Publications by authors named "Ikuma Fujiwara"

60Publications

Clinical Practice Guidelines for Hypophosphatasia.

Clin Pediatr Endocrinol 2020 9;29(1):9-24. Epub 2020 Jan 9.

Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.

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http://dx.doi.org/10.1297/cpe.29.9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958520PMC
January 2020

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

Reprod Toxicol 2020 04 22;93:83-88. Epub 2020 Jan 22.

Centre for Health and Environmental Risk Research, National Institute for Environmental Studies. 16-2 Onogawa, Tsukuba, Ibaraki 305-8506, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.reprotox.2020.01.005DOI Listing
April 2020

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

J Affect Disord 2019 02 5;245:475-483. Epub 2018 Nov 5.

Division of Public Health, Hygiene and Epidemiology, Tohoku Medical and Pharmaceutical University Faculty of Medicine. 1-15-1 Fukumuro, Miyagino-ku, Sendai, Miyagi 983-8536, Japan; Tohoku Medical Megabank Organization, Tohoku University. 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.jad.2018.11.061DOI Listing
February 2019

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

Clin Pediatr Endocrinol 2018 30;27(1):53-57. Epub 2018 Jan 30.

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1297/cpe.27.53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792822PMC
January 2018

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

J Bone Miner Metab 2018 May 20;36(3):344-351. Epub 2017 May 20.

Department of Pediatric Endocrinology and Environmental Medicine, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1007/s00774-017-0840-9DOI Listing
May 2018

Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion Syndrome.

Cytogenet Genome Res 2017 3;151(1):1-4. Epub 2017 Mar 3.

Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1159/000458469DOI Listing
September 2017

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

Diabetes Res Clin Pract 2016 Oct 9;120:132-41. Epub 2016 Aug 9.

Environment and Genome Research Center, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan; Department of Gynecology and Obstetrics, Tohoku University Graduate School of Medicine, 1-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan; Department of Community Medical Supports, Tohoku Medical Megabank Organization, Tohoku University, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan.

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http://dx.doi.org/10.1016/j.diabres.2016.07.020DOI Listing
October 2016

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

J Affect Disord 2016 Jan 28;190:341-348. Epub 2015 Oct 28.

Department of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, 1-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan; Environment and Genome Research Center, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan; Tohoku Medical Megabank Organization, Tohoku University, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan.

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http://dx.doi.org/10.1016/j.jad.2015.10.024DOI Listing
January 2016

A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.

Am J Med Genet A 2015 Nov 30;167A(11):2851-4. Epub 2015 Jun 30.

Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

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http://dx.doi.org/10.1002/ajmg.a.37231DOI Listing
November 2015

Mutations in PIGL in a patient with Mabry syndrome.

Am J Med Genet A 2015 Apr 23;167A(4):777-85. Epub 2015 Feb 23.

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1002/ajmg.a.36987DOI Listing
April 2015

Heterozygous defects in PAX6 gene and congenital hypopituitarism.

Eur J Endocrinol 2015 Jan 23;172(1):37-45. Epub 2014 Oct 23.

Department of Endocrinology and MetabolismTokyo Metropolitan Children's Medical Center, Tokyo, JapanDepartment of PediatricsSchool of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, JapanDivision of PediatricsDepartment of Homeostatic Regulation and Development, Graduate School of Medicine and Dental Sciences, Niigata University, Niigata, JapanDepartment of PediatricsSchool of Medicine, Tohoku University, Miyagi, JapanDepartment of Endocrinology and MetabolismKanagawa Children's Medical Center, Yokohama, Japan

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http://dx.doi.org/10.1530/EJE-14-0255DOI Listing
January 2015

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

Clin Pediatr Endocrinol 2013 Oct 26;22(4):77-81. Epub 2013 Oct 26.

Department of Pediatrics, Tohoku University Hospital, Sendai, Japan.

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http://dx.doi.org/10.1292/cpe.22.77DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809734PMC
October 2013

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

Clin Pediatr Endocrinol 2012 Jul 25;21(3):45-52. Epub 2012 Jul 25.

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1297/cpe.21.45DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687649PMC
July 2012

Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndrome.

J Neurol Sci 2012 Apr 12;315(1-2):77-81. Epub 2011 Dec 12.

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1016/j.jns.2011.11.025DOI Listing
April 2012

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

J Neurol Sci 2011 Jan 29;300(1-2):179-81. Epub 2010 Sep 29.

Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Yumoto Akiumachi, Taihaku-ku, Sendai 982-0241, Japan.

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http://dx.doi.org/10.1016/j.jns.2010.09.009DOI Listing
January 2011

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

Metabolism 2010 Feb 29;59(2):275-8. Epub 2009 Sep 29.

Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.

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http://dx.doi.org/10.1016/j.metabol.2009.07.024DOI Listing
February 2010

Hypospadias in a male patient with 21-hydroxylase deficiency.

Endocr J 2008 Dec 22;55(6):1051-4. Epub 2008 Aug 22.

Department of Pediatrics, Tohoku University Hospital, Aoba-ku, Sendai, Miyagi, Japan.

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http://dx.doi.org/10.1507/endocrj.k07e-175DOI Listing
December 2008

Ultrasound appearance of thyroid tissue in hypothyroid infants.

J Pediatr 2008 Jul 8;153(1):101-4. Epub 2008 Feb 8.

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1016/j.jpeds.2007.12.015DOI Listing
July 2008

Reduced exposure to mercury in patients receiving enteral nutrition.

Tohoku J Exp Med 2006 Nov;210(3):209-12

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1620/tjem.210.209DOI Listing
November 2006

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

Endocr J 2006 Dec 7;53(6):741-3. Epub 2006 Sep 7.

Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1507/endocrj.k06-099DOI Listing
December 2006

[Vitamin D-dependent rickets type I, II].

Authors:
Ikuma Fujiwara

Nihon Rinsho 2006 Jun;Suppl 2:113-5

Department of Pediatrics, Tohoku University Hospital.

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June 2006

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

J Clin Endocrinol Metab 2006 Jul 11;91(7):2643-9. Epub 2006 Apr 11.

Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, 2-10-1 Ohkura, Setagaya, Tokyo 157-8535, Japan.

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http://dx.doi.org/10.1210/jc.2005-2460DOI Listing
July 2006

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

Pediatr Blood Cancer 2007 Dec;49(7):990-3

Department of Pediatrics, Tohoku University School of Medicine, Aoba-ku, Sendai, Japan.

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http://dx.doi.org/10.1002/pbc.20782DOI Listing
December 2007

Subacute thyroiditis in children: patient report and review of the literature.

J Pediatr Endocrinol Metab 2003 Jul-Aug;16(6):897-900

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1515/jpem.2003.16.6.897DOI Listing
March 2004

Hypophosphatemia in juvenile patients with systemic lupus erythematosus.

Pediatr Int 2003 Feb;45(1):23-30

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1046/j.1442-200x.2003.01665.xDOI Listing
February 2003