Intrajejunal Levodopa Infusion for Parkinson’s Disease over 11 years: A Canadian Experience (P13-11.014)

Autor: Chetan Vekhande, Moath Hamed, Genise Tremain, Jennifer Mah, Aakash Shetty, Adriana Lazarescu, Oksana Suchowersky

Publikováno v: Thursday, April 27.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ad07be51f93124e7dcb4b22c49013647
https://doi.org/10.1212/wnl.0000000000203758

Skin Cancer Detection Using Image Processing: A Review

Autor: Aakash Shetty, Kashish Shah, Mohini Reddy, Rutvik Sanghvi, Siddhesh Save, Yashkumar Patel

Publikováno v: Proceedings of the 2nd International Conference on Recent Trends in Machine Learning, IoT, Smart Cities and Applications ISBN: 9789811664069

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2c47a26ee827f4db53677a1131c51052
https://doi.org/10.1007/978-981-16-6407-6_11

Spinal dural arteriovenous fistula presenting as progressive thoracic myelopathy

Autor: Nabeela Nathoo, Erin F Balcom, Cian O'Kelly, Thomas Yeo, Stephen Joza, Aakash Shetty

Publikováno v: Practical neurology. 21(5)

A 51-year-old man had a 4-month history of back pain and progressive leg weakness. The back pain was on the left side, radiating down his left buttock and leg to the dorsum of the foot. He had gradually developed bilateral leg weakness with a right f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b5c7df256ae1dd73df85375ac317e50
https://pubmed.ncbi.nlm.nih.gov/33850033

Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report

Autor: Mark Buller, Tara Dzwiniel, Lotta Koskinen, Moath Hamed, Oksana Suchowersky, Aakash Shetty

Publikováno v: Mov Disord Clin Pract

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bca900d7622a1457049709a7c9359fe
https://europepmc.org/articles/PMC6962660/

CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia

Autor: Erik-Jan Kamsteeg, Ziv Gan-Or, Setareh Ashtiani, Oksana Suchowersky, Guy A. Rouleau, Bart P.C. van de Warrenburg, Tessa Wassenberg, Jennifer A. Ruskey, Aakash Shetty

Publikováno v: European Journal of Medical Genetics, 62, 12
European Journal of Medical Genetics, 62

Aims and objective To characterize the phenotype of CAPN1 (SPG76) mutations in patients diagnosed with hereditary spastic paraplegia (HSP). Background The CAPN1 gene, located on chromosome 11q13.1, is a protein-coding gene involved in neuronal plasti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed3092bb3194bc0339ed7398d1a60e77
https://doi.org/10.1016/j.ejmg.2018.12.010