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Items: 1 to 50 of 64

1.

Regulatory aspects of quality and safety for live recombinant viral vaccines against infectious diseases in Japan.

Sakurai A, Ogawa T, Matsumoto J, Kihira T, Fukushima S, Miyata I, Shimizu H, Itamura S, Ouchi K, Hamada A, Tani K, Okabe N, Yamaguchi T.

Vaccine. 2019 Oct 8;37(43):6573-6579. doi: 10.1016/j.vaccine.2019.08.031. Epub 2019 Sep 7.

2.

Comparing Antimicrobial Susceptibilities among Mycoplasma pneumoniae Isolates from Pediatric Patients in Japan between Two Recent Epidemic Periods.

Oishi T, Takahashi K, Wakabayashi S, Nakamura Y, Ono S, Kono M, Kato A, Saito A, Kondo E, Tanaka Y, Teranishi H, Akaike H, Tanaka T, Miyata I, Ogita S, Ohno N, Nakano T, Ouchi K.

Antimicrob Agents Chemother. 2019 Jun 24;63(7). pii: e02517-18. doi: 10.1128/AAC.02517-18. Print 2019 Jul.

3.

LAMP-based assay can rectify the diagnosis of Yersinia pseudotuberculosis infections otherwise missed by serology.

Kato A, Miyata I, Tanaka Y, Oishi T, Teranishi H, Akaike H, Ohno N, Nakajima H, Kouguchi Y, Ouchi K.

J Med Microbiol. 2019 Feb;68(2):143-147. doi: 10.1099/jmm.0.000868. Epub 2019 Jan 16.

PMID:
30648936
4.

Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure.

Ono S, Matsuda J, Watanabe E, Akaike H, Teranishi H, Miyata I, Otomo T, Sadahira Y, Mizuochi T, Kusano H, Kage M, Ueno H, Yoshida K, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Hayashi Y, Kanegane H, Ouchi K.

Hum Genome Var. 2019 Jan 7;6:2. doi: 10.1038/s41439-018-0035-5. eCollection 2019.

5.

Incidence of Viremia With DNA Viruses in Oncology Patients With Febrile Neutropenia.

Teranishi H, Ohzono N, Miyata I, Wakabayashi S, Kono M, Ono S, Kato A, Saito A, Kondo E, Tanaka Y, Akaike H, Oishi T, Ohno N, Terada K, Ouchi K.

J Pediatr Hematol Oncol. 2018 Nov;40(8):605-608. doi: 10.1097/MPH.0000000000001300.

PMID:
30188350
6.

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.

Horm Res Paediatr. 2018;90(2):132-137. doi: 10.1159/000491104. Epub 2018 Aug 15.

PMID:
30110704
7.

Discovery of GnIH and Its Role in Hypothyroidism-Induced Delayed Puberty.

Tsutsui K, Son YL, Kiyohara M, Miyata I.

Endocrinology. 2018 Jan 1;159(1):62-68. doi: 10.1210/en.2017-00300. Review.

PMID:
28938445
8.

Macrolide-Resistant Mycoplasma pneumoniae Infection, Japan, 2008-2015.

Tanaka T, Oishi T, Miyata I, Wakabayashi S, Kono M, Ono S, Kato A, Fukuda Y, Saito A, Kondo E, Teranishi H, Tanaka Y, Wakabayashi T, Akaike H, Ogita S, Ohno N, Nakano T, Terada K, Ouchi K.

Emerg Infect Dis. 2017 Oct;23(10):1703-1706. doi: 10.3201/eid2310.170106.

9.

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance.

Hosoe J, Kadowaki H, Miya F, Aizu K, Kawamura T, Miyata I, Satomura K, Ito T, Hara K, Tanaka M, Ishiura H, Tsuji S, Suzuki K, Takakura M, Boroevich KA, Tsunoda T, Yamauchi T, Shojima N, Kadowaki T.

Diabetes. 2017 Oct;66(10):2713-2723. doi: 10.2337/db17-0301. Epub 2017 Aug 1.

10.

Cellular and humoral immunity after vaccination or natural mumps infection.

Terada K, Hagihara K, Oishi T, Miyata I, Akaike H, Ogita S, Ohno N, Ouchi K.

Pediatr Int. 2017 Aug;59(8):885-890. doi: 10.1111/ped.13306. Epub 2017 Jul 14.

PMID:
28432833
11.

A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1.

Tsunogai T, Miyata I, Kotake S, Matsuura R, Takagi K, Nanba H, Takahata N, Tajima T, Wada Y.

Clin Pediatr Endocrinol. 2016 Jul;25(3):111-4. doi: 10.1297/cpe.25.111. Epub 2016 Jul 20. No abstract available.

12.

Atypical clinical features of children with central nervous system tumor: Delayed diagnosis and switch in handedness.

Yokoi K, Yamaoka M, Miyata I, Nonaka Y, Yuza Y, Kawata S, Akiyama M, Yanagisawa T, Ida H.

Pediatr Int. 2016 Sep;58(9):923-6. doi: 10.1111/ped.13024. Epub 2016 Jul 21.

PMID:
27440052
13.

Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.

Ono E, Ariga M, Oshima S, Hayakawa M, Imai M, Ochiai Y, Mochizuki H, Namba N, Ozono K, Miyata I.

Clin Pediatr Endocrinol. 2016 Apr;25(2):23-35. doi: 10.1297/cpe.25.23. Epub 2016 Apr 28.

14.

Helicobacter cinaedi bacteremia resulting from antimicrobial resistance acquired during treatment for X-linked agammaglobulinemia.

Toyofuku M, Tomida J, Kawamura Y, Miyata I, Yuza Y, Horikoshi Y.

J Infect Chemother. 2016 Oct;22(10):704-6. doi: 10.1016/j.jiac.2016.02.008. Epub 2016 Mar 31.

PMID:
27040158
15.

Therapeutic Drug Monitoring in Neonatal HSV Infection on Continuous Renal Replacement Therapy.

Funaki T, Miyata I, Shoji K, Enomoto Y, Sakamoto S, Kasahara M, Miyairi I.

Pediatrics. 2015 Jul;136(1):e270-4. doi: 10.1542/peds.2014-3380.

16.

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

Sato N, Hasegawa T, Hasegawa Y, Arisaka O, Ozono K, Amemiya S, Kikuchi T, Tanaka H, Harada S, Miyata I, Tanaka T.

Clin Pediatr Endocrinol. 2015 Apr;24(2):37-49. doi: 10.1297/cpe.24.37. Epub 2015 May 15.

17.

Serostatus following live attenuated vaccination administered before pediatric liver transplantation.

Funaki T, Shoji K, Miyata I, Sakamoto S, Kasahara M, Yoshii H, Miyairi I, Saitoh A.

Liver Transpl. 2015 Jun;21(6):774-83. doi: 10.1002/lt.24104. Epub 2015 May 4.

18.

Successful detection and genotyping of rubella virus from preserved umbilical cord of patients with congenital rubella syndrome.

Miyata I, Kubo T, Miyairi I, Saitoh A, Morimoto N.

Clin Infect Dis. 2015 Feb 15;60(4):605-7. doi: 10.1093/cid/ciu882. Epub 2014 Nov 6. No abstract available.

PMID:
25378458
19.

Echovirus 3 as another enterovirus causing life-threatening neonatal fulminant hepatitis.

Miyata I, Hanaoka N, Okabe N, Fujimoto T, Sakamoto S, Kasahara M, Saitoh A.

J Clin Virol. 2014 Feb;59(2):132-4. doi: 10.1016/j.jcv.2013.11.015. Epub 2013 Dec 7. No abstract available.

PMID:
24374056
20.

Detection of enteroviral RNA from preserved umbilical cord.

Miyata I, Saitoh A.

J Clin Virol. 2013 Mar;56(3):274-5. doi: 10.1016/j.jcv.2012.11.008. Epub 2012 Dec 5. No abstract available.

PMID:
23218992
21.

Dermatologic manifestations of human parechovirus type 3 infection in neonates and infants.

Shoji K, Komuro H, Miyata I, Miyairi I, Saitoh A.

Pediatr Infect Dis J. 2013 Mar;32(3):233-6. doi: 10.1097/INF.0b013e31827b1fd0.

PMID:
23190775
22.

Atypical Pneumocystis jiroveci pneumonia with multiple nodular granulomas after rituximab for refractory nephrotic syndrome.

Sato M, Ito S, Ogura M, Kamei K, Miyairi I, Miyata I, Higuchi M, Matsuoka K.

Pediatr Nephrol. 2013 Jan;28(1):145-9. doi: 10.1007/s00467-012-2286-6. Epub 2012 Sep 5.

PMID:
22948319
23.

An infant with human parechovirus type 3 infection with a distinctive rash on the extremities.

Shoji K, Komuro H, Kobayashi Y, Shike T, Funaki T, Katsuta T, Miyata I, Saitoh A.

Pediatr Dermatol. 2014 Mar-Apr;31(2):258-9. doi: 10.1111/j.1525-1470.2012.01819.x. Epub 2012 Sep 3.

PMID:
22938181
24.

A Case of Allgrove Syndrome with a Novel IVS7 +1 G>A Mutation of The AAAS Gene.

Ikemoto S, Sakurai K, Kuwashima N, Saito Y, Miyata I, Katsumata N, Ida H.

Clin Pediatr Endocrinol. 2012 Jan;21(1):11-3. doi: 10.1297/cpe.21.11. Epub 2012 Feb 8. No abstract available.

25.

Diagnostic usefulness of 3 tesla MRI of the brain for cushing disease in a child.

Ono E, Ozawa A, Matoba K, Motoki T, Tajima A, Miyata I, Ito J, Inoshita N, Yamada S, Ida H.

Clin Pediatr Endocrinol. 2011 Oct;20(4):89-93. doi: 10.1297/cpe.20.89. Epub 2011 Nov 15.

26.

Seizure-modifying potential of histamine H1 antagonists: a clinical observation.

Miyata I, Saegusa H, Sakurai M.

Pediatr Int. 2011 Oct;53(5):706-708. doi: 10.1111/j.1442-200X.2011.03328.x.

PMID:
21261789
27.

An experience at an ambulatory pediatric clinic during the first week of a confirmed H1N1 influenza outbreak in Kobe, Japan.

Miyata I, Katayama H.

J Infect Chemother. 2010 Apr;16(2):152-3. doi: 10.1007/s10156-010-0027-y. Epub 2010 Feb 5. No abstract available.

PMID:
20130952
28.

A Neonatal Case of Autosomal Dominant Hypoparathyroidism without Mutation of the CASR Gene.

Miyata I, Yoshikawa H, Kurokawa N, Kanno K, Hayashi Y, Eto Y.

Clin Pediatr Endocrinol. 2008;17(1):17-22. doi: 10.1297/cpe.17.17. Epub 2008 Feb 14.

29.

Successful intrauterine therapy for fetal goitrous hypothyroidism during late gestation.

Miyata I, Abe-Gotyo N, Tajima A, Yoshikawa H, Teramoto S, Seo M, Kanno K, Sugiura K, Tanaka T, Eto Y.

Endocr J. 2007 Dec;54(5):813-7. Epub 2007 Oct 3.

30.

Right testicular necrosis and left vanishing testis in a neonate.

Miyata I, Yoshikawa H, Ikemoto M, Eto Y.

J Pediatr Endocrinol Metab. 2007 Mar;20(3):449-54.

PMID:
17451086
31.
32.

Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.

Miyata I, Vallette-Kasic S, Saveanu A, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Reynaud R, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T.

J Clin Endocrinol Metab. 2006 Dec;91(12):4981-7. Epub 2006 Sep 12.

PMID:
16968807
33.

Lymphocytic hypophysitis with central diabetes insipidus and subsequent hypopituitarism masking a suprasellar germinoma in a 13-year-old girl.

Mikami-Terao Y, Akiyama M, Yanagisawa T, Takahashi-Fujigasaki J, Yokoi K, Fukuoka K, Sakuma M, Miyata I, Fujisawa K, Oi S, Eto Y.

Childs Nerv Syst. 2006 Oct;22(10):1338-43. Epub 2006 Mar 25.

PMID:
16565852
34.

A novel mutation of the arginine vasopressin receptor 2 gene in a patient with congenital nephrogenic diabetes insipidus.

Tajima A, Miyata I, Katayama A, Toyoda S, Eto Y.

Clin Pediatr Endocrinol. 2005;14(1):27-33. doi: 10.1297/cpe.14.27. Epub 2005 Feb 14.

35.

Constitutionally tall stature with morphological abnormality of the pituitary gland.

Miyata I, Yoshikawa H, Eto Y.

Endocr J. 2004 Apr;51(2):189-95.

36.

Characteristics of hyaluronate-hydroxyethyl acrylate blend gel and release of cationic amphiphilic solutes.

Jin Y, Yamanaka J, Sato S, Miyata I, Yomota C, Yonese M.

Chem Pharm Bull (Tokyo). 2002 Oct;50(10):1341-8.

37.

Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF).

Miyata I, Eto Y, Kamijo T, Ogawa M, Futrakul A, Phillips JA 3rd.

Endocr J. 1999 Mar;46 Suppl:S71-4. No abstract available.

38.

11-year-old boy with sarcoidosis and generalized brawny induration of muscle.

Akiyama M, Wada Y, Ando K, Miyata I, Usui N, Tanaka H, Inoue K, Eto Y.

Pediatr Int. 2002 Feb;44(1):93-7. No abstract available.

PMID:
11982881
39.

Recyclable characteristics of hyaluronate-polyhydroxyethyl acrylate blend hydrogel for controlled releases.

Jin Y, Yamanaka J, Sato S, Miyata I, Yomota C, Yonese M.

J Control Release. 2001 Jun 15;73(2-3):173-81.

PMID:
11516495
40.

Functional disomy for Xq26.3-qter in a boy with an unbalanced t(X;21)(q26.3;p11.2) translocation.

Akiyama M, Kawame H, Ohashi H, Tohma T, Ohta H, Shishikura A, Miyata I, Usui N, Eto Y.

Am J Med Genet. 2001 Mar 1;99(2):111-4. Review.

PMID:
11241467
41.

Localization and characterization of a short isoform of the corticotropin-releasing factor receptor type 2alpha (CRF(2)alpha-tr) in the rat brain.

Miyata I, Shiota C, Chaki S, Okuyama S, Inagami T.

Biochem Biophys Res Commun. 2001 Jan 19;280(2):553-7.

PMID:
11162554
43.

Intracellular signaling in rat cultured vascular smooth muscle cells: roles of nuclear factor-kappaB and p38 mitogen-activated protein kinase on tumor necrosis factor-alpha production.

Yamakawa T, Eguchi S, Matsumoto T, Yamakawa Y, Numaguchi K, Miyata I, Reynolds CM, Motley ED, Inagami T.

Endocrinology. 1999 Aug;140(8):3562-72.

PMID:
10433212
44.

Cloning and characterization of a short variant of the corticotropin-releasing factor receptor subtype from rat amygdala.

Miyata I, Shiota C, Ikeda Y, Oshida Y, Chaki S, Okuyama S, Inagami T.

Biochem Biophys Res Commun. 1999 Mar 24;256(3):692-6.

PMID:
10080961
45.

Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.

Kishi K, Muromoto N, Nakaya Y, Miyata I, Hagi A, Hayashi H, Ebina Y.

Diabetes. 1998 Apr;47(4):550-8. Erratum in: Diabetes 1998 Jul;47(7):1170.

PMID:
9568686
46.

Detection of growth hormone gene defects by dideoxy fingerprinting (ddF).

Miyata I, Cogan JD, Prince MA, Kamijo T, Ogawa M, Phillips JA 3rd.

Endocr J. 1997 Feb;44(1):149-54.

47.

A case of cytomegalovirus mononucleosis associated with pleural effusion.

Kato Y, Miyata I, Sakuma S, Katayama A, Toyoda S, Kobayashi S, Okabe N, Maekawa K.

Acta Paediatr Jpn. 1994 Jun;36(3):280-3.

PMID:
8091978
48.

[Anterior decompression of the thoracic spine through the posterior approach: its usefulness, indications, technique, and the preservation of postoperative spinal stability].

Nishiura T, Hagihara N, Masaoka T, Miyata I, Ishimitsu H, Harada Y.

No Shinkei Geka. 1994 Apr;22(4):377-82. Japanese.

PMID:
8164806
49.

Pediatric cerebellar infarction caused by atlantoaxial subluxation--case report.

Miyata I, Imaoka T, Masaoka T, Nishiura T, Ishimitsu H.

Neurol Med Chir (Tokyo). 1994 Apr;34(4):241-5. Review.

50.

[Cerebellar hypoperfusion in epileptic children].

Sugama S, Kusano K, Miyata I, Okazaki M, Eto Y, Ito F, Maekawa K.

No To Hattatsu. 1992 May;24(3):298-300. Japanese. No abstract available.

PMID:
1591033

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