Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Congenital Abnormalities/diagnosis"'
Autor:
William Reardon
The Bedside Dysmorphologist is a thoughtful clinical guide to common--and often quite subtle--congenital malformations in clinical exam. Organized by area of the body, each section provides the user with a concise, illustrated roadmap for assessment
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 4, Pp 399-402 (2014)
Unilateral absence of the pulmonary artery and interrupted inferior vena cava are rare congenital disorders. The clinical presentation is variable, and many patients can be asymptomatic for many years and even throughout their lives. We report the ca
Externí odkaz:
https://doaj.org/article/6ed3c1f2c1624eec9cb1b27fb4c93ee1
Akademický článek
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Autor:
Stuart Mires, Samantha E de Jesus, Andrew R Bamber, Andrew Mumford, Beverley Power, Catherine Bradshaw, Deborah Lawlor, Hannah Gill, Karen Luyt, Mai Baquedano, Tim Overton, Massimo Caputo, Clare Skerritt
Publikováno v:
Mires, S, de Jesus, S E, Bamber, A R, Mumford, A, Power, B, Bradshaw, C, Lawlor, D, Gill, H, Luyt, K, Baquedano, M, Overton, T, Caputo, M & Skerritt, C 2022, ' Surgical-PEARL protocol : a multicentre prospective cohort study exploring aetiology, management and outcomes for patients with congenital anomalies potentially requiring surgical intervention ', BMJ Open, vol. 12, no. 12, e066480 . https://doi.org/10.1136/bmjopen-2022-066480
IntroductionCongenital anomalies affect over 2% of pregnancies. Surgical advances have reduced mortality and improved survival for patients with congenital anomalies potentially requiring surgical (CAPRS) intervention. However, our understanding of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0baf1cb7586a907fe653b4ada218533e
https://doi.org/10.1136/bmjopen-2022-066480
https://doi.org/10.1136/bmjopen-2022-066480
Autor:
Natalia Prodan, M. Gallardo Arozena, Veronica Accurti, Karl O. Kagan, M. Rodriguez-Fernandez, F. S. Molina, Ranjit Akolekar, Jader de Jesus Cruz, Petya Chaveeva, Nicola Persico, C. de Paco Matallana, Argyro Syngelaki, K. H. Nicolaides, M. M. Gil, T. Elger
Publikováno v:
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
instname
Objective To estimate the risk of fetal loss associated with chorionic villus sampling (CVS) in twin pregnancy, using propensity score analysis. Methods This was a multicenter cohort study of women with twin pregnancy undergoing ultrasound examinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bd395b2380500b9ba83e15a9bb577eb
https://hdl.handle.net/10641/3022
https://hdl.handle.net/10641/3022
Publikováno v:
Gastroenterology. 159(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc54d5431df5f7e1f3a916903227edb5
https://pubmed.ncbi.nlm.nih.gov/32017909
https://pubmed.ncbi.nlm.nih.gov/32017909
Autor:
Jorieke E. H. Bergman, Ruth Greenlees, David Tucker, Miriam Gatt, Catherine Lynch, Christine Verellen-Dumoulin, Melinda Csáky-Szunyogh, Maria Loane, Ingeborg Barišić, Marie-Claude Addor, Elizabeth S Draper, Diana Wellesley, Helen Dolk, Larraitz Arriola, Kari Klungsøyr, Anke Rissmann, Anna Pierini, Jennifer J Kurinczuk, Joan K. Morris, Vera Nelen, Babak Khoshnood, Amanda J. Neville, Mary O'Mahony, Judith Rankin, Hanitra Randrianaivo, Carlos Matias Dias, Annette Queisser-Luft, R. McDonnell, Ester Garne, Anna Springett
Publikováno v:
PLoS ONE
Morris, J K, Springett, A L, Greenlees, R, Loane, M, Addor, M C, Arriola, L, Barisic, I, Bergman, J E H, Csaky-Szunyogh, M, Dias, C, Draper, E S, Garne, E, Gatt, M, Khoshnood, B, Klungsoyr, K, Lynch, C, McDonnell, R, Nelen, V, Neville, A J, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo, H, Rankin, J, Rissmann, A, Kurinczuk, J, Tucker, D, Verellen-Dumoulin, C, Wellesley, D & Dolk, H 2018, ' Trends in congenital anomalies in Europe from 1980 to 2012 ', PLOS ONE, vol. 13, no. 4, e0194986 . https://doi.org/10.1371/journal.pone.0194986
13:e019
PLoS ONE, 13(4):0194986. PUBLIC LIBRARY SCIENCE
PloS one, vol. 13, no. 4, pp. e0194986
PLoS ONE, Vol 13, Iss 4, p e0194986 (2018)
Morris, J K, Springett, A L, Greenlees, R, Loane, M, Addor, M C, Arriola, L, Barisic, I, Bergman, J E H, Csaky-Szunyogh, M, Dias, C, Draper, E S, Garne, E, Gatt, M, Khoshnood, B, Klungsoyr, K, Lynch, C, McDonnell, R, Nelen, V, Neville, A J, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo, H, Rankin, J, Rissmann, A, Kurinczuk, J, Tucker, D, Verellen-Dumoulin, C, Wellesley, D & Dolk, H 2018, ' Trends in congenital anomalies in Europe from 1980 to 2012 ', PLOS ONE, vol. 13, no. 4, e0194986 . https://doi.org/10.1371/journal.pone.0194986
13:e019
PLoS ONE, 13(4):0194986. PUBLIC LIBRARY SCIENCE
PloS one, vol. 13, no. 4, pp. e0194986
PLoS ONE, Vol 13, Iss 4, p e0194986 (2018)
Background Surveillance of congenital anomalies is important to identify potential teratogens. Methods This study analysed the prevalence of 61 congenital anomaly subgroups (excluding chromosomal) in 25 population-based EUROCAT registries (1980–201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::060abaf83e42c822303c5e60fa4bd528
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Autor:
Pieter In 'T Veld, Robert Hilbrands, Alex Michotte, Annieta Goossens, Kathelijn Keymolen, Miriam Marichal, Jean De Schepper, Filip Cools, Harry Heimberg, Andrew T. Hattersley
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
BMC Medical Genetics
BMC Medical Genetics
Background Pancreatic agenesis is an extremely rare cause of neonatal diabetes mellitus and has enabled the discovery of several key transcription factors essential for normal pancreas and beta cell development. Case presentation We report a case of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0056874051c344b4e2d03179c1dcb7d7
https://doi.org/10.1186/s12881-017-0419-2
https://doi.org/10.1186/s12881-017-0419-2
Autor:
Ragot E., Mabrut J. -Y., Ouaissi M., Sauvanet A., Dokmak S., Nuzzo G., Halkic N., Dubois R., Letoublon C., Cherqui D., Azoulay D., Irtan S., Boudjema K., Pruvot F. -R., Gigot J. -F., Kianmanesh R., Adham M., Doussot A., Branchereau S., Ayav A., Balladur P., Adam R., Troisi R. I., Regimbeau Jean M. -A., Majno P., Sommacale D., Bouzid C., Falconi M.
Publikováno v:
World Journal of Surgery
World Journal of Surgery, Springer Verlag, 2017, 41 (2), pp.538-545. ⟨10.1007/s00268-016-3684-x⟩
World Journal of Surgery, 2017, 41 (2), pp.538-545. ⟨10.1007/s00268-016-3684-x⟩
World Journal of Surgery, Springer Verlag, 2017, 41 (2), pp.538-545. 〈10.1007/s00268-016-3684-x〉
World journal of surgery, vol. 41, no. 2, pp. 538-545
World Journal of Surgery, Springer Verlag, 2017, 41 (2), pp.538-545. ⟨10.1007/s00268-016-3684-x⟩
World Journal of Surgery, 2017, 41 (2), pp.538-545. ⟨10.1007/s00268-016-3684-x⟩
World Journal of Surgery, Springer Verlag, 2017, 41 (2), pp.538-545. 〈10.1007/s00268-016-3684-x〉
World journal of surgery, vol. 41, no. 2, pp. 538-545
Background: Pancreaticobiliary maljunctions (PBMs) are congenital anomalies of the junction between pancreatic and bile ducts, frequently associated with bile duct cyst (BDC). BDC is congenital biliary tree diseases that are characterized by distinct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e305f7e8e2b9e06acf8f3f79967aff
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01447060
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01447060
Autor:
Vera Nelen, Hermien E. K. de Walle, Anke Rissmann, Ben Wreyford, Larraitz Arriola, Anna Latos-Bielenska, Carmel Mullaney, Christine Verellen-Dumoulin, Mary O'Mahony, Annukka Ritvanen, Breidge Boyle, Annette Queisser-Wahrendorf, Martin Haeusler, Natalia Zymak-Zakutnia, Elizabeth S Draper, Judith Rankin, Amanda J. Neville, Karin Källén, Marie-Claude Addor, Helen Dolk, David Tucker, Miriam Gatt, Hanitra Randrianaivo, Carlos Matias Dias, Diana Wellesley, Catherine Rounding, Bob McDonnell, Ester Garne, Ingeborg Barišić, Melinda Csáky-Szunyogh, Fabrizio Bianchi
Publikováno v:
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 103(1), F22-F28. BMJ PUBLISHING GROUP
Archives of Disease in Childhood. Fetal and Neonatal Edition
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2018, ' Estimating Global Burden of Disease due to congenital anomaly : an analysis of European data ', Archives of Disease in Childhood, vol. 103, no. 1, pp. F22-F28 . https://doi.org/10.1136/archdischild-2016-311845
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2017, ' Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data ', Archives of Disease in Childhood-Fetal and Neonatal Edition, vol. 103, pp. f22 . https://doi.org/10.1136/archdischild-2016-311845
Archives of disease in childhood. Fetal and neonatal edition, vol. 103, no. 1, pp. F22-F28
Archives of Disease in Childhood. Fetal and Neonatal Edition
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2018, ' Estimating Global Burden of Disease due to congenital anomaly : an analysis of European data ', Archives of Disease in Childhood, vol. 103, no. 1, pp. F22-F28 . https://doi.org/10.1136/archdischild-2016-311845
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2017, ' Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data ', Archives of Disease in Childhood-Fetal and Neonatal Edition, vol. 103, pp. f22 . https://doi.org/10.1136/archdischild-2016-311845
Archives of disease in childhood. Fetal and neonatal edition, vol. 103, no. 1, pp. F22-F28
ObjectiveTo validate the estimates of Global Burden of Disease (GBD) due to congenital anomaly for Europe by comparing infant mortality data collected by EUROCAT registries with the WHO Mortality Database, and by assessing the significance of stillbi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2193f14916de688b1ec6535fa52e0785
https://www.bib.irb.hr/1170355
https://www.bib.irb.hr/1170355