Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Smadar Horowitz-Cederboim"'
Autor:
Enrico Ammirati, Francesca Raimondi, Nicolas Piriou, Loren Sardo Infirri, Saidi A. Mohiddin, Andrea Mazzanti, Chetan Shenoy, Ugo A. Cavallari, Massimo Imazio, Giovanni Donato Aquaro, Iacopo Olivotto, Patrizia Pedrotti, Neha Sekhri, Caroline M. Van de Heyning, Glenn Broeckx, Giovanni Peretto, Oliver Guttmann, Santo Dellegrottaglie, Alessandra Scatteia, Piero Gentile, Marco Merlo, Randal I. Goldberg, Alex Reyentovich, Christopher Sciamanna, Sabine Klaassen, Wolfgang Poller, Cory R. Trankle, Antonio Abbate, Andre Keren, Smadar Horowitz-Cederboim, Julia Cadrin-Tourigny, Rafik Tadros, Giuseppe A. Annoni, Emanuela Bonoldi, Claire Toquet, Lara Marteau, Vincent Probst, Jean Noël Trochu, Antheia Kissopoulou, Aurelia Grosu, Deni Kukavica, Alessandro Trancuccio, Cristina Gil, Giacomo Tini, Matteo Pedrazzini, Margherita Torchio, Gianfranco Sinagra, Juan Ramón Gimeno, Davide Bernasconi, Maria Grazia Valsecchi, Karin Klingel, Eric D. Adler, Paolo G. Camici, Leslie T. Cooper
Publikováno v:
JACC : heart failure
BACKGROUND The risk of adverse cardiovascular events in patients with acute myocarditis (AM) and desmosomal gene variants (DGV) remains unknown.OBJECTIVES The purpose of this study was to ascertain the risk of death, ventricular arrhythmias, recurren
Autor:
Michal Gur, Orly Elpeleg, Ephrat Levy-Lahad, Hadas Mechoulam, Tamar Harel, Vardiella Meiner, Smadar Horowitz-Cederboim, Muhannad Daana
Publikováno v:
Eur J Hum Genet
The transforming growth factor-beta (TGFβ) signaling pathway is essential for palatogenesis and retinal development. Glycoprotein A repetitions predominant (GARP), encoded by LRRC32, is a TGFβ cell surface receptor that has been studied primarily i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::889b9cd48e3cf65a8b95b00810b129b5
https://europepmc.org/articles/PMC6777458/
https://europepmc.org/articles/PMC6777458/
Autor:
Dan Arbell, Amir Zilkha, Smadar Horowitz Cederboim, Ayelet Gamliel, V.M. Kapuller, Rachel Katz-Brull, Stanley H. Korman, Elite Cohen, Morasha Plesser Duvdevani, Smadar Eventov-Friedman, Vardiella Meiner, Ayala Frumkin, Avraham Shaag, Ehud Banne
Publikováno v:
JIMD Reports ISBN: 9783662498323
Transaldolase (TALDO) deficiency has various clinical manifestations including liver dysfunction, hepatosplenomegaly, anemia, thrombocytopenia, and dysmorphic features. We report a case presenting prenatally with hyperechogenic bowel and intrauterine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9125a607e8896a90e64f6f7cbead3974
https://doi.org/10.1007/8904_2015_474
https://doi.org/10.1007/8904_2015_474