نتائج البحث - "Dagmar Csaicsich"

1

دورية أكاديمية

Addition of Alanyl-Glutamine to Dialysis Fluid Restores Peritoneal Cellular Stress Responses - A First-In-Man Trial.

المؤلفون: Klaus Kratochwill, Michael Boehm, Rebecca Herzog, Katharina Gruber, Anton Michael Lichtenauer, Lilian Kuster, Dagmar Csaicsich, Andreas Gleiss, Seth L Alper, Christoph Aufricht, Andreas Vychytil

المصدر: PLoS ONE, Vol 11, Iss 10, p e0165045 (2016)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

العلاقة: http://europepmc.org/articles/PMC5074513?pdf=renderTest; https://doaj.org/toc/1932-6203Test

الوصول الحر: https://doaj.org/article/7b6215a995bf40719509d89fe3068d0fTest

View record in DOAJ

النص الكامل

2

Clinical Factors and Adverse Kidney Outcomes in Children With Antineutrophil Cytoplasmic Antibody–Associated Glomerulonephritis

المؤلفون: Matko Marlais, Tanja Wlodkowski, Nikoleta Printza, Dorothea Kronsteiner, Regina Krisam, Lukas Sauer, Marina Aksenova, Isa Ashoor, Atif Awan, Justine Bacchetta, Ramnath Balasubramanian, Biswanath Basu, Zivile Bekassy, Olivia Boyer, Eugene Yu-hin Chan, Dagmar Csaicsich, Stéphane Decramer, Eiske Dorresteijn, Magdalena Drozynska-Duklas, Loai Akram Eid, Laura Espinosa, Verónica Ferraris, Hana Flögelová, Jessica Forero-Delgadillo, Alessandra Gianviti, Valentina Gracchi, Mercedes López González, Matthias Hansen, Motoshi Hattori, Xu Hong, Nakysa Hooman, Dmytro Ivanov, Hee Gyung Kang, Vasiliki Karava, Ina Kazyra, Adrian Lungu, Stephen Marks, Andrew Maxted, Anna Moczulska, Rebekka Müller, Tatiana Nastausheva, Mattia Parolin, Carmine Pecoraro, Iliana Principi, Cheryl Sanchez-Kazi, Seha Saygili, Raphael Schild, Mohan Shenoy, Rajiv Sinha, Ana Paula Spizzirri, Maria Stack, Maria Szczepanska, Alexey Tsygin, Julia Tzeng, Vaidotas Urbonas, Carlos Zapata, Jakub Zieg, Franz Schaefer, Marina Vivarelli, Kjell Tullus

المساهمون: Pediatrics

المصدر: American Journal of Kidney Diseases, 81(1), 119-122. W B SAUNDERS CO-ELSEVIER INC
American Journal of Kidney Diseases, 81(1), 119-122. W.B. Saunders

مصطلحات موضوعية: Nephrology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc640c6a57557b2a042fde20cf021eceTest
https://hdl.handle.net/11370/43a69db5-a323-4e1a-98c4-6027d34b50faTest

3

Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients—a pilot study

المؤلفون: Phoebe Uhl, Michael Böhm, Klaus Arbeiter, Andreas Heilos, Krisztina Rusai, Elisabeth Puchhammer-Stöckl, Thomas Müller-Sacherer, Gregor Bond, Dagmar Csaicsich, Christoph Aufricht, Elias L. Meyer

المصدر: Pediatric Nephrology (Berlin, Germany)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37dd51d826a015c5c2ad730b899719e4Test
http://europepmc.org/articles/PMC7701084Test

4

A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up

المؤلفون: Adalbert Raimann, Franco Laccone, Diana-Alexandra Ertl, Janina M. Patsch, Dagmar Csaicsich, Gabriele Haeusler

المصدر: Hormone Research in Paediatrics. 87:196-204

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae9b00abefa4b9dfe72a28a7e3abdb7Test
https://doi.org/10.1159/000450947Test

5

Long-term outcome of pediatric renal transplantation in boys with posterior urethral valves

المؤلفون: Karin Hebenstreit, Doris Hebenstreit, Thomas Müller-Sacherer, Alexander Springer, Gabriela Berlakovich, Dagmar Csaicsich

المصدر: Journal of pediatric surgery. 53(11)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1d0446b881c71aa3a14c0f4efdd7774Test
https://pubmed.ncbi.nlm.nih.gov/32407208Test

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WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease

المساهمون: Medizinische Universität Wien = Medical University of Vienna, Departement of Pathology, Institute of Food Science and Human Nutrition, Génétique Médicale et Génomique Fonctionnelle (GMGF), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Centre National de la Recherche Scientifique (CNRS), Génétique des Anomalies du Développement (GAD), Université de Bourgogne (UB)-IFR100 - Structure fédérative de recherche Santé-STIC, Institute of Human Genetics - Institut für Humangenetik [Essen], Universitätsklinikum Essen [Universität Duisburg-Essen] (Uniklinik Essen)-Universitat Duisberg-Essen, Département de génétique médicale [Hôpital de la Timone - APHM], Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Unité de génétique médicale, Université Saint-Joseph de Beyrouth (USJ)-Institut National de la Santé et de la Recherche Médicale (INSERM), Pediatrics, University of Michigan [Ann Arbor], University of Michigan System-University of Michigan System, Division of Clinical Genetics, Innsbruck Medical University [Austria] (IMU), Institute of Human Genetics, University Hospital Magdeburg, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Innsbruck Medical University = Medizinische Universität Innsbruck (IMU), Medical University of Vienna, Génétique Médicale et Génomique Fonctionnelle ( GMGF ), Aix Marseille Université ( AMU ) -Assistance Publique - Hôpitaux de Marseille ( APHM ) - Hôpital de la Timone [CHU - APHM] ( TIMONE ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), Génétique des Anomalies du Développement ( GAD ), Université de Bourgogne ( UB ) -IFR100 - Structure fédérative de recherche Santé-STIC, Institut für Humangenetik [Essen], Universitätsklinikum Essen, Aix Marseille Université ( AMU ) -Assistance Publique - Hôpitaux de Marseille ( APHM ) - Hôpital de la Timone [CHU - APHM] ( TIMONE ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Université Saint-Joseph de Beyrouth ( USJ ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Innsbruck Medical University [Austria] ( IMU ), Internal Medicine, Clinical Genetics

المصدر: Human Mutation
Human Mutation, Wiley, 2015, 36 (11), pp.1021-1028. ⟨10.1002/humu.22828⟩
Human Mutation, 2015, 36 (11), pp.1021-1028. ⟨10.1002/humu.22828⟩
Human Mutation, Wiley, 2015, 36 (11), pp.1021-1028. 〈10.1002/humu.22828〉
Human Mutation, 36(11), 1021-1028. Wiley-Liss Inc.

مصطلحات موضوعية: Male, Microcephaly, Pathology, Biopsy, DNA Mutational Analysis, Medizin, Cohort Studies, 0302 clinical medicine, Glomerulonephritis, Missense mutation, Child, [ SDV.GEN.GH ] Life Sciences [q-bio]/Genetics/Human genetics, Genetics (clinical), Exome sequencing, ComputingMilieux_MISCELLANEOUS, 0303 health sciences, Brain, 3. Good health, Galloway Mowat syndrome, Pedigree, Phenotype, Child, Preschool, Heredodegenerative Disorders, Nervous System, Nephrosis, Cerebellar atrophy, Female, medicine.symptom, Adult, medicine.medical_specialty, Adolescent, Molecular Sequence Data, Neuroimaging, Biology, Short stature, Article, 03 medical and health sciences, Young Adult, Atrophy, Internal medicine, [ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathology, Genetics, medicine, Humans, Amino Acid Sequence, Genetic Association Studies, 030304 developmental biology, Genetic heterogeneity, Proteins, medicine.disease, Endocrinology, Hernia, Hiatal, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Mutation, Sequence Alignment, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology