Results 171 to 180 of about 675,333 (338)
Advanced Intelligent Systems, EarlyView.Cardiovascular diseases are leading death causes; electrocardiogram (ECG) analysis is slow, motivating machine learning and deep learning. This study compares deep convolutional generative adversarial network, conditional GAN, and Wasserstein GAN with gradient penalty (WGAN‐GP) for synthetic ECG spectrograms; Fréchet Inception Distance (FID) and ...
Giovanny Barbosa‐Casanova +3 more
wiley +1 more source
Sleep Duration and Ambulatory Blood Pressure in Black and White Adolescents [PDF]
, 2012 Elizabeth Mezick +2 more
openalex +1 more source
Antibiotic use in elderly patients in ambulatory care: A comparison between Hungary and Sweden [PDF]
, 2022 Ikhwan Yuda Kusuma +11 more
openalex +1 more source
American Journal of Hematology, EarlyView.ABSTRACT D‐dimer defines degradation products derived from the proteolysis mediated by plasmin on cross‐linked fibrin. The evidence‐based use of D‐dimer in some conditions has been consolidated. Currently, however, there is an entrenched prescription of D‐dimer testing to screen otherwise healthy subjects that may induce prescribing physicians to start
Armando Tripodi +11 more
wiley +1 more source
The use of ambulatory blood pressure monitoring among Medicare beneficiaries in 2007–2010
, 2014 Daichi Shimbo +7 more
openalex +2 more sources
The outcomes of continuous ambulatory and automated peritoneal dialysis are similar [PDF]
, 2009 Rajnish Mehrotra +3 more
openalex +1 more source
Ambulatory Portable Pneumatic Compression Device as Part of a Multimodal Aspirin-Based Approach in Prevention of Venous Thromboembolism in Outpatient Total Knee Arthroplasty [PDF]
, 2020 David A. Crawford +5 more
openalex +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT A de novo, missense variant in ITPR1‐inositol 1,4,5‐trisphosphate receptor type 1 (ITPR1), p.(Tyr567Cys), was identified by trio whole‐genome sequencing in an individual diagnosed with Spinocerebellar ataxia 29 (SCA29) who was affected by cerebral palsy and global developmental delay.
Thania Ordaz +12 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source