Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Vykuntaraju K Gowda"'
Autor:
Vykuntaraju K Gowda, Viveka Santhosh Reddy, Varunvenkat M Srinivasan, Dhananjaya K Vamyanmane
Publikováno v:
Annals of Indian Academy of Neurology, Vol 27, Iss 1, Pp 103-105 (2024)
Externí odkaz:
https://doaj.org/article/3d00a2b6dd8d4e169ce644ea89130b3b
Autor:
Vykuntaraju K Gowda, Arun Y Bylappa, Uddhav Kinhal, Varunvenkat M Srinivasan, Dhananjaya K Vamyanmane
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 6, Pp 977-979 (2023)
Mitochondrial disorders are a group of metabolic disorders with variable presentation and usually affect organs with high energy requirements like the brain, eye, and heart. Seventeen-month-old girl child presented with right hemiparesis and regressi
Externí odkaz:
https://doaj.org/article/9d9761a071d842908ad9eead5e250f68
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 2, Pp 283-285 (2022)
Externí odkaz:
https://doaj.org/article/c3a2d9b7ded64f90841735d67b236b76
Autor:
Vykuntaraju K Gowda, Narmadham K Bharathi, Jamunashree Bettaiah, Maya Bhat, Sanjay K Shivappa
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 3, Pp 347-350 (2021)
Background: Canavan disease (CD) is an autosomal recessively inherited leukodystrophy. It affects one in 6,400 to 13,500 people in the Jewish population. However, prevalence and presentation of the disease in India is largely unknown; hence, we are r
Externí odkaz:
https://doaj.org/article/d33c8d0b53c54373a694e9ee2f0f5166
Autor:
Vykuntaraju K Gowda, Amit Avaragollapuravarga Mathada, Varunvenkat M Srinivasan, Dhananjaya K Vamyanmane
Publikováno v:
Advanced Biomedical Research, Vol 12, Iss 1, Pp 148-148 (2023)
Biotinidase deficiency is a rare autosomal recessive neurometabolic disorder resulting in biotin deficiency. Our patient presented with seizures and developmental delay since infancy and was started on megavitamin supplements. At 14 years, she presen
Externí odkaz:
https://doaj.org/article/02e9bf0368154b1d83679cbc13d876c3
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 5, Pp 799-801 (2021)
Externí odkaz:
https://doaj.org/article/ad5aa884ada748c291b96e66a91d9581
Autor:
Manoj Murhekar, Sanjay Verma, Kuldeep Singh, Ashish Bavdekar, Naveen Benakappa, Sridhar Santhanam, Gajanan Sapkal, Rajlakshmi Viswanathan, Mini P Singh, Vijaya Lakshmi Nag, Sadanand Naik, Munivenkatappa Ashok, Asha Mary Abraham, Devika Shanmugasundaram, R Sabarinathan, Valsan Philip Verghese, Suji George, Ravinder Kaur Sachdeva, Jyoti Kolekar, S Manasa, Jagat Ram, Madhu Gupta, Manoj K Rohit, Praveen Kumar, Parul Chawla Gupta, R K Ratho, Sanjay Kumar Munjal, Urvashi Nehra, Daisy Khera, Neeraj Gupta, Nidhi Kaushal, Pratibha Singh, Ravisekhar Gadepalli, Neelam Vaid, Sandeep Kadam, Sanjay Shah, S Mahantesh, Vykuntaraju K Gowda, Pradeep Haldar, M K Aggarwal, Nivedita Gupta
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 14, Iss 2, p e0007982 (2020)
BACKGROUND:Government of India is committed to eliminate measles and control rubella/congenital rubella syndrome (CRS) by 2020. In 2016, CRS surveillance was established in five sentinel sites. We analyzed surveillance data to describe the epidemiolo
Externí odkaz:
https://doaj.org/article/9f8e4009119c4d4db0e59dbbe3491fda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 942-943 (2021)
Externí odkaz:
https://doaj.org/article/f715b6fef4914d4c8caab84449861723
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 3, Pp 324-328 (2016)
Chromoblastomycosis is a chronic granulomatous infection of the skin and subcutaneous tissue caused by specific group of dematiaceous fungi. The infection results from traumatic injury and is seen more commonly on feet and lower legs. It is rarely se
Externí odkaz:
https://doaj.org/article/1ecdacd37d304b2496c668a887086b29
Autor:
Vykuntaraju K. Gowda, Sandeep Rangaiah, Varunvenkat M. Srinivasan, Dhananjaya Kotebagilu Narayana Vamyanmane
Publikováno v:
Karnataka Paediatric Journal. 37:86-89
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder and the most debilitating condition of heterotopic ossification in humans. Misdiagnosis is common and they suffer from complications of incorrect diagnosis and subsequent inapprop