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المؤلفون: Biondo GF; Departament of Pediatrics, Pediatric Postgraduate Programme, Federal University of Health Science of Porto Alegre (UFCSPA), Porto Alegre, Brazil.; Pediatric Intensive Care and Emergency Medicine Department, Pediatric Emergency Division, Hospital Clinicas (HCPA), Porto Alegre, Brazil., Lorentz BT; Departament of Pediatrics, Pediatric Postgraduate Programme, Federal University of Health Science of Porto Alegre (UFCSPA), Porto Alegre, Brazil., Flores JAM; Department of Pediatrics, Pediatric Emergency Division, Santo Antônio Children's Hospital, Porto Alegre, Brazil.; Department of Pediatrics, Faculty of Medicine, Federal University of Health Science of Porto Alegre (UFCSPA), Porto Alegre, Brazil., Santana JCB; Pediatric Intensive Care and Emergency Medicine Department, Pediatric Emergency Division, Hospital Clinicas (HCPA), Porto Alegre, Brazil., Amantéa SL; Departament of Pediatrics, Pediatric Postgraduate Programme, Federal University of Health Science of Porto Alegre (UFCSPA), Porto Alegre, Brazil.; Department of Pediatrics, Pediatric Emergency Division, Santo Antônio Children's Hospital, Porto Alegre, Brazil.; Department of Pediatrics, Faculty of Medicine, Federal University of Health Science of Porto Alegre (UFCSPA), Porto Alegre, Brazil.

المصدر: Pediatric pulmonology [Pediatr Pulmonol] 2024 Feb; Vol. 59 (2), pp. 442-448. Date of Electronic Publication: 2023 Nov 27.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8510590 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1099-0496 (Electronic) Linking ISSN: 10990496 NLM ISO Abbreviation: Pediatr Pulmonol Subsets: MEDLINE

مواضيع طبية MeSH: Respiratory Syncytial Virus Infections*/diagnostic imaging , Respiratory Syncytial Virus Infections*/therapy , Bronchiolitis, Viral*/diagnostic imaging , Bronchiolitis, Viral*/therapy , Bronchiolitis*/diagnostic imaging , Bronchiolitis*/therapy , Respiratory Syncytial Virus, Human* , Pneumonia*, Child ; Humans ; Male ; Infant ; Aged, 80 and over ; Female ; Cross-Sectional Studies

المؤلفون: da Costa Almeida CB; Department of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Welter AT; Department of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Abech GD; Department of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Brandão GR; Department of Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Flores JAM; Pediatric Radiology Service, Hospital da Criança Santo Antônio/Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil., Schüle B; Department of Genetics and Pediatrics, Stanford University School of Medicine, California, United States., Francke U; Department of Genetics and Pediatrics, Stanford University School of Medicine, California, United States., Fiegenbaum M; Department of Human Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Zen PRG; Department of Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre and Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil.; Department of Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil., Rosa RFM; Department of Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre and Santa Casa de Misericórdia de Porto Alegre, Rio Grande do Sul, Brazil.; Department of Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre, Rio Grande do Sul, Brazil.

المصدر: Journal of pediatric genetics [J Pediatr Genet] 2020 Mar; Vol. 9 (1), pp. 58-62. Date of Electronic Publication: 2019 Sep 03.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Thieme Country of Publication: Germany NLM ID: 101589859 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2146-4596 (Print) Linking ISSN: 2146460X NLM ISO Abbreviation: J Pediatr Genet Subsets: PubMed not MEDLINE

المؤلفون: Pogue R; Graduate Program in Genomic Sciences and Biotechnology, Universidade Católica de Brasília, Brasília, DF, Brazil., Marques FA; Graduate Program in Genomic Sciences and Biotechnology, Universidade Católica de Brasília, Brasília, DF, Brazil.; Biotechnology Laboratory, Universidade CEUMA, São Luis, MA, Brazil.; Department of Biomedicine, Universidade CEUMA, São Luís, MA, Brazil.; Department of Pharmacy, Universidade CEUMA, São Luís, MA, Brazil., Kopacek C; Department of Pediatric Endocrinology, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, RS, Brazil., Rosa RCM; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil., Dorfman LE; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Department of Biomedicine, Universidade do Vale do Rio dos Sinos (UNISINOS), São Leopoldo, RS, Brazil., Mazzeu JF; Graduate Program in Medical Sciences, Universidade de Brasília, Brasília, Brazil., Flores JAM; Department of Pediatric Radiology, Hospital da Criança Santo Antônio (HCSA), Porto Alegre, RS, Brazil., Zen PRG; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Graduate Program in Biosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Department of Clinical Genetics, UFCSPA and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil., Rosa RFM; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Graduate Program in Biosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Department of Clinical Genetics, UFCSPA and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil.; Department of Clinical Genetics, HMIPV, Porto Alegre, RS, Brazil.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2017 May; Vol. 173 (5), pp. 1152-1158. Date of Electronic Publication: 2017 Mar 31.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*physiopathology , Bone Diseases, Developmental/*physiopathology , Dwarfism/*physiopathology , Hand Deformities, Congenital/*physiopathology , Pierre Robin Syndrome/*physiopathology, Abnormalities, Multiple/diagnostic imaging ; Abnormalities, Multiple/genetics ; Bone Diseases, Developmental/diagnosis ; Bone Diseases, Developmental/genetics ; Child ; Consanguinity ; Dwarfism/diagnostic imaging ; Dwarfism/genetics ; Female ; Hand Deformities, Congenital/diagnostic imaging ; Hand Deformities, Congenital/genetics ; Humans ; Karyotype ; Pedigree ; Phenotype ; Pierre Robin Syndrome/diagnostic imaging ; Pierre Robin Syndrome/genetics ; Ribs/diagnostic imaging ; Ribs/pathology ; Ribs/physiopathology ; Siblings

SCR Disease Name: Catel Manzke syndrome