文献
J-GLOBAL ID:201802256445434192
整理番号:18A1155049
脂肪酸酸化欠損が疑われる患者におけるパルミチン酸塩を用いた非侵襲試験:疾患特異的アシルカルニチンパターンは診断を確立することができる【JST・京大機械翻訳】
Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosis
著者 (7件):
Janzen Nils
(Screening Laboratory Hannover, Hannover, Germany)
,
Janzen Nils
(Institute of Clinical Chemistry, Hannover Medical School, Hannover, Germany)
,
Hofmann Alejandro D.
(Center of Pediatric Surgery, Hannover Medical School and Bult Children’s Hospital, Hannover, Germany)
,
Schmidt Gunnar
(Institute of Human Genetics, Hannover Medical School, Hannover, Germany)
,
Das Anibh M.
(Clinic for Pediatric Kidney-, Liver- and Metabolic Diseases, Hannover Medical School, Hannover, Germany)
,
Das Anibh M.
(Centre for Systems Neurosciences at Veterinary School Hannover, Hannover, Germany)
,
Illsinger Sabine
(Clinic for Pediatric Kidney-, Liver- and Metabolic Diseases, Hannover Medical School, Hannover, Germany)
資料名:
Orphanet Journal of Rare Diseases (Web)
(Orphanet Journal of Rare Diseases (Web))
巻:
12
号:
1
ページ:
187
発行年:
2017年
JST資料番号:
U7532A
ISSN:
1750-1172
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)