Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Paul Ramaekers"'
Autor:
Sally Pehrsson, Bruce Eglington, Robert Rainbird, Daniele Regis, Paul Ramaekers, Charlie Jefferson
Publikováno v:
Geological Society, London, Special Publications. 531
Mesoproterozoic orogenesis is well established on the western and southern flanks of Laurentia in the well-known Racklan-Forward and Mazatzal Orogens, but its significance within the previously assembled interior of the supercontinent Nuna has not be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1dedf1aabb14e7d6afaa1487ff3a165
https://doi.org/10.1144/sp531-2022-307
https://doi.org/10.1144/sp531-2022-307
Autor:
Kristof Vandekerckhove, Koen Van Herck, Thierry Bové, Katya De Groote, Paul Ramaekers, Ellen Roets, Hans De Wilde, Ellen Vanhie, Katrien François, Daniël De Wolf, Joseph Panzer
Publikováno v:
Prenatal Diagnosis. 37:983-991
Objective Determine prenatal detection rate, mortality and association with genetic abnormalities in patients with severe CHD. Method Single center retrospective study in patients with severe CHD diagnosed pre or postnatally (2006 to 2014). Results 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8acaad50bfcfa8a00f5477f643a270bb
https://doi.org/10.1002/pd.5117
https://doi.org/10.1002/pd.5117
Autor:
GL Fernandes, M Sanz, Christopher I. Cassady, Daniela Prayer, Paul Ramaekers, Peter Brugger, Boris Tutschek, Laurent Salomon, Michael Weber, Nick Raine-Fenning, A. Millischer, Gerlinde M. Gruber, Sherelle Laifer-Narin, B. De Keersmaecker, Ilan E. Timor-Tritsch, Phyllis Glanc, R Ximenes, Luis F. Goncalves, Wesley Lee, M Molho, Jaladhar Neelavalli, L. De Catte, Lawrence D. Platt, Gustavo Malinger, Diane M. Twickler, Denise Pugash
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 49:671-680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3304abc2e540b87b69644201b0a5ea5c
https://doi.org/10.1002/uog.17412
https://doi.org/10.1002/uog.17412
Autor:
Katya, De Groote, Ellen, Vanhie, Ellen, Roets, Paul, Ramaekers, Hans, De Wilde, Joseph, Panzer, Kristof, Vandekerckhove, Thierry, Bove, Katrien, François, Koen, Van Herck, Daniël, De Wolf
Publikováno v:
Prenatal diagnosis. 37(10)
Determine prenatal detection rate, mortality and association with genetic abnormalities in patients with severe CHD.Single center retrospective study in patients with severe CHD diagnosed prenatally or postnatally (2006 to 2014).A total of 567 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d7cba7726f5b27b4394186e5b7a9ff9
https://pubmed.ncbi.nlm.nih.gov/28727893
https://pubmed.ncbi.nlm.nih.gov/28727893
Autor:
Yves Jacquemyn, Cecile Colpaert, Bart Loeys, Heiko Reutter, Maxim Parizel, Bettina Blaumeiser, Katrien Janssens, Paul Ramaekers, Catharina von Lowtzow, Yves Leroy
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 100:797-800
Background Bladder exstrophy is a rare malformation. Prenatal diagnosis is usually an incidental finding on routine ultrasound examination. Triple-X syndrome (karyotype 47,XXX) is the most frequent sex chromosome aneuploidy in live-born females (appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f146ea6b5275f2f253946729c76d9d3
https://doi.org/10.1002/bdra.23299
https://doi.org/10.1002/bdra.23299
Publikováno v:
BJOG: an international journal of obstetrics and gynaecology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6156d579d1ea9f77373ac63e4cf82215
https://pubmed.ncbi.nlm.nih.gov/26307477
https://pubmed.ncbi.nlm.nih.gov/26307477
Publikováno v:
BMJ case reports
We report a case of bilateral fetal hydrothorax presenting at 20 weeks of pregnancy, spontaneously resolving at 22 weeks and severely relapsing at 28 weeks in a fetus with normal karyotype. The cause was a high-output heart failure caused by vein of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94245126442c343c2eb5cfe12bb2a97a
https://pubmed.ncbi.nlm.nih.gov/25628327
https://pubmed.ncbi.nlm.nih.gov/25628327
Autor:
Paul, Ramaekers, Bart, Loeys, Catharina, von Lowtzow, Heiko, Reutter, Yves, Leroy, Cécile, Colpaert, Bettina, Blaumeiser, Katrien, Janssens, Maxim, Parizel, Yves, Jacquemyn
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 100(10)
Bladder exstrophy is a rare malformation. Prenatal diagnosis is usually an incidental finding on routine ultrasound examination. Triple-X syndrome (karyotype 47,XXX) is the most frequent sex chromosome aneuploidy in live-born females (approximately 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f16d52b13109787dae312c5d099ed8c8
https://pubmed.ncbi.nlm.nih.gov/25200913
https://pubmed.ncbi.nlm.nih.gov/25200913
Autor:
Marie Therèse Van Damme, Paul Ramaekers, Jean Pierre Fryns, Ingrid Witters, Frans Andre Van Assche
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 106:83-85
A male newborn with multiple cutaneous hemangiomatosis is described. Pregnancy was complicated by polyhydramnios and a large placental chorioangioma. After an initial outburst of the hemangiomas in the first two weeks of life, spontaneous and almost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::215da19f2775e01e4690e52a74466e9f
https://doi.org/10.1016/s0301-2115(02)00163-x
https://doi.org/10.1016/s0301-2115(02)00163-x
Autor:
Paul Ramaekers, Kamiel Vandenberghe, Yves Gillerot, Alain Verloes, Eric Legius, Jean-Pierre Fryns
Publikováno v:
Scopus-Elsevier
A newborn boy is described with semilobar holoprosencephaly, cebocephaly with single nostril, median pseudocleft of upper lip, postaxial polydactyly, hypogenitalism, Hischsprung's disease and survival till the age of 13 weeks. Chromosomal analysis on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f51eb138ea9f23ed33bf7b9ef4e3e9e
https://doi.org/10.1016/0028-2243(90)90062-6
https://doi.org/10.1016/0028-2243(90)90062-6