Kiyotaka Zaha

Tokorozawa, 3598513, Japan

Last Updated: 09/26/2026

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Found 9 publications

Usefulness of Fecal Calprotectin Measurement in a Pediatric Patient with Crohn's Disease.

Usefulness of Fecal Calprotectin Measurement in a Pediatric Patient with Crohn's Disease.

Journal: Fukushima journal of medical science

Published: December 11, 2024

Prediction and assessment of acute encephalopathy syndromes immediately after febrile status epilepticus.

Prediction and assessment of acute encephalopathy syndromes immediately after febrile status epilepticus.

Journal: Brain & development

Published: March 29, 2022

Immunodeficiency in a patient with microcephalic osteodysplastic primordial dwarfism type I as compared to Roifman syndrome.

Immunodeficiency in a patient with microcephalic osteodysplastic primordial dwarfism type I as compared to Roifman syndrome.

Journal: Brain & development

Published: March 31, 2020

Transient Marked Increase of γδ T Cells in WHIM Syndrome After Successful HSCT.

Transient Marked Increase of γδ T Cells in WHIM Syndrome After Successful HSCT.

Journal: Journal of clinical immunology

Published: February 23, 2018

TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome.

TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome.

Journal: Brain & development

Published: August 21, 2017

A case of Dravet syndrome complicated by human herpesvirus-6 infection-associated acute encephalopathy and choreoathetosis.

A case of Dravet syndrome complicated by human herpesvirus-6 infection-associated acute encephalopathy and choreoathetosis.

Journal: No to hattatsu = Brain and development

Published: January 01, 2017

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.

Journal: Clinical genetics

Published: March 14, 2016

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.

Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.

Journal: The Journal of allergy and clinical immunology

Published: April 29, 2015

Chromosome 9q33q34 microdeletion with early infantile epileptic encephalopathy, severe dystonia, abnormal eye movements, and nephroureteral malformations.

Chromosome 9q33q34 microdeletion with early infantile epileptic encephalopathy, severe dystonia, abnormal eye movements, and nephroureteral malformations.

Journal: Pediatric neurology

Published: January 12, 2014

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Last Updated: 09/26/2026