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pro vyhledávání: '"Mahadevappa, Manjunath"'
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Akademický článek
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Akademický článek
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Autor:
Atchayaram Nalini, Mahadevappa Manjunath, Narayanappa Gayathri, Saraswati Nashi, Seena Vengalil, Chandrajit Prasad, Archana Natarajan, Rita Christopher, Veeramani Preethish-Kumar, Kiran Polavarapu
Publikováno v:
Neuromuscular Disorders. 27:986-996
Fatty acid oxidation disorders presenting as primary myopathy is relatively rare and also diagnostically challenging. Its association with “dropped head syndrome” is reported till date in single cases of carnitine deficiency and multiple acyl CoA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1868cd22c6b3273f792d15f16329cbd
https://doi.org/10.1016/j.nmd.2017.08.004
https://doi.org/10.1016/j.nmd.2017.08.004
Autor:
Mathew, Thomas, John, Saji K, Sarma, GRK, Nadig, Raghunandan, Kumar R, Shiva, Murgod, Uday, Mahadevappa, Manjunath, Javali, Mahendra, Acharya, Purushottam Thammaya, Hosurkar, Guruprasad, Krishnan, Pramod, Kamath, Vikram, Badachi, Sagar, Souza, Delon D, Iyer, Rajesh B, Nagarajaiah, Rajesh Karalumangala, Anand, Bawani, Kumar, Sujit, Kodapala, Suresh, Shivde, Sonia
Publikováno v:
International Journal of Stroke; Jun2021, Vol. 16 Issue 4, p429-436, 8p
Autor:
Priya Treesa Thomas, Ravinder-Jeet Singh, Kandavel Thennarasu, Kiran Polavarapu, Veeramani Preethish-Kumar, Deepha Sekar, Atchayaram Nalini, Mahadevappa Manjunath, Saraswati Nashi, Narayanappa Gayathri, Seena Vengalil
Publikováno v:
Neurology India. 66(1)
Background: Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy. There are no large studies describing its natural course from India. Materials and Methods: Immunohistochemically/genetically confirmed DMD patients diagnosed betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1674c7ba65e5eefa42771d6d599050cd
https://pubmed.ncbi.nlm.nih.gov/29322964
https://pubmed.ncbi.nlm.nih.gov/29322964
Autor:
Srinivas Dwarakanath, Albert Stezin, Ravi Yadav, A Jafar, Mahadevappa Manjunath, Somanna Sampath, Pramod Kumar Pal, Pratibha Surathi, Abhishek Lenka, Ketan Jhunjhunwala
Publikováno v:
Neurology India. 65(6)
Introduction: Dystonia is one of the most prevalent forms of movement disorders and is characterized by sustained or intermittent muscle contractions causing abnormal, often repetitive, movements, postures, or both. Dystonia causes significant morbid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df0ea5269d1688ebcfe552368ec7769
https://pubmed.ncbi.nlm.nih.gov/29133691
https://pubmed.ncbi.nlm.nih.gov/29133691
Autor:
Mahadevappa Manjunath, Talakad N. Sathyaprabha, Kiran Polavarapu, Priya Treesa Thomas, Veeramani Preethish-Kumar, Atchayaram Nalini, Rose Dawn Bharath, Deepha Sekar, Seena Vengalil
Publikováno v:
Neuromuscular disorders : NMD. 26(11)
The purpose of this study was to describe the pattern of muscle involvement using MRI findings and correlate with functional as well as muscle strength measurements. Fifty genetically confirmed DMD children with a mean age of 7.6 ± 2.8 (4–15 years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86cd6541fc0286874216525636dfeedb
https://pubmed.ncbi.nlm.nih.gov/27666775
https://pubmed.ncbi.nlm.nih.gov/27666775
Autor:
Ravi Yadav, Albert Stezin, Mahadevappa Manjunath, Dwarakanath Srinivas, Ketan Jhunjhunwala, Pramod Kumar Pal, Abhishek Lenka
Publikováno v:
Neurology India. 66:135
Improvement in motor symptoms with levodopa is one of the hallmark features of Parkinson's disease (PD). The response to levodopa may reduce during the course of the illness. Few studies have also reported reduced response to levodopa in patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0d319db8cf8edf4d6a21fbb4f9a52af
https://doi.org/10.4103/0028-3886.226454
https://doi.org/10.4103/0028-3886.226454
Autor:
Ravinder-Jeet Singh, Mahadevappa Manjunath, Veeramani Preethish-Kumar, P Kiran, Atchayaram Nalini, Narayanappa Gayathri
Publikováno v:
Neurology India. 63(1)
Background: Multiplex ligation-dependant probe amplification (MLPA) is a highly sensitive and rapid alternative to multiplex polymerase chain reaction (PCR). Muscle biopsy should be reserved for mutation-negative cases. Materials and Methods: An atte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2237352d8b6d1751274b017826ea5532
https://pubmed.ncbi.nlm.nih.gov/25751470
https://pubmed.ncbi.nlm.nih.gov/25751470