Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ritu Kashikar"'
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 31, Iss 03, Pp 693-696 (2021)
Gallbladder paraganglioma is a very rare condition, and only a few cases have been reported in the literature. Herein, we present and discuss the clinical and radiological findings of a 72-year-old woman who complained of heaviness, pain, and on and
Externí odkaz:
https://doaj.org/article/12de4ce8a71340aa9709ab0993d12f20
Publikováno v:
IP Indian Journal of Neurosciences. 7:52-66
Context/Background: Advanced neuro-imaging like Diffusion Tensor Imaging (DTI) is a non-invasive technique with enormous potential in glioma grading. Aims and Objectives: To assess the diagnostic accuracy of DTI metrics for differentiating low grade
Autor:
Vedam L. Ramprasad, Mukesh Desai, Omkar Hajirnis, Tarishi Nemani, Ritu Kashikar, Thenral S. Geetha, Anaita Udwadia-Hegde, Vishal Patel, Ambreen Pandrowala
Publikováno v:
Journal of Pediatric Neurology. 19:092-101
In this case report, we described a 15-year-old boy who presented with intermittent episodes of ataxia and diplopia since 6.5 years of age. Extensive workup done over several years was negative. Brain biopsy showed a neuroinflammatory disorder, and h
Publikováno v:
Cochlear Implants ISBN: 9789811904516
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b9be8134953e55a476a4ebd696fd96f
https://doi.org/10.1007/978-981-19-0452-3_4
https://doi.org/10.1007/978-981-19-0452-3_4
Publikováno v:
Child Neurology Open, Vol 6 (2019)
Child Neurology Open
Child Neurology Open
CLIPPERS (chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids) is a recently described, rare neuroinflammatory disorder diagnosed by clinical symptoms involving the brain stem with a distinct pattern on neuro
Autor:
Ritu Kashikar, Shrinivas Desai
Publikováno v:
Yearbook of Vascular and Endovascular Surgery 2016
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d3c3bda54cb6aec4feee48d154f8c9f
https://doi.org/10.5005/jp/books/13012_20
https://doi.org/10.5005/jp/books/13012_20
Publikováno v:
JAMA neurology. 73(3)
Wilson disease is an autosomal recessive neurodegenerative disease secondary to abnormal copper metabolism. It is caused by mutations in ATB7B and up to 500 mutations are known to date. Magnetic resonance imaging changes are very common in Wilson dis