Results 161 to 170 of about 80,449 (358)

A 34-Year-Old Thai Man Presenting with Pulmonary Stenosis and Heart Failure 24 Years After Surgical Correction with the Rastelli Procedure for Congenital Dextro-Transposition of the Great Artery, Ventricular Septal Defect, and Pulmonary Atresia

, 2021
Natnicha Pongbangli, Sasivimon Jai-aue, Wannaphorn Rotchanapanya, Wanwarang Wongcharoen   +3 more
openalex   +1 more source

Cardiovascular Health in Women—Across the Lifespan

Clinical Endocrinology, EarlyView.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar, Jessica Yao, Simone Gong, Madhuka Wijayarathne, Monique Watts, Swati Mukherjee   +5 more
wiley   +1 more source

Outcome analysis of major cardiac operations in low weight neonates [PDF]

, 2004
Bové, Thierry, De Groote, Katya, De Wolf, Daniël, Francois, Katrien, Matthys, Dirk, MOERMAN, ANNELIESE, Poelaert, Jan, SUYS, B, Van Nooten, Guido, VANHAESEBROECK, P, Verhaaren, Henri   +10 more
core   +2 more sources

Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes

Clinical Genetics, EarlyView.
In 132 individuals with limb anomalies, diagnostic yield was 36% (47/132), including 25 novel variants, three cases with new phenotypes, and two candidate loci, HOXA11 and a small 2q31.1 deletion. Mouse data and exome‐wide analysis, key in identifying the candidate loci, represent an important opportunity for gene discovery.
Akram Mokhtari, Jade Charbonneau, Valancy Miranda, Khadijé Jizi, Marie‐Ange Delrue, Patricia Egerszegi, Isabelle Thiffault, Philippe M. Campeau   +7 more
wiley   +1 more source

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

Clinical Genetics, EarlyView.
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil, Neta Feinstein‐Goren, Lior Greenbaum, Ortal Barel, Daniel C. Koboldt, Samantha A. Brugmann, Kathryn Nicole Weaver, Anne Slavotinek, Ben Pode‐Shakked, Rolf W. Stottmann   +9 more
wiley   +1 more source

A case of secundum atrial septal defect combined with aortic stenosis and coronary artery disease showing a single second heart sound.

, 1990
Makoto Saitoh, Hiroyuki Miyakoda, Masaharu Fukuki, Junichi Yamasaki, Yukihiro Fujimoto, Junichi Hasegawa, Hiroshi Kotake, Hiroto Mashiba   +7 more
openalex   +2 more sources

Complete heart block associated with device closure of perimembranous ventricular septal defects [PDF]

, 2008
Dragoş Predescu, Rajiv Chaturvedi, Mark K. Friedberg, Lee Benson, Akira Ozawa, Kyong‐Jin Lee   +5 more
openalex   +1 more source

Transcatheter Closure of Atrial Septal Defects with 40 mm Septal Occluder in Shahid Gangalal National Heart Centre, Nepal

, 2021
Chandra Mani Adhikari, Kiran Prasad Acharya, Amrit Bogati, Anjana Acharya, Roshani Shahi, Vijay Ghimire, Dipanker Prajapati   +6 more
openalex   +2 more sources

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson, Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta, Oanh Tran, Daniella Miller, Jeroen Breckpot, Ann Swillen, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Federica Pulvirenti, Bruno Marino, Beverly S. Emanuel, Elaine H. Zackai, Zhengdong D. Zhang, Elizabeth Goldmuntz, Erik Boot, Anne S. Bassett, Bernice E. Morrow, Donna M. McDonald‐McGinn   +22 more
wiley   +1 more source

Long-term follow up after transcatheter closure of atrial septal defect and patent foramen ovale in adults

Zdravniški Vestnik, 2014
Background: The aim of our study was to define long-term electrocardiographic and echocardiographic changes and complications after transcatheter closure of atrial septal defect and patent foramen ovale in adults.Methods: The clinical ...
Jure Dolenc, Andraž Cerar, Marta Cvijić, Katja Prokšelj, Mirta Koželj   +4 more
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