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Mitochondrial Disorders of the Nervous System: A Review

Clinical pediatrics, 2019-04, Vol.58 (4), p.381-394

2019

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Abnormal Language Pathway in Children With Angelman Syndrome

Pediatric neurology, 2011-05, Vol.44 (5), p.350-356

2011

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Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood-Expanding the Phenotype of a Recently Reported Condition

Neuropediatrics, 2019-04, Vol.50 (2), p.122

2019

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Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation

Journal of neurogenetics, 2024-04, Vol.38 (2), p.41-45

2024

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Evaluation of Neuroinflammation in X-Linked Adrenoleukodystrophy

Pediatric neurology, 2011-02, Vol.44 (2), p.143-146

2011

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Advances in Tourette syndrome: diagnoses and treatment

The Pediatric clinics of North America, 2015-06, Vol.62 (3), p.687

2015

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SCN2A Mutation Is Associated With Infantile Spasms and Bitemporal Glucose Hypometabolism

Pediatric neurology, 2013-07, Vol.49 (1), p.46-49

2013

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Exome sequencing and diffusion tensor imaging in developmental disabilities

Pediatric research, 2014-03, Vol.75 (3), p.443-447

2014

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

Pediatric neurology, 2017-06, Vol.71, p.70-72

2017

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Association of Reelin gene polymorphisms with autism

Genomics (San Diego, Calif.), 2006, Vol.87 (1), p.75-83

2006

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Ex vivo and in vivo generation of neutrophil extracellular traps by neutrophils from septic patients

Critical care (London, England), 2015-03, Vol.19 (S1), p.P36-P36, Article P36

2015

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Infantile Spasms Are Associated With Abnormal Copy Number Variations

Journal of child neurology, 2013-10, Vol.28 (10), p.1191-1196

2013

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Homozygous Myotonic Dystrophy With Craniosynostosis

Journal of child neurology, 2008-08, Vol.23 (8), p.930-933

2008

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Association of Y Chromosome Haplotypes With Autism

Journal of child neurology, 2009-10, Vol.24 (10), p.1258-1261

2009

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Episodic Ataxia Type 1 (K‐channelopathy) Manifesting as Paroxysmal Nonkinesogenic Dyskinesia: Expanding the Phenotype

Movement disorders clinical practice (Hoboken, N.J.), 2017-09, Vol.4 (5), p.784-786

2017

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Novel FDG-PET Findings in Anti-NMDA Receptor Encephalitis: A Case Based Report

Journal of Child Neurology, 2011-10, Vol.26 (10), p.1325-1328

2011

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Spectrum of Salivary Gland Lesions in a Tertiary Level Hospital

Mymensingh medical journal : MMJ, 2015-07, Vol.24 (3), p.516

2015

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Vaginal rhinosporidiosis: a case report

Mymensingh medical journal : MMJ, 2014-07, Vol.23 (3), p.572

2014

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X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death

Human molecular genetics, 1997-10, Vol.6 (11), p.1803-1809

1997

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Histopathological analysis of hysterectomy specimens

Mymensingh medical journal : MMJ, 2007, Vol.16 (1), p.81

2007

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A 12 years old boy with carcinoma rectum

Mymensingh medical journal : MMJ, 2010-01, Vol.19 (1), p.116

2010

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Evidence of somatic mosaicism in Sturge-Weber syndrome

Neurology, 2002-09, Vol.59 (5), p.780

2002

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

American journal of medical genetics, 2003-05, Vol.119B (1), p.98-101

2003

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Histopathology based cancer pattern in Mymensingh region of Bangladesh

Mymensingh medical journal : MMJ, 2007-07, Vol.16 (2), p.165

2007

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Sensitivity of splenic and bone marrow aspirate study for diagnosis of kala-azar

Mymensingh medical journal : MMJ, 2004-07, Vol.13 (2), p.130

2004

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Mitochondrial Disorders of the Nervous System: A Review

Abnormal Language Pathway in Children With Angelman Syndrome

Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood-Expanding the Phenotype of a Recently Reported Condition

Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation

Evaluation of Neuroinflammation in X-Linked Adrenoleukodystrophy

Advances in Tourette syndrome: diagnoses and treatment

SCN2A Mutation Is Associated With Infantile Spasms and Bitemporal Glucose Hypometabolism

Exome sequencing and diffusion tensor imaging in developmental disabilities

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

Association of Reelin gene polymorphisms with autism

Ex vivo and in vivo generation of neutrophil extracellular traps by neutrophils from septic patients

Infantile Spasms Are Associated With Abnormal Copy Number Variations

Homozygous Myotonic Dystrophy With Craniosynostosis

Association of Y Chromosome Haplotypes With Autism

Episodic Ataxia Type 1 (K‐channelopathy) Manifesting as Paroxysmal Nonkinesogenic Dyskinesia: Expanding the Phenotype

Novel FDG-PET Findings in Anti-NMDA Receptor Encephalitis: A Case Based Report

Spectrum of Salivary Gland Lesions in a Tertiary Level Hospital

Vaginal rhinosporidiosis: a case report

X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death

Histopathological analysis of hysterectomy specimens

A 12 years old boy with carcinoma rectum

Evidence of somatic mosaicism in Sturge-Weber syndrome

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

Histopathology based cancer pattern in Mymensingh region of Bangladesh

Sensitivity of splenic and bone marrow aspirate study for diagnosis of kala-azar

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