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List of works by Kenji Ihara

A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess

scientific article published on 07 November 2020

A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes

scientific article published on May 16, 2003

A girl with Hajdu-Cheney syndrome and premature ovarian failure

scientific article published on 01 January 2012

A pediatric case with prostaglandin I-associated thyrotoxicosis: Case report and the literature review

article

Acute Liver Failure as the Initial Manifestation of Wilson Disease Triggered by Human Parvovirus B19 Infection

scientific article published on 01 January 2012

An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease

scientific article published on 01 September 1997

Bacterial pericarditis caused by Lactobacillus iners in an infant

scientific article published on July 18, 2012

Balloon‐occluded retrograde transvenous obliteration for congenital portosystemic venous shunt: Report of two cases

scientific article published on 01 June 2012

Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome

scientific article published on November 8, 2012

Biotin Deficiency in a Glycogen Storage Disease Type 1b Girl Fed Only with Glycogen Storage Disease‐Related Formula

scientific article published on 03 March 2011

Coagulopathy in Patients With Late-Onset Ornithine Transcarbamylase Deficiency in Remission State: A Previously Unrecognized Complication

scientific article published on December 3, 2012

Complete immunotolerance induction after FEIBA prophylaxis in a haemophilia A patient with high‐titre inhibitor

scientific article published on March 8, 2012

Congenital multiple pituitary hormone deficiency associated with hyperammonemia: a case report with a short review of the literature

scientific article published on February 1, 2011

Cytokine imbalance in hyper‐IgE syndrome: reduced expression of transforming growth factor β and interferon γ genes in circulating activated T cells

scientific article published on April 1, 2003

Efficacy of bosentan therapy for segmental pulmonary artery hypertension due to major aortopulmonary collateral arteries in children

scientific article published on March 28, 2012

Genetic susceptibility to Kawasaki disease: Analysis of pattern recognition receptor genes

scientific article published on April 13, 2012

HLA-class II and class I genotypes among Japanese children with Type 1A diabetes and their families

scientific article published on November 29, 2011

High expression of platelet‐derived growth factor and transforming growth factor‐β1 in blast cells from patients with Down Syndrome suffering from transient myeloproliferative disorder and organ fibrosis

scientific article published on 01 November 2001

High frequency of fusion transcripts of exon 11 and exon 4/5 in AF-4 gene is observed in cord blood, as well as leukemic cells from infant leukemia patients with t(4;11)(q21;q23)

scientific article published on 01 September 1998

Histo‐blood group gene polymorphisms as potential genetic modifiers of the development of coronary artery lesions in patients with Kawasaki disease

scientific article published on November 25, 2011

Hyperinsulinemic hypoglycemia of infancy in Sotos syndrome

scientific article published on December 13, 2012

Hypothalamic pituitary complications in Kabuki syndrome

scientific article published on June 1, 2013

Hypothyroidism and Levothyroxine-Responsive Liver Dysfunction in a Patient with Ring Chromosome 18 Syndrome

scientific article published on September 4, 2012

Linear nevus sebaceous syndrome with hypophosphatemic rickets with elevated FGF-23

scientific article published on December 29, 2011

Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis

scientific article published on June 29, 2013

Nonsense mutation in exon 4 of human complement C9 gene is the major cause of Japanese complement C9 deficiency

scientific article published on June 1, 1998

Physical Growth and Retinopathy in Preterm Infants: Involvement of IGF-I and GH

scientific article published on 01 December 2001

Preoperative Management With Nitrogen Inhalation Therapy for a Low-Birth Weight Infant With Tetralogy of Fallot and Absent Pulmonary Valve

scientific article published on February 25, 2011

Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (alpha-glucosidase) inhibitor

scientific article published on 01 May 1998

Sensorineural Hearing Loss in Sjögren’s Syndrome

scientific article published in 2022

Serum chemokine levels and developmental outcome in preterm infants

scientific article published on April 14, 2011

Tracheal aspirate gene expression in preterm newborns and development of bronchopulmonary dysplasia

scientific article published on December 28, 2011

Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment

scientific article published on November 16, 2012