يعرض 1 - 10 نتائج من 24 نتيجة بحث عن '"Heart Defects, Congenital physiopathology"', وقت الاستعلام: 1.81s تنقيح النتائج
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    رسالة جامعية

    المؤلفون: Sandberg, Camilla

    المساهمون: Umeå universitet. Institutionen för folkhälsa och klinisk medicin, Umeå universitet. Institutionen för samhällsmedicin och rehabilitering

    Degree: Diss. (sammanfattning) Umeå : Umeå universitet, 2016

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    المصدر: Revista Portuguesa de Cardiologia, Vol 37, Iss 5, Pp 399-405 (2018)
    Revista Portuguesa de Cardiologia (English Edition), Vol 37, Iss 5, Pp 399-405 (2018)
    Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
    Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
    instacron:RCAAP

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    المصدر: Congenital heart disease, vol. 12, no. 5, pp. 570-577

    مصطلحات موضوعية: Heart Defects, Congenital, Male, Inotrope, medicine.medical_specialty, Cardiac output, Cardiotonic Agents, Dopamine, medicine.medical_treatment, Blood Pressure, 030204 cardiovascular system & hematology, Intensive Care Units, Pediatric, Perioperative Care, 03 medical and health sciences, 0302 clinical medicine, Interquartile range, Dobutamine, Internal medicine, Intensive care, Hemofiltration, Adrenergic beta-1 Receptor Agonists/administration & dosage, Blood Pressure/drug effects, Blood Pressure/physiology, Cardiac Output/drug effects, Cardiac Output/physiology, Cardiac Surgical Procedures, Cardiotonic Agents/administration & dosage, Child, Child, Preschool, Dobutamine/administration & dosage, Dopamine/administration & dosage, Dose-Response Relationship, Drug, Female, Follow-Up Studies, Heart Defects, Congenital/diagnosis, Heart Defects, Congenital/physiopathology, Heart Defects, Congenital/therapy, Humans, Infant, Perioperative Care/standards, Quality Improvement, Retrospective Studies, diastolic pressure, intensive care, norepinephrine, pediatric cardiac surgery, perfusion pressure, perioperative care, medicine, Radiology, Nuclear Medicine and imaging, 030212 general & internal medicine, Cardiac Output, business.industry, General Medicine, Cardiac surgery, Blood pressure, Amputation, Adrenergic beta-1 Receptor Agonists, Anesthesia, Pediatrics, Perinatology and Child Health, Cardiology, Surgery, Cardiology and Cardiovascular Medicine, business

    وصف الملف: application/pdf

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    المصدر: Pediatric Cardiology
    Pediatric Cardiology, 40(4), 784. Springer New York

    وصف الملف: application/pdf; fulltext; image/pdf

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    المصدر: Arquivos Brasileiros de Cardiologia
    Arquivos Brasileiros de Cardiologia, Issue: ahead, Published: 21 SEP 2018
    Arquivos Brasileiros de Cardiologia, Volume: 111, Issue: 5, Pages: 674-675, Published: NOV 2018
    Arquivos Brasileiros de Cardiologia, Vol 111, Iss 5, Pp 674-675 (2018)
    Arquivos Brasileiros de Cardiologia, Iss 0 (2018)
    Arquivos Brasileiros de Cardiologia, Volume: 111, Issue: 5, Pages: 666-673, Published: 21 SEP 2018
    Arquivos Brasileiros de Cardiologia v.111 n.5 2018
    Sociedade Brasileira de Cardiologia (SBC)
    instacron:SBC

    مصطلحات موضوعية: Male, Fatores de Risco, lcsh:Diseases of the circulatory (Cardiovascular) system, Pediatrics, Heart Defects, Congenital/surgery, Aorta, Thoracic, Comorbidity, 030204 cardiovascular system & hematology, Infant Newborn/mortality, Hypoplastic left heart syndrome, Cohort Studies, Maternal and Child Health, 0302 clinical medicine, Pregnancy, Risk Factors, Hypoplastic Left Heart Syndrome, Medicine, Oximetry, 030212 general & internal medicine, Planos e Programas de Saúde, Síndrome do Coração Esquerdo Hipoplásico/cirurgia, Infant,Newborn, Heart Defects Congenital/mortality, Aortic Arch Syndromes, Saúde Materno- Infantil, Cardiopatias Congênitas/mortalidade, Mortalidade, Premature Birth, Female, Original Article, Short Editorial, medicine.symptom, Cardiology and Cardiovascular Medicine, Brazil, Cohort study, Heart Defects, Congenital, medicine.medical_specialty, Critical Illness, MEDLINE, Cardiopatias Congênitas/fisiopatologia, Cardiopatias Congênitas/cirurgia, 03 medical and health sciences, Análise de Sobrevida, 030225 pediatrics, Diseases in Twins, Diseases of the circulatory (Cardiovascular) system, Humans, Mortality, Survival analysis, Recém Nascido/mortalidade, Maternal and child health, business.industry, Infant, Newborn, Case-control study, Infant, Low Birth Weight, Heart Defects, Congenital/physiopathology, medicine.disease, Infant newborn, Survival Analysis, Confidence interval, Low birth weight, Recém-Nascido, lcsh:RC666-701, RC666-701, Case-Control Studies, Etiology, Health Programs and Plans, business

    وصف الملف: text/html

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    المساهمون: FHU TRANSLAD, Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand ( CHU Dijon ), Service de génétique médicale, CHU Strasbourg-Hôpital de Hautepierre [Strasbourg], Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Génétique des Anomalies du Développement ( GAD ), IFR100 - Structure fédérative de recherche Santé-STIC-Université de Bourgogne ( UB ), Service de pédiatrie (CHU de Dijon), Service d'Ophtalmologie (CHU de Dijon), Service de Cardiologie (hôpital général, CHU Dijon), Hôpital général (CHU Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)-Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Equipe GAD (LNC - U1231), Lipides - Nutrition - Cancer [Dijon - U1231] (LNC), Université de Bourgogne (UB)-Institut National de la Santé et de la Recherche Médicale (INSERM)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Université de Bourgogne (UB)-Institut National de la Santé et de la Recherche Médicale (INSERM)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement, Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), CHU Strasbourg, Génétique des Anomalies du Développement (GAD), Université de Bourgogne (UB)-IFR100 - Structure fédérative de recherche Santé-STIC, Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), FHU TRANSLAD (CHU de Dijon), IFR100 - Structure fédérative de recherche Santé-STIC-Université de Bourgogne (UB), Service de Cardiologie, Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Bourgogne (UB)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Institut National de la Santé et de la Recherche Médicale (INSERM)

    المصدر: European Journal of Human Genetics, 25(1), 43-51. Nature Publishing Group
    European Journal of Human Genetics, 25, 43-51
    European journal of human genetics: EJHG
    European journal of human genetics: EJHG, Nature, 2016, 25 (1), pp.43-51. 〈http://www.nature.com/ejhg/index.html〉. 〈10.1038/ejhg.2016.133〉
    European Journal of Human Genetics
    European Journal of Human Genetics, Nature Publishing Group, 2017, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
    European Journal of Human Genetics, Nature Publishing Group, 2016, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
    European journal of human genetics
    European Journal of Human Genetics, 25, 1, pp. 43-51

    مصطلحات موضوعية: 0301 basic medicine, Male, MESH: Heart Defects, Congenital / physiopathology, Microcephaly, Pathology, MESH: Heart Defects, Congenital / genetics, MESH: Exome / genetics, 030105 genetics & heredity, MESH: RNA Splicing / genetics, Microphthalmia, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, MESH: Child, Exome, MESH: RNA Splicing Factors / genetics, Child, Frameshift Mutation, MESH: High-Throughput Nucleotide Sequencing, Genetics (clinical), Exome sequencing, Coloboma, MESH: Frameshift Mutation, High-Throughput Nucleotide Sequencing, Microdeletion syndrome, Microcephaly, Verheij syndrome, PUF60, Chemistry, Phenotype, Child, Preschool, DISEASES, Medical genetics, Female, RNA Splicing Factors, medicine.symptom, Chromosome Deletion, Chromosomes, Human, Pair 8, MESH: Dwarfism / genetics, Heart Defects, Congenital, medicine.medical_specialty, GENES, Adolescent, RNA Splicing, MESH: Chromosome Deletion, Dwarfism, Biology, MESH: Phenotype, Short stature, Article, PUF60, 03 medical and health sciences, Internal medicine, Intellectual Disability, [ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathology, Genetics, medicine, Humans, Craniofacial, MESH: Adolescent, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], MESH: Humans, MESH: Child, Preschool, medicine.disease, MESH: Repressor Proteins / genetics, MESH: Male, Repressor Proteins, 030104 developmental biology, Endocrinology, MESH: Chromosomes, Human, Pair 8 / genetics, MESH: Dwarfism / physiopathology, MESH: Intellectual Disability / physiopathology, Human medicine, MESH: Intellectual Disability / genetics, Verheij syndrome, MESH: Female, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

    وصف الملف: pdf