Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dhaivat Joshi"'
Autor:
Robin Pokrzywinski, Asha Hareendran, Luba Nalysnyk, Sandy Cowie, Joslyn Crowe, Justin Hopkin, Dhaivat Joshi, Ruth Pulikottil-Jacob
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Acid sphingomyelinase deficiency (ASMD), historically known as Niemann–Pick disease (NPD) types A, A/B, and B, is a rare, progressive, potentially fatal lysosomal storage disease with a spectrum of phenotypes. Little is known about how ASM
Externí odkaz:
https://doaj.org/article/77977a39f6cc484ea27403ee4ac28ed5
Autor:
Carol Mansfield, Lubomyra Nalysnyk, Dhaivat Joshi, Joshua Coulter, Ruth Pulikottil Pulikottil-Jacob
Publikováno v:
Patient Preference and Adherence.
Carol Mansfield,1 Lubomyra Nalysnyk,2 Dhaivat Joshi,2 Joshua Coulter,1 Ruth Pulikottil-Jacob3 1Health Preference Assessment, RTI Health Solutions, Research Triangle Park, North Carolina, USA; 2Health Economics and Value Assessment, Sanofi, Cambridge,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1fb292e452131c6f5bfc16fc8a75360
https://www.dovepress.com/impact-of-potential-symptoms-and-risks-associated-with-acid-sphingomye-peer-reviewed-fulltext-article-PPA
https://www.dovepress.com/impact-of-potential-symptoms-and-risks-associated-with-acid-sphingomye-peer-reviewed-fulltext-article-PPA
Publikováno v:
bioRxiv
MotivationDetection of structural variants (SV) from the alignment of sample DNA reads to the reference genome is an important problem in understanding human diseases. Long reads that can span repeat regions, along with an accurate alignment of these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9e10f1c2ca1bd313fb3fc509d4adaa
Autor:
Dhaivat Joshi, Justin Hopkin, Ruth Pulikottil-Jacob, Robin Pokrzywinski, Joslyn Crowe, Luba Nalysnyk, Asha Hareendran, Sandy Cowie
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Acid sphingomyelinase deficiency (ASMD), historically known as Niemann–Pick disease (NPD) types A, A/B, and B, is a rare, progressive, potentially fatal lysosomal storage disease with a spectrum of phenotypes. Little is known about how ASMD symptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b671bae445eaacc28fc0c1b4b8b4cee
https://pubmed.ncbi.nlm.nih.gov/34697402
https://pubmed.ncbi.nlm.nih.gov/34697402
Autor:
Ian Tafel, Hasan A. Zaidi, Colleen Smith, Stefania Papatheodorou, Linda S. Aglio, Sanghee Lim, Dhaivat Joshi, Zhonghui Ou, Nayan Lamba, Rania A. Mekary, Timothy R. Smith, Quynh-Anh Vo, Lita Araujo-Lama, Joanne Doucette
Publikováno v:
Journal of spine surgery (Hong Kong). 5(2)
Background: The prevalence of spinal deformities increases with age, affecting between 30% and 68% of the elderly population (ages ≥65). The reported prevalence of complications associated with surgery for spinal deformities in this population rang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cba8f738af98648104b4bbb427cc49e
https://pubmed.ncbi.nlm.nih.gov/31380476
https://pubmed.ncbi.nlm.nih.gov/31380476
Publikováno v:
2017 4th International Conference on Signal Processing and Integrated Networks (SPIN).
The information present in the electromyogram (EMG) signals can be used for the diagnosis of the neuro-muscular abnormalities such as: amyotrophic lateral sclerosis (ALS) and myopathy. In this paper, a technique for detection of ALS and myopathy is p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::349ca3e1321e18dd8452051a6ea3129b
https://doi.org/10.1109/spin.2017.8050010
https://doi.org/10.1109/spin.2017.8050010