Results 121 to 130 of about 2,596 (202)

Cardiopathies congénitales chez le chat de moins de 2 ans : étude rétrospective sur 24 cas présentés au Centre Hospitalier Universitaire Vétérinaire de l’Ecole Nationale Vétérinaire de Toulouse, du 1er janvier 2004 au 31 décembre 2014 [PDF]

open access: yes, 2016
Les cardiopathies congénitales sont relativement mal connues en médecine vétérinaire par rapport à la médecine humaine, et demeurent aujourd’hui peu explorées chez le chat.
Labat, Quentin
core  

Cor triatriatum sinister with non-fenestration in a seven-month-old patient

open access: yesTürk Kardiyoloji Derneği Arşivi, 2013
Yılmaz Yozgat   +3 more
doaj   +1 more source

Cor triatriatum sinister with unusual pulmonary venous return. [PDF]

open access: yesEur Heart J Case Rep, 2022
Clemente A   +4 more
europepmc   +1 more source

Hemoptysis as a rare presentation of cor triatriatum sinister [PDF]

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 2015
Sameh M, Said   +3 more
openaire   +2 more sources

Serce trójprzedsionkowe lewostronne [PDF]

open access: yes, 2001
Przedstawiono obraz echokardiograficzny serca trójprzedsionkowego lewostronnego rozpoznanego u dwóch chłopców w wieku 3 lat. W pierwszym przypadku rozpoznano wadę izolowaną bezobjawowym przebiegu w ciągu 8-letniej obserwacji.
Aleszewicz-Baranowska, Janina   +3 more
core   +2 more sources

[Cor triatriatum sinister in a 19-year-old patient].

open access: yesTurk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, 2008
Cor triatriatum sinister is a rare congenital cardiac anomaly in which the left atrium is divided into two chambers by a fibromuscular septum. Although the disease is generally diagnosed in early childhood, some patients remain asymptomatic until adulthood. A 19-year-old female patient presented with dyspnea that increased in severity for the past year.
GÜNDOĞDU, Fuat   +3 more
openaire   +2 more sources

Cor triatriatum sinistrum – relato de caso [PDF]

open access: yes
O cor triatriatum sinistrum é uma cardiopatia congênita considerada extremamente rara, estimando-se prevalência de menos de 0,1 % das doenças cardíacas congênitas.
Cunha, Nabel Anderson de Lencaster Saldanha da   +5 more
core   +1 more source

Prenatal diagnosis of cor triatriatum sinister associated with early pericardial effusion: A case report. [PDF]

open access: yesWorld J Clin Cases, 2021
Cánovas E   +5 more
europepmc   +1 more source

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