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1دورية أكاديمية
المؤلفون: Mehta PA; Fanconi Anemia Comprehensive Care Center, Cincinnati Children's Hospital Medical Center (CCHMC), Cincinnati, Ohio 45229, USA. Parinda.Mehta@cchmc.org, Ileri T, Harris RE, Williams DA, Mo J, Smolarek T, Auerbach AD, Kelly P, Davies SM
المصدر: Pediatric blood & cancer [Pediatr Blood Cancer] 2007 Jun 15; Vol. 48 (7), pp. 668-72.
نوع المنشور: Case Reports; Journal Article
بيانات الدورية: Publisher: John Wiley Country of Publication: United States NLM ID: 101186624 Publication Model: Print Cited Medium: Print ISSN: 1545-5009 (Print) Linking ISSN: 15455009 NLM ISO Abbreviation: Pediatr Blood Cancer Subsets: MEDLINE
مواضيع طبية MeSH: Antineoplastic Combined Chemotherapy Protocols/*administration & dosage , Fanconi Anemia/*complications , Leukemia, Myeloid/*complications , Leukemia, Myeloid/*therapy , Myelodysplastic Syndromes/*complications , Myelodysplastic Syndromes/*therapy, Acute Disease ; Adolescent ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Leukemia, Myeloid/diagnosis ; Male ; Myelodysplastic Syndromes/diagnosis ; Peripheral Blood Stem Cell Transplantation ; Survival Rate ; Treatment Outcome
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2دورية أكاديمية
المؤلفون: Mehta PA; Cincinnati Children's Hospital and Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229, USA. Parinda.Mehta@cchmc.org, Alonzo TA, Gerbing RB, Elliott JS, Wilke TA, Kennedy RJ, Ross JA, Perentesis JP, Lange BJ, Davies SM
مؤلفون مشاركون: Children's Oncology Group
المصدر: Blood [Blood] 2006 Jan 01; Vol. 107 (1), pp. 39-45. Date of Electronic Publication: 2005 Sep 08.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0006-4971 (Print) Linking ISSN: 00064971 NLM ISO Abbreviation: Blood Subsets: MEDLINE
مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Leukemia, Myeloid/*genetics , Xeroderma Pigmentosum Group D Protein/*genetics, Acute Disease ; Adolescent ; Adult ; Case-Control Studies ; Child ; Child, Preschool ; Female ; Gene Frequency ; Genetic Testing ; Genotype ; Humans ; Infant ; Infant, Newborn ; Leukemia, Myeloid/etiology ; Leukemia, Myeloid/therapy ; Male ; Mutation, Missense ; Survival Analysis ; Treatment Outcome