Results 51 to 60 of about 79,987 (264)

Long-term performance of untreated fresh autologous pericardium as a valve substitute in pulmonary position

Annals of Cardiac Anaesthesia, 2022
Background: Pulmonary regurgitation is imminent after transannular patch (TAP). We analyze the long-term performance of untreated autologous pericardium (UAP) as valve substitute at pulmonary position in patients requiring TAP.
Shantanu Pande, Amitabh Arya, Surendra K Agarwal, Prabhat Tewari, Aditya Kapoor, Neetu Soni, Sunil Kumar   +6 more
doaj   +1 more source

A comparison of clinical paediatric murmur assessment with echocardiography [PDF]

, 2004
Objective: To compare the clinical acumen of paediatric cardiovascular examination between various hospital paediatrician grades. Design: Prospective data collection of clinical and echocardiography findings on paediatric echocardiography referrals ...
Bailey, Mark, Grech, Victor E., Mercieca, Victor, Spiteri, Amaris, Torpiano, John G.   +4 more
core  

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

Persistence Pulmonal Hypertension After Balloon Mitral Valvuiloplasty

Majalah Kardiologi Indonesia, 2013
Background.Pulmonary hypertension frequently complicates mitral stenosis. Increased pulmonary artery pressure results from raised left atrial pressure, pulmonary arteriolar vasoconstriction, and obliterative changes in the pulmonary vascular bed, and ...
doaj   +1 more source

Initial experience with Edwards SAPIEN valve transcatheter implantation in native RVOT in Latvia

Acta Medica Lituanica, 2020
Transcatheter pulmonary valve implantation has been a well-known method for more than a decade, but there are still many challenging cases when a personalized solution is needed.
Luize Auzina, Inguna Lubaua, Elina Ligere, Inga Lace, Inta Bergmane, Baiba Matsone-Matsate, Pauls Silis, Lauris Smits, Normunds Sikora, Lars Søndergaard, Valts Ozolins   +10 more
doaj   +1 more source

Intravascular Lithotripsy for Severe RVOT Calcification to Optimize Transcatheter Pulmonary Valve Replacement

JACC: Case Reports, 2023
The presence of severe right ventricular outflow tract calcification may preclude safe and effective transcatheter pulmonary valve replacement in patients with pulmonary allograft stenosis owing to the risk of conduit tear and suboptimal annular ...
Nabil Sabbak, MD, Kara Denby, MD, Anirudh Kumar, MD, Ghazaleh Goldar, MD, Joanna Ghobrial, MD   +4 more
doaj   +1 more source

Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying Severe Noonan Syndrome With Adult‐Onset Acute Myeloid Leukemia

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan syndrome (NS) is a genetically heterogeneous disorder characterized by a broad spectrum of clinical features resulting from dysregulation of the RAS/MAPK pathway. Although complex genotypes are increasingly recognized in NS, cases harboring two distinct pathogenic variants in different NS genes remain extremely rare.
Francesco Prevedello, Dario Seif Ali, Chiara Piccolo, Chiara Rigon, Monica Forzan, Elena Tacchetto, Roberta Palmitessa, Davide Calosci, Leonardo Salviati, Carmela Gurrieri, Eva Trevisson   +10 more
wiley   +1 more source

Bridging aortic valve surgery to 21st century. what can a surgeon do [PDF]

, 2019
Aortic valve stenosis is the most clinically relevant valvular heart disease in the elderlies. Surgical aortic valve replacement (SAVR) represented, for decades, the standard of care for the treatment of severe aortic stenosis.
Barretta, Antonio, Biondi-Zoccai, Giuseppe, D��Abramo, Mizar, Ferrante, Luisa, Frati, Giacomo, Greco, Ernesto, Guerrera, Manuel, Iaccarino, Alessandra, Marullo, Antonino, Miraldi, Fabio, Peruzzi, Mariangela, Proietti, Piero, Saade, Wael, Sciarretta, Sebastiano   +13 more
core   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Mitral bones in mitral stenosis: A rare presentation

Journal of Dr. NTR University of Health Sciences, 2017
Pulmonary ossification is described as mature bone formation with or without marrow elements in alveolar or interstitial spaces. Pulmonary ossification is a rare late sequelae that is virtually pathognomonic of mitral stenosis. Mitral bone is nothing but
Onteddu Joji Reddy, Polysetty Obuleswar Prasad, Jamkhana Abdul Gafoor, Munirajulu Rajanikanth   +3 more
doaj   +1 more source