Hashimoto M - Search Results

1

Congenital central hypoventilation syndrome: a novel mutation of the RET gene in an isolated case.

Kanai M, Numakura C, Sasaki A, Shirahata E, Akaba K, Hashimoto M, Hasegawa H, Shirasawa S, Hayasaka K. Kanai M, et al. Among authors: hashimoto m. Tohoku J Exp Med. 2002 Apr;196(4):241-6. doi: 10.1620/tjem.196.241. Tohoku J Exp Med. 2002. PMID: 12086152 Free article.

2

Molecular analysis of congenital central hypoventilation syndrome.

Sasaki A, Kanai M, Kijima K, Akaba K, Hashimoto M, Hasegawa H, Otaki S, Koizumi T, Kusuda S, Ogawa Y, Tuchiya K, Yamamoto W, Nakamura T, Hayasaka K. Sasaki A, et al. Among authors: hashimoto m. Hum Genet. 2003 Dec;114(1):22-6. doi: 10.1007/s00439-003-1036-z. Epub 2003 Oct 18. Hum Genet. 2003. PMID: 14566559

3

Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese.

Akaba K, Kimura T, Sasaki A, Tanabe S, Ikegami T, Hashimoto M, Umeda H, Yoshida H, Umetsu K, Chiba H, Yuasa I, Hayasaka K. Akaba K, et al. Among authors: hashimoto m. Biochem Mol Biol Int. 1998 Sep;46(1):21-6. doi: 10.1080/15216549800203512. Biochem Mol Biol Int. 1998. PMID: 9784835

4

New form of platyspondylic lethal chondrodysplasia.

Akaba K, Nishimura G, Hashimoto M, Wakabayashi T, Kanasugi H, Hayasaka K. Akaba K, et al. Among authors: hashimoto m. Am J Med Genet. 1996 Dec 30;66(4):464-7. doi: 10.1002/(SICI)1096-8628(19961230)66:4<464::AID-AJMG16>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8989469

5

Diffuse pachygyria with cerebellar hypoplasia: a milder form of microlissencephaly or a new genetic syndrome?

Kato M, Takizawa N, Yamada S, Ito A, Honma T, Hashimoto M, Saito E, Ohta T, Chikaoka H, Hayasaka K. Kato M, et al. Among authors: hashimoto m. Ann Neurol. 1999 Oct;46(4):660-3. doi: 10.1002/1531-8249(199910)46:4<660::aid-ana17>3.0.co;2-q. Ann Neurol. 1999. PMID: 10514106

6

Spondyloepiphyseal dysplasia with accumulation of glycoprotein in the chondrocytes: spondyloepiphyseal dysplasia, Stanescu type.

Nishimura G, Saitoh Y, Okuzumi S, Imaizumi K, Hayasaka K, Hashimoto M. Nishimura G, et al. Among authors: hashimoto m. Skeletal Radiol. 1998 Apr;27(4):188-94. doi: 10.1007/s002560050363. Skeletal Radiol. 1998. PMID: 9592900

7

Spinal arachnoid cyst in a newborn infant.

Hashimoto K, Hashimoto M, Homma S, Ohsone Y, Hasegawa H, Takei J, Kida Y, Takeuchi Y, Ohba M. Hashimoto K, et al. Among authors: hashimoto m. Acta Paediatr Jpn. 1992 Oct;34(5):547-50. doi: 10.1111/j.1442-200x.1992.tb01005.x. Acta Paediatr Jpn. 1992. PMID: 1442029

8

Barriers to and facilitators of point-of-care ultrasound utilization among physicians, nurse practitioners, and nurses in Japan: a comparative study.

Yamada T, Kimura T, Shigetomi K, Shinohara T, Ouchi S, Mabuchi S, Kusama T, Ishida T, Hashimoto M. Yamada T, et al. Among authors: hashimoto m. Ultrasound J. 2025 Jan 10;17(1):1. doi: 10.1186/s13089-025-00399-4. Ultrasound J. 2025. PMID: 39792301

9

Loss of Cpt1a results in elevated glucose-fueled mitochondrial oxidative phosphorylation and defective hematopoietic stem cells.

Li J, Bai J, Pham VT, Hashimoto M, Sezaki M, Shi Q, Jin Q, He C, Armstrong A, Li T, Pan M, Liu S, Luan Y, Zeng H, Andreassen PR, Huang G. Li J, et al. Among authors: hashimoto m. J Clin Invest. 2025 Jan 9:e184069. doi: 10.1172/JCI184069. Online ahead of print. J Clin Invest. 2025. PMID: 39786963 Free article.

10

An early precursor CD8 T cell that adapts to acute or chronic viral infection.

McManus DT, Valanparambil RM, Medina CB, Scharer CD, McGuire DJ, Sobierajska E, Hu Y, Chang DY, Wieland A, Lee J, Nasti TH, Hashimoto M, Ross JL, Prokhnevska N, Cardenas MA, Gill AL, Clark EC, Abadie K, Kumar A, Kaye J, Au-Yeung BB, Kueh HY, Kissick HT, Ahmed R. McManus DT, et al. Among authors: hashimoto m. Nature. 2025 Jan 8. doi: 10.1038/s41586-024-08562-y. Online ahead of print. Nature. 2025. PMID: 39778710

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