Tamura H - Search Results

1

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: tamura h. Endocr J. 2013;60(4):403-8. doi: 10.1507/endocrj.ej12-0242. Epub 2012 Nov 30. Endocr J. 2013. PMID: 23197114 Free article.

2

Niemann-Pick type C disease: novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency.

Tamura H, Takahashi T, Ban N, Torisu H, Ninomiya H, Takada G, Inagaki N. Tamura H, et al. Mol Genet Metab. 2006 Feb;87(2):113-21. doi: 10.1016/j.ymgme.2005.07.025. Epub 2005 Sep 6. Mol Genet Metab. 2006. PMID: 16143556

3

Niemann-Pick disease type C: cataplexy and hypocretin in cerebrospinal fluid.

Oyama K, Takahashi T, Shoji Y, Oyamada M, Noguchi A, Tamura H, Takada G, Kanbayashi T. Oyama K, et al. Among authors: tamura h. Tohoku J Exp Med. 2006 Jul;209(3):263-7. doi: 10.1620/tjem.209.263. Tohoku J Exp Med. 2006. PMID: 16778374 Free article.

4

Elevation of Serum Acid Sphingomyelinase Activity in Acute Kawasaki Disease.

Konno Y, Takahashi I, Narita A, Takeda O, Koizumi H, Tamura M, Kikuchi W, Komatsu A, Tamura H, Tsuchida S, Noguchi A, Takahashi T. Konno Y, et al. Among authors: tamura h, tamura m. Tohoku J Exp Med. 2015 Oct;237(2):133-40. doi: 10.1620/tjem.237.133. Tohoku J Exp Med. 2015. PMID: 26447086 Free article.

5

Large intracardiac thrombus in a patient with steroid-responsive nephrotic syndrome.

Tamura H, Oyamada J, Shimada S, Okazaki M, Tsuchida S, Toyono M, Takahashi T. Tamura H, et al. Nephrology (Carlton). 2016 Jan;21(1):72. doi: 10.1111/nep.12553. Nephrology (Carlton). 2016. PMID: 26693847 No abstract available.

6

Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.

Kondo D, Noguchi A, Tamura H, Tsuchida S, Takahashi I, Kubota H, Yano T, Oyama C, Sawaishi Y, Moriwaki S, Takahashi T. Kondo D, et al. Among authors: tamura h. Tohoku J Exp Med. 2016 Jul;239(3):231-5. doi: 10.1620/tjem.239.231. Tohoku J Exp Med. 2016. PMID: 27396511 Free article.

7

A novel S269C mutation in fibroblast growth factor receptor 3 in a Japanese child with hypochondroplasia.

Takahashi I, Kondo D, Oyama C, Yano T, Tamura H, Noguchi A, Takahashi T. Takahashi I, et al. Among authors: tamura h. Hum Genome Var. 2018 Apr 12;5:1. doi: 10.1038/s41439-018-0001-2. eCollection 2018. Hum Genome Var. 2018. PMID: 29736252 Free PMC article.

8

Biopsy-proven acute interstitial nephritis due to fosfomycin in a child.

Tamura H, Noguchi A, Takahashi I, Tsuchida S, Takahashi T. Tamura H, et al. Nephrology (Carlton). 2018 Sep;23(9):890. doi: 10.1111/nep.13197. Nephrology (Carlton). 2018. PMID: 30134505 No abstract available.

9

Central fibroma of the jaw bone: a case report.

Tamura H, Nishijima K, Nagahata S, Takahashi T. Tamura H, et al. Acta Med Okayama. 1983 Jun;37(3):265-7. doi: 10.18926/AMO/32438. Acta Med Okayama. 1983. PMID: 6880834 Free article.

10

Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP).

Nakatani S, Kawano H, Sato M, Hoshino J, Nishio S, Miura K, Sekine A, Suwabe T, Hidaka S, Kataoka H, Ishikawa E, Shimazu K, Uchiyama K, Fujimaru T, Moriyama T, Kurashige M, Shimabukuro W, Hattanda F, Kimura T, Ushio Y, Manabe S, Watanabe H, Mitobe M, Seta K, Shimada Y, Kai H, Katayama K, Ichikawa D, Hayashi H, Hanaoka K, Mochizuki T, Nakanishi K, Tsuchiya K, Horie S, Isaka Y, Muto S; JRP collaborators. Nakatani S, et al. Clin Exp Nephrol. 2024 Oct;28(10):1004-1015. doi: 10.1007/s10157-024-02509-3. Epub 2024 May 11. Clin Exp Nephrol. 2024. PMID: 38734869

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