Noguchi A - Search Results

1

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.

2

Successful engraftment and decrease of cytomegalovirus load after cord blood stem cell transplantation in a patient with DiGeorge syndrome.

Ohtsuka Y, Shimizu T, Nishizawa K, Ohtaki R, Someya T, Noguchi A, Shimura N, Kim H, Sugimoto H, Fujita H, Morio T, Yamashiro Y. Ohtsuka Y, et al. Among authors: noguchi a. Eur J Pediatr. 2004 Dec;163(12):747-8. doi: 10.1007/s00431-004-1524-8. Eur J Pediatr. 2004. PMID: 15365824 No abstract available.

3

Novel mutation in the TMPRSS6 gene with iron-refractory iron deficiency anemia.

Kodama K, Noguchi A, Adachi H, Hebiguchi M, Yano M, Takahashi T. Kodama K, et al. Among authors: noguchi a. Pediatr Int. 2014 Aug;56(4):e41-4. doi: 10.1111/ped.12395. Pediatr Int. 2014. PMID: 25252070

4

Clinical and genetic features of lysinuric protein intolerance in Japan.

Noguchi A, Nakamura K, Murayama K, Yamamoto S, Komatsu H, Kizu R, Takayanagi M, Okuyama T, Endo F, Takasago Y, Shoji Y, Takahashi T. Noguchi A, et al. Pediatr Int. 2016 Oct;58(10):979-983. doi: 10.1111/ped.12946. Epub 2016 Jun 8. Pediatr Int. 2016. PMID: 26865117

5

Bronchoalveolar lavage fluid in an infant with perinatal lethal Gaucher disease.

Adachi H, Noguchi A, Ota S, Takahashi T, Nanjo H. Adachi H, et al. Among authors: noguchi a. Pediatr Int. 2017 May;59(5):636-637. doi: 10.1111/ped.13247. Epub 2017 Apr 12. Pediatr Int. 2017. PMID: 28402003 No abstract available.

6

Phenotypic characteristics of pediatric inflammatory bowel disease in Japan: results from a multicenter registry.

Arai K, Kunisaki R, Kakuta F, Hagiwara SI, Murakoshi T, Yanagi T, Shimizu T, Kato S, Ishige T, Aomatsu T, Inoue M, Saito T, Iwama I, Kawashima H, Kumagai H, Tajiri H, Iwata N, Mochizuki T, Noguchi A, Kashiwabara T, Shimizu H, Suzuki Y, Hirano Y, Fujiwara T. Arai K, et al. Among authors: noguchi a. Intest Res. 2020 Oct;18(4):412-420. doi: 10.5217/ir.2019.00130. Epub 2020 Aug 18. Intest Res. 2020. PMID: 32806870 Free PMC article.

7

Early detection of Niemann-pick disease type C with cataplexy and orexin levels: continuous observation with and without Miglustat.

Imanishi A, Kawazoe T, Hamada Y, Kumagai T, Tsutsui K, Sakai N, Eto K, Noguchi A, Shimizu T, Takahashi T, Han G, Mishima K, Kanbayashi T, Kondo H. Imanishi A, et al. Among authors: noguchi a. Orphanet J Rare Dis. 2020 Sep 29;15(1):269. doi: 10.1186/s13023-020-01531-4. Orphanet J Rare Dis. 2020. PMID: 32993765 Free PMC article.

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

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

10

Neonatal transient eosinophilic colitis with single bubble sign.

Ota S, Adachi H, Noguchi A, Arai H, Takahashi T. Ota S, et al. Among authors: noguchi a. Pediatr Int. 2018 Dec;60(12):1092-1093. doi: 10.1111/ped.13713. Pediatr Int. 2018. PMID: 30585403 No abstract available.

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