Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Minal Jain"'
Autor:
Minal Jain, Rajesh S Hiray
Publikováno v:
Journal of Pharmaceutical Care, Vol 12, Iss 1 (2024)
Background: Globally, with the increasing orthopaedic admissions, the management modalities have also been evolving. With the focus mainly on reducing hospital stay and improving quality of life, pharmacotherapy is a keystone in management. Thus, the
Externí odkaz:
https://doaj.org/article/26f214abe79146ab8111c49dca1d8ed3
Autor:
Ondřej Gahura, Alexander Mühleip, Carolina Hierro-Yap, Brian Panicucci, Minal Jain, David Hollaus, Martina Slapničková, Alena Zíková, Alexey Amunts
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-13 (2022)
Mitochondrial ATP synthase assemble into oligomers. Here, authors resolve the structure of trypanosomal ATP synthase, showing that its dimerization is essential for function and evolutionary conserved.
Externí odkaz:
https://doaj.org/article/033e79272bfa4cdc9ca0a33a7abdda7a
Publikováno v:
Cost Effectiveness and Resource Allocation, Vol 16, Iss 1, Pp 1-10 (2018)
Abstract Objective To study cost-effectiveness of an interleukin (IL)-17A inhibitor secukinumab, with other biologics and apremilast in patients with Psoriatic arthritis (PsA) from payer perspective in Finland. Methods In this semi-Markov model, subc
Externí odkaz:
https://doaj.org/article/50254b4c74214241b78c506c7926306f
Autor:
Minal Jain, Dushyant Damania, Anunaya R. Jain, Abhijit R. Kanthala, Latha Ganti, Babak S. Jahromi
Publikováno v:
Western Journal of Emergency Medicine, Vol 15, Iss 3, Pp 267-275 (2014)
Introduction: Conflicting data exist regarding the association between the length of stay (LOS) of critically ill patients in the emergency department (ED) and their subsequent outcome. However, such patients are an overall heterogeneous group, and w
Externí odkaz:
https://doaj.org/article/70884f43f92749d38e54f95c8a2c9c3c
Autor:
Latha Ganti, Anunaya Jain, Neeraja Yerragondu, Minal Jain, M. Fernanda Bellolio, Rachel M. Gilmore, Alejandro Rabinstein
Publikováno v:
Neurology Research International, Vol 2013 (2013)
Objective. To study whether gender influences outcome after intracerebral hemorrhage (ICH). Methods. Cohort study of 245 consecutive adults presenting to the emergency department with spontaneous ICH from January 2006 to December 2008. Patients with
Externí odkaz:
https://doaj.org/article/1f2a51c96bf44dd5ab1d7f1896ec8731
Autor:
Shams Ribault, Pascal Rippert, Minal Jain, Laure Le Goff, Dominique Vincent Genod, Aurélie Barriere, Anne Berruyer, Camille Garde, Marie Tinat, Christelle Pons, Carole Vuillerot
Publikováno v:
Journal of Neuromuscular Diseases. 10:301-314
Background: Recent pharmaceutical breakthroughs in neuromuscular diseases may considerably change the prognosis and natural history these diseases. The ability to measure clinically relevant outcomes such as motor function is critical for the assessm
Autor:
Cesarius Singgih Wahono, Laniyati Hamijoyo, Yuriawati Hendrawan, Liyana Rakinaturia, Neha Mittal, Prabal Khanna, Minal Jain, Harry Isbagio
Publikováno v:
PharmacoEconomics - Open.
Autor:
Christopher Grunseich, M. Waite, Joshua J. Todd, Aneesh Patankar, Jessica W Witherspoon, Katherine G. Meilleur, Irene C Chrismer, Xuemin Zhang, Muslima S Razaqyar, Tokunbor A. Lawal, Minal Jain, Magalie Emile-Backer, Chia-Ying Liu
Publikováno v:
Journal of Neuromuscular Diseases
Background: Ryanodine receptor 1-related myopathy (RYR1-RM) can present with a selective pattern and gradient of intramuscular fatty infiltration (IMFI) on magnetic resonance imaging (MRI). Objective: To demonstrate an automated protocol for quantifi
Autor:
James J, Dowling, Wolfgang, Müller-Felber, Barbara K, Smith, Carsten G, Bönnemann, Nancy L, Kuntz, Francesco, Muntoni, Laurent, Servais, Lindsay N, Alfano, Alan H, Beggs, Deborah A, Bilder, Astrid, Blaschek, Tina, Duong, Robert J, Graham, Minal, Jain, Michael W, Lawlor, Jun, Lee, Julie, Coats, Charlotte, Lilien, Linda P, Lowes, Victoria, MacBean, Sarah, Neuhaus, Mojtaba, Noursalehi, Teresa, Pitts, Caroline, Finlay, Sarah, Christensen, Gerrard, Rafferty, Andreea M, Seferian, Etsuko, Tsuchiya, Emma S, James, Weston, Miller, Bryan, Sepulveda, Maria Candida, Vila, Suyash, Prasad, Salvador, Rico, Perry B, Shieh
Supplementary Material: The supplementary material is available in the electronic version of this article: https://doi.org/10.3233/JND-210871. Copyright © 2022 The authors. Background X-linked myotubular myopathy (XLMTM) is a life-threatening congen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d19b66f308abf8cb99baa6a14e7388
https://bura.brunel.ac.uk/handle/2438/24793
https://bura.brunel.ac.uk/handle/2438/24793
Autor:
Tuyen Tran, Andrei Constantinescu, Minal Jain, Courtney Hum, Nicole Sultanum, James J. Dowling, Casie A. Genetti, Carsten G. Bönnemann, Oscar H. Meyer, Mamadou Diallo, Jahannaz Dastgir, Michael W. Lawlor, Meryl Acker, Michael Brudno, Alan H. Beggs, Leslie Nelson, Michael Glueck, Kimberly Amburgey, Faiza Syed, Samia Saeed, Stacy Hewson, C.H. Wang, Reshma Amin
Publikováno v:
Neurology
article-version (Version of Record) 3
article-version (Version of Record) 3
ObjectiveNemaline myopathy (NM) is a rare neuromuscular condition with clinical and genetic heterogeneity. To establish disease natural history, we performed a cross-sectional study of NM, complemented by longitudinal assessment and exploration of pi