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Milos Ognjanovic

Boston Children's Hospital

6

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98

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G458(P) Would a genetic panel be able to elucidate the cause of a child presenting with severe chronic kidney disease in the near future? a population survey of existing mutations

2017 Archives of Disease in Childhood
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G386 Surveillance biopsies of tacrolimus effect in childhood nephrotic syndrome

2016 Archives of Disease in Childhood
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Domiciliary administration of intravenous albumin in congenital nephrotic syndrome.

2015 Pediatric Nephrology
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Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome.

2013 Developmental Medicine & Child Neurology
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KCNJ10 Mutations Disrupt Function in Patients with EAST Syndrome

2011 Nephron Physiology
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