Furujo M - Search Results

1

Spectrum of mutations associated with methionine adenosyltransferase I/III deficiency among individuals identified during newborn screening in Japan.

Nagao M, Tanaka T, Furujo M. Nagao M, et al. Among authors: furujo m. Mol Genet Metab. 2013 Dec;110(4):460-4. doi: 10.1016/j.ymgme.2013.10.013. Epub 2013 Oct 31. Mol Genet Metab. 2013. PMID: 24231718

2

Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI.

Furujo M, Kubo T, Kosuga M, Okuyama T. Furujo M, et al. Mol Genet Metab. 2011 Dec;104(4):597-602. doi: 10.1016/j.ymgme.2011.08.029. Epub 2011 Aug 28. Mol Genet Metab. 2011. PMID: 21930407

3

S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report.

Furujo M, Kinoshita M, Nagao M, Kubo T. Furujo M, et al. Mol Genet Metab. 2012 Mar;105(3):516-8. doi: 10.1016/j.ymgme.2011.11.192. Epub 2011 Dec 2. Mol Genet Metab. 2012. PMID: 22178350

4

Methionine adenosyltransferase I/III deficiency: neurological manifestations and relevance of S-adenosylmethionine.

Furujo M, Kinoshita M, Nagao M, Kubo T. Furujo M, et al. Mol Genet Metab. 2012 Nov;107(3):253-6. doi: 10.1016/j.ymgme.2012.08.002. Epub 2012 Aug 11. Mol Genet Metab. 2012. PMID: 22951388 Review.

5

Enzyme replacement therapy in two Japanese siblings with Fabry disease, and its effectiveness on angiokeratoma and neuropathic pain.

Furujo M, Kubo T, Kobayashi M, Ohashi T. Furujo M, et al. Mol Genet Metab. 2013 Nov;110(3):405-10. doi: 10.1016/j.ymgme.2013.07.005. Epub 2013 Jul 14. Mol Genet Metab. 2013. PMID: 23906479

6

Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI: 10-Year follow up.

Furujo M, Kosuga M, Okuyama T. Furujo M, et al. Mol Genet Metab Rep. 2017 Sep 14;13:69-75. doi: 10.1016/j.ymgmr.2017.08.007. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 28983456 Free PMC article.

7

Genetic and pharmacological correction of aberrant dopamine synthesis using patient iPSCs with BH4 metabolism disorders.

Ishikawa T, Imamura K, Kondo T, Koshiba Y, Hara S, Ichinose H, Furujo M, Kinoshita M, Oeda T, Takahashi J, Takahashi R, Inoue H. Ishikawa T, et al. Among authors: furujo m. Hum Mol Genet. 2016 Dec 1;25(23):5188-5197. doi: 10.1093/hmg/ddw339. Hum Mol Genet. 2016. PMID: 27798097 Free PMC article.

8

Effect of growth hormone therapy on thyroid function in isolated growth hormone deficient and short small for gestational age children: a two-year study, including on assessment of the usefulness of the thyrotropin-releasing hormone (TRH) stimulation test.

Ebuchi Y, Kubo T, Furujo M, Higuchi Y, Fujinaga S, Tsuchiya H, Urata N, Ochi M, Namba T, Hara N, Kishi M. Ebuchi Y, et al. Among authors: furujo m. J Pediatr Endocrinol Metab. 2020 Nov 26;33(11):1417-1423. doi: 10.1515/jpem-2020-0151. J Pediatr Endocrinol Metab. 2020. PMID: 33035188

9

An infant case of Graves' disease with ophthalmopathy.

Kubo T, Shimizu J, Furujo M, Takeuchi A, Yoshioka-Iwaso H, Eguchi N, Fukuhara S, Koyama T, Kanadani T, Shiraga H, Oshima K. Kubo T, et al. Among authors: furujo m. Endocr J. 2005 Oct;52(5):647-50. doi: 10.1507/endocrj.52.647. Endocr J. 2005. PMID: 16284447 Free article.

10

Predicting obesity in early adulthood in Japanese women.

Kubo T, Furujo M, Ueda Y, Imai K, Tsukahara K, Morita H, Ogura K, Kimura T, Shimizu J, Fukuhara S, Koyama T, Kanadani T, Shiraga H. Kubo T, et al. Among authors: furujo m. J Paediatr Child Health. 2008 Jan;44(1-2):33-7. doi: 10.1111/j.1440-1754.2007.01166.x. Epub 2007 Jul 19. J Paediatr Child Health. 2008. PMID: 17640286

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