Encephalopathies with KCNC1 variants: genotype‐phenotype‐functional correlations
Cameron, Jillian M., Maljevic, Snezana, Nair, Umesh, Aung, Ye Htet, Cogné, Benjamin, Bézieau, Stéphane, Blair, Edward, Isidor, Bertrand, Zweier, Christiane, Reis, André, Koenig, Mary Kay, Maarup, Timothy, Sarco, Dean, Afenjar, Alexandra, Huq, A. H. M. Mahbubul, Kukolich, Mary, Billette de Villemeur, Thierry, Nava, Caroline, Héron, Bénédicte, Petrou, Steven, Berkovic, Samuel F.
Published in Annals of clinical and translational neurology (01.07.2019)
Published in Annals of clinical and translational neurology (01.07.2019)
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Journal Article
Evaluation of Neuroinflammation in X-Linked Adrenoleukodystrophy
Kumar, Ajay, MD, PhD, DNB, Chugani, Harry T., MD, Chakraborty, Pulak, PhD, Huq, A.H.M. Mahbubul, MD, PhD
Published in Pediatric neurology (01.02.2011)
Published in Pediatric neurology (01.02.2011)
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Journal Article
Homozygous myotonic dystrophy with craniosynostosis
Cerghet, Mirela, Tapos, Daniela, Serajee, Fatema J, Mahbubul Huq, A H M
Published in Journal of child neurology (01.08.2008)
Published in Journal of child neurology (01.08.2008)
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Journal Article
Advances in Tourette syndrome: diagnoses and treatment
Serajee, Fatema J, Mahbubul Huq, A H M
Published in The Pediatric clinics of North America (01.06.2015)
Published in The Pediatric clinics of North America (01.06.2015)
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Journal Article
Association of Reelin gene polymorphisms with autism
Serajee, Fatema J., Zhong, Hailang, Mahbubul Huq, A.H.M.
Published in Genomics (San Diego, Calif.) (2006)
Published in Genomics (San Diego, Calif.) (2006)
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Journal Article
X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death
Mahbubul Huq, A. H. M., Lovell, Rhonda S., Ou, Ching-Nan, Beaudet, Arthur L., Craigen, William J.
Published in Human molecular genetics (01.10.1997)
Published in Human molecular genetics (01.10.1997)
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Journal Article
Evidence of somatic mosaicism in Sturge-Weber syndrome
Huq, A H M Mahbubul, Chugani, Diane C, Hukku, Bharati, Serajee, Fatema Jahan
Published in Neurology (10.09.2002)
Published in Neurology (10.09.2002)
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Journal Article
Stroke in sickle cell disease
Serajee, Fatema J., Sarnaik, Sharada A., Altinok, Deniz, Huq, A.H.M. Mahbubul
Published in Journal of pediatric neurology (01.09.2010)
Published in Journal of pediatric neurology (01.09.2010)
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Journal Article
The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism
Serajee, F J, Zhong, H, Nabi, R, Huq, A H M Mahbubul
Published in Journal of medical genetics (01.04.2003)
Published in Journal of medical genetics (01.04.2003)
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Journal Article
No association between the EN2 gene and autistic disorder
Zhong, H, Serajee, F J, Nabi, R, Huq, A H M Mahbubul
Published in Journal of medical genetics (01.01.2003)
Published in Journal of medical genetics (01.01.2003)
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Journal Article
Isolation, Mapping, and Functional Expression of the Mouse X Chromosome Glycerol Kinase Gene
Huq, A.H.M.Mahbubul, Lovell, Rhonda S., Sampson, Margaret J., Decker, William K., Dinulos, Mary Beth, Disteche, Christine M., Craigen, William J.
Published in Genomics (San Diego, Calif.) (15.09.1996)
Published in Genomics (San Diego, Calif.) (15.09.1996)
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Journal Article
Demonstration of an Unstable Variant of Pyruvate Dehydrogenase Protein (E1) in Cultured Fibroblasts from a Patient with Congenital Lactic Acidemia
MAHBUBUL HUQ, A. H. M., ITO, MICHINORI, NAITO, ETSUO, SAIJO, TAKAHIKO, TAKEDA, EIJI, KURODA, YASUHIRO
Published in Pediatric research (01.07.1991)
Published in Pediatric research (01.07.1991)
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Journal Article