戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 uding fructose intolerance, xanthinuria, and carnitine deficiency.
2 ave been identified as the cause for primary carnitine deficiency.
3 ransporter OCTN2 are responsible for primary carnitine deficiency.
4 carnitine treatment is effective in systemic carnitine deficiency.
5 leads to renal carnitine wasting and primary carnitine deficiency.
6 tam antibiotic, in humans is associated with carnitine deficiency.
7  clinical relevance to patients with primary carnitine deficiency because whereas each and every muta
8  test the causative role of OCTN2 in primary carnitine deficiency by searching for mutations in this
9         Here we report two new patients with carnitine deficiency caused by mutations affecting tyros
10                                    Myopathic carnitine deficiency could be due to an increase in effl
11 452K) identified in one patient with primary carnitine deficiency did not affect membrane targeting,
12                                      Primary carnitine deficiency is a disorder of fatty acid oxidati
13                                      Primary carnitine deficiency is an autosomal recessive disorder
14                                      Primary carnitine deficiency is an autosomal recessive disorder
15 A potential mechanism for the development of carnitine deficiency is competition between cephaloridin
16 cephaloridine and that cephaloridine-induced carnitine deficiency is likely to be due to inhibition o
17       Fibroblasts from patients with primary carnitine deficiency lacked mediated carnitine transport
18 ic Acid-1 and - 3; p = 0.056 and p = 0.014), carnitine deficiency (p = 0.002) and alanine abundancy (
19 cyl-CoA dehydrogenase deficiency and primary carnitine deficiency, respectively.
20                                     Systemic carnitine deficiency (SCD) is a rare autosomal recessive
21  and substrate oxidation in conjunction with carnitine deficiency were investigated in experimental r
22                                    Secondary carnitine deficiency, which is frequently observed in he