AH, Lovell RS, Ou CN, Beaudet AL, Craigen WJ (1997). X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death. Human molecular genetics.

Huq AH, Braverman RM, Greenberg F, Bacino CA, Rimoin DL, Lachman RS, Levin ML (1997). The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties. American journal of medical genetics.

Huq AH, Sutcliffe JS, Nakao M, Shen Y, Gibbs RA, Beaudet AL (1997). Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity. Genome research.

Huq AH, Lovell RS, Sampson MJ, Decker WK, Dinulos MB, Disteche CM, Craigen WJ (1996). Isolation, mapping, and functional expression of the mouse X chromosome glycerol kinase gene. Genomics.

Ito M, Kobashi H, Naito E, Saijo T, Takeda E, Huq AH, Kuroda Y (1992). Decrease of pyruvate dehydrogenase phosphatase activity in patients with congenital lactic acidemia. Clinica chimica acta; international journal of clinical chemistry.

Ito M, Huq AH, Naito E, Saijo T, Takeda E, Kuroda Y (1992). 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.

Saijo T, Ito M, Takeda E, Huq AH, Naito E, Yokota I, Sone T, Pike JW, Kuroda Y (1991). 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.

Huq AH, Ito M, Naito E, Saijo T, Takeda E, Kuroda Y (1991). Demonstration of an unstable variant of pyruvate dehydrogenase protein (E1) in cultured fibroblasts from a patient with congenital lactic acidemia. Pediatric research.

Takeda E, Hashimoto T, Tayama M, Miyazaki M, Shirakawa E, Shiino Y, Saijo T, Ito M, Naito E, Huq AH (1991). Diagnosis of atlantoaxial subluxation in Morquio's syndrome and spondyloepiphyseal dysplasia congenita. Acta paediatrica Japonica : Overseas edition.

Y. Kawano, T. Abe, T. Suzue, J. Satoh,, K. Kamata, M. A.H.M. Huq, T. Ninomiya, T. Watanabe, Y. Kuroda, T. Koyama, T. Shimokawa (1989). Recovery kinetics of hematopoiesis after peripheral blood stem cell autotransplantation Gan to kagaku ryoho. Cancer & chemotherapy.

Y Takaue, T Koyama, Y Kawano, J Satoh, M A Huq,, T Ninomiya, Y Kuroda, T Ueda, K Hiura (1989). Rapid and complete hematopoietic reconstitution following peripheral blood stem cell autotransplantation in a child with T cell acute lymphoblastic leukemia Rinsho Ketsueki.

Ninomiya T, , , , . , Koyama T,, Watanabe T, Kawano Y, Huq AHM M, Kuroda Y (1989). Diagnosis of systemic fungal infection by Limulus test Pediatric Clinic of Japan.

Watanabe T, Takaue Y, Kawano Y, Koyama T, Huq MA, Shimokawa T, Ninomiya T, Aga Y, Inai T, Hino M (1989). Peripheral blood stem cell autotransplantation in treatment of childhood cancer. Bone marrow transplantation.

Y Takaue, T Watanabe, Y Kawano, T Koyama, T Abe, T Suzue, J Satoh, M A Huq, T Ohuchi, T Ninomiya, et al. (1988). Separation of circulating stem cells on discontinuous percoll gradients Rinsho Ketsueki. Journal of Clinical hematology.

Y Takaue, T Watanabe, Y Kawano, T Koyama, T Abe, T Suzue, J Satoh, M A Huq, T Ohuchi, T Ninomiya, et al. (1988). Cryopreservation of circulating stem cells in large quantities Gan To Kagaku Ryoho ..

T Watanabe, Y Takaue, A H Mahbubul Huq, T Koyama, Y Kawano, J Sato, T Ninomiya, M Hino, H Takehara, N Komi (1988). Attempted marrow rescue with cryopreserved circulating stem cells following high-dose chemotherapy Gan To Kagaku Ryoho.

Watanabe T, Taguchi Y, Huq AHM M, Kawano Y, Takaue Y, Ninomiya T, Kuroda Y, Satoh J, and Sakamoto F. (1988). Successful treatment of cytomegalovirus pneumonitis in acute lymphoblastic leukemia with CMV immunoglobin. Rinsho Ketsueki. Journal of Clinical hematology.

Huq AH, Matsuoka S, Kurahashi Y, Kuroda Y, Ma SJ, Ohuchi T, Oka M (1988). Dopamine 4-sulfate: effects on isolated perfused rat heart and role of atria. Life sciences.

Takaue Y, Watanabe T, Kawano Y, Koyama T, Abe T, Suzue T, Satoh J, Huq AHM M, I. Kawano, Y Kurahashi, Kuroda Y. (1988). Successful reconstitution of hematopoiesis with cryopreserved circulating stem cells following marrow ablative chemotherapy in a child with recurrent malignant lymphoma. Japanese Journal of Pediatrics.
Miki Koraku Award for Excellence in Research
Research Awards for Clinical Trainees
Best Medical Graduate (Gold Medal)
M.B.B.S., Dhaka University/Mymensingh Medical College, Bangladesh
Ph.D., Tokushima Bunri University