نتایج جستجو برای: آیة 21
تعداد نتایج: 248346 فیلتر نتایج به سال:
Purpose of developing the guidelines: The first guidelines for diagnosis and treatment of 21-hydroxylase deficiency (21-OHD) were published as a diagnostic handbook in Japan in 1989, with a focus on patients with severe disease. The "Guidelines for Treatment of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Found in Neonatal Mass Screening (1999 revision)" published in 1999 were rev...
We report two Japanese women with androgen excess symptoms. Analyses of 21-hydroxylase gene demonstrated that a 24-year-old Japanese woman had a homozygous mutation of IVS2-13 A/C>G, while a 25-year-old Japanese woman had a compound heterozygous mutation of I172N and E245del1nt, a novel mutation which would result in completely nonfunctional enzyme due to a frame shift. As IVS2-13 A/C>G and I17...
We report Zeeman infra-red spectroscopy of electronic-nuclear levels 5I8 →5I7 transitions Ho3+ in the C4v(F−) centre CaF2 with magnetic field along ⟨111⟩ direction crystal. Transitions to lowest 5I7 state, an isolated electronic doublet, and next group states, a pseudo-quadruplet consisting doublet two nearby singlets, exhibit strongly non-linear splittings intensity variations. Simulated spect...
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