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Necessity of genetic testing on asymptomatic proteinuria before the progression of nephrotic syndrome in children with focal segmental glomerulosclerosis.
Fujinaga, Shuichiro; Oba, Daiju.
Affiliation
  • Fujinaga S; Division of Nephrology, Saitama Children's Medical Center, 1-2 Shintoshin, Chuo-Ku, Saitama City, Saitama, 330-8777, Japan. f_shuich@d2.dion.ne.jp.
  • Oba D; Division of Medical Genetics, Saitama Children's Medical Center, Saitama, Japan.
Pediatr Nephrol ; 38(9): 3199-3200, 2023 09.
Article in En | MEDLINE | ID: mdl-37162573
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glomerulosclerosis, Focal Segmental / Nephrotic Syndrome Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Child / Humans Language: En Journal: Pediatr Nephrol Journal subject: NEFROLOGIA / PEDIATRIA Year: 2023 Document type: Article Affiliation country: Japón Country of publication: Alemania
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glomerulosclerosis, Focal Segmental / Nephrotic Syndrome Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Child / Humans Language: En Journal: Pediatr Nephrol Journal subject: NEFROLOGIA / PEDIATRIA Year: 2023 Document type: Article Affiliation country: Japón Country of publication: Alemania