Lista de obras -

A case of aphallia

artículo científico publicado en 1996

A nationwide attempt to standardize growth hormone assays

artículo científico publicado en 2005

A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).

artículo científico

Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylase

article

Adult heights of 258 girls with turner syndrome on low dose of growth hormone therapy in Japan

artículo científico publicado en 2010

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

artículo científico publicado en 2004

Clinical characteristics, etiologies and pathophysiology of patients with severe short stature with severe GH deficiency: questionnaire study on the data registered with the foundation for growth science, Japan

artículo científico publicado en 2006

Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome.

artículo científico publicado en 2004

Congenital absence of the portal vein: clinical and radiologic findings

artículo científico publicado en 2002

Continuing efforts to standardize measured serum growth hormone values in Japan

artículo científico publicado en 2016

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

artículo científico publicado en 2004

Dose-dependent changes in body composition during growth hormone (GH) treatment in Japanese patients with adult GH deficiency: a randomized, placebo-controlled trial

artículo científico publicado en 2010

Evaluation of Quality of Life in Children with GH Deficiency and Idiopathic Short Stature Using the Child Behavior Checklist

artículo científico publicado en 2009

Favorable impact of growth hormone treatment on cholesterol levels in turner syndrome

artículo científico publicado en 2012

Follow-Up Study of Children with Precocious Puberty Treated with Cyproterone Acetate

artículo científico publicado en 1997

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

artículo científico publicado en 2015

Generalized skeletal dysplasia in mother and daughter with 22q11 deletion syndrome

artículo científico publicado en 2003

Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation

artículo científico

Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome

artículo científico publicado en 2006

No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment

artículo científico publicado en 2006

Ovarian function in three female patients with McCune-Albright syndrome with persistent autonomous ovarian activity

artículo científico publicado en 2002

Possible linkage between specific histological structures and aberrant reactivation of the Wnt pathway in adamantinomatous craniopharyngioma

artículo científico publicado en 2004

Premature thelarche in Rubinstein-Taybi syndrome

scientific article published on 01 April 2002

Results of long-term follow-up after treatment of central precocious puberty with leuprorelin acetate: evaluation of effectiveness of treatment and recovery of gonadal function. The TAP-144-SR Japanese Study Group on Central Precocious Puberty

artículo científico publicado en 2004

Standardization of blood growth hormone levels measured by different kits using a linear structural relationship

artículo científico publicado en 2006

Standardized centile curves and reference intervals of serum insulin-like growth factor-I (IGF-I) levels in a normal Japanese population using the LMS method

artículo científico publicado en 2012

Studies of very severe short stature with severe GH deficiency: from the data registered with the foundation for growth science

artículo científico publicado en 2005

The Third International Congress of the GRS and the IGF Society, November 11-15, 2006, Kobe, Japan

artículo científico publicado en 2007

Usefulness of pancreatic ultrasonography in the diagnosis of Shwachman-Bodian-Diamond syndrome

artículo científico publicado en 2005

XI International Congress of AUXOLOGY, September 9-12, 2007, Tokyo, Japan.

artículo científico publicado en 2008

Lista de obras de

A case of aphallia

A nationwide attempt to standardize growth hormone assays

A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).

Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylase

Adult heights of 258 girls with turner syndrome on low dose of growth hormone therapy in Japan

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Clinical characteristics, etiologies and pathophysiology of patients with severe short stature with severe GH deficiency: questionnaire study on the data registered with the foundation for growth science, Japan

Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome.

Congenital absence of the portal vein: clinical and radiologic findings

Continuing efforts to standardize measured serum growth hormone values in Japan

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

Dose-dependent changes in body composition during growth hormone (GH) treatment in Japanese patients with adult GH deficiency: a randomized, placebo-controlled trial

Evaluation of Quality of Life in Children with GH Deficiency and Idiopathic Short Stature Using the Child Behavior Checklist

Favorable impact of growth hormone treatment on cholesterol levels in turner syndrome

Follow-Up Study of Children with Precocious Puberty Treated with Cyproterone Acetate

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

Generalized skeletal dysplasia in mother and daughter with 22q11 deletion syndrome

Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation

Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome

No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment

Ovarian function in three female patients with McCune-Albright syndrome with persistent autonomous ovarian activity

Possible linkage between specific histological structures and aberrant reactivation of the Wnt pathway in adamantinomatous craniopharyngioma

Premature thelarche in Rubinstein-Taybi syndrome

Results of long-term follow-up after treatment of central precocious puberty with leuprorelin acetate: evaluation of effectiveness of treatment and recovery of gonadal function. The TAP-144-SR Japanese Study Group on Central Precocious Puberty

Standardization of blood growth hormone levels measured by different kits using a linear structural relationship

Standardized centile curves and reference intervals of serum insulin-like growth factor-I (IGF-I) levels in a normal Japanese population using the LMS method

Studies of very severe short stature with severe GH deficiency: from the data registered with the foundation for growth science

The Third International Congress of the GRS and the IGF Society, November 11-15, 2006, Kobe, Japan

Usefulness of pancreatic ultrasonography in the diagnosis of Shwachman-Bodian-Diamond syndrome

XI International Congress of AUXOLOGY, September 9-12, 2007, Tokyo, Japan.