Kobayashi H - Search Results

1

The role of native T1 values on the evaluation of cardiac manifestation in Japanese Fabry disease patients.

Anan I, Sakuma T, Fukuro E, Morimoto S, Nojiri A, Kawai M, Sakurai K, Kobayashi M, Kobayashi H, Ida H, Ohashi T, Yoshimura M, Eto Y, Hongo K. Anan I, et al. Among authors: kobayashi h, kobayashi m. Mol Genet Metab Rep. 2022 Mar 16;31:100858. doi: 10.1016/j.ymgmr.2022.100858. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35782602 Free PMC article.

2

pH dependence of the function of sodium ion extrusion systems in Escherichia coli.

Sakuma T, Yamada N, Saito H, Kakegawa T, Kobayashi H. Sakuma T, et al. Among authors: kobayashi h. Biochim Biophys Acta. 1998 Mar 25;1363(3):231-7. doi: 10.1016/s0005-2728(97)00102-3. Biochim Biophys Acta. 1998. PMID: 9518629 Free article.

3

A pathogenic role of Th2 cells and their cytokine products on the pulmonary metastasis of murine B16 melanoma.

Kobayashi M, Kobayashi H, Pollard RB, Suzuki F. Kobayashi M, et al. Among authors: kobayashi h. J Immunol. 1998 Jun 15;160(12):5869-73. J Immunol. 1998. PMID: 9637498

4

[Multiple sulfatase deficiency].

Eto Y, Ito T, Kobayashi H. Eto Y, et al. Among authors: kobayashi h. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):385-8. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645088 Review. Japanese. No abstract available.

5

Reduction of lysosomal storage in murine mucopolysaccharidosis type VII by transplantation of normal and genetically modified macrophages.

Ohashi T, Yokoo T, Iizuka S, Kobayashi H, Sly WS, Eto Y. Ohashi T, et al. Among authors: kobayashi h. Blood. 2000 Jun 1;95(11):3631-3. Blood. 2000. PMID: 10828055 Free article.

6

A botulism case of a 12-year-old girl caused by intestinal colonization of Clostridium botulinum type Ab.

Kobayashi H, Fujisawa K, Saito Y, Kamijo M, Oshima S, Kubo M, Eto Y, Monma C, Kitamura M. Kobayashi H, et al. Jpn J Infect Dis. 2003 Apr;56(2):73-4. Jpn J Infect Dis. 2003. PMID: 12824692

7

Neonatal gene transfer using lentiviral vector for murine Pompe disease: long-term expression and glycogen reduction.

Kyosen SO, Iizuka S, Kobayashi H, Kimura T, Fukuda T, Shen J, Shimada Y, Ida H, Eto Y, Ohashi T. Kyosen SO, et al. Among authors: kobayashi h. Gene Ther. 2010 Apr;17(4):521-30. doi: 10.1038/gt.2009.160. Epub 2009 Dec 24. Gene Ther. 2010. PMID: 20033064

8

Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case.

Kobayashi H, Shimada Y, Ikegami M, Kawai T, Sakurai K, Urashima T, Ijima M, Fujiwara M, Kaneshiro E, Ohashi T, Eto Y, Ishigaki K, Osawa M, Kyosen SO, Ida H. Kobayashi H, et al. Mol Genet Metab. 2010 May;100(1):14-9. doi: 10.1016/j.ymgme.2010.01.015. Epub 2010 Feb 4. Mol Genet Metab. 2010. PMID: 20202878

9

Pathology of the first autopsy case diagnosed as mucolipidosis type III α/β suggesting autophagic dysfunction.

Kobayashi H, Takahashi-Fujigasaki J, Fukuda T, Sakurai K, Shimada Y, Nomura K, Ariga M, Ohashi T, Eto Y, Otomo T, Sakai N, Ida H. Kobayashi H, et al. Mol Genet Metab. 2011 Feb;102(2):170-5. doi: 10.1016/j.ymgme.2010.09.014. Epub 2010 Nov 3. Mol Genet Metab. 2011. PMID: 21051253

10

Oral administration of recombinant human acid α-glucosidase reduces specific antibody formation against enzyme in mouse.

Ohashi T, Iizuka S, Shimada Y, Eto Y, Ida H, Hachimura S, Kobayashi H. Ohashi T, et al. Among authors: kobayashi h. Mol Genet Metab. 2011 May;103(1):98-100. doi: 10.1016/j.ymgme.2011.01.009. Epub 2011 Jan 27. Mol Genet Metab. 2011. PMID: 21320791

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