I. Fujiwara

C. Shimizu, T. Ogata, K. Ozono, 2017, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Gonadal function, fertility, and reproductive medicine in childhood and adolescent cancer patients: a national survey of Japanese pediatric endocrinologists

C. Shimizu, T. Ogata, K. Ozono, 2016, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Coordinated Maturational Regulation of PHEX and Renal Phosphate Transport Inhibitory Activity: Evidence for the Pathophysiological Role of PHEX in X‐Linked Hypophosphatemia

R. Thomas, L. Quarles, M. Drezner, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation

S. Kure, T. Yorifuji, I. Fujiwara, 2012, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfecta

S. Kure, I. Fujiwara, Akiko Saito-hakoda, 2018, Journal of Bone and Mineral Metabolism.

Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan.

H. Tsukahara, K. Ihara, K. Ozono, 2018, Endocrine journal.

Higher prevalence of hypertensive disorders of pregnancy in women who smoke: the Japan environment and children’s study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2019, Hypertension Research.

Incidence of Domestic Violence Against Pregnant Females After the Great East Japan Earthquake in Miyagi Prefecture: The Japan Environment and Children’s Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2016, Disaster Medicine and Public Health Preparedness.

Preconception dysmenorrhea as a risk factor for psychological distress in pregnancy: The Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, N. Yaegashi, 2019, Journal of affective disorders.

Clinical Practice Guidelines for Hypophosphatasia*

K. Ozono, T. Kubota, T. Michigami, 2020, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

First‐in‐Asian Phase I Study of the Anti‐Fibroblast Growth Factor 23 Monoclonal Antibody, Burosumab: Safety and Pharmacodynamics in Adults With X‐linked Hypophosphatemia

H. Cheong, Hiroyuki Tanaka, K. Ozono, 2018, JBMR plus.

Testosterone-Induced Changes in Markers of Bone Turnover in Adolescent Boys with Testicular Dysfunction

K. Iinuma, I. Fujiwara, E. Ogawa, 2003 .

Phenotype variability in nephrogenic diabetes insipidus due to p.D85N mutation in the arginine vasopressin receptor 2 gene

H. Mugishima, T. Morimoto, Y. Kondo, 2013, Nephrology.

Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiency.

N. Katsumata, I. Fujiwara, E. Ogawa, 2010, Metabolism: clinical and experimental.

Normal pituitary function in a Japanese patient with Barth syndrome

S. Miyabayashi, S. Yamaguchi, K. Iinuma, 2001, European Journal of Pediatrics.

Update on the prevalence and determinants of folic acid use in Japan evaluated with 91,538 pregnant women: the Japan Environment and Children’s Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Prevalence and determinants of inadequate use of folic acid supplementation in Japanese pregnant women: the Japan Environment and Children’s Study (JECS)

S. Kuriyama, H. Nishigori, N. Yaegashi, 2017, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Brain White Matter Abnormality in a Newborn Infant with Congenital Adrenal Hyperplasia

S. Kure, M. Uematsu, I. Fujiwara, 2013, Clinical Pediatric Endocrinology.

Brain white matter abnormality in a newborn infant with congenital adrenal hyperplasia.

S. Kure, M. Uematsu, I. Fujiwara, 2013, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri–Weill dyschondrosteosis

T. Ogata, Hiroyuki Tanaka, Y. Matsubara, 2016, Journal of Human Genetics.

Ultrasound appearance of thyroid tissue in hypothyroid infants.

I. Fujiwara, E. Ogawa, Kanako Kojima‐Ishii, 2008, The Journal of pediatrics.

Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone.

T. Ogata, T. Hasegawa, T. Nagai, 2006, The Journal of clinical endocrinology and metabolism.

PTHrP‐independent hypercalcemia with increased proinflammatory cytokines and bone resorption in two children with CD19‐negative precursor B acute lymphoblastic leukemia

M. Imaizumi, K. Fujii, A. Sato, 2007, Pediatric blood & cancer.

Heterozygous defects in PAX6 gene and congenital hypopituitarism.

Y. Hasegawa, K. Muroya, T. Hasegawa, 2014, European journal of endocrinology.

[Precocious puberty caused by hCG-producing germinoma involving the bilateral basal ganglia and cerebral white matter without 1ypical radiologic findings: case report].

T. Tominaga, M. Fujimura, T. Kumabe, 2006, No shinkei geka. Neurological surgery.

A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1

M. Igarashi, I. Fujiwara, M. Fukami, 2019, Sexual Development.

Identification of clinical factors related to antibody‐mediated immune response to the subfornical organ

E. Hoorn, N. Goshima, T. Yorifuji, 2022, Clinical endocrinology.

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome.

A. Utani, H. Tsutsumi, T. Nakahata, 2004, Blood.

Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation.

T. Ogata, K. Kosaki, I. Fujiwara, 2006, Endocrine journal.

Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation

Gabriele Gillessen-Kaesbach, Dagmar Wieczorek, Albert David, 2010, Human mutation.

Hypophosphatemia in juvenile patients with systemic lupus erythematosus

Y. Kondo, K. Iinuma, T. Ohura, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

R. Hennekam, L. Biesecker, J. Graham, 2010, Human mutation.

Oral-facial-digital syndrome with hypothalamic hamartoma, postaxial ray hypoplasia of the limbs, and vagino-cystic communication: a new variant?

K. Iinuma, I. Fujiwara, Y. Kondo, 1999, American journal of medical genetics.

Interannual Changes in the Prevalence of Intimate Partner Violence Against Pregnant Women in Miyagi Prefecture After the Great East Japan Earthquake: The Japan Environment and Children’s Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2019, Journal of Interpersonal Violence.

A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly

G. Nishimura, Y. Hasegawa, T. Hasegawa, 2015, American journal of medical genetics. Part A.

Suppressive effects of RXR agonist PA024 on adrenal CYP11B2 expression, aldosterone secretion and blood pressure

A. Sugawara, S. Ito, R. Ito, 2017, PLoS ONE.

A novel intronic mutation of the TAZ (G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon

S. Miyabayashi, K. Iinuma, O. Sakamoto, 2001, Human Genetics.

The risk of secondary sex ratio imbalance and increased monozygotic twinning after blastocyst transfer: data from the Japan Environment and Children’s Study

M. Shima, T. Kawamoto, S. Kuriyama, 2019, Reproductive Biology and Endocrinology.

Hypercalcemia due to all‐trans retinoic acid therapy for acute promyelocytic leukemia: A case report of effective treatment with bisphosphonate

M. Imaizumi, S. Tsuchiya, K. Iinuma, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

Familial Paget’s disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27)

F. Katsuoka, Yu Yokoyama, Noriko Himori, 2022, Journal of Bone and Mineral Metabolism.

Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes

H. Ohashi, Y. Matsubara, N. Okamoto, 2018, Human Genetics.

A case with central and peripheral hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) plus cataract

I. Nonaka, H. Osaka, S. Okahashi, 2011, Journal of the Neurological Sciences.

Ultrasonographic Findings in Neonates Screened for Congenital Hypothyroidism

K. Iinuma, T. Ohura, I. Fujiwara, 2002 .

A comparison of pituitary-adrenal responses to corticotropin-releasing hormone, hypoglycaemia and metyrapone in children with brain tumours and growth hormone deficiency

I. Fujiwara, E. Ogawa, Y. Igarashi, 1995, European Journal of Pediatrics.

Intravenous pamidronate treatment in osteogenesis imperfecta.

I. Fujiwara, E. Ogawa, A. Asanuma, 1998, European journal of pediatrics.

The association between gestational use of personal care products and neonatal urological abnormality at birth: The Japan Environment and Children's Study.

N. Yaegashi, S. Nakayama, A. Takeuchi, 2020, Reproductive toxicology.

Effects of RXR Agonists on Cell Proliferation/Apoptosis and ACTH Secretion/Pomc Expression

A. Sugawara, S. Ito, T. Yoshikawa, 2015, PloS one.

Brief Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor- (cid:1) B activation: common genetic etiology with Blau syndrome

A. Utani, H. Tsutsumi, T. Nakahata, 2005 .

Psychological distress during pregnancy in Miyagi after the Great East Japan Earthquake: The Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, N. Yaegashi, 2016, Journal of Affective Disorders.

Secondhand smoke exposure is associated with the risk of hypertensive disorders of pregnancy: the Japan Environment and Children’s Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2023, Hypertension Research.

Safety and efficacy of treatment with asfotase alfa in patients with hypophosphatasia: Results from a Japanese clinical trial

T. Ogata, K. Ozono, S. Okada, 2017, Clinical endocrinology.

Mutations in PIGL in a patient with Mabry syndrome

K. Nakayama, T. Kinoshita, Y. Matsubara, 2015, American journal of medical genetics. Part A.

Preconception folic acid supplementation use and the occurrence of neural tube defects in Japan: A nationwide birth cohort study of the Japan Environment and Children's Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2018, Congenital anomalies.

Reduced exposure to mercury in patients receiving enteral nutrition.

K. Haginoya, Yasuko Kobayashi, S. Tsuchiya, 2006, The Tohoku journal of experimental medicine.

Association between social capital and the prevalence of gestational diabetes mellitus: An interim report of the Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, H. Inadera, 2016, Diabetes research and clinical practice.

Methionine Enkephalin Suppresses Osteocyte Apoptosis Induced by Compressive Force through Regulation of Nuclear Translocation of NFATc1

T. Takano-Yamamoto, S. Kure, I. Fujiwara, 2019, JBMR plus.

Fermented Food Consumption and Psychological Distress in Pregnant Women: A Nationwide Birth Cohort Study of the Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, N. Yaegashi, 2016, Tohoku journal of experimental medicine.

Effect of Parenteral Hyperalimentation on Growth in Glycogen Storage Disease Type IA

I. Fujiwara, Y. Igarashi, D. Abukawa, 1994 .

Abnormal Regulation of Renal 25‐Hydroxyvitamin D‐1α‐Hydroxylase Activity in X‐Linked Hypophosphatemia: A Translational or Post‐Translational Defect

M. Drezner, I. Fujiwara, Ron Horst, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Subacute Thyroiditis in Children: Patient Report and Review of the Literature

K. Iinuma, I. Fujiwara, E. Ogawa, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in INSR

S. Kure, A. Kikuchi, I. Fujiwara, 2018, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Psychological distress during pregnancy in Miyagi after the Great East Japan Earthquake: The Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, N. Yaegashi, 2016, Journal of affective disorders.

Preconception dysmenorrhea as a risk factor for psychological distress in pregnancy: The Japan Environment and Children's Study.

S. Kuriyama, H. Nishigori, N. Yaegashi, 2019, Journal of affective disorders.

Pregnant Women’s Awareness of Social Capital in the Great East Japan Earthquake-Affected Areas of Miyagi Prefecture: The Japan Environment and Children’s Study

S. Kuriyama, H. Nishigori, N. Yaegashi, 2017, Disaster Medicine and Public Health Preparedness.

Ultrasound appearance of thyroid tissue in hypothyroid infants.

I. Fujiwara, E. Ogawa, Kanako Kojima‐Ishii, 2008, The Journal of pediatrics.

Heterozygous defects in PAX6 gene and congenital hypopituitarism.

Y. Hasegawa, K. Muroya, T. Hasegawa, 2014, European journal of endocrinology.

syndrome B activation: common genetic etiology with Blau κ nuclear factor- Early-onset sarcoidosis and CARD15 mutations with constitutive

A. Utani, H. Tsutsumi, T. Nakahata, 2013 .