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Publications by Marjo Kestilä

Congenital Nephrotic Syndrome (NPHS1): Features Resulting From Different Mutations in Finnish Patients

Kidney International

English

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Two Novel NPHS1 Mutations in a Chinese Family With Congenital Nephrotic Syndrome

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Novel NPHS1 Splice Site Mutations in a Chinese Child With Congenital Nephrotic Syndrome

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OC8 High Prevalence Ofwt1gene Mutations in Patients With Steroid-Resistant Nephrotic Syndrome

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Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

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Histopathological Features of Primary Nephrotic Syndrome in Children

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Congenital Aortic Stenosis Resulting From a Unicommissural Valve: Clinical and Anatomic Features in Twenty-One Adult Patients

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Editorial: Nephrotic Syndrome in Pediatric Patients

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Anesthetic Management of Bilateral Nephrectomy in Children With Congenital Nephrotic Syndrome.

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Congenital Nephrotic Syndrome and Recurrence of Proteinuria After Renal Transplantation

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