O. Nose

发表

Difference Between Japanese and Caucasian Populations in the Allelic Frequency of Growth Hormone Receptor Polymorphisms

K. Chihara, K. Iida, Yutaka Takahashi, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical utility of insulin-like growth factor binding protein-3 in the evaluation and treatment of short children with suspected growth hormone deficiency.

Y. Hasegawa, T. Tanaka,, S. Yokoya, 1994, European journal of endocrinology.

Multiple associated endocrine abnormalities in a patient with pseudohypoparathyroidism type 1a

Y. Seino, T. Saito, H. Yabuuchi, 1988, European Journal of Pediatrics.

Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT).

N. Amino, K. Tatsumi, O. Nose, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Effects of alternate and simultaneous administrations of calcium and phosphorus on calcium metabolism in children receiving total parenteral nutrition.

Y. Seino, A. Okada, H. Yabuuchi, 1986, JPEN. Journal of parenteral and enteral nutrition.

The Silver‐Russell Syndrome: A Case with Hypergonadotropic Hypogonadism

S. Okada, H. Yabuuchi, T. Harada, 1980 .

Watery diarrhoea with a vasoactive intestinal peptide-producing ganglioneuroblastoma.

P. K. Lee, K. Kakudo, O. Nose, 1980, Archives of disease in childhood.

Watery diarrhoea withavasoactive intestinal peptide-producin g ganglioneuroblas toma

Takesada Mori, N. Yanaihara, O. Nose, 1980 .

Analysis of steroid 21-hydroxylase gene in five unrelated Japanese patients with 21-hydroxylase deficiency.

T. Honjo, J. Nakura, P. White, 1987, Endocrinologia japonica.

HLA-A and -B antigens in Japanese patients with congenital hypothyroidism and their parents.

N. Amino, K. Miyai, T. Fukunishi, 2008, Tissue antigens.

The study of organic acids metabolism in a patient with ornithine transcarbamylase (OTC) deficiency.

H. Kodama, S. Okada, S. Okada, 1982, Advances in experimental medicine and biology.

Effect of the Energy Source on Changes in Energy Expenditure, Respiratory Quotient, and Nitrogen Balance during Total Parenteral Nutrition in Children

M. Ament, H. Yabuuchi, O. Nose, 1987, Pediatric Research.

Elevated Adrenocorticotropic Hormone-Stimulated 17-Hydroxypregnenolone/17-Hydroxyprogesterone in Japanese Children with Premature Pubarche, Hirsutism, Acne and/or Accelerated Growth

T. Tezuka, K. Fujieda, Toshiaki Tanaka, 1996 .

Novel compound heterozygous mutations of growth hormone (GH) receptor gene in a patient with GH insensitivity syndrome.

K. Iida, Yutaka Takahashi, H. Kaji, 1997, The Journal of clinical endocrinology and metabolism.

Recent Advances in the Diagnosis of PIT1 Abnormality

Y. Wada, N. Okamoto, N. Amino, 1994 .

Metabolic changes following gastroplasty in Prader-Willi syndrome —A case report

Y. Kawashima, M. Miyata, T. Harada, 1990, The Japanese journal of surgery.

Prediction of later development of thyrotoxicosis or central hypothyroidism from the cord serum thyroid-stimulating hormone level in neonates born to mothers with Graves disease.

Y. Iwatani, N. Amino, J. Tachi, 1989, The Journal of pediatrics.

Usefulness and limitation of measurement of insulin-like growth factor binding protein-3 (IGFBP-3) for diagnosis of growth hormone deficiency.

Y. Hasegawa, T. Tanaka,, Y. Ohyama, 1992, Endocrinologia japonica.

Prevalence of lactose malabsorption in Japanese children and adults

H. Yabuuchi, T. Harada, O. Nose, 2006 .

Breath hydrogen test for detecting lactose malabsorption in infants and children. Prevalence of lactose malabsorption in Japanese children and adults.

H. Yabuuchi, T. Harada, O. Nose, 1979, Archives of disease in childhood.

Comparison between insulin-like growth factor-I (IGF-I) and IGF binding protein-3 (IGFBP-3) measurement in the diagnosis of growth hormone deficiency.

Y. Hasegawa, T. Tanaka,, Y. Ohyama, 1993, Endocrine journal.

A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect.

N. Amino, K. Tatsumi, M. Kimura, 2000, Thyroid : official journal of the American Thyroid Association.

Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect.

N. Amino, K. Tatsumi, K. Miki, 1998, The Journal of clinical endocrinology and metabolism.

Functional characterization of truncated growth hormone (GH) receptor-(1-277) causing partial GH insensitivity syndrome with high GH-binding protein.

K. Iida, H. Kaji, Y. Okimura, 1999, The Journal of clinical endocrinology and metabolism.

Serum levels of vitamin D metabolites in children receiving total parenteral nutrition.

Y. Seino, H. Yabuuchi, K. Yamaoka, 1986, JPEN. Journal of parenteral and enteral nutrition.

Enzyme immunoassay of thyroxin-binding globulin in dried blood samples on filter paper.

K. Miyai, N. Hata, M. Ito, 1983, Clinical chemistry.

The effect of thyroid hormone on the activities of lactase in the culture of fetal rat intestine.

O. Nose, K. Shimizu, S. Okada, 1990, Cell biology international reports.

Hypothalamic-pituitary functions in patients with idiopathic pituitary dwarfism

K. Miyai, S. Okada, H. Yabuuchi, 1978, European Journal of Pediatrics.

Effective Method for Prediction of Transient Hypothyroidism in Neonates Born to Mothers with Chronic Thyroiditis

Y. Iwatani, N. Amino, K. Miyai, 1989, American journal of perinatology.

Universal predictive criteria for neonatal overt thyrotoxicosis requiring treatment.

Y. Iwatani, N. Amino, K. Miyai, 1988, American journal of perinatology.

Transient infantile hyperthyrotrophinaemia.

K. Miyai, H. Yabuuchi, K. Miki, 1989, Archives of disease in childhood.

Human herpesvirus-6 infection with liver injury in neonatal hepatitis

H. Tajiri, K. Baba, S. Okada, 1990, The Lancet.

Massive Intestinal Albumin Loss after Fontan Operation

T. Sano, T. Matsushita, S. Okada, 1991, Acta paediatrica Japonica : Overseas edition.

Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain.

K. Iida, H. Kaji, Y. Okimura, 1998, The Journal of clinical endocrinology and metabolism.

Thyroid Hormones in Human Milk and their Influence on Thyroid Function of Breast-Fed Babies

K. Ichihara, N. Amino, K. Miyai, 1983, Pediatric Research.

Seasonality of birth in sporadic cretinism.

K. Ichihara, N. Amino, K. Miyai, 1979, Early Human Development.

Transient neonatal hypothyroidism probably related to immaturity of thyroidal iodine organification.

K. Miyai, N. Hata, H. Yabuuchi, 1986, The Journal of pediatrics.

Rubella antibody in neonatal hypothyroidism due to thyroid dysgenesis.

K. Miyai, O. Nose, T. Tsuruhara, 1981, Early human development.

Increased frequency of HLA-Aw24 in congenital hypothyroidism in Japan.

K. Miyai, T. Fukunishi, T. Hirai, 1980, The New England journal of medicine.

A new method of paired thyrotropin assay as a screening test for neonatal hypothyroidism.

K. Nakatani, K. Ichihara, N. Amino, 1978, The Journal of clinical endocrinology and metabolism.

The Boy:Girl Ratio of Children Diagnosed with Growth Hormone Deficiency-Induced Short Stature Is Associated with the Boy:Girl Ratio of Children Visiting Short Stature Clinics

M. Murashita, S. Kitanaka, T. Tanizawa, 2021, Hormone Research in Paediatrics.

Female pseudohermaphroditism caused by maternal congenital adrenal hyperplasia.

J. Ono, H. Yabuuchi, T. Harada, 1979, The Journal of pediatrics.

DIET AND SERUM LIPIDS IN JAPANESE CHILDREN

T. Sano, M. Ogawa, H. Yabuuchi, 1984 .

Treatment of a Patient with Ornithine Transcarbamylase Deficiency with Essential Amino Acids and Sodium Benzoate

H. Kodama, H. Yabuuchi, H. Tajiri, 1983 .

Does CSF copper level in Wilson disease reflect copper accumulation in the brain?

H. Kodama, K. Nomiyama, H. Nomiyama, 1988, Pediatric Neurology.

Application of the New Oral Pancreatic Exocrine Function Test “PFD” Test in Children—Normal Values in Children—

Y. Yamashiro, T. Konno, Y. Tazawa, 1984 .

Enzyme immunoassay of free thyroxin in dried blood samples on filter paper.

N. Amino, K. Miyai, Y. Endo, 1985, Clinical chemistry.

Measurement of “Free Thyroxine” in Dried Blood Samples on Filter Paper by Radio- and Enzyme-Immunoassay for Monitoring Thyroid Function

K. Miyai, Y. Endo, N. Hata, 1986 .

A case of mucolipidosis II: Biochemical, nutritional, and immunological studies

Masahiro Kato, S. Okada, S. Kojima, 1979, Brain and Development.

Vitamin D metabolism in biliary atresia: intestinal absorptions of 25-hydroxyvitamin D3 and 1,25-dihydroxyvitamin D3.

H. Tanaka, Y. Seino, H. Yabuuchi, 1988, Journal of pediatric gastroenterology and nutrition.

Semiautomated Enzyme Immunoassay of Thyrotropin as a Mass Screening Test for Neonatal Hypothyroidism

K. Miyai, S. Kusuda, T. Oura, 1984, Pediatric Research.

Radioimmunoassay of "free thyroxin" in dried blood spots on filter paper - preliminary observations on the effective differentiation of subjects with congenital hypothyroidism from those with subnormal thyroxin-binding globulin and normal subjects.

K. Ichihara, N. Amino, K. Miyai, 1982, Clinical chemistry.

Activity of the glycine cleavage system in hyperammonemia treated with benzoate.

S. Kamoshita, H. Tajiri, Y. Motokawa, 1983, The Tohoku journal of experimental medicine.

When and how to combine growth hormone with a luteinizing hormone‐releasing hormone analogue

A. Tanae, R. Horikawa, N. Katsumata, 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Urinary iodide excretion measured with an iodide-selective ion electrode: studies on normal subjects of varying ages and patients with thyroid diseases.

K. Miyai, Y. Endo, Y. Iijima, 1988, Endocrinologia japonica.

Efficacy of a multiple insulin injection regimen in teenagers with insulin-dependent diabetes. Carbohydrate and lipid oxidation measured by continuous indirect calorimetry.

M. Shichiri, H. Yabuuchi, H. Tajiri, 1987, Diabetes research and clinical practice.

Breath hydrogen test for detecting lactose malabsorption in infants and children. Prevalence of lactose malabsorption in Japanese children and adults.

H. Yabuuchi, T. Harada, O. Nose, 1979, Archives of disease in childhood.