Results 221 to 230 of about 75,748 (340)

Wartość diagnostyczna pomiaru NT-proBNP w rozpoznawaniu izolowanej dysfunkcji rozkurczowej lewej komory wśród pacjentów z udokumentowaną chorobą wieńcową

, 2006
Krystian Wita, Artur Filipecki, Wojciech Wróbel, Jolanta Krauze, Agnieszka Drzewiecka-Gerber, Anna Rybicka-Musialik, Mariola Nowak, Zbigniew Tabor, Michał Lelek, Wojciech Kwaśniewski i Maria Trusz-Gluza   +9 more
openalex   +1 more source

Correction to ‘Early experience of Sacubitril–Valsartan in heart failure with reduced ejection fraction in real‐world clinical setting’

ESC Heart Failure, Volume 12, Issue 2, Page 1525-1525, April 2025.
wiley   +1 more source

Genetic and Clinical Spectrum of Hereditary Transthyretin Amyloidosis in Brazil

Journal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background Transthyretin hereditary amyloidosis (ATTRv) clinical variability has been widely reported, not only across countries and variants but also among families and distinct regions within a single nation. One of the principal challenges in disease management is the accurate determination of age of onset (AOO), which is heterogeneous and ...
Gustavo Maximiano‐Alves, Carolina Lavigne‐Moreira, Marcus Vinicius Simões, Adilson Junior Pinto Galvão, Flavio Henrique Valicelli, Fernando Saraiva Coneglian, Elisa Vegezzi, Pedro Manoel Marques Garibaldi, Pedro José Tomaselli, Andrea Cortese, Wilson Marques Jr   +10 more
wiley   +1 more source

Navigating the challenges of NT-proBNP result disclosure in clinical research. [PDF]

J Clin Transl Sci
Kent DA, Villegas-Downs M, Wilson A, Krishnan J, Gerald L.   +4 more
europepmc   +1 more source

Correction to ‘Increase of serum pancreatic enzymes during hospitalization for acute heart failure’

ESC Heart Failure, Volume 12, Issue 2, Page 1526-1526, April 2025.
wiley   +1 more source

The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 407-418, February 2026.
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, Outi Elomaa, Sirpa Kivirikko, Leila Jeskanen, Katriina Lappalainen, Nelli Sjöblom, Juha Kere, Katariina Hannula‐Jouppi, Liisa Harjama   +10 more
wiley   +1 more source

NT-proBNP testing for heart failure diagnosis in people with atrial fibrillation: A diagnostic accuracy study. [PDF]

PLoS Med
Jones NR, Taylor KS, Ordóñez-Mena JM, Goyder CR, Hobbs FDR, Taylor CJ.   +5 more
europepmc   +1 more source

N-terminal pro B-type natriuretic peptide (NT-proBNP) hos hundar med kronisk mitralisklaffdegeneration

, 2011
Hanna Olson
openalex   +1 more source

Risk Factors Associated With Sarcopenia in Patients With Chronic Kidney Disease: A Systematic Review and Meta‐Analysis

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 1, February 2026.
ABSTRACT Background Sarcopenia is an age‐related degenerative disorder characterized by a progressive decline in skeletal muscle mass, strength, and function with high prevalence in chronic kidney disease (CKD). Identifying clinical and epidemiological factors of sarcopenia in patients with CKD is essential to enable early recognition and appropriate ...
Kaili Jin, Xiaoyan Li, Yiqin Ma, Dan Yang, Xiaoxue Tan, Qiuhua Sun, Rongyun Wang   +6 more
wiley   +1 more source

A Rapid Method Based on Colloidal Selenium Nanoparticle to Detect NT-proBNP Antigen in Serum for Monitoring Acute Heart Failure. [PDF]

Int J Nanomedicine
Tang C, Xiang H, Zhu J, Chen T, Shao J, Gu L, Shen Y, Zhu Y.   +7 more
europepmc   +1 more source