Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chikkanna Govindaraju"'
Autor:
Arumugam Paramasivam, J.N. Jessiena Ponmalar, Rakesh Kumar, Parayil Sankaran Bindu, Madhu Nagappa, Kumarasamy Thangaraj, V.P. Vandana, Vandana Nunia, Arun B. Taly, Sanjib Sinha, H R Arvinda, Narayanappa Gayathri, Chikkanna Govindaraju, Shwetha Chiplunkar, Mariyamma Philip, M.M. Srinivas Bharath, Chetan Chandrakanth Vekhande, Nahid Akhtar Khan, Periyasamy Govindaraj, Kothari Sonam
Publikováno v:
Clinical Neurology and Neurosurgery. 164:182-189
Objectives Studies exploring the outcome of epilepsy in patients with mitochondrial disorders are limited. This study examined the outcome of epilepsy in patients with mitochondrial disorders and its relation with the clinical phenotype, genotype and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc89a7da5969aa1d3da27bab52d59f8e
https://doi.org/10.1016/j.clineuro.2017.12.010
https://doi.org/10.1016/j.clineuro.2017.12.010
Autor:
Madhu Nagappa, Kumarasamy Thangaraj, Nahid Akthar Khan, Parayil Sankaran Bindu, Sanjib Sinha, Chikkanna Govindaraju, H R Arvinda, Narayanappa Gayathri, Periyasamy Govindaraj, Kothari Sonam, Arun B Taly
Publikováno v:
Neuropediatrics. 46:277-281
Mutations in the mitochondrial-encoded nicotinamide adenine dinucleotide dehydrogenase 5 gene ( MT-ND5 ) has been implicated as an important genetic cause of childhood mitochondrial encephalomyopathies. This study reports the clinical and magnetic re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66ab4a73ac3605ec196303660a601c80
https://doi.org/10.1055/s-0035-1550149
https://doi.org/10.1055/s-0035-1550149
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations
Autor:
Madhu Nagappa, Kumarasamy Thangaraj, M.M. Srinivas Bharath, Sanjib Sinha, Nahid Akthar Khan, Narayanappa Gayathri, Kothari Sonam, Arun B Taly, Chikkanna Govindaraju, H R Arvinda, Parayil Sankaran Bindu
Publikováno v:
Brain and Development. 36:807-812
Background: Mutation in the SURF1 is one of the most common nuclear mutations associated with Leigh syndrome and cytochrome c oxidase deficiency. This study aims to describe the phenotypic and imaging features in four patients with Leigh syndrome and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ee245ae2fced1b9770b588f26266a2d
https://doi.org/10.1016/j.braindev.2013.10.012
https://doi.org/10.1016/j.braindev.2013.10.012
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 2, Pp 217-221 (2014)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Two adult men presented with the rare Hoffmann's syndrome (HS). Case 1: A 35-year-old male patient had progressive stiffness of lower limbs of 13 years and generalized muscle hypertrophy and myalgia of 3 years duration. Had periorbital edema, dry ski
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc6baf1d060d58d380039496ee4d8921
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Autor:
Kumaraswamy Thangaraj, Chikkanna Govindaraju, Kothari Sonam, Nahid Akthar Khan, Arun B Taly, Hanumanthapura R. Aravinda, Parayil Sankaran Bindu, Atchayaram Nalini, Narayanappa Gayathri
Publikováno v:
Journal of clinical neuromuscular disease. 16(2)
Mitochondrial disorders resulting from an isolated deficiency of complex II of the respiratory chain is rarely reported. The phenotypic spectrum associated with these disorders is heterogeneous and still expanding. This report describes a patient who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a2ce094f946dab5ba96a6b6005bc41e
https://pubmed.ncbi.nlm.nih.gov/25415517
https://pubmed.ncbi.nlm.nih.gov/25415517
Autor:
Chikkanna Govindaraju, Narayanappa Gayathri, Sanjib Sinha, H R Arvinda, Madhu Nagappa, Kumarasamy Thangaraj, V.P. Vandana, Periyasamy Govindaraj, Parayil Sankaran Bindu, Arun B. Taly, Shwetha Chiplunkar, Kothari Sonam
Publikováno v:
Clinical neurology and neurosurgery. 148
Objectives Reports of audiological manifestations in specific subgroups of mitochondrial disorders are limited. This study aims to describe the audiological findings in patients with MELAS syndrome and m.3243A>G mutation. Patients & methods Audiologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8612ce994c3299318e183c2fba6f56fe
https://pubmed.ncbi.nlm.nih.gov/27359089
https://pubmed.ncbi.nlm.nih.gov/27359089
Autor:
Kothari Sonam, A B Taly, D Ranjith, Swapnil Sinha, Parayil Sankaran Bindu, M.M. Srinivas Bharath, Madhu Nagappa, Nahid Akhtar Khan, Kumarasamy Thangaraj, H R Arvinda, Narayanappa Gayathri, Chikkanna Govindaraju
Publikováno v:
The British Journal of Radiology. 87:20130478
Bilateral hypertrophic olivary degeneration on brain MRI has been reported in a few metabolic, genetic and neurodegenerative disorders, including mitochondrial disorders. In this report, we sought to analyse whether bilateral symmetrical inferior oli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73c94052f97dd7e6e3e8ecadb9b8c769
https://doi.org/10.1259/bjr.20130478
https://doi.org/10.1259/bjr.20130478