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1Academic Journal
المؤلفون: Nathalie Lelong, Babak Khoshnood, David Tucker, Mika Gissler, Maria Loane, Ingeborg Barisic, Miriam Gatt, Kari Klungsoyr, Amanda Neville, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Joan K Morris, Paula Braz, Vera Nelen, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Silvia Baldacci, Michele Santoro, Alessio Coi, Lorena Mezzasalma, Daniel Thayer, Svetlana V Glinianaia, Hermien de Walle, Guy Thys, Anna Latos-Bielenska, Aurora Puccini, Elisa Ballardini, Wladimir Wertelecki, Carlos Matias Dias, Gianni Astolfi, James Densem, Joachim Tan, Joanne Emma Given, Hugh Claridge, Abigail Reid, Liz Limb, Gillian Briggs, Nicholas Connor, Stine Kjaer Urhoj, Mads Damkjær, Christina Neergaard Pedersen, Annarita Armaroli, Ljubica Boban, L Renée Lutke, Nicole H A Siemensma-Mühlenberg, Nathalie Bertille, Makan Rahshenas, Clara Cavero Carbonell, Laia Barrachina Bonet, Laura García Villodre, Anna Jamry-Dziurla, Sonja Kiuru-Kuhlefelt, Lyubov Yevtushok, Nataliia Zymak-Zakutnia, Diana Akhmedzhanova, Lyubov Ostapchuk, Oksana Tsizh, Serhii Lapchenko, Ausenda Machado, Ana João Santos, Liliana Antunes, Hanitra Randrianaivo-Ranjatoelina, Elly Den Hond, Olatz Mokoroa Carollo, Ieuan Scanlon
المصدر: BMJ Open, Vol 11, Iss 6 (2021)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
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المؤلفون: Hanitra Randrianaivo‐Ranjatoelina, Christian Gachet, Arnaud Dupuis, Mathieu Fiore, Marie‐Line Jacquemont, Cécile Lavenu-Bombled, Marie Dreyfus, François Lanza, Céline De Thoré, Renhao Li, Marie-Jeanne Baas
المصدر: Br J Haematol
مصطلحات موضوعية: Adult, Male, Adolescent, Biology, GP1BB Gene, Bernard–Soulier syndrome, Article, Young Adult, medicine, Prevalence, Humans, Child, Genetics, High prevalence, Infant, Newborn, Bernard-Soulier Syndrome, Infant, Hematology, Middle Aged, medicine.disease, Platelet Glycoprotein GPIb-IX Complex, Child, Preschool, Mutation (genetic algorithm), Mutation, Female, France, Genetic isolate, Reunion
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المؤلفون: Judith Rankin, David Tucker, Olatz Mokoroa, Miriam Gatt, Anke Rissmann, Mary O'Mahony, Catherine Lynch, Amanda J. Neville, Marie-Claude Addor, Monica Lanzoni, Ester Garne, Hanitra Randrianaivo-Ranjatoelina, Ingeborg Barišić, Joan K. Morris, Vera Nelen, Natalya Zymak-Zakutnia, Fabrizio Bianchi, Maria Loane, H. E. K. De Walle
المساهمون: Reproductive Origins of Adult Health and Disease (ROAHD)
المصدر: Morris, J K, Garne, E, Loane, M, Addor, M C, Barisic, I, Bianchi, F, Gatt, M, Lanzoni, M, Lynch, C, Mokoroa, O, Nelen, V, Neville, A, O'Mahony, M T, Randrianaivo-Ranjatoelina, H, Rissmann, A, Tucker, D, de Walle, H E K, Zymak-Zakutnia, N & Rankin, J 2018, ' Prevalence of valproate syndrome in Europe from 2005 to 2014 : A registry based multi-centre study ', European Journal of Medical Genetics, vol. 61, no. 9, pp. 479-482 . https://doi.org/10.1016/j.ejmg.2018.05.008
European journal of medical genetics, 61(9), 479-482. ELSEVIER SCIENCE BVمصطلحات موضوعية: Adult, Pediatrics, medicine.medical_specialty, medicine.medical_treatment, Population, Congenital anomaly, Sodium valproate, Valproic acid, CHILDREN, Congenital Abnormalities, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Pregnancy, 030225 pediatrics, Statistical significance, Genetics, medicine, Humans, Cognitive Dysfunction, Registries, Multi centre, education, Genetics (clinical), education.field_of_study, Spina bifida, business.industry, MAJOR CONGENITAL-MALFORMATIONS, Valproic Acid, ANTIEPILEPTIC DRUGS, WOMEN, General Medicine, Syndrome, medicine.disease, TRENDS, Europe, Pregnancy Complications, Increased risk, Anticonvulsant, Anticonvulsants, Female, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf
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المؤلفون: Ingeborg Barišić, Judith Rankin, Anna Pierini, Anke Rissmann, Vera Nelen, Elisa Calzolari, Ester Garne, Hanitra Randrianaivo-Ranjatoelina, Carlos Matias Dias, Awi Wiesel, Kari Klyungsoyr Melve, Maria Loane, Bérénice Doray, Marian K. Bakker, Helen Dolk, Christine Verellun-Dumoulin, Mary O'Mahony, Marie-Claude Addor, David Tucker, Larraitz Arriola, Miriam Gatt
المساهمون: Methods in Medicines evaluation & Outcomes research (M2O), Reproductive Origins of Adult Health and Disease (ROAHD)
المصدر: Birth Defects Research. Part A: Clinical and Molecular Teratology, 94(3), 134-140. Wiley-Blackwell
Garne, E, Loane, M, Dolk, H, Barisic, I, Addor, M-C, Arriola, L, Bakker, M, Calzolari, E, Matias Dias, C, Doray, B, Gatt, M, Melve, K K, Nelen, V, O'Mahony, M, Pierini, A, Randrianaivo-Ranjatoelina, H, Rankin, J, Rissmann, A, Tucker, D, Verellun-Dumoulin, C & Wiesel, A 2012, ' Spectrum of congenital anomalies in pregnancies with pregestational diabetes ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 94, no. 3, pp. 134-40 . https://doi.org/10.1002/bdra.22886مصطلحات موضوعية: Male, Embryology, Pediatrics, Pregestational Diabetes, Pregnancy in Diabetics, MELLITUS, Pregnancy, Risk Factors, Neural Tube Defects, Registries, Livebirths, RISK, education.field_of_study, OUTCOMES, livebirths, WOMEN, Ear, General Medicine, ASSOCIATION, Congenital Anomalies, Europe, Anotia, Population Surveillance, Female, NEURAL-TUBE DEFECTS, Live Birth, Hernia, Umbilical, Adult, Heart Defects, Congenital, medicine.medical_specialty, Population, Population Based, population based, Congenital Abnormalities, Young Adult, Diabetes mellitus, Anencephaly, BIRTH-DEFECTS, medicine, Diabetes Mellitus, Humans, MALFORMATIONS, Risk factor, education, TYPE-1, Congenital Microtia, Omphalocele, Spina bifida, business.industry, congenital anomalies, Infant, Newborn, Odds ratio, NATIONWIDE, medicine.disease, Estados de Saúde e de Doença, pregestational diabetes, Pregnancy Complications, Pediatrics, Perinatology and Child Health, business, Developmental Biology
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المؤلفون: Anna Latos-Bielenska, Patricia A. Boyd, Christine Verellen-Dumoulin, Carmel Mullaney, Karin Källén, Bérénice Doray, Marian K. Bakker, Vera Nelen, Babak Khoshnood, Antonin Sipek, Stein Emil Vollset, Annukka Ritvanen, Bob McDonnell, Ester Garne, Hanitra Randrianaivo-Ranjatoelina, Anna Materna-Kiryluk, Annette Queisser-Luft, Joaquin Salvador, Amanda J. Neville, Emmanuelle Amar, Anke Rissmann, David Tucker, Martin Haeusler, Miriam Gatt, Elizabeth S Draper, Elisa Calzolari, Ruth Greenlees, Anna Pierini, Mary O'Mahony, Larraitz Arriola, Wladimir Wertelecki, Judith Rankin, Marie-Claude Addor, Diana Wellesley, Carlos Matias Dias, Ingeborg Barišić, María Luisa Martínez-Frías
المصدر: Greenlees, R, Neville, A, Addor, M-C, Amar, E, Arriola, L, Bakker, M, Barisic, I, Boyd, P A, Calzolari, E, Doray, B, Draper, E, Vollset, S E, Garne, E, Gatt, M, Haeusler, M, Kallen, K, Khoshnood, B, Latos-Bielenska, A, Martinez-Frias, M-L, Materna-Kiryluk, A, Dias, C M, McDonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo-Ranjatoélina, H, Rankin, J, Rissmann, A, Ritvanen, A, Salvador, J, Sipek, A, Tucker, D, Verellen-Dumoulin, C, Wellesley, D & Wertelecki, W 2011, ' Paper 6: EUROCAT member registries: organization and activities ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 91 Suppl 1, pp. S51-S100 . https://doi.org/10.1002/bdra.20775
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instnameمصطلحات موضوعية: Embryology, Pediatrics, Databases, Factual, ENGLAND, Multiple congenital anomaly, Age limit, 0302 clinical medicine, Pregnancy, Prenatal Diagnosis, Prevalence, Confidentiality, 030212 general & internal medicine, Registries, RISK, 0303 health sciences, education.field_of_study, Fetal death, 030305 genetics & heredity, congenital anomaly registries, General Medicine, organization, Stillbirth, ascertainment, 3. Good health, Computer algorithm, Europe, CONGENITAL-ANOMALIES, Prenatal screening, Evaluation Studies as Topic, Population Surveillance, Committee Membership, Female, Medical emergency, medicine.medical_specialty, Population, Population based, Congenital Abnormalities, 03 medical and health sciences, medicine, Humans, education, Fetal Death, Internet, business.industry, RENAC, Abortion, Induced, Estados de Saúde e de Doença, medicine.disease, population-based, congenital anomalies, multiple congenital anomaly, computer algorithm, classification, surveillance, etiology, Pediatrics, Perinatology and Child Health, business, Developmental Biology
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