長谷川 奉延

研究成果

年別の研究成果 1986 2004 2006 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021 2022

• 6871 被引用数
• 44 h-index
• 323 Article
• 25 Letter
• 13 Review article
• 8 Comment/debate
• 2 その他
  • 2 Chapter

年別の研究成果

年別の研究成果

検索結果

• 2018

  Adrenocortical carcinoma characterized by gynecomastia: A case report

  Takeuchi, T., Yoto, Y., Ishii, A., Tsugawa, T., Yamamoto, M., Hori, T., Kamasaki, H., Nogami, K., Oda, T., Nui, A., Kimura, S., Yamagishi, T., Homma, K., Hasegawa, T., Fukami, M., Watanabe, Y., Sasamoto, H. & Tsutsumi, H., 2018, In: clinical pediatric endocrinology. 27, 1, p. 9-18 10 p.

  研究成果: Article › 査読

  • Gynecomastia 100%
  • Adrenocortical Carcinoma 98%
  • Virilism 59%
  • Testosterone 38%
  • Estradiol 37%
  4 被引用数 (Scopus)

• An association with hypopituitarism and 9q subtelomere deletion syndrome

  Higuchi, S., Takagi, M., Takeda, R., Yoshihashi, H., Narumi, S. & Hasegawa, T., 2018 12月, In: Clinical Case Reports. 6, 12, p. 2371-2375 5 p.

  研究成果: Article › 査読

  Open Access

  • Hypopituitarism 100%

• A Novel Mutation in NKX2-1 Shows Dominant-Negative Effects only in the Presence of PAX8

  Shinohara, H., Takagi, M., Ito, K., Shimizu, E., Fukuzawa, R. & Hasegawa, T., 2018 8月, In: Thyroid. 28, 8, p. 1071-1073 3 p.

  研究成果: Article › 査読

  • Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress 100%
  • Mutation 81%
  • Haploinsufficiency 31%
  • Homeobox Genes 28%
  • In Vitro Techniques 10%
  6 被引用数 (Scopus)

• A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination

  Takagi, M., Shimomura, S., Fukuzawa, R., Narumi, S., Nishimura, G. & Hasegawa, T., 2018 12月 1, In: Journal of Human Genetics. 63, 12, p. 1277-1281 5 p.

  研究成果: Article › 査読

  • Spondylocarpotarsal synostosis 100%
  • Tarsal Coalition 27%
  • Mutation 27%
  • Lordosis 20%
  • Scoliosis 17%
  1 被引用数 (Scopus)

• A pediatric case of pheochromocytoma without apparent hypertension associated with von hippel-lindau disease

  Igaki, J., Nishi, A., Sato, T. & Hasegawa, T., 2018, In: clinical pediatric endocrinology. 27, 2, p. 87-93 7 p.

  研究成果: Article › 査読

  • von Hippel-Lindau Disease 100%
  • Pheochromocytoma 80%
  • Hypertension 47%
  • Pediatrics 46%
  • Tachycardia 42%
  2 被引用数 (Scopus)

• Association between monoallelic TSHR mutations and congenital hypothyroidism: A statistical approach

  Abe, K., Narumi, S., Suwanai, A. S., Adachi, M., Muroya, K., Asakura, Y., Nagasaki, K., Abe, T. & Hasegawa, T., 2018 2月, In: European journal of endocrinology. 178, 2, p. 137-144 8 p.

  研究成果: Article › 査読

  • Congenital Hypothyroidism 100%
  • Neonatal Screening 43%
  • Mutation 41%
  • Dual Oxidases 26%
  • Heterozygote 22%
  14 被引用数 (Scopus)

• Comparison of serum 25-hydroxyvitamin D levels between radioimmunoassay and liquid chromatography-tandem mass spectrometry in infants and postpartum women

  Hara, K., Ikeda, K., Koyama, Y., Wada, Y. & Hasegawa, T., 2018 10月 1, In: Journal of Pediatric Endocrinology and Metabolism. 31, 10, p. 1105-1111 7 p.

  研究成果: Article › 査読

  • 25-hydroxyvitamin D 100%
  • Tandem Mass Spectrometry 93%
  • Liquid Chromatography 88%
  • Postpartum Period 81%
  • Radioimmunoassay 80%
  4 被引用数 (Scopus)

• Cover Image, Volume 176A, Number 1, January 2018

  Ikenoue, S., Miyakoshi, K., Ishii, T., Sato, Y., Otani, T., Akiba, Y., Kasuga, Y., Ochiai, D., Matsumoto, T., Ichihashi, Y., Matsuzaki, Y., Tachikawa, K., Michigami, T., Nishimura, G., Ikeda, K., Hasegawa, T. & Tanaka, M., 2018 1月 1, In: American journal of medical genetics. Part A. 176, 1, p. i

  研究成果: Article › 査読

  • Hypophosphatasia 100%
  • Phenotype 37%

• Discordant fetal phenotype of hypophosphatasia in two siblings

  Ikenoue, S., Miyakoshi, K., Ishii, T., Sato, Y., Otani, T., Akiba, Y., Kasuga, Y., Ochiai, D., Matsumoto, T., Ichihashi, Y., Matsuzaki, Y., Tachikawa, K., Michigami, T., Nishimura, G., Ikeda, K., Hasegawa, T. & Tanaka, M., 2018 1月, In: American Journal of Medical Genetics, Part A. 176, 1, p. 171-174 4 p.

  研究成果: Article › 査読

  • Hypophosphatasia 100%
  • Siblings 57%
  • Pregnancy 37%
  • Phenotype 37%
  • Newborn Infant 36%
  8 被引用数 (Scopus)

• Efficacy and safety of denosumab therapy for osteogenesis imperfecta patients with osteoporosis—Case series

  Kobayashi, T., Nakamura, Y., Suzuki, T., Yamaguchi, T., Takeda, R., Takagi, M., Hasegawa, T., Kosho, T. & Kato, H., 2018 12月 1, In: Journal of Clinical Medicine. 7, 12, 479.

  研究成果: Article › 査読

  Open Access

  • Denosumab 100%
  • Osteogenesis Imperfecta 94%
  • Bone Density 64%
  • Safety 41%
  • Osteoporosis 21%
  13 被引用数 (Scopus)

• Fetal goitrous hypothyroidism and polyhydramnios in a patient with compound heterozygous DUOXA2 Mutations

  Tanase-Nakao, K., Miyata, I., Terauchi, A., Saito, M., Wada, S., Hasegawa, T. & Narumi, S., 2018 10月 1, In: Hormone Research in Paediatrics. 90, 2, p. 132-137 6 p.

  研究成果: Article › 査読

  • Dual Oxidases 100%
  • Polyhydramnios 82%
  • Hypothyroidism 61%
  • Mutation 33%
  • Goiter 19%
  5 被引用数 (Scopus)

• Identification of compound heterozygous TSHR mutations (R109Q and R450H) in a patient with nonclassic TSH resistance and functional characterization of the mutant receptors

  Sugisawa, C., Abe, K., Sunaga, Y., Taniyama, M., Hasegawa, T. & Narumi, S., 2018, In: clinical pediatric endocrinology. 27, 3, p. 123-130 8 p.

  研究成果: Article › 査読

  Open Access

  • Mutation 42%
  • Congenital Hypothyroidism 33%
  • Phenotype 15%
  • Iodine 13%
  • Missense Mutation 12%
  4 被引用数 (Scopus)

• Longitudinal serum and urine steroid metabolite profiling in a 46,XY infant with prenatally identified POR deficiency

  Ono, H., Numakura, C., Homma, K., Hasegawa, T., Tsutsumi, S., Kato, F., Fujisawa, Y., Fukami, M. & Ogata, T., 2018 4月, In: Journal of Steroid Biochemistry and Molecular Biology. 178, p. 177-184 8 p.

  研究成果: Article › 査読

  • Antley-Bixler Syndrome Phenotype 100%
  • Dihydrotestosterone 64%
  • Steroid 49%
  • Androgen 48%
  • Steroids 40%
  1 被引用数 (Scopus)

• Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signature

  Narumi, S., Matsubara, K., Ishii, T. & Hasegawa, T., 2018, In: clinical pediatric endocrinology. 27, 4, p. 235-238 4 p.

  研究成果: Article › 査読
  3 被引用数 (Scopus)

• MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency

  Shima, H., Hayashi, M., Tachibana, T., Oshiro, M., Amano, N., Ishii, T., Haruna, H., Igarashi, M., Kon, M., Fukuzawa, R., Tanaka, Y., Fukami, M., Hasegawa, T. & Narumi, S., 2018 11月, In: PloS one. 13, 11, e0206184.

  研究成果: Article › 査読

  • 46,XY Disorders of Sex Development 100%
  • Adrenal Insufficiency 83%
  • Gestational Age 56%
  • Placenta 13%
  • Virulence 12%
  15 被引用数 (Scopus)

• Prevalence of central fatness in 1992–1994: 40% of Japanese boys 6–17 years

  Inokuchi, M., Matsuo, N., Takayama, J. I. & Hasegawa, T., 2018, In: Endocrine journal. 65, 2, p. 213-220 8 p.

  研究成果: Article › 査読

  • Body Mass Index 100%
  • Waist Circumference 70%
  • Body Size 26%
  • Ilium 26%
  • Pediatric Obesity 25%
  4 被引用数 (Scopus)

• Prevalence of diverse complications and its association with karyotypes in Japanese adult women with turner syndrome—a questionnaire survey by the foundation for growth science—

  Hanew, K., Tanaka, T., Horikawa, R., Hasegawa, T. & Yokoya, S., 2018, In: Endocrine journal. 65, 5, p. 509-519 11 p.

  研究成果: Article › 査読

  • Karyotype 100%
  • Turner Syndrome 71%
  • Growth 49%
  • Epilepsy 47%
  • Metabolic Bone Diseases 45%
  8 被引用数 (Scopus)

• Safety Outcomes during Pediatric GH Therapy: Final Results from the Prospective GeNeSIS Observational Program

  Child, C. J., Zimmermann, A. G., Chrousos, G. P., Cummings, E., Deal, C. L., Hasegawa, T., Jia, N., Lawrence, S., Linglart, A., Loche, S., Maghnie, M., Sánchez, J. P., Polak, M., Predieri, B., Richter-Unruh, A., Rosenfeld, R. G., Yeste, D., Yorifuji, T. & Blum, W. F., 2018 11月 9, In: Journal of Clinical Endocrinology and Metabolism. 104, 2, p. 379-389 11 p.

  研究成果: Article › 査読

  • Neuroendocrinology 100%
  • Safety 54%
  • Observational Studies 49%
  • Pediatrics 40%
  • Intracranial 33%
  28 被引用数 (Scopus)

• Serum 25-hydroxyvitamin D ₃ levels of one-month-old term infants in Tokyo using liquid chromatography tandem mass spectrometry

  Hara, K., Ikeda, K., Koyama, Y., Wada, Y. & Hasegawa, T., 2018 3月, In: Acta Paediatrica, International Journal of Paediatrics. 107, 3, p. 532-533 2 p.

  研究成果: Article › 査読
  1 被引用数 (Scopus)

• Spontaneous virilization around puberty in nr5a1-related 46,xy sex reversal: Additional case and a literature review

  Adachi, M., Hasegawa, T., Tanaka, Y., Asakura, Y., Hanakawa, J. & Muroya, K., 2018, In: Endocrine journal. 65, 12, p. 1187-1192 6 p.

  研究成果: Article › 査読

  • Virilism 100%
  • Puberty 76%
  • Leydig Cells 68%
  • 46,XY Disorders of Sex Development 66%
  • Hyperplasia 25%
  6 被引用数 (Scopus)

• Trismus-pseudocamptodactyly syndrome with bilateral hypoplastic mandibular condyles and shallow mandibular fossa: A case report

  Kusano, C., Hori, N., Izawa, K., Kosaki, R., Nishimura, G. & Hasegawa, T., 2018 7月, In: Oral Science International. 15, 2, p. 90-92 3 p.

  研究成果: Article › 査読

  Open Access

  • Hecht syndrome 100%
  • Mandibular Condyle 65%
  • Arthrogryposis 13%
  • Trismus 13%
  • Genetic Databases 12%

• Two novel mutations of COMP in Japanese boys with pseudoachondroplasia

  Ichihashi, Y., Takagi, M., Ishii, T., Watanabe, K., Nishimura, G. & Hasegawa, T., 2018 12月 1, In: Human Genome Variation. 5, 1, 12.

  研究成果: Article › 査読

  Open Access

  • Pseudoachondroplasia 100%
  • Cartilage Oligomeric Matrix Protein 86%
  • Osteochondrodysplasias 55%
  • Mutation 47%
  • Thrombospondins 25%
  1 被引用数 (Scopus)

• WHO 2006 Child Growth Standards overestimate short stature and underestimate overweight in Japanese children

  Inokuchi, M., Matsuo, N., Takayama, J. I. & Hasegawa, T., 2018 1月 26, In: Journal of Pediatric Endocrinology and Metabolism. 31, 1, p. 33-38 6 p.

  研究成果: Article › 査読

  • Overweight 100%
  • Weights and Measures 71%
  • Growth 56%
  • Child 49%
  • Japan 37%
  9 被引用数 (Scopus)
• 2017

  A novel case of somatic KCNJ5 mutation in pediatric-onset aldosterone-producing adenoma

  Uchida, N., Amano, N., Yamaoka, Y., Uematsu, A., Sekine, Y., Suzuki, M., Watanabe, J., Nishimoto, K., Mukai, K., Fukuzawa, R., Hasegawa, T. & Ishii, T., 2017 8月, In: Journal of the Endocrine Society. 1, 8, p. 1056-1061 6 p.

  研究成果: Article › 査読

  Open Access

  • Aldosterone 100%
  • Adenoma 90%
  • Pediatrics 62%
  • Mutation 54%
  • Adrenocorticotropic Hormone 17%
  2 被引用数 (Scopus)

• A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency

  Takagi, M., Dobashi, K., Nagahara, K., Kato, M., Nishimura, G., Fukuzawa, R., Narumi, S. & Hasegawa, T., 2017 4月 1, In: American Journal of Medical Genetics, Part A. 173, 4, p. 1071-1076 6 p.

  研究成果: Article › 査読

  • Megalencephaly 100%
  • Germ-Line Mutation 79%
  • Growth Hormone 67%
  • Gain of Function Mutation 31%
  • Thymoma 28%
  5 被引用数 (Scopus)

• A novel mutation in the C-propeptide of COL2A1 causes atypical spondyloepiphyseal dysplasia congenita

  Kusano, C., Takagi, M., Hori, N., Murotsuki, J., Nishimura, G. & Hasegawa, T., 2017 3月 2, In: Human Genome Variation. 4, 17003.

  研究成果: Article › 査読

  Open Access

  • Congenita Spondyloepiphyseal dysplasia 100%
  • Mutation 45%
  • Pubic Bone 36%
  • Genetic Databases 35%
  • Missense Mutation 27%
  3 被引用数 (Scopus)

• Clinical practice guidelines for congenital hyperinsulinism

  Yorifuji, T., Horikawa, R., Hasegawa, T., Adachi, M., Soneda, S., Minagawa, M., Ida, S., Yonekura, T., Kinoshita, Y., Kanamori, Y., Kitagawa, H., Shinkai, M., Sasaki, H. & Nio, M., 2017, In: clinical pediatric endocrinology. 26, 3, p. 127-152 26 p.

  研究成果: Article › 査読

  • Congenital Hyperinsulinism 100%
  • Practice Guidelines 60%
  • Pediatrics 41%
  • Guidelines 41%
  • Surgeons 22%
  35 被引用数 (Scopus)

• FGFR1 Analyses in Four Patients with Hypogonadotropic Hypogonadism with Split-Hand/Foot Malformation: Implications for the Promoter Region

  Ohtaka, K., Fujisawa, Y., Takada, F., Hasegawa, Y., Miyoshi, T., Hasegawa, T., Miyoshi, H., Kameda, H., Kurokawa-Seo, M., Fukami, M. & Ogata, T., 2017 5月, In: Human mutation. 38, 5, p. 503-506 4 p.

  研究成果: Article › 査読

  • Receptor, Fibroblast Growth Factor, Type 1 100%
  • Hypogonadism 80%
  • Genetic Promoter Regions 65%
  • Foot 57%
  • Hand 51%
  4 被引用数 (Scopus)

• Genetic defects in pediatric-onset adrenal insufficiency in Japan

  Amano, N., Narumi, S., Hayashi, M., Takagi, M., Imai, K., Nakamura, T., Hachiya, R., Sasaki, G., Homma, K., Ishii, T. & Hasegawa, T., 2017 8月, In: European journal of endocrinology. 177, 2, p. 187-194 8 p.

  研究成果: Article › 査読

  • Adrenal Insufficiency 100%
  • Addison Disease 83%
  • Japan 64%
  • Pediatrics 50%
  • Mineralocorticoids 22%
  25 被引用数 (Scopus)

• Histological changes in autoimmune hepatitis with graves’ disease: A child case report

  Yamada, M., Shibata, H., Masugi, Y., Ishi, T., Kameyama, K., Ebinuma, H. & Hasegawa, T., 2017, In: Internal Medicine. 56, 16, p. 2139-2143 5 p.

  研究成果: Article › 査読

  Open Access

  • Autoimmune Hepatitis 100%
  • Graves Disease 90%
  • Child 34%
  • Biopsy 28%
  • Transaminases 16%
  2 被引用数 (Scopus)

• Hormonal treatment of disorders of sex development

  Toki, M. & Hasegawa, T., 2017, In: Japanese Journal of Clinical Urology. 71, 10, p. 784-789 6 p.

  研究成果: Article › 査読

• Incidence of diabetes mellitus and neoplasia in japanese short-statured children treated with growth hormone in the Genetics and Neuroendocrinology of Short Stature International Study (GeNeSIS)

  Yokoya, S., Hasegawa, T., Ozono, K., Tanaka, H., Kanzaki, S., Tanaka, T., Chihara, K., Jia, N., Child, C. J., Ihara, K., Funai, J., Iwamoto, N. & Seino, Y., 2017, In: clinical pediatric endocrinology. 26, 4, p. 229-241 13 p.

  研究成果: Article › 査読

  • Neuroendocrinology 100%
  • Growth Hormone 60%
  • Diabetes Mellitus 50%
  • Incidence 30%
  • Child 27%
  3 被引用数 (Scopus)

• Mild thyroid peroxidase deficiency caused by TPO mutations with residual activity: Correlation between clinical phenotypes and enzymatic activity

  Narumi, S., Fox, L. A., Fukudome, K., Sakaguchi, Z., Sugisawa, C., Abe, K., Kameyama, K. & Hasegawa, T., 2017, In: Endocrine journal. 64, 11, p. 1087-1097 11 p.

  研究成果: Article › 査読

  • Thyroid Dyshormonogenesis 2A 100%
  • Iodide Peroxidase 57%
  • Phenotype 26%
  • Mutation 24%
  • Serum 20%
  7 被引用数 (Scopus)

• Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica

  Takeda, R., Takagi, M., Shinohara, H., Futagawa, H., Narumi, S., Hasegawa, T., Nishimura, G. & Yoshihashi, H., 2017 12月, In: European Journal of Medical Genetics. 60, 12, p. 635-638 4 p.

  研究成果: Article › 査読

  • Gerodermia osteodysplastica 100%
  • Whole Exome Sequencing 57%
  • Mutation 26%
  • Diphosphonates 26%
  • Cutis Laxa 19%
  3 被引用数 (Scopus)

• Population Pharmacokinetics of Diazoxide in Children with Hyperinsulinemic Hypoglycemia

  Kizu, R., Nishimura, K., Sato, R., Kosaki, K., Tanaka, T., Tanigawara, Y. & Hasegawa, T., 2017 11月 1, In: Hormone Research in Paediatrics. 88, 5, p. 316-323 8 p.

  研究成果: Article › 査読

  • Diazoxide 100%
  • Hypoglycemia 70%
  • Pharmacokinetics 55%
  • Child 31%
  • Population 28%
  7 被引用数 (Scopus)

• Severe hypertriglyceridemia during treatment of acute lymphoblastic leukemia associated with type III hyperlipoproteinemia

  Yamada, Y., Shima, H., Shibata, H., Ishii, T., Hasegawa, T. & Shimada, H., 2017, (Accepted/In press) In: Pediatric Blood and Cancer.

  研究成果: Article › 査読

• Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX

  Takagi, M., Yagi, H., Fukuzawa, R., Narumi, S. & Hasegawa, T., 2017 4月 13, In: Human Genome Variation. 4, 17012.

  研究成果: Article › 査読

  Open Access

  • Disorders of Sex Development 100%
  • Genitalia 69%
  • ATR-X syndrome 65%
  • Disorder 64%
  • Mutation 63%
  3 被引用数 (Scopus)

• The response to growth hormone treatment in prepubertal children with growth hormone deficiency in japan: Comparing three consecutive years of treatment data of the foundation for growth science in Japan between the 1990s and 2000s

  Isojima, T., Hasegawa, T., Yokoya, S. & Tanaka, T., 2017, In: Endocrine journal. 64, 9, p. 851-858 8 p.

  研究成果: Article › 査読

  • Growth Hormone 100%
  • Japan 86%
  • Growth 53%
  • Child 45%
  • Therapeutics 17%
  4 被引用数 (Scopus)

• Three-Quarters Adrenalectomy for Infantile-Onset Cushing Syndrome due to Bilateral Adrenal Hyperplasia in McCune-Albright Syndrome

  Itonaga, T., Goto, H., Toujigamori, M., Ohno, Y., Korematsu, S., Izumi, T., Narumi, S., Hasegawa, T. & Ihara, K., 2017 10月 1, In: Hormone Research in Paediatrics. 88, 3-4, p. 285-290 6 p.

  研究成果: Article › 査読

  • Polyostotic Fibrous Dysplasia 100%
  • Cushing Syndrome 78%
  • Adrenalectomy 75%
  • Hyperplasia 58%
  • Abdominal Obesity 12%
  3 被引用数 (Scopus)

• Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with turner syndrome

  Isojima, T., Sakazume, S., Hasegawa, T., Ogata, T., Nakanishi, T., Nagai, T. & Yokoya, S., 2017, In: clinical pediatric endocrinology. 26, 3, p. 153-164 12 p.

  研究成果: Article › 査読

  • Noonan Syndrome 100%
  • Turner Syndrome 86%
  • Reference Values 54%
  • Growth 34%
  • Child 29%
  1 被引用数 (Scopus)
• 2016

  A case of mature teratoma with a falsely high serum estradiol value measured with an immunoassay

  Hosokawa, M., Shibata, H., Ishii, T., Fujino, A., Kuroda, T., Kosaki, K., Kameyama, K. & Hasegawa, T., 2016, In: Journal of Pediatric Endocrinology and Metabolism. 29, 6, p. 737-739 3 p.

  研究成果: Article › 査読

  • Teratoma 100%
  • Immunoassay 87%
  • Estradiol 76%
  • Serum 39%
  • Liquid Chromatography 22%
  2 被引用数 (Scopus)

• A case of transient neonatal diabetes due to a novel mutation in ABCC8

  Takagi, M., Takeda, R., Yagi, H., Ariyasu, D., Fukuzawa, R. & Hasegawa, T., 2016, In: clinical pediatric endocrinology. 25, 4, p. 139-141 3 p.

  研究成果: Article › 査読
  4 被引用数 (Scopus)

• A novel mutation of the THRB gene in a japanese family with resistance to thyroid hormone

  Ito, J., Narumi, S., Nishizawa, K., Kamimaki, T., Hori, N. & Hasegawa, T., 2016 1月 30, In: clinical pediatric endocrinology. 25, 1, p. 19-22 4 p.

  研究成果: Article › 査読
  1 被引用数 (Scopus)

• A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation

  Mitani, M., Furuichi, M., Narumi, S., Hasegawa, T., Chiga, M., Uchida, S. & Sato, S., 2016, In: clinical pediatric endocrinology. 25, 4, p. 127-134 8 p.

  研究成果: Article › 査読

  • Hypopituitarism 78%
  • Mutation 34%
  • Acidosis 31%
  • Hyperkalemia 25%
  • Growth 20%
  4 被引用数 (Scopus)

• Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in japanese infants by urinary steroid metabolites

  Koyama, Y., Homma, K., Fukami, M., Miwa, M., Ikeda, K., Ogata, T., Murata, M. & Hasegawa, T., 2016 4月 28, In: clinical pediatric endocrinology. 25, 2, p. 37-44 8 p.

  研究成果: Article › 査読

  • Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 100%
  • tetrahydroaldosterone 66%
  • Oxidoreductases 64%
  • Steroids 52%
  • Tetrahydrocortisone 41%
  5 被引用数 (Scopus)

• Co-Administration of the CYP3A4 Inhibitor Diltiazem Counteracts Mitotane-Induced Clearance of Glucocorticoids and Antihypertensives in a Patient with Adrenocortical Carcinoma

  Minami, I., Yoshimoto, T., Tsujimoto, K., Homma, K., Hasegawa, T. & Ogawa, Y., 2016 12月 1, In: AACE Clinical Case Reports. 2, 1, p. e36-e40

  研究成果: Article › 査読

  Open Access

  • Mitotane 100%
  • Cytochrome P-450 CYP3A Inhibitors 93%
  • Adrenocortical Carcinoma 87%
  • Diltiazem 77%
  • Cytochrome P-450 CYP3A 63%
  1 被引用数 (Scopus)

• Criteria for radiologic diagnosis of hypochondroplasia in neonates

  Saito, T., Nagasaki, K., Nishimura, G., Wada, M., Nyuzuki, H., Takagi, M., Hasegawa, T., Amano, N., Murotsuki, J., Sawai, H., Yamada, T., Sato, S. & Saitoh, A., 2016 4月 1, In: Pediatric Radiology. 46, 4, p. 513-518 6 p.

  研究成果: Article › 査読

  • Hypochondroplasia 100%
  • Femur 39%
  • Ilium 32%
  • Receptor, Fibroblast Growth Factor, Type 3 21%
  • Acetabulum 17%
  6 被引用数 (Scopus)

• Diagnosis and treatment of adrenal insufficiency including adrenal crisis: A japan endocrine society clinical practice guideline

  Yanase, T., Tajima, T., Katabami, T., Iwasaki, Y., Tanahashi, Y., Sugawara, A., Hasegawa, T., Mune, T., Oki, Y., Nakagawa, Y., Miyamura, N., Shimizu, C., Otsuki, M., Nomura, M., Akehi, Y., Tanabe, M. & Kasayama, S., 2016, In: Endocrine journal. 63, 9, p. 765-784 20 p.

  研究成果: Article › 査読

  • Adrenal Insufficiency 100%
  • Practice Guidelines 73%
  • Hydrocortisone 69%
  • Japan 64%
  • Adrenocorticotropic Hormone 44%
  53 被引用数 (Scopus)

• Effects of financial support on treatment of adolescents with growth hormone deficiency: A retrospective study in Japan

  Maeda, E., Higashi, T., Hasegawa, T., Yokoya, S., Mochizuki, T., Ishii, T., Ito, J., Kanzaki, S., Shimatsu, A., Takano, K., Tajima, T., Tanaka, H., Tanahashi, Y., Teramoto, A., Nagai, T., Hanew, K., Horikawa, R., Yorifuji, T., Wada, N. & Tanaka, T., 2016 10月 21, In: BMC Health Services Research. 16, 1, 602.

  研究成果: Article › 査読

  • Financial Support 100%
  • Growth Hormone 72%
  • Japan 62%
  • Retrospective Studies 50%
  • adolescent 44%

• Feminizing adrenocortical carcinoma with distinct histopathological findings

  Hatano, M., Takenaka, Y., Inoue, I., Homma, K., Hasegawa, T., Sasano, H., Awata, T. & Katayama, S., 2016, In: Internal Medicine. 55, 22, p. 3301-3307 7 p.

  研究成果: Article › 査読

  • Adrenocortical Carcinoma 100%
  • Adosterol 32%
  • estradiol sulfate 31%
  • Iodine-131 25%
  • Gynecomastia 25%
  4 被引用数 (Scopus)