高ピルビン酸血症
WordNet
- a blood disorder characterized by an increased concentration of hydrogen ions in the blood (which falls below 7 on the pH scale)
UpToDate Contents
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- 1. 有機酸血症 organic acidemias
- 2. 先天性代謝異常：代謝性救急疾患 inborn errors of metabolism metabolic emergencies
- 3. 先天性代謝異常：分類 inborn errors of metabolism classification
- 4. 先天性代謝異常：疫学、病因、および臨床的特徴 inborn errors of metabolism epidemiology pathogenesis and clinical features
- 5. 臍帯血酸塩基分析 umbilical cord blood acid base analysis
English Journal
- [Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)].
- Wendel U, Przyrembel H, Becker K, Walther B, Berger R, Bremer HJ.
- Monatsschrift für Kinderheilkunde.Monatsschr Kinderheilkd.1978 Mar;126(3):140-7.
- The course of pyruvate dehydrogenase deficiency in an infant is described. During pregnancy fetal movements were reduced, and since birth severe neurologic involvement was noticed. Permanent metabolic acidosis due to lactic acidemia as well as hyperpyruvic acidemia and hyperalaninemia were present.
- PMID 417240
- Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria.
- Lonsdale D, Faulkner WR, Price JW, Smeby RR.
- Pediatrics.Pediatrics.1969 Jun;43(6):1025-34.
- PMID 5786203
Related Links
- 1. Pediatrics. 1969 Jun;43(6):1025-34. Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria. Lonsdale D, Faulkner WR, Price JW, Smeby RR. PMID: 5786203 [PubMed - indexed ...
- Publication » Transient Hyperalaninemia and Hyperpyruvic Acidemia. Article Transient Hyperalaninemia and Hyperpyruvic Acidemia Y. Oka I. Matsuda S. Arashima M. Anakura T. Mitsuyama H. Nambu ...
★リンクテーブル★
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- 英
- hyperpyruvic acidemia
- 関
- ピルビン酸デヒドロゲナーゼ