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Cytokine & Growth Factor Reviews|August 1, 2025
Mechanisms and routes of G-protein coupled receptor-mediated Tau degradation in Alzheimer's diseaseVaishnavi Ananthanarayana, Hariharakrishnan Chidamabram, Periyasamy Govindaraj, et al.Neurochemistry International|September 14, 2020
Exposure to the neurotoxin 3-nitropropionic acid in neuronal cells induces unique histone acetylation pattern: Implications for neurodegenerationS Ranganayaki, Periyasamy Govindaraj, N Gayathri, et al.The Indian Journal of Medical Research|April 11, 2015
Mitochondrial disorders: challenges in diagnosis & treatmentNahid Akhtar Khan, Periyasamy Govindaraj, Angamuthu Kannan Meena, et al.American Journal of Medical Genetics. Part A|July 1, 2024
A unique case of hyperammonemia due to CA5A deficiency: Impact of coexisting gene mutations, pseudogene, and microdeletionRohan Peter Mathew, Prashanth Ranya Raghavendra, Biradar Disha, et al.American Journal of Medical Genetics. Part A|January 28, 2026
Expanding the Phenotype of STAMBP-Related Microcephaly-Capillary Malformation SyndromeVykuntaraju K Gowda, Amaresh Roy, B Disha, et al.Molecular Vision|June 28, 2013
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 neuropathyNahid Akhtar Khan, Periyasamy Govindaraj, Vuskamalla Jyothi, et al.Annals of Human Genetics|November 22, 2024
Intermittent episodes of acute severe encephalomyopathy and early death in two siblings caused by biallelic likely pathogenic variants in FASTKD2: Expanding phenotype and literature reviewNamanpreet Kaur, Puneeth H Somashekar, Sekar Deepha, et al.Mitochondrion|December 17, 2009
Mitochondrial DNA haplogroup 'R' is associated with Noonan syndrome of south IndiaDeepa Selvi Rani, Perundurai S Dhandapany, Pratibha Nallari, et al.Annals of Hematology|March 12, 2013
Mitochondrial DNA variations in myelodysplastic syndromeMaya Gupta, Manisha Madkaikar, Vundinti Babu Rao, et al.Journal of Child Neurology|March 18, 2020
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene PanelBindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.Pageof 7