Ozono K - Search Results

1

Progeroid syndrome patients with ZMPSTE24 deficiency could benefit when treated with rapamycin and dimethylsulfoxide.

Akinci B, Sankella S, Gilpin C, Ozono K, Garg A, Agarwal AK. Akinci B, et al. Among authors: ozono k. Cold Spring Harb Mol Case Stud. 2017 Jan;3(1):a001339. doi: 10.1101/mcs.a001339. Cold Spring Harb Mol Case Stud. 2017. PMID: 28050601 Free PMC article.

2

Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings.

Miyoshi Y, Akagi M, Agarwal AK, Namba N, Kato-Nishimura K, Mohri I, Yamagata M, Nakajima S, Mushiake S, Shima M, Auchus RJ, Taniike M, Garg A, Ozono K. Miyoshi Y, et al. Among authors: ozono k. Clin Genet. 2008 Jun;73(6):535-44. doi: 10.1111/j.1399-0004.2008.00992.x. Epub 2008 Apr 22. Clin Genet. 2008. PMID: 18435794 Free PMC article.

3

SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome.

Hashimoto N, Kagitani-Shimono K, Sakai N, Otomo T, Tominaga K, Nabatame S, Mogami Y, Takahashi Y, Imai K, Yanagihara K, Okinaga T, Nagai T, Taniike M, Ozono K. Hashimoto N, et al. Among authors: ozono k. J Hum Genet. 2011 Dec;56(12):846-51. doi: 10.1038/jhg.2011.115. Epub 2011 Oct 20. J Hum Genet. 2011. PMID: 22011817

4

Antifungal prophylaxis with micafungin in patients treated for childhood cancer.

Kusuki S, Hashii Y, Yoshida H, Takizawa S, Sato E, Tokimasa S, Ohta H, Ozono K. Kusuki S, et al. Among authors: ozono k. Pediatr Blood Cancer. 2009 Oct;53(4):605-9. doi: 10.1002/pbc.22140. Pediatr Blood Cancer. 2009. PMID: 19533659

5

Long-term developmental outcome in patients with West syndrome after epilepsy surgery.

Iwatani Y, Kagitani-Shimono K, Tominaga K, Okinaga T, Mohri I, Kishima H, Kato A, Sanefuji W, Yamamoto T, Tatsumi A, Murata E, Taniike M, Nagai T, Ozono K. Iwatani Y, et al. Among authors: ozono k. Brain Dev. 2012 Oct;34(9):731-8. doi: 10.1016/j.braindev.2012.01.008. Epub 2012 Feb 14. Brain Dev. 2012. PMID: 22336751

6

Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.

Miura K, Kim OH, Lee HR, Namba N, Michigami T, Yoo WJ, Choi IH, Ozono K, Cho TJ. Miura K, et al. Among authors: ozono k. Am J Med Genet A. 2014 Jan;164A(1):156-63. doi: 10.1002/ajmg.a.36218. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259409

7

Elimination of protein aggregates prevents premature senescence in human trisomy 21 fibroblasts.

Nawa N, Hirata K, Kawatani K, Nambara T, Omori S, Banno K, Kokubu C, Takeda J, Nishimura K, Ohtaka M, Nakanishi M, Okuzaki D, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K. Nawa N, et al. Among authors: ozono k. PLoS One. 2019 Jul 29;14(7):e0219592. doi: 10.1371/journal.pone.0219592. eCollection 2019. PLoS One. 2019. PMID: 31356639 Free PMC article.

8

Hepatitis C virus infection and interferon therapy in patients with Down syndrome.

Miyoshi Y, Tajiri H, Okaniwa M, Terasawa S, Fujisawa T, Iizuka T, Ozono K. Miyoshi Y, et al. Among authors: ozono k. Pediatr Int. 2008 Feb;50(1):7-11. doi: 10.1111/j.1442-200X.2007.02515.x. Pediatr Int. 2008. PMID: 18279197

9

Effect of single oral phosphate loading on vitamin D metabolites in normal subjects and in X-linked hypophosphatemic rickets.

Yamaoka K, Tanaka H, Kurose H, Shima M, Ozono K, Nakajima S, Seino Y. Yamaoka K, et al. Among authors: ozono k. Bone Miner. 1989 Sep;7(2):159-69. doi: 10.1016/0169-6009(89)90073-1. Bone Miner. 1989. PMID: 2804451

10

Hypercalcemia associated with infantile fibrosarcoma producing parathyroid hormone-related protein.

Michigami T, Yamato H, Mushiake S, Nakayama M, Yoneda A, Satomura K, Imura K, Ozono K. Michigami T, et al. Among authors: ozono k. J Clin Endocrinol Metab. 1996 Mar;81(3):1090-5. doi: 10.1210/jcem.81.3.8772581. J Clin Endocrinol Metab. 1996. PMID: 8772581

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