Results 101 to 110 of about 28,021 (274)

Surface visualization of the brain regions exhibiting significant between-state differences in nodal efficiency for the three comparisons, VSW-RS, VSD-VSW, and VSD-RS.

, 2015
The node size is proportional to the relative significance of each between-state comparison (two-tailed paired t-test, p < 0.05, FDR correction). The node colors indicate the node belonging to the six different modules according to the brain template [35]
Xue Wen (498444), Zengjian Wang (765806), Ming Liu (105953), Junjing Wang (498446), Bishan Liang (633594), Ruiwang Huang (276738), Ruibin Zhang (498445), Delong Zhang (276735)   +7 more
core   +1 more source

Isolierter muskulärer VSD, diagnostiziert in der Fetalperiode: Bedeutung für Schwangerschaft, Geburt und postnatales Outcome [PDF]

, 2017
Als häufigster angeborener Herzfehler kommt dem Ventrikel-Septum-Defekt (VSD) in der Pränataldiagnostik eine besondere Bedeutung zu. Diagnostizierte fetale Auffälligkeiten beunruhigen die werdenden Eltern; betreuende Ärzte benötigen klare Zahlen für die ...
Brenner, Martina
core   +1 more source

Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1608-1618, July 2026.
ABSTRACT RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS‐mitogen‐activated protein kinase (RAS–MAPK) signaling pathway, often presenting with congenital heart defects, craniofacial dysmorphisms, and developmental delays. To assess the diagnostic yield of genetic testing in patients with suspected RASopathies and to
Emanuele Bobbio, Martina Caiazza, Emanuele Monda, Giustina Aruta, Alberto Budillon, Augusto Esposito, Adelaide Fusco, Annapaola Cirillo, Marta Rubino, Immacolata Viscovo, Gioacchino Scarano, Matteo Della Monica, Vincenzo Nigro, Giulio Piluso, Leandro Pecchia, Maria Giovanna Russo, Giuseppe Limongelli   +16 more
wiley   +1 more source

BAV and VSD in Alk2/Gata5-Cre mutants.

, 2012
BAV and VSD in Alk2/Gata5-Cre mutants.
Penny S. Thomas (170077), Vesa Kaartinen (38989), Somyoth Sridurongrit (170083), Pilar Ruiz-Lozano (35887)   +3 more
core   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Overlooked Ventricular Septal Defect Post-Myocardial Infarction and Coronary Artery Bypass Grafting

Clinical Medicine Insights: Case Reports
Ventricular septal defect (VSD) represents a severe complication that may manifest after a myocardial infarction (MI), typically occurring between 2 and 7 days later.
Nderim Rexha, Xhevdet Krasniqi, Agnesa Dervishaj Rexha, Aurora Bakalli   +3 more
doaj   +1 more source

Explanatory deep learning to predict elevated pulmonary artery pressure in children with ventricular septal defects using standard chest x-rays: a novel approach

Frontiers in Cardiovascular Medicine
ObjectiveEarly risk assessment of pulmonary arterial hypertension (PAH) in patients with congenital heart disease (CHD) is crucial to ensure timely treatment. We hypothesize that applying artificial intelligence (AI) to chest x-rays (CXRs) could identify
Zhixin Li, Gang Luo, Zhixian Ji, Sibao Wang, Silin Pan   +4 more
doaj   +1 more source

Vasodilators in VSDs. [PDF]

Circulation, 1977
R, Macri, S, Redaelli
openaire   +2 more sources

Target genes associated with cardiac development predicted for 8 differentially expressed miRNAs in patients with VSD.

, 2014
miRNA, microRNA; VSD, ventricular septal defect.Target genes associated with cardiac development predicted for 8 differentially expressed miRNAs in patients with VSD.
Qiang Sun (225630), Lianbo Liu (622764), Haifeng Hou (622765), Zhongtang Zhao (520419), Yizhi Liu (90863), Kunkun Yu (622766), Dong Li (212687), Long Ji (622763)   +7 more
core   +1 more source

Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation

The Laryngoscope, Volume 136, Issue 7, Page 3240-3245, July 2026.
We report the first documented case of airway involvement in Conradi–Hünermann–Happle syndrome (CDPX2), an X‐linked dominant form of chondrodysplasia punctata caused by pathogenic variants in EBP. A 2‐month‐old female with genetically confirmed CDPX2 developed severe subglottic stenosis and persistent respiratory distress requiring CPAP; cross ...
Enrique G. Villarreal, Jackie Chiang, Evan J. Propst, Nikolaus E. Wolter   +3 more
wiley   +1 more source