author-photo

Nahid Akhtar Khan

Centre for Cellular and Molecular Biology

14

Papers

153

Citations

Citation Trend

Filter By

Papers (13) Sort By

Journal Conference Others

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate

2018 Investigative Ophthalmology & Visual Science
Show All
- Source
- Cite
- Save
Citations (1)
Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations

2018 Clinical Neurology and Neurosurgery
Show All
- Source
- Cite
- Save
Citations (11)
Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India

2017 Mitochondrion
Show All
- Source
- Cite
- Save
Citations (12)
Mitochondrial disorders: Challenges in diagnosis & treatment

2015 Indian Journal of Medical Research
Show All
- Source
- Cite
- Save
Citations (35)
Mitochondrial DNA variations associated with hypertrophic cardiomyopathy

2014 Mitochondrion
Show All
- Source
- Cite
- Save
Citations (21)
Figure 1 from The "double panda" sign in Leigh disease. - Semantic Scholar

2014
Show All
- Source
- Cite
- Save
Citations (0)
The “Double Panda” Sign in Leigh Disease

2014 Journal of Child Neurology
Show All
- Source
- Cite
- Save
Citations (5)
The "double panda" sign in Leigh disease. - Semantic Scholar

2014
Show All
- Source
- Cite
- Save
Citations (0)
Mitochondrial DNA variations in Madras motor neuron disease

2013 Mitochondrion
Show All
- Source
- Cite
- Save
Citations (5)
Haplogroup Heterogeneity of LHON Patients Carrying the m.14484T>C Mutation in India

2013 Investigative Ophthalmology & Visual Science
Show All
- Source
- Cite
- Save
Citations (16)