Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Abhimanyu S. Ahuja"'
Autor:
Abhimanyu S. Ahuja, Bryce W. Polascik, Divyesh Doddapaneni, Eamonn S. Byrnes, Jayanth Sridhar
Publikováno v:
Integrative Medicine Research, Vol 12, Iss 1, Pp 100917- (2023)
Externí odkaz:
https://doaj.org/article/7db8d29cfcb04a52907bf39d5aec0a5f
Publikováno v:
Integrative Medicine Research, Vol 11, Iss 4, Pp 100888- (2022)
Externí odkaz:
https://doaj.org/article/c2ea38415fd04f499e633ac1e5c53165
Publikováno v:
Integrative Medicine Research, Vol 9, Iss 3, Pp 100434- (2020)
Externí odkaz:
https://doaj.org/article/d58eae306c4742f9a67651b72a9e5afe
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-3 (2019)
Abstract Background To describe a patient with sleep alleviated episodic ataxia type 2 with a novel CACNA1A pathogenic variant and provide a possible link to sleep responsive migraine. Case presentation A 26-year-old woman with recurrent attacks of d
Externí odkaz:
https://doaj.org/article/b6d115d8f93248a9ae13996f4cc4c563
Autor:
Abhimanyu S. Ahuja
Publikováno v:
PeerJ, Vol 7, p e7702 (2019)
The practice of medicine is changing with the development of new Artificial Intelligence (AI) methods of machine learning. Coupled with rapid improvements in computer processing, these AI-based systems are already improving the accuracy and efficienc
Externí odkaz:
https://doaj.org/article/a5e1af317c3b477da5c1f3d1ce8ef6fc
Autor:
Abhimanyu S. Ahuja
Publikováno v:
PeerJ, Vol 6, p e4790 (2018)
Mitochondria are small, energy-producing structures vital to the energy needs of the body. Genetic mutations cause mitochondria to fail to produce the energy needed by cells and organs which can cause severe disease and death. These genetic mutations
Externí odkaz:
https://doaj.org/article/07a5e43309a0444d997a97f8626c6930
Publikováno v:
Seminars in Ophthalmology. :1-4
Autor:
Pavalan Selvam, Angita Jain, Jessica Abbott, Abhimanyu S. Ahuja, Anvir Cheema, Katelyn A. Bruno, Herjot Atwal, Irman Forghani, Thomas Caulfield, Paldeep S. Atwal
Publikováno v:
Molecular Syndromology. :1-8
In this report, we describe phenotypic features of a patient with mucopolysaccharidosis type IVA (Morquio syndrome) harboring a novel exon 1 deletion in GALNS with enzymatic confirmation consistent with Morquio syndrome. To our knowledge, this is the
Publikováno v:
Clinical Ophthalmology.
Syril Dorairaj,1 Leticia A Checo,1 Isabella V Wagner,1 Richard D Ten Hulzen,1 Abhimanyu S Ahuja2 1Department of Ophthalmology, Mayo Clinic, Jacksonville, FL, USA; 2Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, U
Publikováno v:
Journal of Neuro-Ophthalmology. 41:e153-e156