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References in periodicals archive ?
Dohi, "A multi-factor software reliability model based on logistic regression," in Proceedings of the 2010 IEEE 21st International Symposium on Software Reliability Engineering (ISSRE '10), pp.
(29.) Iwano M, Dohi K, Hirata E, Kurumatani N, Horii Y, Shiiki H, et al.
Dyschromatosis symmetrica hereditaria (DSH), also known as acropigmentation of Dohi, was first described by Toyama in 1910 as an unknown hyperpigmentation disorder of the distal extremities [4].
Dohi et al., "Gender-based outcomes among patients with diabetes mellitus after percutaneous coronary intervention in the drug-eluting stent era," International Heart Journal, vol.
Dohi, "Primary Sjogren's syndrome presenting as hypokalaemic periodic paralysis and respiratory arrest," Clinical Rheumatology, vol.
[17] Okamura Hiroyuki, Tadashi Dohi and Shunji Osaki, "Software reliability growth models with normal failure time distributions," Reliability Engineering & System Safety, vol.
It comprises of a spectrum of diseases which include dyschromatosis universalis hereditaria (DUH) or acropigmentation of Dohi and segmental form called unilateral dermatomal pigmentary dermatosis (UDPD).1,2,3 Dyschromatosis symmetrica hereditaria (DSH) was first reported as a clinical entity by Toyama in 1929.4 It is characterized by symmetrical distribution of hyperpigmented and hypopigmented macules on the extremities more so over the dorsum of hands and feet.
The source noted that "the body of Dohi and the military leaders arrived in to forensic medicine of Mosul.