RESPIRATORY CHAIN DEFICIENCY PRESENTING AS DIFFUSE MESANGIAL SCLEROSIS WITH NPHS3 MUTATION

Ítems similars

• Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
  per: Heeringa, Saskia F., et al.
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• Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome Patients
  per: Ovunc, Bugsu, et al.
  Publicat: (2012)
• Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome
  per: Chernin, Gil, et al.
  Publicat: (2008)
• Diffuse mesangial sclerosis – Report of two cases
  per: Vankalakunti, M., et al.
  Publicat: (2012)
• Posterior reversible leukoencephalopathy syndrome in children with hematologic disorders
  per: Barış Malbora, et al.
  Publicat: (2010-09-01)