Zobrazeno 1 - 10
of 168
pro vyhledávání: '"González de Garibay AS"'
Autor:
Dubucs, Charlotte, Caillet, Anthony, Frémont, Félix, Delteil, Laurane, N'Go, Van, Neville, Amanda Julie, Ballardini, Elisa, Dolk, Helen, Loane, Maria, Garne, Ester, Khoshnood, Babak, Lelong, Nathalie, Rissmann, Anke, O'Mahony, Mary, Pierini, Anna, Gatt, Miriam, Bergman, Jorieke, Krawczynski, Maciej Robert, Latos Bielenska, Anna, Echevarría González de Garibay, Luis Javier
Publikováno v:
Birth Defects Research; Nov2024, Vol. 116 Issue 11, p1-16, 16p
Autor:
Juan Rico, Luis Javier Echevarría-González de Garibay, María García-López, Sandra Guardiola-Vilarroig, Luis Alberto Maceda-Roldán, Óscar Zurriaga, Clara Cavero-Carbonell
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Abstract Background Rare diseases present a wide spectrum of clinical manifestations and severity levels and are often poorly known and underrepresented, making them difficult to classify. Diagnoses are usually coded using the International Classific
Externí odkaz:
https://doaj.org/article/182ad1398fca4ceb877ea58695f2dddf
Akademický článek
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Autor:
Jorieke E. H. Bergman, Ingeborg Barišić, Marie‐Claude Addor, Paula Braz, Clara Cavero‐Carbonell, Elizabeth S. Draper, Luis J. Echevarría‐González‐de‐Garibay, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Jennifer J. Kurinczuk, Anna Latos‐Bielenska, Karen Luyt, Danielle Martin, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary T. O'Mahony, Isabelle Perthus, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Anke Rissmann, Florence Rouget, Gerardine Sayers, Bruno Schaub, Sarah Stevens, David Tucker, Christine Verellen‐Dumoulin, Awi Wiesel, Erica H. Gerkes, Annie Perraud, Maria A. Loane, Diana Wellesley, Hermien E. K. de Walle
Publikováno v:
American Journal of Medical Genetics. Part A.
American Journal of Medical Genetics. Part A, 191(4), 995-1006. Wiley
Bergman, J E H, Barišić, I, Addor, M C, Braz, P, Cavero-Carbonell, C, Luyt, K & et, A 2022, ' Amniotic band syndrome and limb body wall complex in Europe 1980–2019 ', American Journal of Medical Genetics . https://doi.org/10.1002/ajmg.a.63107
American Journal of Medical Genetics. Part A
American Journal of Medical Genetics. Part A, 191(4), 995-1006. Wiley
Bergman, J E H, Barišić, I, Addor, M C, Braz, P, Cavero-Carbonell, C, Luyt, K & et, A 2022, ' Amniotic band syndrome and limb body wall complex in Europe 1980–2019 ', American Journal of Medical Genetics . https://doi.org/10.1002/ajmg.a.63107
American Journal of Medical Genetics. Part A
Amniotic band syndrome (ABS) and limb body wall complex (LBWC) have an overlapping phenotype of multiple congenital anomalies and their etiology is unknown. We aimed to determine the prevalence of ABS and LBWC in Europe from 1980 to 2019and to descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8ac8e4bea146e488a17fe65be1c0707
https://doi.org/10.1002/ajmg.a.63107
https://doi.org/10.1002/ajmg.a.63107
Autor:
Teichteil-Königsbuch, Florent, Povéda, Guillaume, González de Garibay Barba, Guillermo, Luchterhand, Tim, Thiébaux, Sylvie
Publikováno v:
Proc. International Conference on Automated Planning and Scheduling (ICAPS)
33rd International Conference on Automated Planning and Scheduling (ICAPS)
33rd International Conference on Automated Planning and Scheduling (ICAPS), Jul 2023, Prague, Czech Republic
33rd International Conference on Automated Planning and Scheduling (ICAPS)
33rd International Conference on Automated Planning and Scheduling (ICAPS), Jul 2023, Prague, Czech Republic
International audience; Resource-Constrained Project Scheduling Problems (RCPSPs) are NP-complete, which makes it challenging to efficiently solve large instances and robustify solutions in the presence of uncertainty. To remedy this, we learn to eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9d0e1a5ecb209870e77cbb09b8c71a84
https://hal.laas.fr/hal-04141504/document
https://hal.laas.fr/hal-04141504/document
Akademický článek
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Autor:
Chrysovalanto Mamasoula, Theophile Bigirumurame, Thomas Chadwick, Marie‐Claude Addor, Clara Cavero‐Carbonell, Carlos M. Dias, Luis‐Javier Echevarría‐González‐de‐Garibay, Miriam Gatt, Babak Khoshnood, Kari Klungsoyr, Kay Randall, Sylvia Stoianova, Martin Haeusler, Vera Nelen, Amanda J. Neville, Isabelle Perthus, Anna Pierini, Bénédicte Bertaut‐Nativel, Anke Rissmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Natalya Zymak‐Zakutnia, Ingeborg Barisic, Hermien E.K. de Walle, Monica Lanzoni, Gerardine Sayers, Carmel Mullaney, Lindsay Pennington, Judith Rankin
Publikováno v:
Birth Defects Research
Birth Defects Research, 2023, 115 (6), pp.583-594. ⟨10.1002/bdr2.2152⟩
Birth Defects Research, 2023, 115 (6), pp.583-594. ⟨10.1002/bdr2.2152⟩
Background Evidence on the direction and strength of association between maternal age and the prevalence of congenital heart defects (CHD) in different age group categories is conflicting. Some studies have illustrated different trends with an increa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e0a4d59eeb0a4a225fbcc74a6bfbb83
https://hdl.handle.net/11250/3064913
https://hdl.handle.net/11250/3064913
Autor:
Rico, Juan1 (AUTHOR), Echevarría-González de Garibay, Luis Javier2 (AUTHOR), García-López, María3 (AUTHOR), Guardiola-Vilarroig, Sandra1,4 (AUTHOR), Maceda-Roldán, Luis Alberto5 (AUTHOR), Zurriaga, Óscar1,4,6 (AUTHOR), Cavero-Carbonell, Clara1 (AUTHOR) cavero_cla@gva.es
Publikováno v:
Orphanet Journal of Rare Diseases. 3/9/2021, Vol. 16 Issue 1, p1-13. 13p.
Autor:
Joan K. Morris, Diana Wellesley, Elizabeth Limb, Jorieke E. H. Bergman, Agnieszka Kinsner‐Ovaskainen, Marie Claude Addor, Jennifer M. Broughan, Clara Cavero‐Carbonell, Carlos M. Dias, Luis‐Javier Echevarría‐González‐de‐Garibay, Miriam Gatt, Martin Haeusler, Ingeborg Barisic, Kari Klungsoyr, Nathalie Lelong, Anna Materna‐Kiryluk, Amanda Neville, Vera Nelen, Mary T. O'Mahony, Isabelle Perthus, Anna Pierini, Judith Rankin, Anke Rissmann, Florence Rouget, Geraldine Sayers, Sarah Stevens, David Tucker, Ester Garne
Publikováno v:
Birth defects research, 114(20), 1417-1426. Wiley
Birth Defects Research
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Birth Defects Research
r-FISABIO. Repositorio Institucional de Producción Científica
instname
[Corrections added after online publication, 16 November 2022: The last name of Dr. Jennifer M. Broughan was incorrectly spelled in the initial publication. It has been corrected.] Background: Younger mothers are at a greater risk of having a pregnan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c102c9464c324fb641783ed33d64ecdc
https://research.rug.nl/en/publications/65d07439-9406-4c1e-b5e6-1b0283131f71
https://research.rug.nl/en/publications/65d07439-9406-4c1e-b5e6-1b0283131f71
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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