Lista de obras - Ken Saida - Dominio Público Uruguay

A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child

artículo científico publicado en 2013

A case of adult Dent disease in Japan with advanced chronic kidney disease.

artículo científico publicado en 2013

A simple refined approach for renovascular hypertension in children: a ten-year experience

artículo científico publicado en 2020

Ampicillin- and ampicillin/sulbactam-resistant Escherichia coli infection in a neonatal intensive care unit in Japan.

artículo científico publicado en 2016

Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report

scientific article published on 18 April 2018

De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder

artículo científico publicado en 2018

Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports.

artículo científico publicado en 2017

Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan

artículo científico publicado en 2015

Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants

artículo científico publicado en 2014

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.

artículo científico publicado en 2013

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

artículo científico publicado en 2021

Novel CLTC variants cause new brain and kidney phenotypes

artículo científico publicado en 2021

Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene.

artículo científico publicado en 2018

Preoperative left ventricular internal dimension in end-diastole as earlier identification of early patent ductus arteriosus operation and postoperative intensive care in very low birth weight infants

artículo científico publicado en 2013

Right-to-left shunting in the ductus arteriosus is induced readily by intense crying and rapid postural change in neonates with meconium-stained amniotic fluid

scientific article published on 01 January 2012

Rituximab-associated agranulocytosis in children with refractory idiopathic nephrotic syndrome: case series and review of literature.

artículo científico publicado en 2014

SOFT syndrome in a patient from Chile

artículo científico publicado en 2018

Successful therapy switch from eculizumab to mycophenolate mofetil in a girl with DEAP-HUS

artículo científico publicado en 2017

Successful unrelated cord blood transplantation using a reduced-intensity conditioning regimen in a 6-month-old infant with congenital neutropenia complicated by severe pneumonia.

artículo científico publicado en 2004

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan

artículo científico publicado en 2015

Treatment of hemolytic uremic syndrome related to Bordetella pertussis infection -is plasma exchange or eculizumab use necessary?

artículo científico publicado en 2018

Lista de obras de Ken Saida

A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child

A case of adult Dent disease in Japan with advanced chronic kidney disease.

A simple refined approach for renovascular hypertension in children: a ten-year experience

Ampicillin- and ampicillin/sulbactam-resistant Escherichia coli infection in a neonatal intensive care unit in Japan.

Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report

De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder

Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports.

Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan

Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

Novel CLTC variants cause new brain and kidney phenotypes

Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene.

Preoperative left ventricular internal dimension in end-diastole as earlier identification of early patent ductus arteriosus operation and postoperative intensive care in very low birth weight infants

Right-to-left shunting in the ductus arteriosus is induced readily by intense crying and rapid postural change in neonates with meconium-stained amniotic fluid

Rituximab-associated agranulocytosis in children with refractory idiopathic nephrotic syndrome: case series and review of literature.

SOFT syndrome in a patient from Chile

Successful therapy switch from eculizumab to mycophenolate mofetil in a girl with DEAP-HUS

Successful unrelated cord blood transplantation using a reduced-intensity conditioning regimen in a 6-month-old infant with congenital neutropenia complicated by severe pneumonia.

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan

Treatment of hemolytic uremic syndrome related to Bordetella pertussis infection -is plasma exchange or eculizumab use necessary?