Nahid A. Khan
Hyderabad, TG, India
Last Updated: 09/26/2026
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Found 11 publications
Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate.
Journal: Investigative ophthalmology & visual science
Published: January 19, 2018
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.
Journal: Clinical neurology and neurosurgery
Published: August 16, 2017
Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
Journal: Investigative ophthalmology & visual science
Published: August 03, 2017
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.
Journal: Mitochondrion
Published: July 23, 2016
Mitochondrial disorders: challenges in diagnosis & treatment.
Journal: The Indian journal of medical research
Published: April 11, 2015
Response to letter to the editor "mitochondrial haplogroups are associated with hypertrophic cardiomyopathy in the Indian population".
Journal: Mitochondrion
Published: July 24, 2014
Mitochondrial DNA variations associated with hypertrophic cardiomyopathy.
Journal: Mitochondrion
Published: August 24, 2013
Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
Journal: Investigative ophthalmology & visual science
Published: May 16, 2013
The "double panda" sign in Leigh disease.
Journal: Journal of child neurology
Published: February 17, 2013
Mitochondrial DNA variations in Madras motor neuron disease.
Journal: Mitochondrion
Published: November 09, 2012
Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
Journal: Molecular vision
Published: August 13, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026