Matsumoto S - Search Results

1

Outcomes of pediatric obesity-related lifestyle disease screenings in Kumamoto.

Nagamatsu F, Kido J, Suginohara Y, Nakamura T, Nakamura R, Komatsu N, Miyamoto D, Hamada Y, Kashiwagi T, Sugino S, Kiyohara H, Nakamura K, Matsumoto S. Nagamatsu F, et al. Among authors: matsumoto s. Pediatr Int. 2023 Jan-Dec;65(1):e15442. doi: 10.1111/ped.15442. Pediatr Int. 2023. PMID: 36560886

2

Flow cytometric isolation of endodermal progenitors from mouse salivary gland differentiate into hepatic and pancreatic lineages.

Hisatomi Y, Okumura K, Nakamura K, Matsumoto S, Satoh A, Nagano K, Yamamoto T, Endo F. Hisatomi Y, et al. Among authors: matsumoto s. Hepatology. 2004 Mar;39(3):667-75. doi: 10.1002/hep.20063. Hepatology. 2004. PMID: 14999685

3

Gene expression profiles of homogentisate-treated Fah-/- Hpd-/-mice using DNA microarrays.

Tanaka Y, Nakamura K, Matsumoto S, Kimoto Y, Tanoue A, Tsujimoto G, Endo F. Tanaka Y, et al. Among authors: matsumoto s. Mol Genet Metab. 2006 Nov;89(3):203-9. doi: 10.1016/j.ymgme.2005.09.022. Epub 2006 Aug 8. Mol Genet Metab. 2006. PMID: 16899383

4

Glycine regulates proliferation and differentiation of salivary-gland-derived progenitor cells.

Nakamura Y, Matsumoto S, Mochida T, Nakamura K, Takehana K, Endo F. Nakamura Y, et al. Among authors: matsumoto s. Cell Tissue Res. 2009 May;336(2):203-12. doi: 10.1007/s00441-009-0767-0. Epub 2009 Mar 17. Cell Tissue Res. 2009. PMID: 19290545

5

Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes.

Kido J, Nakamura K, Matsumoto S, Mitsubuchi H, Ohura T, Shigematsu Y, Yorifuji T, Kasahara M, Horikawa R, Endo F. Kido J, et al. Among authors: matsumoto s. J Hum Genet. 2013 May;58(5):285-92. doi: 10.1038/jhg.2013.17. Epub 2013 Mar 14. J Hum Genet. 2013. PMID: 23486339

6

VLCAD deficiency in a patient who recovered from ventricular fibrillation, but died suddenly of a respiratory syncytial virus infection.

Yamamoto A, Nakamura K, Matsumoto S, Iwai M, Shigematsu Y, Tajima G, Tsumura M, Okada S, Mitsubuchi H, Endo F. Yamamoto A, et al. Among authors: matsumoto s. Pediatr Int. 2013 Dec;55(6):775-8. doi: 10.1111/ped.12111. Pediatr Int. 2013. PMID: 24330285

7

Biochemical and clinical features of hereditary hyperprolinemia.

Mitsubuchi H, Nakamura K, Matsumoto S, Endo F. Mitsubuchi H, et al. Among authors: matsumoto s. Pediatr Int. 2014 Aug;56(4):492-6. doi: 10.1111/ped.12420. Pediatr Int. 2014. PMID: 24931297 Free PMC article.

8

Diagnosis and treatment of hereditary tyrosinemia in Japan.

Nakamura K, Matsumoto S, Mitsubuchi H, Endo F. Nakamura K, et al. Among authors: matsumoto s. Pediatr Int. 2015;57(1):37-40. doi: 10.1111/ped.12550. Pediatr Int. 2015. PMID: 25443793 Review.

9

Early intervention for late-onset ornithine transcarbamylase deficiency.

Fujisawa D, Mitsubuchi H, Matsumoto S, Iwai M, Nakamura K, Hoshide R, Harada N, Yoshino M, Endo F. Fujisawa D, et al. Among authors: matsumoto s. Pediatr Int. 2015;57(1):e1-3. doi: 10.1111/ped.12457. Pediatr Int. 2015. PMID: 25711267

10

Clinical manifestations and growth of patients with urea cycle disorders in Japan.

Nakamura K, Kido J, Matsumoto S, Mitsubuchi H, Endo F. Nakamura K, et al. Among authors: matsumoto s. J Hum Genet. 2016 Jul;61(7):613-6. doi: 10.1038/jhg.2016.17. Epub 2016 Mar 3. J Hum Genet. 2016. PMID: 26935171

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