Results 201 to 210 of about 2,830,227 (287)

Polymeric Heart Valves: Do They Represent a Reliable Alternative to Current Prosthetic Devices? [PDF]

Polymers (Basel)
Todesco M, Lezziero G, Gerosa G, Bagno A.   +3 more
europepmc   +1 more source

Effects of valve geometry and tissue anisotropy on the radial stretch and coaptation area of tissue-engineered heart valves.

Journal of Biomechanics, 2013
S. Loerakker, G. Argento, C.W.J. Oomens, F. Baaijens   +3 more
semanticscholar   +1 more source

Review Article: Contemporary Transcatheter Heart Valves for TAVI in Bicuspid Aortic Anatomy. [PDF]

J Clin Med
Simopoulou C, Oliva O, Cesario V, Dumonteil N, Tchetche D, De Biase C.   +5 more
europepmc   +1 more source

Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies

American Journal of Medical Genetics Part A, EarlyView.
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

Comparison of Latest Generation Intra- and Supra-Annular Self-Expanding Transcatheter Heart Valves for Aortic Valve-in-Valve Procedures. [PDF]

Catheter Cardiovasc Interv
Stötzel AK, Bhadra OD, Waldschmidt L, Demal TJ, Grundmann D, Voigtländer L, Blankenberg S, Reichenspurner H, Schofer N, Schaefer A.   +9 more
europepmc   +1 more source

SUTURELESS PROSTHETIC HEART VALVES

The Journal of Thoracic and Cardiovascular Surgery, 1963
G J, MAGOVERN, H W, CROMIE
openaire   +2 more sources

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

American Journal of Medical Genetics Part A, EarlyView.
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

Pregnant Woman in Outcomes with Prosthetic Heart Valves. [PDF]

J Cardiovasc Dev Dis
Sefiyeva G, Shadrina U, Vavilova T, Sirotkina O, Bautin A, Chynybekova A, Pozhidaeva A, Stepanovykh E, Starshinova A, Kudlay D, Irtyuga O.   +10 more
europepmc   +1 more source

Therapy for Myhre Syndrome: Goals, Misconceptions, and Current Agents

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre Syndrome (MYHRS, MIM #139210) is a rare, multisystem connective tissue disorder caused by recurrent heterozygous gain‐of‐function pathogenic variants in the SMAD4 gene, a key player in TGF‐β signaling and a regulator of extracellular matrix homeostasis.
Alessandro De Falco, Alfonso Manuel D'Alessio, Nicola Brunetti‐Pierri   +2 more
wiley   +1 more source

Rethinking mechanical heart valves in the aortic position: new paradigms in design and testing. [PDF]

Front Cardiovasc Med
Chakraborty S, Simon MG, Bellofiore A.
europepmc   +1 more source