Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Lokesh, Lingappa"'
Publikováno v:
Annals of Indian Academy of Neurology, Vol 27, Iss 5, Pp 593-595 (2024)
Externí odkaz:
https://doaj.org/article/985dbc07f20945c78bd1c5b53355d541
Autor:
Kevin A. Strauss, Vincent J. Carson, Emilienne Bolettieri, Mariah Everett, Ashton Bollinger, Lauren E. Bowser, Keturah Beiler, Millie Young, Simon Edvardson, Nitay Fraenkel, Adele D'Amico, Enrico Bertini, Lokesh Lingappa, Devyani Chowdhury, Linda P. Lowes, Megan Iammarino, Lindsay N. Alfano, Karlla W. Brigatti
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 11, Pp 1972-1984 (2023)
ABSTRACT Objective We created WiTNNess as a hybrid prospective/cross‐sectional observational study to simulate a clinical trial for infantile‐onset TNNT1 myopathy. Our aims were to identify populations for future trial enrollment, rehearse outcom
Externí odkaz:
https://doaj.org/article/aed2e23aa754450b8426dda69cb75b30
Autor:
Tejanjani Vathada, Lokesh Lingappa
Publikováno v:
Annals of Child Neurology, Vol 31, Iss 2, Pp 97-102 (2023)
Purpose Developmental delay (DD) is reported to be frequent in developing countries, such as India. Hence, this study was carried out to evaluate preventable risk factors that can predispose children to DD, through observations of pediatric neurology
Externí odkaz:
https://doaj.org/article/87b2417173f9470a9c3fc8248f5e0b87
Autor:
Sirisharani Siddiahgari, Santosh Kumar Soma, Chandravathi Penmetcha, Sandhya Vaddadi, Varshini Bandi, Lokesh Lingappa
Publikováno v:
Indian Journal of Dermatology, Vol 67, Iss 2, Pp 164-168 (2022)
Background: Silvery Hair Syndromes (SHS), an autosomal recessive inherited disorder, includes Chediak–Higashi syndrome (CHS), Griscelli syndrome (GS), Hermansky–Pudlak syndrome (HPS), and Elejalde syndrome. Associated immunological and neurologic
Externí odkaz:
https://doaj.org/article/cad55a2e1ac6499faab41e66cbd14101
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2592-2594 (2022)
Externí odkaz:
https://doaj.org/article/da089e3bd1124b56ab46908a6c23256e
Autor:
Lokesh Lingappa, Ramesh Konanki, Ravi Varma, Nikit Shah, Subodh Raju, Sukumar Sura, Leenatha Reddy, Sirisha Rani
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 4, Pp 545-548 (2020)
We present the case of a 5-year-old girl who had six episodes of meningitis. She also had panhypopituitarism and was found to have a persistent craniopharyngeal canal (CPC) as the cause of her recurrent meningitis. Role of neuroradiology and a high i
Externí odkaz:
https://doaj.org/article/1ebace26eb744b99b4275ec04e6cfbfb
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S40- (2022)
Externí odkaz:
https://doaj.org/article/396ebf530e5340d19483e13393f82637
Autor:
Lokesh Lingappa, Shoji Ichikawa, Amie K Gray, Dena Acton, Michael J Evans, Rajsekara Chakravarthi Madarasu, Ramesh Kekunnaya, Sirisharani Siddaiahagari
Publikováno v:
Annals of Indian Academy of Neurology, Vol 22, Iss 3, Pp 327-331 (2019)
Hyperphosphatemia in the absence of renal failure is an unusual occurrence, particularly in children, but is a common primary feature of familial hyperphosphatemic tumor calcinosis. We report a child with hyperphosphatemia who presented with multiple
Externí odkaz:
https://doaj.org/article/9d3a70904c754868a61718fb43dd867e
Autor:
Sundaram Challa, Monalisa Hui, Saumya Jakati, Megha Shantveer Uppin, Liza Rajasekhar, Meena Angamuthu Kannan, Lokesh Lingappa, Murthy Murali Krishna Jagarlapudi
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 1, Pp 61-66 (2019)
Background: Juvenile idiopathic inflammatory myopathies (JIIM) are rare and heterogeneous. Subtype identification is important for treatment. Materials and Methods: Patients below 18 years diagnosed as idiopathic inflammatory myopathy (IIM) according
Externí odkaz:
https://doaj.org/article/3a07e6afb24f4026a58ba0e532d159f8
Publikováno v:
Asian Journal of Neurosurgery. 18:062-069
Objective Fourth ventricular and juxta fourth ventricular arachnoid cysts (ACs) are rare clinical entities. Conventionally, ACs are managed with either micro-surgical excision or cerebrospinal fluid (CSF) diversionary procedures such as a shunt. Effe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41c495351f59bb0e93a9321a6bb38042
https://doi.org/10.1055/s-0043-1760858
https://doi.org/10.1055/s-0043-1760858