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22,470 results

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Page 1
Genetic heterogeneity in 26 infants with a hypomyelinating leukodystrophy.
Arai-Ichinoi N, Uematsu M, Sato R, Suzuki T, Kudo H, Kikuchi A, Hino-Fukuyo N, Matsumoto M, Igarashi K, Haginoya K, Kure S. Arai-Ichinoi N, et al. Among authors: suzuki t. Hum Genet. 2016 Jan;135(1):89-98. doi: 10.1007/s00439-015-1617-7. Epub 2015 Nov 23. Hum Genet. 2016. PMID: 26597493
Panax ginseng: a newly identified cause of gynecomastia.
Kakisaka Y, Ohara T, Tozawa H, Sato S, Katayama S, Suzuki T, Hino-Fukuyo N, Kure S. Kakisaka Y, et al. Among authors: suzuki t. Tohoku J Exp Med. 2012 Oct;228(2):143-5. doi: 10.1620/tjem.228.143. Tohoku J Exp Med. 2012. PMID: 23006978 Free article.
Lower back pain as a symptom of migrainous corpalgia.
Kakisaka Y, Ohara T, Katayama S, Suzuki T, Hino-Fukuyo N, Uematsu M, Kure S. Kakisaka Y, et al. Among authors: suzuki t. J Child Neurol. 2013 May;28(5):676-7. doi: 10.1177/0883073813478170. Epub 2013 Feb 26. J Child Neurol. 2013. PMID: 23446803
A case series of CAEBV of children and young adults treated with reduced-intensity conditioning and allogeneic bone marrow transplantation: a single-center study.
Watanabe Y, Sasahara Y, Satoh M, Looi CY, Katayama S, Suzuki T, Suzuki N, Ouchi M, Horino S, Moriya K, Nanjyo Y, Onuma M, Kitazawa H, Irie M, Niizuma H, Uchiyama T, Rikiishi T, Kumaki S, Minegishi M, Wada T, Yachie A, Tsuchiya S, Kure S. Watanabe Y, et al. Among authors: suzuki n, suzuki t. Eur J Haematol. 2013 Sep;91(3):242-248. doi: 10.1111/ejh.12151. Epub 2013 Jun 28. Eur J Haematol. 2013. PMID: 23734904
Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome.
Hino-Fukuyo N, Kikuchi A, Arai-Ichinoi N, Niihori T, Sato R, Suzuki T, Kudo H, Sato Y, Nakayama T, Kakisaka Y, Kubota Y, Kobayashi T, Funayama R, Nakayama K, Uematsu M, Aoki Y, Haginoya K, Kure S. Hino-Fukuyo N, et al. Among authors: suzuki t. Hum Genet. 2015 Jun;134(6):649-58. doi: 10.1007/s00439-015-1553-6. Epub 2015 Apr 16. Hum Genet. 2015. PMID: 25877686 Clinical Trial.
Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation.
Hino-Fukuyo N, Kikuchi A, Iwasaki M, Sato Y, Kubota Y, Kobayashi T, Nakayama T, Haginoya K, Arai-Ichinoi N, Niihori T, Sato R, Suzuki T, Kudo H, Funayama R, Nakayama K, Aoki Y, Kure S. Hino-Fukuyo N, et al. Among authors: suzuki t. Brain Dev. 2017 Apr;39(4):337-340. doi: 10.1016/j.braindev.2016.11.006. Brain Dev. 2017. PMID: 27916450
Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early-onset Refractory Diarrhea.
Uchida T, Suzuki T, Kikuchi A, Kakuta F, Ishige T, Nakayama Y, Kanegane H, Etani Y, Mizuochi T, Fujiwara SI, Nambu R, Suyama K, Tanaka M, Yoden A, Abukawa D, Sasahara Y, Kure S. Uchida T, et al. Among authors: suzuki t. J Pediatr Gastroenterol Nutr. 2020 Sep;71(3):333-339. doi: 10.1097/MPG.0000000000002796. J Pediatr Gastroenterol Nutr. 2020. PMID: 32487952
22,470 results
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