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Future Cardiology
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July 25, 2024
Making a case for mitochondria in hypertrophic cardiomyopathy
Pankaj Prasun, Utkarsh Kohli
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 26, 2025
<i>ANKS1B</i> is a potential candidate gene for short stature and failure to thrive in children
Pankaj Prasun, Rebecca C Pulvermacher
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 9, 2025
<i>GNB1</i> haploinsufficiency presents as monogenic obesity syndrome
Pankaj Prasun, Katelyn J Watkin
Journal of the Neurological Sciences
|
November 25, 2011
Fatal acute encephalopathy in two siblings: a distinct hereditary entity?
Pankaj Prasun, David W Stockton
Journal of Neurology
|
July 16, 2014
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation
Pankaj Prasun, Dwight D Koeberl
Molecular Syndromology
|
June 29, 2026
Novel Clinical and Genetic Findings in Laurin-Sandrow Syndrome: A Case Report
Pankaj Prasun, Katelyn J Watkin
The Journal of Pediatrics
|
January 31, 2012
Declining school performance as a harbinger of a treatable neurodegenerative condition
Pankaj Prasun, Vinod K Misra
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Late onset Leigh syndrome mimicking central nervous system vasculitis
Pankaj Prasun, Loren Del Mar Pena
American Journal of Medical Genetics. Part A
|
June 4, 2025
Chromosome 3q22.2-q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, Pierre Robin Sequence, and Recurrent Infections
Pankaj Prasun, Sonja Henry, Vivek Balasubramaniam
Translational Gastroenterology and Hepatology
|
January 13, 2021
Mitochondrial dysfunction in nonalcoholic fatty liver disease and alcohol related liver disease
Pankaj Prasun, Ilona Ginevic, Kimihiko Oishi
Page
of 5
Search research articles
Search
Showing results (11-20 of 46) with videos related to
Sort By:
Page
of 5
Future Cardiology
|
July 25, 2024
Making a case for mitochondria in hypertrophic cardiomyopathy
Pankaj Prasun, Utkarsh Kohli
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 26, 2025
<i>ANKS1B</i> is a potential candidate gene for short stature and failure to thrive in children
Pankaj Prasun, Rebecca C Pulvermacher
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 9, 2025
<i>GNB1</i> haploinsufficiency presents as monogenic obesity syndrome
Pankaj Prasun, Katelyn J Watkin
Journal of the Neurological Sciences
|
November 25, 2011
Fatal acute encephalopathy in two siblings: a distinct hereditary entity?
Pankaj Prasun, David W Stockton
Journal of Neurology
|
July 16, 2014
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation
Pankaj Prasun, Dwight D Koeberl
Molecular Syndromology
|
June 29, 2026
Novel Clinical and Genetic Findings in Laurin-Sandrow Syndrome: A Case Report
Pankaj Prasun, Katelyn J Watkin
The Journal of Pediatrics
|
January 31, 2012
Declining school performance as a harbinger of a treatable neurodegenerative condition
Pankaj Prasun, Vinod K Misra
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Late onset Leigh syndrome mimicking central nervous system vasculitis
Pankaj Prasun, Loren Del Mar Pena
American Journal of Medical Genetics. Part A
|
June 4, 2025
Chromosome 3q22.2-q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, Pierre Robin Sequence, and Recurrent Infections
Pankaj Prasun, Sonja Henry, Vivek Balasubramaniam
Translational Gastroenterology and Hepatology
|
January 13, 2021
Mitochondrial dysfunction in nonalcoholic fatty liver disease and alcohol related liver disease
Pankaj Prasun, Ilona Ginevic, Kimihiko Oishi
Page
of 5