Haseena Sait

Raebareli Road
Lucknow, UP, India

Last Updated: 09/26/2026

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Found 29 publications

Corrigendum to "Nuances in ATP7B Genetic Testing and Interpretation in India" [J Clin Exp Hepatol 16 (1) (2026) 103205].

Corrigendum to "Nuances in ATP7B Genetic Testing and Interpretation in India" [J Clin Exp Hepatol 16 (1) (2026) 103205].

Journal: Journal of clinical and experimental hepatology

Published: June 30, 2026

Nuances in ATP7B Genetic Testing and Interpretation in India.

Nuances in ATP7B Genetic Testing and Interpretation in India.

Journal: Journal of clinical and experimental hepatology

Published: August 07, 2025

Genotypic and Phenotypic Profile of Hereditary Spastic Paraplegia in Children: A Single-Centre Study from Northern India.

Genotypic and Phenotypic Profile of Hereditary Spastic Paraplegia in Children: A Single-Centre Study from Northern India.

Journal: Indian pediatrics

Published: July 23, 2025

Molecular and Clinical Landscape of Osteogenesis Imperfecta: Unraveling Autosomal Recessive Forms, Therapeutic Outcomes, and Bone Mineral Density in Carriers.

Molecular and Clinical Landscape of Osteogenesis Imperfecta: Unraveling Autosomal Recessive Forms, Therapeutic Outcomes, and Bone Mineral Density in Carriers.

Journal: Clinical genetics

Published: April 11, 2025

Gonadal mosaicism and paradoxical phenotype in NEXMIF encephalopathy: a case report of two siblings.

Gonadal mosaicism and paradoxical phenotype in NEXMIF encephalopathy: a case report of two siblings.

Journal: Journal of genetics

Published: April 02, 2025

Spectrum of Inherited Childhood-Onset Dystonia: Case Series of 19 Families With Genotype and Phenotype Characterization Highlighting the Treatable Causes.

Spectrum of Inherited Childhood-Onset Dystonia: Case Series of 19 Families With Genotype and Phenotype Characterization Highlighting the Treatable Causes.

Journal: Clinical genetics

Published: February 10, 2025

Clinical and Radiological Characterization of TEFM-Associated Neurological Disorder.

Clinical and Radiological Characterization of TEFM-Associated Neurological Disorder.

Journal: American journal of medical genetics. Part A

Published: January 25, 2025

Immune dysregulation in a dysmorphic child with 6q23.3 deletion: a single case report.

Immune dysregulation in a dysmorphic child with 6q23.3 deletion: a single case report.

Journal: Clinical dysmorphology

Published: October 02, 2024

COQ7 splice site variant causing a spastic paraparesis phenotype in siblings.

COQ7 splice site variant causing a spastic paraparesis phenotype in siblings.

Journal: Journal of genetics

Published: July 31, 2024

Effect of Maternal Iodine Excess during Pregnancy on Neonatal Thyroid Function and Neurodevelopmental Status at 12 Weeks.

Effect of Maternal Iodine Excess during Pregnancy on Neonatal Thyroid Function and Neurodevelopmental Status at 12 Weeks.

Journal: Journal of the ASEAN Federation of Endocrine Societies

Published: February 15, 2024

Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening: an initial perspective.

Anastrozole-mediated modulation of mitochondrial activity by inhibition of mitochondrial permeability transition pore opening: an initial perspective.

Journal: Journal of biomolecular structure & dynamics

Published: February 23, 2023

Neurodegeneration with brain iron accumulation: a case series highlighting phenotypic and genotypic diversity in 20 Indian families.

Neurodegeneration with brain iron accumulation: a case series highlighting phenotypic and genotypic diversity in 20 Indian families.

Journal: Neurogenetics

Published: November 07, 2022

Showing 1-12 of 29

Last Updated: 09/26/2026