Atsuko Noguchi[Author] - Search Results

Year	Number of Results
2002	1
2004	1
2005	1
2006	2
2008	1
2010	2
2012	2
2013	3
2014	4
2015	1
2016	4
2017	9
2018	9
2019	2
2020	4
2021	1
2022	5
2023	5
2024	2

1

Rare diseases presenting with hemophagocytic lymphohistiocytosis.

Kanegane H, Noguchi A, Yamada Y, Yasumi T. Kanegane H, et al. Among authors: noguchi a. Pediatr Int. 2023 Jan-Dec;65(1):e15516. doi: 10.1111/ped.15516. Pediatr Int. 2023. PMID: 36843347 Review.

2

Overview of symptoms and treatment for lysinuric protein intolerance.

Noguchi A, Takahashi T. Noguchi A, et al. J Hum Genet. 2019 Sep;64(9):849-858. doi: 10.1038/s10038-019-0620-6. Epub 2019 Jun 18. J Hum Genet. 2019. PMID: 31213652 Review.

3

Clinical outcome of ulcerative colitis with severe onset in children: a multicenter prospective cohort study.

Nambu R, Arai K, Kudo T, Murakoshi T, Kunisaki R, Mizuochi T, Kato S, Kumagai H, Inoue M, Ishige T, Saito T, Noguchi A, Yodoshi T, Hagiwara SI, Iwata N, Nishimata S, Kakuta F, Tajiri H, Hiejima E, Toita N, Mochizuki T, Shimizu H, Iwama I, Hirano Y, Shimizu T; JPIBD-R. Nambu R, et al. Among authors: noguchi a. J Gastroenterol. 2023 May;58(5):472-480. doi: 10.1007/s00535-023-01972-1. Epub 2023 Mar 8. J Gastroenterol. 2023. PMID: 36884071

4

Barth Syndrome: Different Approaches to Diagnosis.

Imai-Okazaki A, Kishita Y, Kohda M, Yatsuka Y, Hirata T, Mizuno Y, Harashima H, Hirono K, Ichida F, Noguchi A, Yoshida M, Tokorodani C, Nishiuchi R, Takeda A, Nakaya A, Sakata Y, Murayama K, Ohtake A, Okazaki Y. Imai-Okazaki A, et al. Among authors: noguchi a. J Pediatr. 2018 Feb;193:256-260. doi: 10.1016/j.jpeds.2017.09.075. Epub 2017 Dec 15. J Pediatr. 2018. PMID: 29249525

5

Alpha1-antitrypsin deficiency recognized by failure to gain weight in infancy.

Sakano M, Suzuki M, Nakano S, Noguchi A, Shimizu T. Sakano M, et al. Among authors: noguchi a. Pediatr Int. 2022 Jan;64(1):e14874. doi: 10.1111/ped.14874. Pediatr Int. 2022. PMID: 35072963 No abstract available.

6

A child with branchio-oto-renal spectrum disorder carrying an SIX1 variant.

Arai H, Noguchi A, Shina K, Otaka S, Takahashi I, Kosaki K, Takahashi T. Arai H, et al. Among authors: noguchi a. Pediatr Int. 2023 Jan-Dec;65(1):e15638. doi: 10.1111/ped.15638. Pediatr Int. 2023. PMID: 37795857 No abstract available.

7

Identification of small-sized intrachromosomal segments at the ends of INV-DUP-DEL patterns.

Shimojima Yamamoto K, Tamura T, Okamoto N, Nishi E, Noguchi A, Takahashi I, Sawaishi Y, Shimizu M, Kanno H, Minakuchi Y, Toyoda A, Yamamoto T. Shimojima Yamamoto K, et al. Among authors: noguchi a. J Hum Genet. 2023 Nov;68(11):751-757. doi: 10.1038/s10038-023-01181-x. Epub 2023 Jul 10. J Hum Genet. 2023. PMID: 37423943

8

Response to "AAT deficiency: PI*Mpalermo and PI*Siiyama, current diagnosis and future risk".

Suzuki M, Noguchi A, Shimizu T. Suzuki M, et al. Among authors: noguchi a. Pediatr Int. 2022 Jan;64(1):e15306. doi: 10.1111/ped.15306. Pediatr Int. 2022. PMID: 36114160 No abstract available.

9

A Survey of Genetic Counseling for Non-invasive Prenatal Testing Examinees in Akita.

Onodera Y, Miura H, Fujishima A, Notomi R, Noguchi A, Takahashi I, Sato A, Takahashi T, Terada Y. Onodera Y, et al. Among authors: noguchi a. JMA J. 2022 Jul 15;5(3):349-355. doi: 10.31662/jmaj.2022-0030. Epub 2022 Jun 17. JMA J. 2022. PMID: 35992285 Free PMC article.

10

Precocious puberty in a case of Simpson-Golabi-Behmel syndrome with a de novo 240-kb deletion including GPC3.

Watanabe K, Noguchi A, Takahashi I, Yamada M, Suzuki H, Takenouchi T, Kosaki K, Takahashi T. Watanabe K, et al. Among authors: noguchi a. Hum Genome Var. 2022 Jun 9;9(1):23. doi: 10.1038/s41439-022-00196-8. Hum Genome Var. 2022. PMID: 35680838 Free PMC article.

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