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1دورية أكاديميةBrazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case report.
المؤلفون: de Souza Timoteo AR; Departamento de Biologia Celular e Genética, Universidade Federal do Rio Grande do Norte, Av. Senador Salgado Filho, s/n, Natal, 59078-970, RN, Brazil., Pinheiro de Almeida IC; Hospital Liga contra o Câncer, Av. Miguel Castro, Natal, 1355, 59062-000, RN, Brazil., Yurchenko AA; Cancer Genomics Lab, B2M, Gustave Roussy Cancer Campus, 114 rue Edouard Vaillant, Villejuif, 94805, France., de Miranda Henriques SR; Hospital Liga contra o Câncer, Av. Miguel Castro, Natal, 1355, 59062-000, RN, Brazil., de Souza Segundo P; Hospital Universitário Onofre Lopes, Universidade Federal do Rio Grande do Norte, Av. Nilo Peçanha, 620, 59012-300, RN, Natal, Brazil., Rajabi F; Cancer Genomics Lab, B2M, Gustave Roussy Cancer Campus, 114 rue Edouard Vaillant, Villejuif, 94805, France., Nikolaev S; Cancer Genomics Lab, B2M, Gustave Roussy Cancer Campus, 114 rue Edouard Vaillant, Villejuif, 94805, France., Petta TB; Departamento de Biologia Celular e Genética, Universidade Federal do Rio Grande do Norte, Av. Senador Salgado Filho, s/n, Natal, 59078-970, RN, Brazil. tirzah.petta@usc.edu.; Keck School of Medicine, Department of Pathology, University of Southern California, HMR 315, 2011, Zonal Avenue, Los Angeles, CA, 90089-9092, USA. tirzah.petta@usc.edu.
المصدر: BMC medical genomics [BMC Med Genomics] 2023 Aug 12; Vol. 16 (1), pp. 186. Date of Electronic Publication: 2023 Aug 12.
نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE
مواضيع طبية MeSH: Xeroderma Pigmentosum*/genetics , Xeroderma Pigmentosum*/epidemiology , Xeroderma Pigmentosum*/pathology , COVID-19*/epidemiology , Melanoma*/genetics , Skin Neoplasms*/genetics, Male ; Female ; Humans ; Brazil ; Pandemics ; Siblings ; DNA Repair ; DNA-Binding Proteins/genetics
SCR Disease Name: Xeroderma Pigmentosum, Complementation Group E
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2دورية أكاديمية
المؤلفون: Furlanetto G; Furlanetto Institute, São Paulo, Brazil furlanettoglaucio@gmail.com., Furlanetto BH; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Henriques SR; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Lopes LM; Real e Benemérita Associação Portuguesa, São Paulo, Brazil., Miranda ET; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Porto CM; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Pereira ME; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Davini C; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil., Espinosa EC; Instituto Furlanetto - Real e Benemérita Associação Portuguesa de Beneficência, São Paulo, Brazil.
المصدر: World journal for pediatric & congenital heart surgery [World J Pediatr Congenit Heart Surg] 2015 Jan; Vol. 6 (1), pp. 26-32.
نوع المنشور: Evaluation Study; Journal Article
بيانات الدورية: Publisher: Sage Publications Country of Publication: United States NLM ID: 101518415 Publication Model: Print Cited Medium: Internet ISSN: 2150-136X (Electronic) Linking ISSN: 21501351 NLM ISO Abbreviation: World J Pediatr Congenit Heart Surg Subsets: MEDLINE
مواضيع طبية MeSH: Abnormalities, Multiple/*surgery , Heart Defects, Congenital/*surgery , Pulmonary Veins/*abnormalities , Vascular Malformations/*surgery, Abnormalities, Multiple/mortality ; Cardiopulmonary Bypass ; Female ; Heart Defects, Congenital/mortality ; Humans ; Infant ; Infant, Newborn ; Male ; Pulmonary Veins/surgery ; Retrospective Studies ; Tomography, X-Ray Computed ; Treatment Outcome ; Vascular Malformations/mortality
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3دورية أكاديمية
عنوان ترانسليتريتد: Quilotórax iatrogénico: una complicación del tubo de drenaje pleural.
المؤلفون: Sebastiao Porto A; Servicios de Cirugía y Pediatría. Hospital Universitario Alzira Velano. Facultad de Ciencias Médicas. Universidad de Alfenas. Brasil. profporto@hotmail.com.br, Ocáriz Bazzano FC, Henrique Paiva A, Marti Traver LA, Celeste Henriques SR
المصدر: Anales espanoles de pediatria [An Esp Pediatr] 2000 Nov; Vol. 53 (5), pp. 492-4.
نوع المنشور: Case Reports; Comparative Study; Journal Article
بيانات الدورية: Publisher: Doyma Country of Publication: Spain NLM ID: 0420463 Publication Model: Print Cited Medium: Print ISSN: 0302-4342 (Print) Linking ISSN: 03024342 NLM ISO Abbreviation: An Esp Pediatr Subsets: MEDLINE
مواضيع طبية MeSH: Chest Tubes/*adverse effects , Chylothorax/*etiology , Drainage/*adverse effects , Drainage/*instrumentation , Pneumothorax/*surgery, Follow-Up Studies ; Humans ; Iatrogenic Disease ; Infant ; Male ; Pneumothorax/diagnostic imaging ; Radiography, Thoracic ; Time Factors