Results 11 to 20 of about 12,584,325 (355)

2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS)

Revista Española de Cardiología, 2021
2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS)
G. Hindricks, T. Potpara, N. Dagres, E. Arbelo, Jeroen J. Bax, C. Blomström-Lundqvist, G. Boriani, M. Castellà, G. Dan, P. Dilaveris, L. Fauchier, G. Filippatos, J. Kalman, M. la Meir, D. Lane, J. Lebeau, M. Lettino, G. Lip, F. Pinto, G. Thomas, M. Valgimigli, I. V. van Gelder, B. V. Van putte, C. Watkins   +23 more
semanticscholar   +1 more source

2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes-2023.

Diabetes Care, 2022
The American Diabetes Association (ADA) "Standards of Care in Diabetes" includes the ADA's current clinical practice recommendations and is intended to provide the components of diabetes care, general treatment goals and guidelines, and tools to evaluate
Nuha A. ElSayed, G. Aleppo, V. Aroda, Raveendhara R. Bannuru, F. Brown, Dennis Bruemmer, B. Collins, M. Hilliard, Diana M. Isaacs, Eric L. Johnson, S. Kahan, K. Khunti, Jose Leon, S. Lyons, M. L. Perry, P. Prahalad, R. Pratley, J. Seley, R. Stanton, R. Gabbay   +19 more
semanticscholar   +1 more source

2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure

European Journal of Heart Failure, 2022
Document Reviewers: Rudolf A. de Boer (CPG Review Coordinator) (Netherlands), P. Christian Schulze (CPG Review Coordinator) (Germany), Magdy Abdelhamid (Egypt), Victor Aboyans (France), Stamatis Adamopoulos (Greece), Stefan D.
T. McDonagh, M. Metra, M. Adamo, R. Gardner, A. Baumbach, M. Böhm, H. Burri, J. Butler, J. Čelutkienė, O. Chioncel, J. Cleland, A. Coats, M. Crespo-Leiro, D. Farmakis, M. Gilard, S. Heymans, A. Hoes, T. Jaarsma, E. Jankowska, M. Lainščak, C. Lam, A. Lyon, J. McMurray, A. Mebazaa, R. Mindham, C. Muneretto, Massimo Francesco Piepoli, S. Price, G. Rosano, F. Ruschitzka, Anne Kathrine Skibelund   +30 more
semanticscholar   +1 more source

Sarcopenia: revised European consensus on definition and diagnosis

Age and Ageing, 2018
Background in 2010, the European Working Group on Sarcopenia in Older People (EWGSOP) published a sarcopenia definition that aimed to foster advances in identifying and caring for people with sarcopenia.
A. Cruz-Jentoft, G. Bahat, J. Bauer, Y. Boirie, O. Bruyère, T. Cederholm, C. Cooper, F. Landi, Y. Rolland, A. Sayer, S. Schneider, C. Sieber, E. Topinkova, M. Vandewoude, M. Visser, M. Zamboni, I. Bautmans, J. Baeyens, M. Cesari, A. Cherubini, J. Kanis, M. Maggio, F. Martin, J. Michel, K. Pitkala, J. Reginster, R. Rizzoli, D. Sánchez-Rodríguez, J. Schols   +28 more
semanticscholar   +1 more source

2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism developed in collaboration with the European Respiratory Society (ERS)

European Respiratory Journal, 2019
New @ESCardio Guidelines for the Diagnosis and Management of Acute #PulmonaryEmbolism developed in collaboration with @EuroRespSoc now available: #cardiotwitter @erspublications http://bit.ly ...
S. Konstantinides, G. Meyer, C. Becattini, H. Bueno, G. Geersing, V. Harjola, M. Huisman, M. Humbert, C. Jennings, D. Jiménez, N. Kucher, I. Lang, M. Lankeit, R. Lorusso, L. Mazzolai, N. Meneveau, F. Áinle, P. Prandoni, P. Pruszczyk, M. Righini, A. Torbicki, E. Van Belle, J. Zamorano   +22 more
semanticscholar   +1 more source

Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array

Molecular Cytogenetics, 2021
Background The phenotypes of uniparental disomy (UPD) are variable, which may either have no clinical impact, lead to clinical signs and symptoms. Molecular analysis is essential for making a correct diagnosis.
Lili Zhou, Zhaoke Zheng, Yunzhi Xu, Xiaoxiao Lv, Chenyang Xu, Xueqin Xu   +5 more
doaj   +1 more source

Genetic testing in Marfan syndrome [PDF]

, 2016
Genetic testing is aiding rapid diagnosis of Marfan syndrome as a basis for management of eye, heart and skeletal disease. The affected patient's mutation can be used as a basis for prenatal or postnatal diagnosis of offspring.
Aragon-Martin, JA, Child, AH, Sage, K
core   +1 more source

Risk of Suicide After Cancer Diagnosis in England

JAMA psychiatry, 2018
Importance A diagnosis of cancer carries a substantial risk of psychological distress. There has not yet been a national population-based study in England of the risk of suicide after cancer diagnosis. Objectives To quantify suicide risk in patients with
Katherine E Henson, R. Brock, J. Charnock, B. Wickramasinghe, O. Will, A. Pitman   +5 more
semanticscholar   +1 more source

Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array

Molecular Cytogenetics, 2023
Background With the application of chromosome microarray, next-generation sequencing and other highly sensitive genetic techniques in disease diagnosis, the detection of mosaicism has become increasingly prevalent.
Lili Zhou, Huanzheng Li, Chenyang Xu, Xueqin Xu, Zhaoke Zheng, Shaohua Tang   +5 more
doaj   +1 more source

Diagnosis in vascular dementia, applying ‘Cochrane diagnosis rules’ to ‘dementia diagnostic tools’ [PDF]

, 2017
In this issue of Clinical Science, Biesbroek and colleagues describe recent work on magnetic resonance imaging (MRI)-based cerebral lesion location and its association with cognitive decline.
McCleery, Jenny, Quinn, Terence J.
core   +1 more source