Serajee, Fatema
M.D.
Associate Professor
More about Fatema Serajee
Publications & Presentations
Serajee F, Salman Rashid, Huq AM (2024). Carbamazepine responsive Episodic Dystonia and Hallucination due to Pyruvate Dehy-drogenase E2 (DLAT) gene mutation Neurogenetics.
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.
Ueda K, Serajee F, Huq AM (2018). Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation. Pediatrics.
Set KK, Weber ARB, Serajee FJ, Huq AM (2018). Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss. Neurology.
Serajee FJ (2017). Narcolepsy without Cataplexy Mimicking Psychiatric Illness J Pediatr Neurol.
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.
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).
Ueda K, Serajee F, Rajlich J, Taraman S, Steckling L, Huq AM (2017). Sibling response to initial antiepileptic medication predicts treatment success. Epilepsy research.
Rashid S, Dean M, Serajee F (2016). "Molar Tooth Sign" Reveals the Cause of Apnea in a Term Neonate. The Journal of pediatrics.
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.
Serajee FJ, Mahbubul Huq AH (2015). Advances in Tourette syndrome: diagnoses and treatment. Pediatric clinics of North America.
Agarwal R, Davis C, Altinok D, Serajee FJ (2014). Posterior reversible encephalopathy and cerebral vasoconstriction in a patient with hemolytic uremic syndrome. Pediatric neurology.
Omar J, Agarwal R, Serajee F (2014). Case 2: An 11-year-old girl with aggressive behaviour and intellectual impairment. Paediatrics & child health.
Veeravigrom M, Serajee F (2012). A case of isolated oculomotor nerve palsy in a girl. J Pediatric Neurology.
Sarnaik SA, Altinock D, Huq AM (2010). Stroke in sickle cell disease J Pediatric Neurology.
Serajee FJ, Mahbubul Huq AH (2009). Association of Y chromosome haplotypes with autism. Journal of child neurology.
Cerghet M, Tapos D, Serajee FJ, Mahbubul Huq AH (2008). Homozygous myotonic dystrophy with craniosynostosis. Journal of child neurology.
Serajee FJ, Zhong H, Mahbubul Huq AH (2006). Association of Reelin gene polymorphisms with autism. Genomics.
Serajee FJ, Nabi R, Zhong H, Huq M (2004). Polymorphisms in xenobiotic metabolism genes and autism. Journal of child neurology.
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, 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, 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.
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, 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.
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.
Ueda K, Serajee F, Huq AM (2018). Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation. Pediatrics.
Set KK, Weber ARB, Serajee FJ, Huq AM (2018). Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss. Neurology.
Serajee FJ (2017). Narcolepsy without Cataplexy Mimicking Psychiatric Illness J Pediatr Neurol.
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.
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).
Ueda K, Serajee F, Rajlich J, Taraman S, Steckling L, Huq AM (2017). Sibling response to initial antiepileptic medication predicts treatment success. Epilepsy research.
Rashid S, Dean M, Serajee F (2016). "Molar Tooth Sign" Reveals the Cause of Apnea in a Term Neonate. The Journal of pediatrics.
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.
Serajee FJ, Mahbubul Huq AH (2015). Advances in Tourette syndrome: diagnoses and treatment. Pediatric clinics of North America.
Agarwal R, Davis C, Altinok D, Serajee FJ (2014). Posterior reversible encephalopathy and cerebral vasoconstriction in a patient with hemolytic uremic syndrome. Pediatric neurology.
Omar J, Agarwal R, Serajee F (2014). Case 2: An 11-year-old girl with aggressive behaviour and intellectual impairment. Paediatrics & child health.
Veeravigrom M, Serajee F (2012). A case of isolated oculomotor nerve palsy in a girl. J Pediatric Neurology.
Sarnaik SA, Altinock D, Huq AM (2010). Stroke in sickle cell disease J Pediatric Neurology.
Serajee FJ, Mahbubul Huq AH (2009). Association of Y chromosome haplotypes with autism. Journal of child neurology.
Cerghet M, Tapos D, Serajee FJ, Mahbubul Huq AH (2008). Homozygous myotonic dystrophy with craniosynostosis. Journal of child neurology.
Serajee FJ, Zhong H, Mahbubul Huq AH (2006). Association of Reelin gene polymorphisms with autism. Genomics.
Serajee FJ, Nabi R, Zhong H, Huq M (2004). Polymorphisms in xenobiotic metabolism genes and autism. Journal of child neurology.
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, 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, 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.
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, 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.
Credentials, Certifications & Awards
Resident Research Award
Education
M.B.B.S., Dhaka University/Mymensingh Medical College, Bangladesh