بدائل البحث:
significant challenges » significant challenge (توسيع البحث), significant changes (توسيع البحث)
challenges decrease » challenges case (توسيع البحث)
greater decrease » greatest decrease (توسيع البحث), greater increase (توسيع البحث), greater disease (توسيع البحث)
we decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), nn decrease (توسيع البحث)
significant challenges » significant challenge (توسيع البحث), significant changes (توسيع البحث)
challenges decrease » challenges case (توسيع البحث)
greater decrease » greatest decrease (توسيع البحث), greater increase (توسيع البحث), greater disease (توسيع البحث)
we decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), nn decrease (توسيع البحث)
-
141
App user onboarding trends.
منشور في 2025"…<div><p>Background</p><p>Skin-related neglected tropical diseases (sNTDs) remain a significant public health challenge in Cameroon, where limited resources, training, and infrastructure hinder early diagnosis and management. …"
-
142
App user base growth trends.
منشور في 2025"…<div><p>Background</p><p>Skin-related neglected tropical diseases (sNTDs) remain a significant public health challenge in Cameroon, where limited resources, training, and infrastructure hinder early diagnosis and management. …"
-
143
Table 1_Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.docx
منشور في 2025"…</p>Objective<p>This study aims to elucidate the clinical implications of concurrent AICDA and IKBKB homozygous variants in a pediatric patient diagnosed with hyper-IgM syndrome.</p>Methods<p>We present immunological and genetic analysis of a Tunisian patient with two homozygous variants of uncertain significance (VUSs) in the IKBKB and AICDA genes, suspected of causing hyper-IgM and immune deficiency. …"
-
144
-
145
-
146
-
147
-
148
-
149
-
150
-
151
Data Sheet 1_Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.pdf
منشور في 2025"…</p>Objective<p>This study aims to elucidate the clinical implications of concurrent AICDA and IKBKB homozygous variants in a pediatric patient diagnosed with hyper-IgM syndrome.</p>Methods<p>We present immunological and genetic analysis of a Tunisian patient with two homozygous variants of uncertain significance (VUSs) in the IKBKB and AICDA genes, suspected of causing hyper-IgM and immune deficiency. …"
-
152
-
153
-
154
-
155
-
156
-
157
-
158
-
159
-
160