Zobrazeno 1 - 10
of 13
pro vyhledávání: '"LVNC, left ventricular noncompaction"'
Publikováno v:
JACC Case Reports
Uhl’s anomaly is a rare congenital heart disease characterized by partial or complete absence of the right ventricle myocardium. We report the first case, in a 21-year-old man, of Uhl’s anomaly–associated left ventricular noncompaction. This as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0d761b435269d01acba4316ff94615
http://europepmc.org/articles/PMC8446256
http://europepmc.org/articles/PMC8446256
Publikováno v:
JACC: Case Reports, Vol 2, Iss 13, Pp 2085-2089 (2020)
JACC Case Reports
JACC Case Reports
Left ventricular noncompaction cardiomyopathy (LVNC) was diagnosed in a 59-year-old woman, based on echocardiography. Later, diagnostic criteria were also found positive by cardiac magnetic resonance (CMR). However, coronary angiography revealed theb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4bbf97bd7821c2cf7eefe8f75886da4
https://doi.org/10.1016/j.jaccas.2020.09.027
https://doi.org/10.1016/j.jaccas.2020.09.027
Autor:
Jérôme Garot, Philippe Charron, Flavie Ader, Lise Legrand, Julie Proukhnitzky, Céline Bordet, Pascale Richard
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 8, Pp 1205-1209 (2020)
JACC: Case Reports, Vol 2, Iss 8, Pp 1205-1209 (2020)
Saw-tooth cardiomyopathy is a very rare disease, and only few cases have been published since its first description 10 years ago. We report the clinical presentation, imaging features and genetic analysis of a saw-tooth cardiomyopathy and argues that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::304df67a6aba065f78c00a0820acd914
http://europepmc.org/articles/PMC8311883
http://europepmc.org/articles/PMC8311883
Autor:
Haiwei Du, Jian Huang, Haizhou Pan, Ranxu Zhao, Yingjie Wei, Yanfen Li, Chunyan Li, Shenghua Liu, Fan Liu, Yuanyuan Xie
Publikováno v:
EBioMedicine
EBioMedicine, Vol 53, Iss, Pp-(2020)
EBioMedicine, Vol 53, Iss, Pp-(2020)
Background: Left ventricular noncompaction cardiomyopathy (LVNC) is a hereditary heart disease characterized by an excessive trabecular meshwork of deep intertrabecular recesses within the ventricular myocardium. The guidelines for management of LVNC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce280af46ff90fdc043cd8f2be666438
http://europepmc.org/articles/PMC7058526
http://europepmc.org/articles/PMC7058526
Publikováno v:
HeartRhythm Case Reports
HeartRhythm Case Reports, Vol 2, Iss 1, Pp 92-97 (2016)
HeartRhythm Case Reports, Vol 2, Iss 1, Pp 92-97 (2016)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef23ab0976fe146ed960d8e1f8ce55af
http://europepmc.org/articles/PMC5412645
http://europepmc.org/articles/PMC5412645
Autor:
Damien Voilliot, Nicolas Sadoul, Clément Venner, Pierre-Yves Marie, Yves Juillière, Etienne Aliot, Zied Frikha, Béatrice Brembilla-Perrot, Christine Selton-Suty, Olivier Huttin
Publikováno v:
Scipedia Open Access
Scipedia SL
International Journal of Cardiology. Heart & Vasculature
International Journal of Cardiology: Heart & Vasculature, Vol 5, Iss C, Pp 9-14 (2014)
Scipedia SL
International Journal of Cardiology. Heart & Vasculature
International Journal of Cardiology: Heart & Vasculature, Vol 5, Iss C, Pp 9-14 (2014)
Introduction Left ventricular (LV) systolic dysfunction is the most frequent initial presentation of patient with LV noncompaction (NC). Our objectives were to evaluate myocardial contraction properties in patients with LVNC and the relationship of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f617f893db8e4cdbc5a3b05a2c1a21e
Autor:
Sawada Y; 1Laboratory of Laboratory Animal Science, Azabu University, School of Veterinary Medicine, Sagamihara, Kanagawa, Japan., Kaneko A; 2Center for the Evolutionary Origins of Human Behavior (EHUB), Kyoto University, Inuyama, Aichi, Japan., Koie H; 3College of Bioresource Science, Nihon University, Fujisawa, Kanagawa, Japan; and., Nakayama S; 3College of Bioresource Science, Nihon University, Fujisawa, Kanagawa, Japan; and., Tsukamoto A; 1Laboratory of Laboratory Animal Science, Azabu University, School of Veterinary Medicine, Sagamihara, Kanagawa, Japan., Nakamura S; 1Laboratory of Laboratory Animal Science, Azabu University, School of Veterinary Medicine, Sagamihara, Kanagawa, Japan., Miyabe-Nishiwaki T; 2Center for the Evolutionary Origins of Human Behavior (EHUB), Kyoto University, Inuyama, Aichi, Japan., Ageyama N; 4Tsukuba Primate Research Center, National Institutes of Biomedical Innovation, Health and Nutrition, Tsukuba, Ibaraki, Japan.
Publikováno v:
Comparative medicine [Comp Med] 2024 Oct 31; Vol. 74 (5), pp. 360-366. Date of Electronic Publication: 2024 Oct 31 (Print Publication: 2024).
Autor:
Mohammad A; Department of Internal Medicine, Loma Linda University Health, Loma Linda, California, USA., Parwani P; Department of Cardiology, Loma Linda University Health, Loma Linda, California, USA., Manalo C; Department of Radiology, Loma Linda University Health, Loma Linda, California, USA., Gordon BM; Department of Pediatric Cardiology, Loma Linda University Health, Loma Linda, California, USA., Kheiwa A; Department of Cardiology, Loma Linda University Health, Loma Linda, California, USA.
Publikováno v:
JACC. Case reports [JACC Case Rep] 2021 Sep 15; Vol. 3 (12), pp. 1463-1467. Date of Electronic Publication: 2021 Sep 15 (Print Publication: 2021).
Autor:
Stämpfli SF; Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland., De Boeck BW; Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland., Cuculi F; Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland., Kobza R; Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland.
Publikováno v:
JACC. Case reports [JACC Case Rep] 2020 Nov 18; Vol. 2 (13), pp. 2085-2089. Date of Electronic Publication: 2020 Nov 18 (Print Publication: 2020).
Autor:
Proukhnitzky J; APHP, Département de Génétique & Département de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires ou Rares, Hôpital Pitié-Salpêtrière, Paris, France., Garot J; Institut Cardiovasculaire Paris Sud, Hôpital Privé Jacques Cartier, Ramsay Santé Massy, France., Bordet C; APHP, Département de Génétique & Département de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires ou Rares, Hôpital Pitié-Salpêtrière, Paris, France., Legrand L; APHP, Département de Génétique & Département de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires ou Rares, Hôpital Pitié-Salpêtrière, Paris, France., Ader F; Sorbonne Université, INSERM, UMR_S 1166 and ICAN Institute for Cardiometabolism and Nutrition, Paris, France.; APHP, UF Cardiogénétique et Myogénétique Moléculaire et Cellulaire, Service de Biochimie Métabolique, Hôpitaux Universitaires de la Pitié-Salpêtrière-Charles Foix, Paris, France., Richard P; APHP, Département de Génétique & Département de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires ou Rares, Hôpital Pitié-Salpêtrière, Paris, France.; Sorbonne Université, INSERM, UMR_S 1166 and ICAN Institute for Cardiometabolism and Nutrition, Paris, France.; APHP, UF Cardiogénétique et Myogénétique Moléculaire et Cellulaire, Service de Biochimie Métabolique, Hôpitaux Universitaires de la Pitié-Salpêtrière-Charles Foix, Paris, France., Charron P; APHP, Département de Génétique & Département de Cardiologie, Centre de Référence des Maladies Cardiaques Héréditaires ou Rares, Hôpital Pitié-Salpêtrière, Paris, France.; Sorbonne Université, INSERM, UMR_S 1166 and ICAN Institute for Cardiometabolism and Nutrition, Paris, France.
Publikováno v:
JACC. Case reports [JACC Case Rep] 2020 Jul 15; Vol. 2 (8), pp. 1205-1209. Date of Electronic Publication: 2020 Jul 15 (Print Publication: 2020).