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Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?
Kisla Ekinci, Rabia Miray; Altun, Ibrahim; Bisgin, Atil; Atmis, Bahriye; Altintas, Derya Ufuk; Balci, Sibel.
Afiliação
  • Kisla Ekinci RM; Department of Pediatric Rheumatology, Faculty of Medicine, Cukurova University, Saricam, Adana, 01331, Turkey. mir_kisla@hotmail.com.
  • Altun I; Department of Pediatrics, Faculty of Medicine, Cukurova University, Adana, Turkey.
  • Bisgin A; Department of Medical Genetics, Faculty of Medicine, Cukurova University, Adana, Turkey.
  • Atmis B; Department of Pediatric Nephrology, Faculty of Medicine, Cukurova University, Adana, Turkey.
  • Altintas DU; Department of Pediatric Allergy and Immunology, Faculty of Medicine, Cukurova University, Adana, Turkey.
  • Balci S; Department of Pediatric Rheumatology, Faculty of Medicine, Cukurova University, Saricam, Adana, 01331, Turkey.
CEN Case Rep ; 9(4): 344-346, 2020 11.
Article em En | MEDLINE | ID: mdl-32372346
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complemento C2 / Doenças da Deficiência Hereditária de Complemento / Hematúria Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Adolescent / Humans / Male Idioma: En Revista: CEN Case Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Turquia
Texto completo
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Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complemento C2 / Doenças da Deficiência Hereditária de Complemento / Hematúria Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Adolescent / Humans / Male Idioma: En Revista: CEN Case Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Turquia