K. Onigata

发表

Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese

H. Togari, Yukari Sugiyama, H. Mizuno, 2006, Endocrine.

Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

S. Kusuda, R. Horikawa, T. Tajima, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Background factors associated with academic motivation for attending medical school immediately after admission in Japan: A single‐center study

T. Watari, K. Onigata, Nobuhiro Nagai, 2022, Journal of general and family medicine.

Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome

K. Tachibana, Hiroyuki Tanaka, K. Fujieda, 2012, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Identification of a gain-of-function mutation in the HNF-1β gene in a Japanese family with MODY

Y. Matsuzawa, Q. Zhu, K. Yamagata, 2002, Diabetologia.

Detection of Point Mutation for Human Growth Hormone in Patients with Anti-Pituitary Antibody Positive Type 1 Diabetes Mellitus

T. Suzuki, T. Kanda, I. Kobayashi, 2001, The Journal of international medical research.

Association of the CTLA-4 gene 49 A/G polymorphism with type 1 diabetes and autoimmune thyroid disease in Japanese children.

S. Amemiya, A. Kasuga, Kisho Kobayashi, 2003, Diabetes care.

Role of Serum Leptin in the Regulation of Weight Gain in Early Infancy

A. Morikawa, K. Onigata, K. Nagashima, 1999, Neonatology.

The Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT): initial aims and impact of the family history of type 1 diabetes mellitus in Japanese children

K. Tachibana, Toshikazu Takahashi, I. Yokota, 2001, Pediatric diabetes.

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas

K. Yamazawa, T. Ogata, K. Matsuoka, 2008, Journal of Molecular Medicine.

Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.

L. Persani, S. Mora, S. Refetoff, 2008, The Journal of clinical endocrinology and metabolism.

Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin.

A. Morikawa, T. Nagashima, M. Murakami, 2001, Thyroid : official journal of the American Thyroid Association.

Survey of potentially inappropriate prescriptions for common cold symptoms in Japan: A cross-sectional study

T. Watari, K. Adachi, Kenji Watanabe, 2022, PloS one.

A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency.

A. Morikawa, T. Nagashima, K. Nagashima, 1998, The Journal of clinical endocrinology and metabolism.

Lipoprotein(a) Levels in Japanese Children With IDDM

K. Onigata, K. Nagashima, T. Kuroume, 1993, Diabetes Care.

Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation

Yoshiro Saito, Hironori Kobayashi, T. Hamajima, 2012 .

Detection of skewed X-inactivation in two female carriers of vasopressin type 2 receptor gene mutation.

A. Morikawa, H. Mochizuki, T. Nagashima, 1997, The Journal of clinical endocrinology and metabolism.

Relationship Between Serum Levels of Methylguanidine and Glycemic Control in IDDM Children

K. Onigata, K. Nagashima, T. Kuroume, 1993, Diabetes Care.

Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature

A. Morikawa, T. Nagashima, K. Onigata, 1999, Journal of Human Genetics.

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.

G. Rappold, B. Niesler, T. Reinehr, 2002, The Journal of clinical endocrinology and metabolism.

Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation.

Yoshiro Saito, Hironori Kobayashi, T. Hamajima, 2012, European journal of endocrinology.

Resistance to thyroid hormone.

G. Szinnai, K. Onigata, 2014, Endocrine development.

Trends in the Incidence of Duodenal Ulcers Among Children in Gunma Prefecture

T. Tomomasa, A. Morikawa, H. Kaneko, 2003 .

A Cross-Sectional Study of The Background Factors Associated With Academic Motivation Upon Admission To A Medical School in Japan

T. Watari, K. Onigata, Kaori Kono, 2021 .

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

S. Kusuda, R. Horikawa, T. Tajima, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Identification of novel human GH-1 gene polymorphisms that are associated with growth hormone secretion and height.

K. Tachibana, Y. Hasegawa, T. Tanaka,, 2000, The Journal of clinical endocrinology and metabolism.

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

K. Tachibana, Hiroyuki Tanaka, K. Ozono, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects.

Y. Matsuzawa, M. Kanamori, D. Moore, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Sequence analysis of thyroid transcription factor-1 gene reveals absence of mutations in patients with thyroid dysgenesis but presence of polymorphisms in the 5' flanking region and intron.

T. Ieiri, A. Hishinuma, K. Nagashima, 1998, Endocrine journal.

Clinical case seminar in pediatric thyroid disease.

M. Polak, R. Elisei, G. Szinnai, 2014, Endocrine development.

Cognitive Bias and Diagnostic Errors among Physicians in Japan: A Self-Reflection Survey

Y. Tokuda, H. Kanda, T. Watari, 2022, International journal of environmental research and public health.

Identification and functional analysis of novel inactivating thyrotropin receptor mutations in patients with thyrotropin resistance.

K. Tsunekawa, A. Morikawa, M. Murakami, 2006, Thyroid : official journal of the American Thyroid Association.

Familial congenital hypopituitarism with central diabetes insipidus.

K. Onigata, K. Nagashima, S. Tamai, 1994, The Journal of clinical endocrinology and metabolism.

Anterior Pituitary Dysfunction in Children with Idiopathic Central Diabetes Insipidus

A. Morikawa, T. Nagashima, K. Onigata, 1995 .

Longitudinal Evaluation of Patients with a Homozygous R450H Mutation of the TSH Receptor Gene

H. Togari, I. Kato, Yukari Sugiyama, 2009, Hormone Research in Paediatrics.

Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.

R. Weiss, S. Refetoff, O. Ercan, 2012, The Journal of clinical endocrinology and metabolism.

A Child with Necrotizing Infundibulo-Hypophysitis?

T. Nagashima, K. Onigata, K. Nagashima, 1994 .

Gradual improvement of liver function after administration of ursodeoxycholic acid in an infant with a novel ABCB11 gene mutation with phenotypic continuum between BRIC2 and PFIC2

H. Kuwano, M. Hasegawa, T. Tomomasa, 2007, European journal of gastroenterology & hepatology.

A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

T. Taketani, R. Maruyama, N. Ishikawa, 2017, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Development of growth hormone and adrenocorticotropic hormone deficiencies in patients with prenatal or perinatal-onset hypothalamic hypopituitarism having invisible or thin pituitary stalk on magnetic resonance imaging.

K. Tachibana, Y. Hasegawa, E. Kinoshita, 2001, Endocrine journal.

Distal renal tubular acidosis associated with hypercalcemia and nephrocalcinosis in an infant

K. Maruyama, M. Shinohara, K. Onigata, 2002, Pediatric Nephrology.

Reversible secondary pseudohypoaldosteronism due to pyelonephritis

K. Maruyama, K. Onigata, Hiroyuki Watanabe, 2002, Pediatric Nephrology.

Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX.

G. Rappold, T. Ogata, N. Matsuo, 2001, Endocrine journal.

Identification of Mutations in the Hepatocyte Nuclear Factor (HNF)-1α Gene in Japanese Subjects With IDDM

T. Utsugi, T. Maruyama, T. Yanagawa, 1997, Diabetes.

A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormone.

R. Weiss, S. Refetoff, R. Couch, 1997, Thyroid : official journal of the American Thyroid Association.