Serajee, Fatema J.: search on Z-Library

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1

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

Rafiqun Nabi, Hailang Zhong, Fatema J Serajee, AHM Mahbubul Huq

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2003

Language:

english

File:

PDF, 54 KB

english, 2003

2

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism

Rafiqun Nabi, Fatema J. Serajee, Diane C. Chugani, Hailang Zhong, A.H.M. Mahbubul Huq

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 77 KB

english, 2004

3

Association of Reelin gene polymorphisms with autism

Fatema J. Serajee, Hailang Zhong, A.H.M. Mahbubul Huq

Journal:

Year:

2006

Language:

english

File:

PDF, 183 KB

english, 2006

4

Posterior Reversible Encephalopathy and Cerebral Vasoconstriction in a Patient With Hemolytic Uremic Syndrome

Agarwal, Rajkumar, Davis, Cresha, Altinok, Deniz, Serajee, Fatema J.

Journal:

Pediatric Neurology

Year:

2014

Language:

english

File:

PDF, 1.05 MB

english, 2014

5

Advances in Tourette Syndrome

Serajee, Fatema J., Mahbubul Huq, A.H.M.

Journal:

Pediatric Clinics of North America

Year:

2015

Language:

english

File:

PDF, 351 KB

english, 2015

6

Homozygous Mutation in Synaptic Vesicle Glycoprotein 2A Gene Results in Intractable Epilepsy, Involuntary Movements, Microcephaly, and Developmental and Growth Retardation

Serajee, Fatema J., Huq, Ahm M.

Journal:

Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 974 KB

english, 2015

7

“Molar Tooth Sign” Reveals the Cause of Apnea in a Term Neonate

Rashid, Salman, Dean, Marissa, Serajee, Fatema

Journal:

The Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 258 KB

english, 2016

8

Narcolepsy without Cataplexy Mimicking Psychiatric Illness

Ueda, Keisuke, Serajee, Fatema

Journal:

Journal of Pediatric Neurology

Year:

2016

Language:

english

File:

PDF, 66 KB

english, 2016

9

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

Tripathi, Richa, Serajee, Fatema, Jiang, Huiyuan, Huq, A.H.M. Mahbubul

Journal:

Pediatric Neurology

Year:

2017

Language:

english

File:

PDF, 284 KB

english, 2017

10

Sibling response to initial antiepileptic medication predicts treatment success

Ueda, Keisuke, Serajee, Fatema, Rajlich, Jan, Taraman, Sharief, Steckling, Lindsey, Huq, Ahm M.

Journal:

Epilepsy Research

Year:

2017

Language:

english

File:

PDF, 194 KB

english, 2017

11

Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss

Set, Kallol K., Weber, Amanda R.B., Serajee, Fatema J., Huq, Ahm M.

Journal:

Year:

2018

Language:

english

File:

PDF, 410 KB

english, 2018

12

Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation

Ueda, Keisuke, Serajee, Fatema, Huq, Ahm M.

Journal:

Year:

2018

Language:

english

File:

PDF, 1.01 MB

english, 2018

13

Exome Sequencing Identifying Dual Mutations in Calcium Signaling Genes GNAO1 and ATP2B3 in a Patient with Early Infantile Epileptic Encephalopathy

Ueda, Keisuke, Serajee, Fatema, Huq, Ahm

Journal:

Journal of Pediatric Neurology

Year:

2017

Language:

english

File:

PDF, 3.46 MB

english, 2017

14

O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling

Selvan, Nithya, George, Stephan, Serajee, Fatema J, Shaw, Marie, Hobson, Lynne, Kalscheuer, Vera M, Prasad, Nripesh, Levy, Shawn E, Taylor, Juliet, Afitmos, Salim, Schwartz, Charles E., Huq, Ahm M, Ge

Journal:

Journal of Biological Chemistry

Year:

2018

Language:

english

File:

PDF, 3.59 MB

english, 2018

15

A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions

Ueda, Keisuke, Serajee, Fatema, Huq, Ahm M.

Journal:

Journal of Clinical Neurology

Year:

2017

Language:

english

File:

PDF, 1.05 MB

english, 2017

16

Case 2: An 11-year-old girl with aggressive behaviour and intellectual impairment

Omar, Jasmine, Agarwal, Rajkumar, Serajee, Fatema

Journal:

Paediatrics & child health

Year:

2014

Language:

english

File:

PDF, 742 KB

english, 2014

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