Results 121 to 130 of about 39,627 (309)

Cardiovascular computed tomography versus transoesophageal echocardiography after cryptogenic ischaemic stroke – a pilot study of 12 patients

Journal of International Medical Research, 2020
Objective Transoesophageal echocardiography (TEE) is the gold standard for the detection of cardiac emboli sources in ischaemic stroke patients, but new computed tomography (CT) scanners are able to visualize the heart.
Mette Sørensen Resen, Mai Bang Poulsen, Karsten Overgaard, Rune Skovgaard Rasmussen, Anne Merete Boas Soja, Brian Nilsson, Mariana Obreja Kristensen, Christina Kruuse, Peter Sommer Ulriksen   +8 more
doaj   +1 more source

Transcatheter closure of Ventricular Septal defects in Malta : initial experience [PDF]

, 2005
Ventricular septal defects (VSD) consist of deficiencies of the wall separating the two ventricles. VSDs are the commonest congenital cardiac defects. Small VSDs rarely require intervention, however, larger defects cause ventricular volume overload with ...
Aquilina, Oscar, DeGiovanni, Joseph V., Fenech, Albert, Formosa Gouder, Mireille, Grech, Victor E., Magic, Jadran, Manche, Alexander   +6 more
core  

Het platypneu-orthodeoxiesyndroom bij de geriatrische patiënt : presentatie, diagnostiek en therapie

, 2020
De ziektegeschiedenis van een 85-jarige vrouw met als klinische presentatie een triade van een longembolie, een ischemisch cerebrovasculair accident (CVA) en het platypneu-orthodeoxiesyndroom (POS) wordt beschreven.
Bultynck, Céline, De Smet, Sanne, Demuynck, Mathias, Desimpelaere, Patrick, Petrovic, Mirko   +4 more
core   +1 more source

Cardiac hemangioma of the right atrium in a neonate : fetal management and expedited surgical resection [PDF]

, 2005
Cardiac hemangioma is a rare tumor with a reported incidence of 1-2%. We describe the case of a neonate with a right atrial mass that was diagnosed prenatally. The fetus developed a supraventricular tachycardia and was delivered by cesarean section in
Campbell, A., Costello, C., D’Cruz, C.A., Einzig, Stanley, Kula, Monika, Sebastian, Vinod A.   +5 more
core   +1 more source

Genotype–Phenotype Correlation in TTC7A ‐Associated Gastrointestinal Defects and Immunodeficiency Syndrome 1

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff, Hans Christian Schmidt, Matthias Hans Belau, Johanna Hagens, Mario Lange, Daniel Tegtmeyer, Konrad Reinshagen, Frederike Leonie Harms, Christian Tomuschat   +8 more
wiley   +1 more source

Spanish cardiac catheterization in congenital heart diseases registry. Fourth official report from the ACI-SEC and the GTH SECPCC (2023)

REC: Interventional Cardiology (English Ed.)
RESUMEN Introduction and objectives: The Interventional Cardiology Association of the Spanish Society of Cardiology (ACI-SEC) and the Interventional Working Group of the Spanish Society of Pediatric Cardiology (GTH-SECPCC) present their 2023 annual ...
Fernando Ballesteros Tejerizo, Félix Coserría Sánchez, Teresa Bastante, Ana Belén Cid Álvarez, María Álvarez-Fuente, Enrique Balbacid Domingo, Pedro Betrián Blasco, Roberto Blanco Mata, José Ignacio Carrasco, Juan Manuel Carretero Bellón, Juana María Espín López, Marta Flores Fernández, Alfredo Gómez-Jaume, Beatriz Insa Albert, Santiago Jiménez Valero, Luis Andrés Lalaguna, Soledad Ojeda Pineda, Ainhoa Pérez Guerrero, Alejandro Rasines Rodríguez, Joaquín Sánchez Gila, Ricardo Sanz-Ruiz, María Eugenia Vázquez-Álvarez, Juan Ignacio Zabala Argüelles   +22 more
doaj   +1 more source

Liver and brain abscess caused by Aggregatibacter paraphrophilus in association with a large patent foramen ovale: a case report [PDF]

, 2012
RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'.
Ariyaratnam, Shaumya, Carmichael, Andrew, Dickinson, Richard J, Gajendragadkar, Parag R, Harris, Kathryn, Karas, Johannis A, Roberts, Phil   +6 more
core   +2 more sources

Poland Anomaly and Atretic Cephalocele in the Same Child: Coincidence or Association?

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Poland Anomaly is a rare congenital disorder typically characterized by hypoplasia or agenesis of pectoral muscle with or without ipsilateral limb hypoplasia. The association of central nervous system malformation with Poland Anomaly has been rarely reported and includes craniofacial dysplasia, microcephaly, and Dandy‐Walker malformation ...
Alessandra Greta Grassi, Silvia Pontesilli, Laura Demelas, Francesca Vigliani, Massimo Agosti, Angelo Selicorni   +5 more
wiley   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim, Kristen N. Lee, Amanda B. Pritchard   +2 more
wiley   +1 more source

Case of Great Hypertrophy of the Heart and Open Foramen Ovale, without Cyanosis. [PDF]

Medical examiner (Philadelphia, Pa.)
J.Douglas White, James Bryan
openalex   +2 more sources