Výsledky vyhledávání - "R M F, Berger"

Akademický článek

Cardiac Function and Serum Biomarkers throughout Staged Fontan Palliation: A Prospective Observational Study

Autor: J. P. G. van der Ven, V P. Kamphuis, E van den Bosch, D Gnanam, C Terol, A J. J. C. Bogers, J. M. P. J. Breur, R. M. F. Berger, N. A. Blom, A. D. J. ten Harkel, L. Koopman, W. A. Helbing

Publikováno v: Journal of Cardiovascular Development and Disease, Vol 10, Iss 7, p 289 (2023)

Fontan patients undergo multiple cardiothoracic surgeries in childhood. Following these procedures, ventricular function is temporarily decreased, and recovers over months. This is presumably related to cardiopulmonary bypass, but this is incompletel

Externí odkaz: https://doaj.org/article/e676cd2ac66548dc94dd295dff7beceb

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Cardiac Function and Serum Biomarkers throughout Staged Fontan Palliation: A Prospective Observational Study

Autor: Helbing, J. P. G. van der Ven, V P. Kamphuis, E van den Bosch, D Gnanam, C Terol, A J. J. C. Bogers, J. M. P. J. Breur, R. M. F. Berger, N. A. Blom, A. D. J. ten Harkel, L. Koopman, W. A.

Publikováno v: Journal of Cardiovascular Development and Disease; Volume 10; Issue 7; Pages: 289

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=multidiscipl::ab1a4fc46c47a418ec96c84964ad29a4

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Akademický článek

Patient Characteristics in Persistent Pulmonary Hypertension of the Newborn

Autor: M. T. R. Roofthooft, A. Elema, K. A. Bergman, R. M. F. Berger

Publikováno v: Pulmonary Medicine, Vol 2011 (2011)

Objective. To assess the impact of PPHN on mortality, morbidity, and behavioural skills. Methods. A retrospective observational study of 143 newborns with PPHN, over an 11-year period, using objective health-status data from medical records and famil

Externí odkaz: https://doaj.org/article/cd2441d0a3f64ffe931360169d50113a

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Validation of Fick cardiac output calculated with assumed oxygen consumption: a study of cardiac output during epoprostenol

Autor: A, Bergstra, A F M, van den Heuvel, F, Zijlstra, R M F, Berger, G A, Mook, D J, van Veldhuisen

Publikováno v: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation. 12(5)

To test the validity of using assumed oxygen consumption for Fick cardiac output during administration of epoprostenol.In 24 consecutive patients Fick cardiac output calculated with assumed oxygen consumption according to LaFarge and Miettinen (COLM)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::89fc1eee09b1af79bfbafd589ae092c4
https://pubmed.ncbi.nlm.nih.gov/25696328

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Transcatheter pulmonary valve perforation and balloon dilatation in neonates with pulmonary atresia and intact ventricular septum

Autor: C G, Gerestein, R M F, Berger, M, Dalinghaus, A J J C, Bogers, M, Witsenburg

Publikováno v: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation. 11(11)

Pulmonary atresia and intact ventricular septum is characterised by a great morphological variety. Treatment is not uniform.To evaluate our experience with transcatheter valvotomy and balloon dilatation in neonates with pulmonary atresia and intact v

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3459b90b1b5d17c586a9a0393325a923
https://pubmed.ncbi.nlm.nih.gov/25696158

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Primaire pulmonale hypertensie op de kinderleeftijd

Autor: R. M. F. Berger, P. P. Roeleveld, M. Jongejan

Publikováno v: Tijdschrift voor Kindergeneeskunde, 70, 68-74. Bohn Stafleu van Loghum

Primaire pulmonale hypertensie is een zeldzame en levensbedreigende longvaataandoening met onbekende pathogenese, die zich op de kinderleeftijd op verschillende manieren kan presenteren. Er bestaat geen causale behandeling en tot voor kort was alleen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33dda61b0c3c870f61924dceae59edb7
https://doi.org/10.1007/bf03061407

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Enhanced expression of vascular endothelial growth factor in pulmonary plexogenic arteriopathy due to congenital heart disease

Autor: Hari S. Sharma, R. Geiger, John Hess, Ad J.J.C. Bogers, R. M. F. Berger, Wolter J. Mooi

Publikováno v: Journal of Pathology, 191, 202-207. John Wiley & Sons Ltd.

Congenital heart disease (CHD) leading to increased pulmonary blood pressure and flow is an important cause of pulmonary plexogenic arteriopathy (PPA). This type of arteriopathy tends to progress to an irreversible stage, hallmarked histologically by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0df0af0cca22099b96160358d0cde8e3
https://pure.eur.nl/en/publications/cc593c28-d708-4b7a-b33d-70b606af9b2e

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