Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Bartłomiej, Mroziński"'
Autor:
Zuzanna Kozłowska, Zuzanna Owsiańska, Joanna P. Wroblewska, Apolonia Kałużna, Andrzej Marszałek, Yogen Singh, Bartłomiej Mroziński, Qian Liu, Justyna A. Karolak, Paweł Stankiewicz, Gail Deutsch, Marta Szymankiewicz-Bręborowicz, Tomasz Szczapa
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Alveolar capillary dysplasia (ACD) is a rare cause of severe pulmonary hypertension and respiratory failure in neonates. The onset of ACD is usually preceded by a short asymptomatic period. The condition is refractory to all avail
Externí odkaz:
https://doaj.org/article/76cc8384c7354543b6c9647b65fc9007
Autor:
Gazala Abdulaziz-Opiela, Anna Sobieraj, Greta Sibrecht, Julia Bajdor, Bartłomiej Mroziński, Zuzanna Kozłowska, Rafał Iciek, Katarzyna Wróblewska-Seniuk, Ewa Wender-Ożegowska, Tomasz Szczapa
Publikováno v:
International Journal of Molecular Sciences. 24:7629
Neonatal venous thrombosis is a rare condition that can be iatrogenic or occur due to viral infections or genetic mutations. Thromboembolic complications are also commonly observed as a result of SARS-CoV-2 infections. They can affect pediatric patie
Autor:
Bartłomiej Mroziński, Zuzanna Owsiańska, Justyna A. Karolak, Andrzej Marszałek, Joanna Wróblewska, Apolonia Kaluzna, Tomasz Szczapa, Gail H. Deutsch, Marta Szymankiewicz-Bręborowicz, Pawel Stankiewicz, Zuzanna Kozłowska, Qian Liu, Yogen Singh
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
Background Alveolar capillary dysplasia (ACD) is a rare cause of severe pulmonary hypertension and respiratory failure in neonates. The onset of ACD is usually preceded by a short asymptomatic period. The condition is refractory to all available ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eba88dbd41fd971028f772ce557516d4
Autor:
Magdalena Janus, Katarzyna Karmelita-Katulska, Małgorzata Pyda, Justyna Rajewska-Tabor, Bartłomiej Mroziński, Szymon Rozmiarek, Andrzej Siniawski, Barbara Rabska-Pietrzak, Agnieszka Graczyk-Szuster, Marek Niedziela, Monika Obara-Moszynska, Anna Kociemba
Publikováno v:
Frontiers in Endocrinology
Frontiers in Endocrinology, Vol 9 (2018)
Frontiers in Endocrinology, Vol 9 (2018)
Cardiovascular defects occur in 50% of patients with Turner syndrome (TS). The aim of the study was to estimate the usefulness of cardiac magnetic resonance imaging (CMR) and magnetic resonance angiography (angio-MR) as diagnostics in children and ad
Publikováno v:
Kardiochirurgia i Torakochirurgia Polska = Polish Journal of Cardio-Thoracic Surgery
The paper presents the management of a child born with pulmonary valve atresia, a single (double-inlet) ventricle, right ventricular hypoplasia, and perimembranous septal defect. The first stage of treatment consisted in a Blalock-Taussig shunt. Cont
Autor:
Michał Wojtalik, Artur Baszko, Aldona Siwińska, Bartłomiej Mroziński, Tomasz Moszura, Rafał Surmacz, Waldemar Bobkowski
Publikováno v:
Advances in Interventional Cardiology. 3:261-264
In case of significant hypoxia in the course of congenital heart defect, when definite surgery is difficult, various palliative procedures are performed. One of the most frequently used is a modified Blalock-Taussig (BT) anastomosis. The BT anastomos
Publikováno v:
Fetal Diagnosis and Therapy. 31:69-72
We report the case of fetal goiter which occurred in two consecutive pregnancies in the same patients. The first one, due to too late diagnosis and no intrauterine treatment, contributed to the immediate postnatal death of the newborn; the second one
Publikováno v:
Pediatria Polska. 82:619-623
Cel pracy Celem pracy byla ocena skuteczności i bezpieczenstwa stosowania flekainidu w leczeniu profilaktycznym czestoskurczu nadkomorowego (SVT) u noworodkow i niemowląt. Material i metody Badaniami objeto populacje 20 dzieci w 1 roku zycia, 17 no
Autor:
Aldona Siwińska, Michał Wojtalik, Bartłomiej Mroziński, Waldemar Bobkowski, Tomasz Moszura, Rafał Surmacz, Oskar Jaremba
Publikováno v:
Kardiologia Polska. 71:396-398
Despite marked improvement in the cardiosurgery, total repair of interrupted aortic arch with coexisting risk factors in neonatal or early infancy is associated with high mortality. We present a patient treated by an alternative hybrid procedure with
Publikováno v:
Fetal diagnosis and therapy. 34(1)