Kugo M - Search Results

1

Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation.

Ogino W, Takeshima Y, Nishiyama A, Okizuka Y, Yagi M, Tsuneishi S, Saiki K, Kugo M, Matsuo M. Ogino W, et al. Among authors: kugo m. Kobe J Med Sci. 2007;53(5):229-40. Kobe J Med Sci. 2007. PMID: 18204299 Free article.

2

[A case of perinatal cytomegalovirus infection with severe progressive brain atrophy].

Nabetani M, Tsuneishi S, Kugo M, Konishi H, Yamazaki T. Nabetani M, et al. Among authors: kugo m. No To Hattatsu. 1993 Jan;25(1):76-80. No To Hattatsu. 1993. PMID: 8380111 Japanese.

3

Severe neonatal nemaline myopathy with delayed maturation of muscle.

Wada H, Nishio H, Kugo M, Waku S, Ikeda K, Takada S, Murakami R, Itoh H, Matsuo M, Nakamura H. Wada H, et al. Among authors: kugo m. Brain Dev. 1996 Mar-Apr;18(2):135-8. doi: 10.1016/0387-7604(95)00131-x. Brain Dev. 1996. PMID: 8733906

4

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.

Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M. Nozu K, et al. Among authors: kugo m. J Clin Endocrinol Metab. 2010 Dec;95(12):E511-8. doi: 10.1210/jc.2010-0392. Epub 2010 Sep 1. J Clin Endocrinol Metab. 2010. PMID: 20810575

5

Culture-proven neonatal sepsis in Japanese neonatal care units in 2006-2008.

Morioka I, Morikawa S, Miwa A, Minami H, Yoshii K, Kugo M, Kitsunezuka Y, Enomoto M, Jikimoto T, Nakamura M, Yokoyama N, Nishio H, Matsuo M, Yamada H. Morioka I, et al. Among authors: kugo m. Neonatology. 2012;102(1):75-80. doi: 10.1159/000337833. Epub 2012 May 16. Neonatology. 2012. PMID: 22614023

6

A Case of an Extremely Preterm Infant with Intussusception Triggered by Acquired Cytomegalovirus Infection.

Naito S, Fukushima S, Ioroi T, Sakata C, Kurokawa D, Egawa T, Tsuruno Y, Okamoto M, Fukuzawa H, Kugo M. Naito S, et al. Among authors: kugo m. Kobe J Med Sci. 2024 Jun 12;70(2):E66-E69. doi: 10.24546/0100489974. Kobe J Med Sci. 2024. PMID: 38936880 Free PMC article.

7

Comprehensive stratum corneum ceramide profiling reveals reduced acylceramides in ichthyosis patient with CERS3 mutations.

Yamamoto M, Sassa T, Kyono Y, Uemura H, Kugo M, Hayashi H, Imai Y, Yamanishi K, Kihara A. Yamamoto M, et al. Among authors: kugo m. J Dermatol. 2021 Apr;48(4):447-456. doi: 10.1111/1346-8138.15725. Epub 2021 Jan 25. J Dermatol. 2021. PMID: 33492757 Free article.

8

Superoxide dismutase in polymorphonuclear leukocytes of term newborn infants and very low birth weight infants.

Kugo M, Sano K, Uetani Y, Nakamura H. Kugo M, et al. Pediatr Res. 1989 Sep;26(3):227-31. doi: 10.1203/00006450-198909000-00014. Pediatr Res. 1989. PMID: 2587125

9

Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics.

Horinouchi T, Nozu K, Hamahira K, Inaguma Y, Abe J, Nakajima H, Kugo M, Iijima K. Horinouchi T, et al. Among authors: kugo m. BMC Pediatr. 2015 Nov 11;15:177. doi: 10.1186/s12887-015-0497-2. BMC Pediatr. 2015. PMID: 26561332 Free PMC article. Clinical Trial.

10

Combination of furosemide and fludrocortisone as a loading test for diagnosis of distal renal tubular acidosis in a pediatric case.

Kyono Y, Nozu K, Nakagawa T, Takami Y, Fujita H, Ioroi T, Kugo M, Iijima K, Kamiyoshi N. Kyono Y, et al. Among authors: kugo m. CEN Case Rep. 2020 Feb;9(1):81-86. doi: 10.1007/s13730-019-00432-1. Epub 2019 Nov 8. CEN Case Rep. 2020. PMID: 31705302 Free PMC article.

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