Sasai H - Search Results

1

Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutation.

Lee T, Misaki M, Shimomura H, Tanaka Y, Yoshida S, Murayama K, Nakamura K, Fujiki R, Ohara O, Sasai H, Fukao T, Takeshima Y. Lee T, et al. Among authors: sasai h. Hum Genome Var. 2018 Aug 16;5:22. doi: 10.1038/s41439-018-0022-x. eCollection 2018. Hum Genome Var. 2018. PMID: 30131866 Free PMC article.

2

Diffuse large B-cell lymphoma presenting with osteolytic lesions in the bilateral femur.

Funato M, Kato H, Sasai H, Kubota K, Ozeki M, Kato Z, Kaneko H, Fukao T, Kondo N. Funato M, et al. Among authors: sasai h. Eur J Haematol. 2009 Nov;83(5):502. doi: 10.1111/j.1600-0609.2009.01300.x. Epub 2009 Jun 22. Eur J Haematol. 2009. PMID: 19548918 No abstract available.

3

Translocation (1;10)(p34;p15) in infant acute myeloid leukemia with extramedullary infiltration in multiple sites.

Funato M, Fukao T, Sasai H, Hori T, Terazawa D, Ozeki M, Orii K, Teramoto T, Kaneko H, Kondo N. Funato M, et al. Among authors: sasai h. Cancer Genet Cytogenet. 2009 Jul 15;192(2):86-9. doi: 10.1016/j.cancergencyto.2009.04.010. Cancer Genet Cytogenet. 2009. PMID: 19596261

4

Congenital inner ear malformations without sensorineural hearing loss in children.

Ozeki M, Kato Z, Sasai H, Kubota K, Funato M, Orii K, Kaneko H, Fukao T, Kondo N. Ozeki M, et al. Among authors: sasai h. Int J Pediatr Otorhinolaryngol. 2009 Oct;73(10):1484-7. doi: 10.1016/j.ijporl.2009.07.013. Epub 2009 Aug 19. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19695719 Review.

5

Refractory chronic pleurisy caused by Helicobacter equorum-like bacterium in a patient with X-linked agammaglobulinemia.

Funato M, Kaneko H, Ohkusu K, Sasai H, Kubota K, Ohnishi H, Kato Z, Fukao T, Kondo N. Funato M, et al. Among authors: sasai h. J Clin Microbiol. 2011 Sep;49(9):3432-5. doi: 10.1128/JCM.00478-11. Epub 2011 Jun 15. J Clin Microbiol. 2011. PMID: 21677071 Free PMC article.

6

Successful treatment of pediatric immune thrombocytopenic purpura associated with ulcerative colitis.

Funato M, Fukao T, Sasai H, Hori T, Terazawa D, Kubota K, Ozeki M, Orii K, Kaneko H, Kondo N. Funato M, et al. Among authors: sasai h. Pediatr Int. 2011 Oct;53(5):771-773. doi: 10.1111/j.1442-200X.2010.03308.x. Pediatr Int. 2011. PMID: 21955013 No abstract available.

7

Paclitaxel-based chemotherapy for aggressive kaposiform hemangioendothelioma of the temporomastoid region: Case report and review of the literature.

Funato M, Fukao T, Sasai H, Hori T, Terazawa D, Kanda K, Ozeki M, Mizuta K, Hirose Y, Kaneko H, Kondo N. Funato M, et al. Among authors: sasai h. Head Neck. 2013 Aug;35(8):E258-61. doi: 10.1002/hed.23107. Epub 2012 Aug 21. Head Neck. 2013. PMID: 22907922 Review.

8

Successive MRI Findings of Reversible Cerebral White Matter Lesions in a Patient with Cystathionine β-Synthase Deficiency.

Sasai H, Shimozawa N, Asano T, Kawamoto N, Yamamoto T, Kimura T, Kawamoto M, Matsui E, Fukao T. Sasai H, et al. Tohoku J Exp Med. 2015 Dec;237(4):323-7. doi: 10.1620/tjem.237.323. Tohoku J Exp Med. 2015. PMID: 26639091 Free article.

9

Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) Without Neurological Regression.

Akagawa S, Fukao T, Akagawa Y, Sasai H, Kohdera U, Kino M, Shigematsu Y, Aoyama Y, Kaneko K. Akagawa S, et al. Among authors: sasai h. JIMD Rep. 2017;32:81-85. doi: 10.1007/8904_2016_570. Epub 2016 Jun 16. JIMD Rep. 2017. PMID: 27306202 Free PMC article.

10

Exon 10 skipping in ACAT1 caused by a novel c.949G>A mutation located at an exonic splice enhancer site.

Otsuka H, Sasai H, Nakama M, Aoyama Y, Abdelkreem E, Ohnishi H, Konstantopoulou V, Sass JO, Fukao T. Otsuka H, et al. Among authors: sasai h. Mol Med Rep. 2016 Nov;14(5):4906-4910. doi: 10.3892/mmr.2016.5819. Epub 2016 Oct 10. Mol Med Rep. 2016. PMID: 27748876

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