Zobrazeno 1 - 10
of 1 283
pro vyhledávání: '"Sheela, A."'
Autor:
Emily E. Wiloch, Geof W. Smith, James L. Yeatts, Enoch B. de S. Meira, Farha Ferdous Sheela, Ronald E. Baynes, Emma Nixon
Publikováno v:
Journal of Dairy Science. 105:549-559
Flunixin is a nonsteroidal anti-inflammatory drug approved for use in cattle to manage pyrexia associated with bovine respiratory disease, mastitis, and endotoxemia. In the United States, no nonsteroidal anti-inflammatory drugs are approved for use i
Autor:
Sheela Kumar Gujjari, Avinash Bettahalli Shivamallu, Pratibha Shashikumar, Manish Kumar Yadav, Akila Prashant, Swet Nisha
Publikováno v:
J Oral Biol Craniofac Res
INTRODUCTION: Periodontitis causes oxidative stress and reduce total antioxidant levels. The aim of this study was to determine the effect of non-surgical periodontal treatment on leptin levels and total antioxidant capacity in chronic periodontitis.
Autor:
Sheela T. Patel, Rahul Kar
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 7, Iss 4, Pp 772-777 (2021)
Journal of Vascular Surgery Cases, Innovations and Techniques
Journal of Vascular Surgery Cases, Innovations and Techniques
A 50-year-old man with a history of coil embolization of a symptomatic 5.3-cm hepatic artery aneurysm 6 years previously presented with a massive gastrointestinal bleed. He was found to have embolization coils extruding into the duodenum from a hepat
Autor:
Diksha Brahmbhatt, Sheela Maru, Teresa Janevic, Simone A. Reynolds, Lauren Birnie, Kizzi Belfon, Max Hadler, Lily Glenn
Publikováno v:
Journal of Urban Health : Bulletin of the New York Academy of Medicine
Immigrant women represent half of New York City (NYC) births, and some immigrant groups have elevated risk for poor maternal health outcomes. Disparities in health care utilization across the maternity care spectrum may contribute to differential mat
Autor:
Chaitanya Datar, Nutan Kamath, Mamta N. Muranjan, Katta M. Girisha, Gandham SriLakshmi Bhavani, Anju Shukla, Shubha R. Phadke, Hitesh Shah, Chelna Galada, Sheela Nampoothiri, Prince Jacob
Publikováno v:
American Journal of Medical Genetics Part A. 188:751-759
Pseudoachondroplasia (PSACH) is an autosomal dominant disorder characterized by rhizomelic short-limbed skeletal dysplasia. The primary clinical and radiographic features include disproportionate dwarfism, joint laxity and hyperextensibility, exagger
Autor:
Suzanne M. Simkovich, Lindsay J. Underhill, Miles A. Kirby, Mary E. Crocker, Dina Goodman, John P. McCracken, Lisa M. Thompson, Anaité Diaz-Artiga, Adly Castañaza-Gonzalez, Sarada S. Garg, Kalpana Balakrishnan, Gurusamy Thangavel, Ghislaine Rosa, Jennifer L. Peel, Thomas F. Clasen, Eric D. McCollum, William Checkley, Vigneswari Aravindalochanan, Dana B. Barr, Vanessa Burrowes, Devan Campbell, Eduardo Canuz, Howard Chang, Yunyun Chen, Marilú Chiang, Maggie L. Clark, Rachel Craik, Victor Dávila-Román, Lisa de las Fuentes, Oscar De Léon, Ephrem Dusabimana, Lisa Elon, Juan Gabriel Espinoza, Irma S. Pineda Fuentes, Savannah Gupton, Meghan Hardison, Stella Hartinger, Steven A. Harvey, Mayari Hengstermann, Phabiola Herrera, Shakir Hossen, Penelope Howards, Lindsay Jaacks, Shirin Jabbarzadeh, Michael A. Johnson, Abigail Jones, Katherine Kearns, Jacob Kremer, Margaret Laws, Patricia M. Lenzen, Jiawen Liao, Amy Lovvorn, Fiona Majorin, Julia McPeek, Rachel M. Meyers, J. Jaime Miranda, Erick Mollinedo, Lawrence Moulton, Krishnendu Mukhopadhyay, Luke Naeher, Abidan Nambajimana, Florien Ndagijimana, Azhar Nizam, Jean de Dieu Ntivuguruzwa, Aris Papageorghiou, Ricardo Piedrahita, Ajay Pillarisetti, Naveen Puttaswamy, Elisa Puzzolo, Ashlinn Quinn, Sarah Rajkumar, Usha Ramakrishnan, Davis Reardon, Joshua Rosenthal, P. Barry Ryan, Zoe Sakas, Sankar Sambandam, Jeremy Sarnat, Sheela Sinharoy, Kirk R. Smith, Kyle Steenland, Damien Swearing, Ashley K. Toenjes, Jean Damascene Uwizeyimana, Viviane Valdes, Amit Verma, Lance Waller, Megan Warnock, Kendra Williams, Wenlu Ye, Bonnie Young
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
RATIONALE: Pneumonia is the leading cause of death in children worldwide. Identifying and appropriately managing severe pneumonia in a timely manner improves outcomes. Little is known about the readiness of healthcare facilities to manage severe pedi
Autor:
Donata Orioli, Maria Accadia, Anja Raams, Sarah Giachetti, Sigrid M.A. Swagemakers, Wim Vermeulen, Dhanya Yesodharan, Arjan F. Theil, Giuseppina Caligiuri, Elena Botta, Alan R. Lehmann, Desirée E.C. Smith, Tomoo Ogi, Marisa I. Mendes, Sheela Nampoothiri, Silvia Bione, Gajja S. Salomons, Anita Lombardi, Peter J. van der Spek, Jan H.J. Hoeijmakers
Publikováno v:
Human Molecular Genetics, 30(18), 1711-1720. Oxford University Press
Botta, E, Theil, A F, Raams, A, Caligiuri, G, Giachetti, S, Bione, S, Accadia, M, Lombardi, A, Smith, D E C, Mendes, M I, Swagemakers, S M A, van der Spek, P J, Salomons, G S, Hoeijmakers, J H J, Yesodharan, D, Nampoothiri, S, Ogi, T, Lehmann, A R, Orioli, D & Vermeulen, W 2021, ' Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy ', Human Molecular Genetics, vol. 30, no. 18, pp. 1711-1720 . https://doi.org/10.1093/hmg/ddab123
Human molecular genetics, 30(18), 1711-1720. Oxford University Press
Human Molecular Genetics
Botta, E, Theil, A F, Raams, A, Caligiuri, G, Giachetti, S, Bione, S, Accadia, M, Lombardi, A, Smith, D E C, Mendes, M I, Swagemakers, S M A, van der Spek, P J, Salomons, G S, Hoeijmakers, J H J, Yesodharan, D, Nampoothiri, S, Ogi, T, Lehmann, A R, Orioli, D & Vermeulen, W 2021, ' Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy ', Human Molecular Genetics, vol. 30, no. 18, pp. 1711-1720 . https://doi.org/10.1093/hmg/ddab123
Human molecular genetics, 30(18), 1711-1720. Oxford University Press
Human Molecular Genetics
Trichothiodystrophy (TTD) is a rare hereditary neurodevelopmental disorder defined by sulfur-deficient brittle hair and nails and scaly skin, but with otherwise remarkably variable clinical features. The photosensitive TTD (PS-TTD) forms exhibits in
Publikováno v:
Biomedicine. 41:431-438
Introduction and Aim:Preeclampsia is a pregnancy specific hypertensive disorder and its complications are associated with maternal morbidity and mortality. The intention of the study is to determine early placental and endothelial dysfunction markers
Autor:
Katharina Beyer, Sara J. MacLennan, Lisa Moris, Michael Lardas, Ken Mastris, Gary Hooker, Robert Greene, Erik Briers, Muhammad Imran Omar, Jemma Healey, Sheela Tripathee, Giorgio Gandaglia, Lionne D.F. Venderbos, Emma J. Smith, Josefine Bjorkqvist, Alex Asiimwe, Johannes Huber, Monique J. Roobol, Jihong Zong, Anders Bjartell, James N’Dow, Alberto Briganti, Steven MacLennan, Mieke Van Hemelrijck, Emma Jane Smith, James N'Dow, Karin Plass, Maria Ribal, Nicolas Mottet, Robert Shepherd, Thomas Van den Broeck, Peter-Paul Willemse, Riccardo Campi, Mauro Gacci, LU Susan Evans-Axelsson, Daniele Crosti, Massimiliano Meoni, Roberto Garzonio, Chris Bangma, Monique Roobol, Sebastiaan Remmers, Derya Tilki, Anssi Auvinen, Teemu Murtola, Tapio Visakorpi, Kirsi Talala, Teuvo Tammela, Aino Siltari, Stephane Lejeune, Femke van Diggelen, Sophie Byrne, Luz Fialho, Antonella Cardone, Paulina Gono, Bertrand De Meulder, Charles Auffray, Irina-Afrodita Balaur, Nesrine Taibi, Shaun Power, Nazanin Zounemat Kermani, Kees van Bochove, Elisa Cirillo, Maxim Moinat, Emma Voss, Denis Horgan, Louise Fullwood, Marc Holtorf, Doron Lancet, Gabi Bernstein, Imran Omar, Sara MacLennan, Manfred Wirth, Michael Froehner, Beate Brenner, Angelika Borkowetz, Christian Thomas, Friedemann Horn, Kristin Reiche, Markus Kreuz, Andreas Josefsson, Delila Gasi Tandefelt, Jonas Hugosson, Jack Schalken, Henkjan Huisman, Thomas Hofmarcher, Peter Lindgren, Emelie Andersson, Adam Fridhammar, Frank Verholen, John-Edward Butler-Ransohoff, Todd Williamson, Kumari Chandrawansa, Reg Waldeck, Megan Molnar, Amanda Bruno, Ronald Herrera, Ekaterina Nevedomskaya, Samuel Fatoba, Niculae Constantinovici, Ateesha Mohamed, Carl Steinbeißer, Siddhanth Kedhagae, Monika Maass, Patrizia Torremante, Marc Dietrich Voss, Zsuzsanna Devecseri, Tom Abbott, Amit Kiran, Chad Dau, Kishore Papineni, Jing Wang-silvanto, Steve Hass, Robert Snijder, Verena Doyé, Xuewei Wang, Andy Garnham, Mark Lambrecht, Russ Wolfinger, Stijn Rogiers, Angela Servan, Joaquin Casariego, Mohamed Samir, Katie Pascoe, Paul Robinson, Christian Reich, Shilpa Ratwani, Elaine Longden-Chapman, Danny Burke, Paul Agapow, Sahra Derkits, Muriel Licour, Michelle Ang, Sarah Payne, Alan Yong, Lucy Thompson, Sophia Le Mare, Michael Bussmann, Inken Köhler, Guido Juckeland, Daniel Kotik
Publikováno v:
European Urology Focus
European Urology Focus, 7(5), 943-946. Elsevier
European Urology Focus, 7, 5, pp. 943-946
European Urology Focus, 7, 943-946
European Urology Focus, 7(5), 943-946. Elsevier
European Urology Focus, 7, 5, pp. 943-946
European Urology Focus, 7, 943-946
Contains fulltext : 244306.pdf (Publisher’s version ) (Open Access) Patients are the stewards of their own care and hence their voice is important when designing and implementing research. Patients should be involved not only as participants in res
Publikováno v:
Journal of Drug Delivery and Therapeutics. 11:48-53
Asthma and Chronic Obstructive Pulmonary Disease (COPD) are two of the leading causes of morbidity, mortality and economic burden worldwide. The burden of chronic respiratory disease has major adverse effects on the quality of life and ability of aff