Physician

Pediatric Cardiology

Dr. Ryuichi Kuromaru, MD

Dr. Ryuichi Kuromaru practices Pediatric Cardiology. Ryuichi Kuromaru is a published MD as well. He has 34 publications published. The latest was: Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib.

Publications

The Leu544Ile polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency.
PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children.
Late-onset ornithine transcarbamylase deficiency in male patients: prognostic factors and characteristics of plasma amino acid profile.
A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl-phosphate synthetase-1 activity in liver: a pitfall in enzymatic diagnosis for hyperammonaemia.
Improved diabetes control by using ''close adjustment algorithms''.
Association study of human MTH1 gene polymorphisms with type 1 diabetes mellitus.
Identification of a novel type 1 diabetes susceptibility gene, T-bet.
Quantification of circulating varicella zoster virus-DNA for the early diagnosis of visceral varicella.
A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes.
Association study between interleukin-12 receptor beta1/beta2 genes and type 1 diabetes or asthma in the Japanese population.
Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes.
Changes in adiposity and excess body weight correlate with growth responses but not with decreases in low-density lipoprotein cholesterol levels during GH treatment in...
Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese population.
A case of growth hormone and gonadotropin deficiency associated with unilateral anophthalmia, microphallus, cryptorchidism, and mental retardation.
Association between birthweight and body mass index at 3 years of age.
Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with type 1 diabetes in the Japanese population.
Juvenile idiopathic arthritis associated with autoimmune thyroid disorders and autoimmune cholangitis.
Premature mortality and hypopituitarism.
Growth hormone treatment and type 2 diabetes.
Hypothalamic hamartoma associated with an arachnoid cyst.
Association of interleukin-4 receptor and interleukin-4 promoter gene polymorphisms with systemic lupus erythematosus.
Rubinstein-Taybi syndrome: a girl with a history of neuroblastoma and premature thelarche.
Long-term effect of growth hormone (GH) treatment on body composition in children with GH deficiency.
High-intensity basal ganglia lesions on T1-weighted images in two toddlers with elevated blood manganese with portosystemic shunts.
Long-term prospective study of body composition and lipid profiles during and after growth hormone (GH) treatment in children with GH deficiency: gender-specific metab...
Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib.
Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (alpha-glucosidase) inhibitor.
An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme: a carboxylase deficiency detected by newborn screening for maple syrup urine disease.
A simple WWW interface and quick response system-information query system for cross-sectional body dimensions.
The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients.
Body composition, atherogenic risk factors and apolipoproteins following growth hormone treatment.
Lipoprotein (a) changes during growth hormone treatment.
Monozygotic twins with discordant sex.

Doctors Specialties

Pediatrics
Pediatric Cardiology

Accepted Insurances

Education

Case Western Reserve University - University Hospitals
University of Hawaii

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