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Page 1
A novel PHKA2 variant in a Japanese boy with glycogen storage diseases type IXa.
Pediatr Int. 2022 Jan;64(1):e14839. doi: 10.1111/ped.14839. Epub 2021 Nov 27.
Pediatr Int. 2022.
PMID: 34837663
No abstract available.
Early Detection and Diagnosis of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency Missed by Newborn Screening Using Tandem Mass Spectrometry.
Shigetomi H, Tanaka T, Nagao M, Tsutsumi H.
Shigetomi H, et al.
Int J Neonatal Screen. 2018 Jan 16;4(1):5. doi: 10.3390/ijns4010005. eCollection 2018 Mar.
Int J Neonatal Screen. 2018.
PMID: 33072931
Free PMC article.
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Abnormal spermatogenesis in mice unable to synthesize ascorbic acid.
Yazama F, Furuta K, Fujimoto M, Sonoda T, Shigetomi H, Horiuchi T, Yamada M, Nagao N, Maeda N.
Yazama F, et al. Among authors: shigetomi h.
Anat Sci Int. 2006 Jun;81(2):115-25. doi: 10.1111/j.1447-073X.2006.00139.x.
Anat Sci Int. 2006.
PMID: 16800296
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[A case of acute lymphotic leukemia which was difficult to make a diagnosis of CRMO for moving arthralgia and periarticular swelling].
Kizawa T, Katou S, Shigetomi H, Tanaka T, Iida K, Nagai K, Igarashi K, Yamamoto M, Hatakeyama N, Suzuki N, Tsutsumi H.
Kizawa T, et al. Among authors: shigetomi h.
Nihon Rinsho Meneki Gakkai Kaishi. 2012;35(2):150-5. doi: 10.2177/jsci.35.150.
Nihon Rinsho Meneki Gakkai Kaishi. 2012.
PMID: 22576573
Free article.
Japanese.
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