المؤلفون: van Dooijeweert B; Department of Pediatric Hematology, University Medical Center Utrecht, Utrecht, The Netherlands., van Ommen CH; Department of Pediatric Hematology, Erasmus Medical Center, Rotterdam, The Netherlands., Smiers FJ; Department of Pediatric Hematology, Leiden University Medical Center, Leiden, The Netherlands., Tamminga RYJ; Department of Pediatric Hematology, University Medical Center Groningen, Groningen, The Netherlands., Te Loo MW; Department of Pediatric Hematology, Radboud University Medical Center, Nijmegen, The Netherlands., Donker AE; Department of Pediatrics, Maxima Medical Center, Veldhoven, The Netherlands., Peters M; Department of Pediatric Hematology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands., Granzen B; Department of Pediatric Hematology, Maastricht University Medical Center, Maastricht, The Netherlands., Gille HJJP; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Bierings MB; Department of Pediatric Hematology, University Medical Center Utrecht, Utrecht, The Netherlands., MacInnes AW; Laboratory Genetic Metabolic Diseases, Academic Medical Center Amsterdam, Amsterdam, The Netherlands., Bartels M; Department of Pediatric Hematology, University Medical Center Utrecht, Utrecht, The Netherlands.

المصدر: European journal of haematology [Eur J Haematol] 2018 Feb; Vol. 100 (2), pp. 163-170. Date of Electronic Publication: 2017 Dec 01.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0609 (Electronic) Linking ISSN: 09024441 NLM ISO Abbreviation: Eur J Haematol Subsets: MEDLINE

مواضيع طبية MeSH: Anemia, Diamond-Blackfan/*diagnosis , Anemia, Diamond-Blackfan/*genetics, Adolescent ; Anemia, Diamond-Blackfan/epidemiology ; Anemia, Diamond-Blackfan/therapy ; Child ; Child, Preschool ; Combined Modality Therapy ; Congenital Abnormalities/diagnosis ; Congenital Abnormalities/genetics ; Female ; Follow-Up Studies ; Genetic Association Studies ; Genetic Testing ; Genetic Variation ; Genotype ; Humans ; Infant ; Infant, Newborn ; Male ; Netherlands/epidemiology ; Phenotype ; Polymorphism, Single Nucleotide ; Registries

المؤلفون: Hagleitner MM; Department of Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands., Coenen MJ; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Patino-Garcia A; Department of Pediatrics, University of Navarra and University Clinic, Pamplona, Spain., de Bont ES; Department of Pediatric Hematology and Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Gonzalez-Neira A; Human Genotyping Unit-CeGen, Spanish National Cancer Research Center, Madrid, Spain., Vos HI; Department of Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands., van Leeuwen FN; Department of Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands., Gelderblom H; Department of Clinical Oncology, Leiden University Medical Center, Leiden, The Netherlands., Hoogerbrugge PM; Department of Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands., Guchelaar HJ; Department of Clinical Pharmacy & Toxicology, Leiden University Medical Center, Leiden, The Netherlands., Te Loo MW; Department of Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.

المصدر: PloS one [PLoS One] 2014 Dec 31; Vol. 9 (12), pp. e115869. Date of Electronic Publication: 2014 Dec 31 (Print Publication: 2014).

نوع المنشور: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

مواضيع طبية MeSH: Catechol O-Methyltransferase/*genetics , Cisplatin/*adverse effects , Hearing Loss/*chemically induced , Hearing Loss/*genetics , Methyltransferases/*genetics, Adolescent ; Adult ; Antineoplastic Agents/adverse effects ; Antineoplastic Agents/therapeutic use ; Bone Neoplasms/drug therapy ; Child ; Child, Preschool ; Cisplatin/therapeutic use ; Female ; Genotype ; Humans ; Male ; Netherlands ; Osteosarcoma/drug therapy ; Polymorphism, Single Nucleotide ; Spain ; Young Adult

المؤلفون: Fernández GC; División Inmunología, IIHEMA, Academia Nacional de Medicina, Buenos Aires, Argentina. gfernandez@hematologia.anm.edu.ar, Te Loo MW, van der Velden TJ, van der Heuvel LP, Palermo MS, Monnens LL

المصدر: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2003 Oct; Vol. 18 (10), pp. 1066-8. Date of Electronic Publication: 2003 Aug 12.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0931-041X (Print) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE

مواضيع طبية MeSH: Endothelium, Vascular/*metabolism , Glomerular Mesangium/*blood supply , Hemolytic-Uremic Syndrome/*etiology , Hemolytic-Uremic Syndrome/*metabolism , Thrombomodulin/*metabolism, Cells, Cultured ; Endothelial Cells/cytology ; Endothelial Cells/metabolism ; Endothelium, Vascular/cytology ; Humans ; Inflammation Mediators/metabolism ; Leucine/pharmacokinetics ; Microcirculation ; Shiga Toxin 2/pharmacology ; Tritium

المؤلفون: Kapojos JJ; Department of Pathology and Laboratory Medicine, University of Groningen, Groningen, The Netherlands., van den Berg A, van Goor H, te Loo MW, Poelstra K, Borghuis T, Bakker WW

المصدر: Kidney international [Kidney Int] 2003 May; Vol. 63 (5), pp. 1681-6.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 0323470 Publication Model: Print Cited Medium: Print ISSN: 0085-2538 (Print) Linking ISSN: 00852538 NLM ISO Abbreviation: Kidney Int Subsets: MEDLINE

مواضيع طبية MeSH: Antineoplastic Agents/*pharmacology , Glomerular Mesangium/*cytology , Glomerular Mesangium/*physiology , Hemopexin/*genetics , Tumor Necrosis Factor-alpha/*pharmacology, Anti-Inflammatory Agents/pharmacology ; Cells, Cultured/drug effects ; Cells, Cultured/physiology ; Gene Expression/drug effects ; Humans ; Nephrotic Syndrome/physiopathology ; Prednisolone/pharmacology