コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ut PS-exposed autophagic vesicles because of asplenia.
2 Q) in a child with both severe 46,XY-DSD and asplenia.
3 7.1 years and 64% had functional or anatomic asplenia.
4 ciency causes organ growth defects including asplenia.
5 eptibility to infection caused by functional asplenia.
6 e molecular determinants of human congenital asplenia.
7 t underlie spleen development and congenital asplenia, a condition linked to increased risk of overwh
9 s, we searched for patients with and without asplenia and community-acquired severe sepsis/septic sho
10 ctive lateralization including dextrocardia, asplenia and intestinal malrotation, suggesting that BCO
13 or C3 deficiencies, 1 of isolated congenital asplenia, and 2 of Bruton disease (X-linked agammaglobul
16 esis and the etiology of isolated congenital asplenia (ICA), a life-threatening human condition, are
18 n proposed in the pathogenesis of congenital asplenia in patients carrying mutations of the gene-enco
22 quently in OPSI patients (42% vs 12% without asplenia; P < .001) and more frequently manifested as bl
24 iary and organ laterality defects as well as asplenia, paralleling symptoms of the human condition ri
25 g chronic mucocutaneous candidiasis, AI, and asplenia, respectively, in 49 of 121 (40%) and 10 of 121
30 by a perinatal lethal skeletal dysplasia and asplenia, with severe malformation or absence of specifi
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。