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The ratio of glycated albumin to hemoglobin A1c measured in IFCC units accurately represents the glycation gap.
Akatsuka J, Mochizuki M, Musha I, Ohtake A, Kobayashi K, Kikuchi T, Kikuchi N, Kawamura T, Urakami T, Sugihara S, Hoshino T, Amemiya S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes. Akatsuka J, et al. Among authors: ohtake a. Endocr J. 2015;62(2):161-72. doi: 10.1507/endocrj.EJ14-0066. Epub 2014 Nov 2. Endocr J. 2015. PMID: 25367400 Free article.
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes.
Okuno M, Ayabe T, Yokota I, Musha I, Shiga K, Kikuchi T, Kikuchi N, Ohtake A, Nakamura A, Nakabayashi K, Okamura K, Momozawa Y, Kubo M, Suzuki J, Urakami T, Kawamura T, Amemiya S, Ogata T, Sugihara S, Fukami M; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes. Okuno M, et al. Among authors: ohtake a. Diabet Med. 2018 Mar;35(3):376-380. doi: 10.1111/dme.13566. Epub 2018 Jan 3. Diabet Med. 2018. PMID: 29247561
Estimation of glycaemic control in the past month using ratio of glycated albumin to HbA1c.
Musha I, Mochizuki M, Kikuchi T, Akatsuka J, Ohtake A, Kobayashi K, Kikuchi N, Kawamura T, Yokota I, Urakami T, Sugihara S, Amemiya S; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes. Musha I, et al. Among authors: ohtake a. Diabet Med. 2018 Jul;35(7):855-861. doi: 10.1111/dme.13640. Epub 2018 May 2. Diabet Med. 2018. PMID: 29653463
[Galactosemia].
Ohtake A, Amemiya S. Ohtake A, et al. Nihon Rinsho. 2006 Sep 28;Suppl 3:215-9. Nihon Rinsho. 2006. PMID: 17022534 Review. Japanese. No abstract available.
Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.
Tajima G, Hara K, Tsumura M, Kagawa R, Okada S, Sakura N, Maruyama S, Noguchi A, Awaya T, Ishige M, Ishige N, Musha I, Ajihara S, Ohtake A, Naito E, Hamada Y, Kono T, Asada T, Sasai H, Fukao T, Fujiki R, Ohara O, Bo R, Yamada K, Kobayashi H, Hasegawa Y, Yamaguchi S, Takayanagi M, Hata I, Shigematsu Y, Kobayashi M. Tajima G, et al. Among authors: ohtake a. Mol Genet Metab. 2017 Nov;122(3):67-75. doi: 10.1016/j.ymgme.2017.07.011. Epub 2017 Jul 31. Mol Genet Metab. 2017. PMID: 28801073
Macroscopic Characteristics of the Native Liver in Children With MPV17-Related Mitochondrial DNA Depletion Syndrome: An Indication for Performing Liver Transplantation?
Kasahara M, Sakamoto S, Fukuda A, Horikawa R, Ito R, Uchida H, Yanagi Y, Shimizu S, Nakao T, Mimori K, Haga C, Schlegel A, Ohtake A, Shimura M, Fushimi T, Ichimoto K, Matsunaga A, Murayama K. Kasahara M, et al. Among authors: ohtake a. Liver Transpl. 2022 Mar;28(3):497-500. doi: 10.1002/lt.26296. Epub 2021 Oct 12. Liver Transpl. 2022. PMID: 34536975 No abstract available.
Need for strict clinical management of patients with carnitine palmitoyltransferase II deficiency: Experience with two cases detected by expanded newborn screening.
Bo R, Musha I, Yamada K, Kobayashi H, Hasegawa Y, Awano H, Arao M, Kikuchi T, Taketani T, Ohtake A, Yamaguchi S, Iijima K. Bo R, et al. Among authors: ohtake a. Mol Genet Metab Rep. 2020 May 27;24:100611. doi: 10.1016/j.ymgmr.2020.100611. eCollection 2020 Sep. Mol Genet Metab Rep. 2020. PMID: 32489884 Free PMC article.
Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: focusing on mitochondrial DNA depletion syndrome.
Yamazaki T, Murayama K, Compton AG, Sugiana C, Harashima H, Amemiya S, Ajima M, Tsuruoka T, Fujinami A, Kawachi E, Kurashige Y, Matsushita K, Wakiguchi H, Mori M, Iwasa H, Okazaki Y, Thorburn DR, Ohtake A. Yamazaki T, et al. Among authors: ohtake a. Pediatr Int. 2014 Apr;56(2):180-7. doi: 10.1111/ped.12249. Epub 2014 Mar 6. Pediatr Int. 2014. PMID: 24266892
271 results