Kang D - Search Results

1

[Diagnosis and management of early-onset thrombophilia/thrombosis: a review].

Ohga S, Egami N, Ishimura M, Yamamura K, Ochiai M, Kang D. Ohga S, et al. Among authors: kang d. Rinsho Ketsueki. 2020;61(9):1373-1381. doi: 10.11406/rinketsu.61.1373. Rinsho Ketsueki. 2020. PMID: 33162538 Review. Japanese.

2

Protein S and protein C gene mutations in Japanese deep vein thrombosis patients.

Kinoshita S, Iida H, Inoue S, Watanabe K, Kurihara M, Wada Y, Tsuda H, Kang D, Hamasaki N. Kinoshita S, et al. Among authors: kang d. Clin Biochem. 2005 Oct;38(10):908-15. doi: 10.1016/j.clinbiochem.2005.05.006. Clin Biochem. 2005. PMID: 15978566

3

Thromboembolic complications in splenectomized patients with dominantly inherited beta-thalassemia.

Ohga S, Ideguchi H, Kato J, Ishimura M, Takada H, Harada N, Kawanaka H, Hattori Y, Kang D, Hamasaki N, Hara T. Ohga S, et al. Among authors: kang d. Acta Haematol. 2008;120(1):31-5. doi: 10.1159/000151601. Epub 2008 Aug 27. Acta Haematol. 2008. PMID: 18728358 No abstract available.

4

Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy.

Ishimura M, Saito M, Ohga S, Hoshina T, Baba H, Urata M, Kira R, Takada H, Kusuhara K, Kang D, Hara T. Ishimura M, et al. Among authors: kang d. Eur J Pediatr. 2009 Jun;168(6):673-7. doi: 10.1007/s00431-008-0816-9. Epub 2008 Aug 27. Eur J Pediatr. 2009. PMID: 18751723

5

Protein C deficiency as the major cause of thrombophilias in childhood.

Ohga S, Ishiguro A, Takahashi Y, Shima M, Taki M, Kaneko M, Fukushima K, Kang D, Hara T; Japan Childhood Thrombophilia Study Group. Ohga S, et al. Among authors: kang d. Pediatr Int. 2013 Jun;55(3):267-71. doi: 10.1111/ped.12102. Pediatr Int. 2013. PMID: 23521084 Review.

6

Staphylococcal endocarditis as the first manifestation of heritable protein S deficiency in childhood.

Hoshina T, Nakashima Y, Sato D, Nanishi E, Nishio H, Nagata H, Yamamura K, Doi T, Shiokawa Y, Koga Y, Kang D, Ohga S, Hara T. Hoshina T, et al. Among authors: kang d. J Infect Chemother. 2014 Feb;20(2):128-30. doi: 10.1016/j.jiac.2013.08.002. Epub 2013 Dec 11. J Infect Chemother. 2014. PMID: 24462440

7

Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency.

Ichiyama M, Ohga S, Ochiai M, Fukushima K, Ishimura M, Torio M, Urata M, Hotta T, Kang D, Hara T. Ichiyama M, et al. Among authors: kang d. Brain Dev. 2016 Feb;38(2):253-6. doi: 10.1016/j.braindev.2015.07.004. Epub 2015 Aug 4. Brain Dev. 2016. PMID: 26250584

8

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism.

Ichiyama M, Ohga S, Ochiai M, Tanaka K, Matsunaga Y, Kusuda T, Inoue H, Ishimura M, Takimoto T, Koga Y, Hotta T, Kang D, Hara T. Ichiyama M, et al. Among authors: kang d. Pediatr Res. 2016 Jan;79(1-1):81-6. doi: 10.1038/pr.2015.180. Epub 2015 Sep 15. Pediatr Res. 2016. PMID: 26372516

9

Blood Reference Intervals for Preterm Low-Birth-Weight Infants: A Multicenter Cohort Study in Japan.

Ochiai M, Matsushita Y, Inoue H, Kusuda T, Kang D, Ichihara K, Nakashima N, Ihara K, Ohga S, Hara T; Kyushu University High-Risk Neonatal Clinical Research Network, Japan. Ochiai M, et al. Among authors: kang d. PLoS One. 2016 Aug 23;11(8):e0161439. doi: 10.1371/journal.pone.0161439. eCollection 2016. PLoS One. 2016. PMID: 27552225 Free PMC article.

10

The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.

Inoue H, Terachi SI, Uchiumi T, Sato T, Urata M, Ishimura M, Koga Y, Hotta T, Hara T, Kang D, Ohga S. Inoue H, et al. Among authors: kang d. Pediatr Blood Cancer. 2017 Jul;64(7). doi: 10.1002/pbc.26404. Epub 2017 Jan 23. Pediatr Blood Cancer. 2017. PMID: 28111891

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