Takahashi T - Search Results

1

Genetic Ablation of Pyruvate Dehydrogenase Kinase Isoform 4 Gene Enhances Recovery from Hyperoxic Lung Injury: Insights into Antioxidant and Inflammatory Mechanisms.

Watanabe K, Kato A, Adachi H, Noguchi A, Arai H, Ito M, Namba F, Takahashi T. Watanabe K, et al. Among authors: takahashi t. Biomedicines. 2024 Mar 27;12(4):746. doi: 10.3390/biomedicines12040746. Biomedicines. 2024. PMID: 38672101 Free PMC article.

2

Low level of tracheal cellular fibronectin in extremely premature infants with funisitis: relationship with respiratory distress 1 month after birth.

Arai H, Ito T, Adachi H, Goto R, Takahashi T. Arai H, et al. Among authors: takahashi t. Pediatr Pulmonol. 2014 Sep;49(9):905-10. doi: 10.1002/ppul.22910. Epub 2013 Oct 24. Pediatr Pulmonol. 2014. PMID: 24155097

3

Neonatal transient eosinophilic colitis with single bubble sign.

Ota S, Adachi H, Noguchi A, Arai H, Takahashi T. Ota S, et al. Among authors: takahashi t. Pediatr Int. 2018 Dec;60(12):1092-1093. doi: 10.1111/ped.13713. Pediatr Int. 2018. PMID: 30585403 No abstract available.

4

Overview of symptoms and treatment for lysinuric protein intolerance.

Noguchi A, Takahashi T. Noguchi A, et al. Among authors: takahashi t. J Hum Genet. 2019 Sep;64(9):849-858. doi: 10.1038/s10038-019-0620-6. Epub 2019 Jun 18. J Hum Genet. 2019. PMID: 31213652 Review.

5

A Japanese Patient with Genitopatellar Syndrome Transiently Presenting with Cardiac Intramural Cavity during the Neonatal Period.

Takahashi K, Adachi H, Toyono M, Ito M, Kato A, Noguchi A, Takahashi T. Takahashi K, et al. Among authors: takahashi t. Case Rep Genet. 2020 Aug 29;2020:1731720. doi: 10.1155/2020/1731720. eCollection 2020. Case Rep Genet. 2020. PMID: 32908725 Free PMC article.

6

Detection of Pathologic Heart Murmurs Using a Piezoelectric Sensor.

Takahashi K, Ono K, Arai H, Adachi H, Ito M, Kato A, Takahashi T. Takahashi K, et al. Among authors: takahashi t. Sensors (Basel). 2021 Feb 16;21(4):1376. doi: 10.3390/s21041376. Sensors (Basel). 2021. PMID: 33669261 Free PMC article.

7

An Early-Onset Neuronopathic Form of Acid Sphingomyelinase Deficiency: A SMPD1 p.C133Y Mutation in the Saposin Domain of Acid Sphingomyelinase.

Ota S, Noguchi A, Kondo D, Nakajima Y, Ito T, Arai H, Takahashi T. Ota S, et al. Among authors: takahashi t. Tohoku J Exp Med. 2020 Jan;250(1):5-11. doi: 10.1620/tjem.250.5. Tohoku J Exp Med. 2020. PMID: 31941852 Free article.

8

Bronchoalveolar lavage fluid in an infant with perinatal lethal Gaucher disease.

Adachi H, Noguchi A, Ota S, Takahashi T, Nanjo H. Adachi H, et al. Among authors: takahashi t. Pediatr Int. 2017 May;59(5):636-637. doi: 10.1111/ped.13247. Epub 2017 Apr 12. Pediatr Int. 2017. PMID: 28402003 No abstract available.

9

Monochorionic diamniotic twins without twin-twin transfusion syndrome: Severe brain damage in the larger infant.

Arai H, Sawaishi Y, Kato A, Ito T, Takahashi T. Arai H, et al. Among authors: takahashi t. Pediatr Int. 2019 Sep;61(9):924-925. doi: 10.1111/ped.13926. Epub 2019 Sep 11. Pediatr Int. 2019. PMID: 31512301 No abstract available.

10

Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome.

Adachi H, Takahashi I, Higashimoto K, Tsuchida S, Noguchi A, Tamura H, Arai H, Ito T, Masue M, Nishibori H, Takahashi T, Soejima H. Adachi H, et al. Among authors: takahashi i, takahashi t. Endocr J. 2013;60(4):403-8. doi: 10.1507/endocrj.ej12-0242. Epub 2012 Nov 30. Endocr J. 2013. PMID: 23197114 Free article.

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