بدائل البحث:
largest decrease » largest decreases (توسيع البحث), marked decrease (توسيع البحث)
larger decrease » marked decrease (توسيع البحث)
i largest » _ largest (توسيع البحث), i large (توسيع البحث)
i larger » _ larger (توسيع البحث), i large (توسيع البحث), _ large (توسيع البحث)
c cases » ic cases (توسيع البحث), _ cases (توسيع البحث), 3 cases (توسيع البحث)
1 cases » 19 cases (توسيع البحث), 16 cases (توسيع البحث), _ cases (توسيع البحث)
largest decrease » largest decreases (توسيع البحث), marked decrease (توسيع البحث)
larger decrease » marked decrease (توسيع البحث)
i largest » _ largest (توسيع البحث), i large (توسيع البحث)
i larger » _ larger (توسيع البحث), i large (توسيع البحث), _ large (توسيع البحث)
c cases » ic cases (توسيع البحث), _ cases (توسيع البحث), 3 cases (توسيع البحث)
1 cases » 19 cases (توسيع البحث), 16 cases (توسيع البحث), _ cases (توسيع البحث)
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161
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162
Case primary tumour does not decline.
منشور في 2019"…High turnover cases have (<i>β</i><sub>0</sub> = 1.0, <i>δ</i><sub>0</sub> = 0.6) and low turnover cases (<i>β</i><sub>0</sub> = 0.42, <i>δ</i><sub>0</sub> = 0.02), treatment strength Δ = 0.2. …"
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163
Image_1_Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series.JPEG
منشور في 2022"…At the presentation at ages 17 (Case 1) and 18 years (Case 2), both had reduced visual acuity (Snellen): (Case 1) right eye (RE):CF 3m, left eye (LE):0.6, (Case 2) RE:0.2, LE:0.15; and color vision (Ishihara): (Case 1) 1/15 and 13/15; (Case 2) 2/15 and 3/15. …"
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164
Table_1_Case report: Long-term follow-up of two patients with LHON caused by DNAJC30:c.152G>A pathogenic variant-case series.DOCX
منشور في 2022"…At the presentation at ages 17 (Case 1) and 18 years (Case 2), both had reduced visual acuity (Snellen): (Case 1) right eye (RE):CF 3m, left eye (LE):0.6, (Case 2) RE:0.2, LE:0.15; and color vision (Ishihara): (Case 1) 1/15 and 13/15; (Case 2) 2/15 and 3/15. …"
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165
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166
Table1_Case report: A case of new mutation in SERPINC1 leading to thrombotic microangiopathy.DOCX
منشور في 2023"…However, thrombotic microangiopathy (TMA) caused by hereditary antithrombin deficiency is rare.</p><p>Case Presentation: We reported the case of a 32-year-old Chinese female patient with TMA with renal injury caused by decreased antithrombin-III activity due to a new mutation (chr1-173884049 c.50A>G) in SERPINC1, which encodes antithrombin-III. …"
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167
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Human coccidioidomycosis cases from 1995 to 2020 as part of reference diagnostic service.
منشور في 2021الموضوعات: "…human coccidioidomycosis cases…"
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172
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