Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ginette M Ecury-Goossen"'
Autor:
Roelof van Ewijk, Minke H. W. Huibers, Meindert E. Manshande, Ginette M. Ecury-Goossen, Ashley J. Duits, Job C. Calis, Aleid G. van Wassenaer-Leemhuis
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Perinatally chikungunya infected neonates have been reported to have high rates of post-infection neurologic sequelae, mainly cognitive problems. In older children and adults chikungunya does not appear to have sequelae, but data
Externí odkaz:
https://doaj.org/article/e960b71c59b4412382097872bba40e7a
Autor:
Eline A. Verberne, Shirley M. Lo‐A‐Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L. G. Wever, Eric Arends, Hilda Holtsema, Petra J. Hajenius, Daphne Moreta, Ginette M. Ecury‐Goossen, Marcel M. A. M. Mannens, Hermien E. K. de Walle, Jorieke E. H. Bergman, Mieke M. van Haelst
Publikováno v:
Birth defects research. John Wiley and Sons Ltd
Birth defects research, 115(6), 595-604. John Wiley and Sons Ltd
Verberne, E A, Lo-A-Njoe, S M, van Ginkel, M, Zwolsman, J, Nikkels, S, Clement, L, de Vroomen, M, Wever, M L G, Arends, E, Holtsema, H, Hajenius, P J, Moreta, D, Ecury-Goossen, G M, Mannens, M M A M, de Walle, H E K, Bergman, J E H & van Haelst, M M 2023, ' Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao ', Birth defects research, vol. 115, no. 6, pp. 595-604 . https://doi.org/10.1002/bdr2.2153, https://doi.org/10.1002/bdr2.2153
Birth defects research, 115(6), 595-604. John Wiley and Sons Ltd
Verberne, E A, Lo-A-Njoe, S M, van Ginkel, M, Zwolsman, J, Nikkels, S, Clement, L, de Vroomen, M, Wever, M L G, Arends, E, Holtsema, H, Hajenius, P J, Moreta, D, Ecury-Goossen, G M, Mannens, M M A M, de Walle, H E K, Bergman, J E H & van Haelst, M M 2023, ' Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao ', Birth defects research, vol. 115, no. 6, pp. 595-604 . https://doi.org/10.1002/bdr2.2153, https://doi.org/10.1002/bdr2.2153
Background: Congenital anomalies represent an important global health issue. Data on the prevalence and pattern of congenital anomalies in the Caribbean region are scarce and lacking altogether in Aruba, Bonaire and Curaçao (ABC islands). Methods: W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0da354a8c2f480402eb96e4020ae7f05
https://doi.org/10.1002/bdr2.2153
https://doi.org/10.1002/bdr2.2153
Autor:
Inez M Vanholder, Ginette M Ecury‐Goossen, Jop Admiraal, Leendert Porcelijn, Rosalina ML van Spaendonk, Samantha C Gouw
Publikováno v:
Journal of paediatrics and child health, 58(12), 2319-2321. Wiley-Blackwell
Journal of Paediatrics and Child Health, 58(12), 2319-2321. Wiley-Blackwell
Journal of Paediatrics and Child Health, 58(12), 2319-2321. WILEY
Vanholder, I M, Ecury-Goossen, G M, Admiraal, J, Porcelijn, L, van Spaendonk, R M L & Gouw, S C 2022, ' Congenital amegakaryocytic thrombocytopenia presenting with a new thrombopoietin receptor (MPL) pathogenic variant : An instructive neonatal case ', Journal of Paediatrics and Child Health, vol. 58, no. 12, pp. 2319-2321 . https://doi.org/10.1111/jpc.16168
Journal of paediatrics and child health
Journal of Paediatrics and Child Health, 58(12), 2319-2321. Wiley-Blackwell
Journal of Paediatrics and Child Health, 58(12), 2319-2321. WILEY
Vanholder, I M, Ecury-Goossen, G M, Admiraal, J, Porcelijn, L, van Spaendonk, R M L & Gouw, S C 2022, ' Congenital amegakaryocytic thrombocytopenia presenting with a new thrombopoietin receptor (MPL) pathogenic variant : An instructive neonatal case ', Journal of Paediatrics and Child Health, vol. 58, no. 12, pp. 2319-2321 . https://doi.org/10.1111/jpc.16168
Journal of paediatrics and child health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c82c356aa631c3a667dacb5f491d444
https://hdl.handle.net/1887/3566398
https://hdl.handle.net/1887/3566398
Autor:
Eline A. Verberne, Jonne M. Westermann, Tamar I. Vries, Ginette M. Ecury‐Goossen, Shirley M. Lo‐A‐Njoe, Meindert E. Manshande, Sonja Faries, Hans D. Veenhuis, Patricia Philippi, Farah A. Falix, Irsa Rosina‐Angelista, Maria Ponson‐Wever, Louise Rafael‐Croes, Patricia Thorsen, Eric Arends, Maartje Vroomen, Sietse Q. Nagelkerke, Martijn Tilanus, Lars T. Veken, Karin Huijsdens‐van Amsterdam, Anne‐Marie Kevie‐Kersemaekers, Mariëlle Alders, Marcel M. A. M. Mannens, Mieke M. Haelst
Publikováno v:
American Journal of Medical Genetics Part A, 188(6), 1777-1791. Wiley-Liss Inc.
American journal of medical genetics. Part A, 188(6), 1777-1791. Wiley-Liss Inc.
Verberne, E A, Westermann, J M, de Vries, T I, Ecury-Goossen, G M, Lo-A-Njoe, S M, Manshande, M E, Faries, S, Veenhuis, H D, Philippi, P, Falix, F A, Rosina-Angelista, I, Ponson-Wever, M, Rafael-Croes, L, Thorsen, P, Arends, E, de Vroomen, M, Nagelkerke, S Q, Tilanus, M, van der Veken, L T, Huijsdens-van Amsterdam, K, van der Kevie-Kersemaekers, A-M, Alders, M, Mannens, M M A M & van Haelst, M M 2022, ' Genetic care in geographically isolated small island communities : 8 years of experience in the Dutch Caribbean ', American Journal of Medical Genetics Part A, vol. 188, no. 6, pp. 1777-1791 . https://doi.org/10.1002/ajmg.a.62708
American journal of medical genetics. Part A, 188(6), 1777-1791. Wiley-Liss Inc.
Verberne, E A, Westermann, J M, de Vries, T I, Ecury-Goossen, G M, Lo-A-Njoe, S M, Manshande, M E, Faries, S, Veenhuis, H D, Philippi, P, Falix, F A, Rosina-Angelista, I, Ponson-Wever, M, Rafael-Croes, L, Thorsen, P, Arends, E, de Vroomen, M, Nagelkerke, S Q, Tilanus, M, van der Veken, L T, Huijsdens-van Amsterdam, K, van der Kevie-Kersemaekers, A-M, Alders, M, Mannens, M M A M & van Haelst, M M 2022, ' Genetic care in geographically isolated small island communities : 8 years of experience in the Dutch Caribbean ', American Journal of Medical Genetics Part A, vol. 188, no. 6, pp. 1777-1791 . https://doi.org/10.1002/ajmg.a.62708
Worldwide, there are large inequalities in genetic service delivery. In 2011, we established a bi-annual joint pediatric-genetics clinic with a visiting clinical geneticist in the Dutch Caribbean. This retrospective study evaluates the yield of diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3113ee3583a01686e46a6357e683726c
https://pubmed.ncbi.nlm.nih.gov/35253369
https://pubmed.ncbi.nlm.nih.gov/35253369
Autor:
Fleur A. Camfferman, Ginette M. Ecury-Goossen, Jhuresy E. La Roche, Nico ede Jong, Willem evan 't Leven, Hendrik J. Vos, Martin D. Verweij, Kazem eNasserinejad, Filip eCools, Paul eGovaert, Jeroen eDudink
Publikováno v:
Frontiers in Human Neuroscience, Vol 8 (2015)
Introduction. Preterm infants are born during critical stages of brain development, in which the adaptive capacity of the fetus to extra-uterine environment is limited. Inadequate brain perfusion has been directly linked to preterm brain damage. Adva
Externí odkaz:
https://doaj.org/article/1a683f0fa187456dbab4ea66c9c97e89
Autor:
Maria Ponson-Wever, Lidewij Henneman, Meindert E. Manshande, Ginette M. Ecury-Goossen, Mieke M. van Haelst, Marcel M.A.M. Mannens, Eline A. Verberne, Martijn Tilanus, Maartje de Vroomen
Publikováno v:
Verberne, E A, Ecury-Goossen, G M, Manshande, M E, Ponson-Wever, M, de Vroomen, M, Tilanus, M, Mannens, M M A M, Henneman, L & van Haelst, M M 2021, ' Clinical and community genetics services in the Dutch Caribbean ', Journal of Community Genetics, vol. 12, no. 3, pp. 497-501 . https://doi.org/10.1007/s12687-021-00515-6, https://doi.org/10.1007/s12687-021-00515-6
Journal of Community Genetics
Journal of Community Genetics, 12(3), 497-501. Springer Verlag
Journal of community genetics, 12(3), 497-501. Springer Verlag
Journal of Community Genetics
Journal of Community Genetics, 12(3), 497-501. Springer Verlag
Journal of community genetics, 12(3), 497-501. Springer Verlag
The Caribbean part of the Kingdom of the Netherlands consists of six islands: Aruba, Bonaire, Curaçao, St. Maarten, St. Eustatius, and Saba. Because of their small size and relative remoteness, they face several economic and healthcare challenges, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdead96b8491eb891a37246f61bb5782
https://research.vumc.nl/en/publications/48ed84af-2ba5-4a0d-8d29-e536484feaa0
https://research.vumc.nl/en/publications/48ed84af-2ba5-4a0d-8d29-e536484feaa0
Autor:
Irsa Rosina-Angelista, Ginette M. Ecury-Goossen, Karolien Van De Maele, Charlotte A. Smulders, Mieke M. van Haelst, Egbert J.W. Redeker
Publikováno v:
Clinical Dysmorphology, 28(2), 57-62. Lippincott Williams and Wilkins
van de Maele, K, Smulders, C, Ecury-Goossen, G, Rosina-Angelista, I, Redeker, E & van Haelst, M 2019, ' Stuve-Wiedemann syndrome : Recurrent neonatal infections caused by impairment of JAK/STAT 3 pathway ', Clinical Dysmorphology, vol. 28, no. 2, pp. 57-62 . https://doi.org/10.1097/MCD.0000000000000255
Clinical dysmorphology, 28(2), 57-62. Lippincott Williams and Wilkins
van de Maele, K, Smulders, C, Ecury-Goossen, G, Rosina-Angelista, I, Redeker, E & van Haelst, M 2019, ' Stuve-Wiedemann syndrome : Recurrent neonatal infections caused by impairment of JAK/STAT 3 pathway ', Clinical Dysmorphology, vol. 28, no. 2, pp. 57-62 . https://doi.org/10.1097/MCD.0000000000000255
Clinical dysmorphology, 28(2), 57-62. Lippincott Williams and Wilkins
Stüve-Wiedemann syndrome (OMIM #601559) is a rare, autosomal recessive disorder characterized by skeletal dysplasia, consecutive infections, feeding difficulties and autonomic dysregulation. We present an Afro-Caribbean family with two siblings diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::511533a1d761090aff5a2aefc3ef548c
https://doi.org/10.1097/mcd.0000000000000255
https://doi.org/10.1097/mcd.0000000000000255
Autor:
Ashley J. Duits, Meindert E. Manshande, Roelof van Ewijk, Job C. J. Calis, Minke H. W. Huibers, Aleid G. van Wassenaer-Leemhuis, Ginette M. Ecury-Goossen
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-8 (2021)
BMC Infectious Diseases
BMC Infectious Diseases
Background Perinatally chikungunya infected neonates have been reported to have high rates of post-infection neurologic sequelae, mainly cognitive problems. In older children and adults chikungunya does not appear to have sequelae, but data on postna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62c368d1cf2dde255b5f2182f22561da
https://doi.org/10.1186/s12879-021-05876-4
https://doi.org/10.1186/s12879-021-05876-4
Autor:
Ginette M Ecury-Goossen, Paul Govaert, Joost van Rosmalen, Jeroen Dudink, Marlou M. A. Raets, Fleur A. Camfferman, Rik H. J. Vos, Irwin K M Reiss
Publikováno v:
Pediatric Radiology, 46(9), 1291-1300. Springer-Verlag
Pediatric Radiology
Pediatric Radiology, 46(9), 1291–1300. Springer Verlag
Pediatric Radiology
Pediatric Radiology, 46(9), 1291–1300. Springer Verlag
BACKGROUND: Little is known about cerebral artery resistive index values in infants born extremely preterm. OBJECTIVE: To report resistive index values in various cerebral arteries in a prospective cohort of preterm infants born at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fc207a18a1f53390304a6fbc09661e5
https://doi.org/10.1007/s00247-016-3615-x
https://doi.org/10.1007/s00247-016-3615-x
Autor:
Jeroen Dudink, Freek E. Hoebeek, Ginette M Ecury-Goossen, Aicha B. C. Dijkshoorn, Manon J.N.L. Benders, Lisa M. Hortensius, Sylke J. Steggerda
Publikováno v:
Pediatrics, 142(5). American Academy of Pediatrics
Pediatrics, 142(5)
Pediatrics, 142(5):e20180609. American Academy of Pediatrics
Pediatrics, 142(5)
Pediatrics, 142(5):e20180609. American Academy of Pediatrics
CONTEXT: The effect of neonatal cerebellar hemorrhage on neurodevelopmental outcome (NDO) in the absence of supratentorial injury is still largely unknown. OBJECTIVE: To evaluate the influence of isolated neonatal cerebellar hemorrhage on cognitive,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea6b52ba0e40e6ca875a63c50f511ac
https://pubmed.ncbi.nlm.nih.gov/30341153
https://pubmed.ncbi.nlm.nih.gov/30341153