## Abstract Individuals with maple syrup urine disease (MSUD) have an inherited metabolic disorder resulting in a deficiency in the branched‐chain keto‐acid dehydrogenase complex. As a result, these individuals have elevated concentrations of the branched‐chain amino acids valine, isoluecine, allo‐
✦ LIBER ✦
Measurement of urinary CDH and CTH by tandem mass spectrometry in patients hemizygous and heterozygous for Fabry disease
✍ Scribed by K. Mills; P. Morris; P. Lee; A. Vellodi; S. Waldek; E. Young; B. Winchester
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 216 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0141-8955
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Quantification of branched-chain amino a
✍
John Sowell; Laura Pollard; Tim Wood
📂
Article
📅
2011
🏛
John Wiley and Sons
🌐
English
⚖ 365 KB
👁 1 views
In situ derivatization–liquid liquid ext
✍
Jana Cimlová; Pavla Kružberská; Zdeněk Švagera; Petr Hušek; Petr Šimek
📂
Article
📅
2012
🏛
John Wiley and Sons
🌐
English
⚖ 1005 KB
Polar analytes that possess protic functional groups have often been treated with alkyl chloroformates to decrease their polarity and increase their volatility prior to gas chromatography-mass spectrometry analysis. This derivatization reaction has two distinct advantages. It proceeds smoothly in aq
Stir-bar-sorptive extraction, with in-si
✍
Migaku Kawaguchi; Rie Ito; Norihiro Sakui; Noriya Okanouchi; Koichi Saito; Yasuo
📂
Article
📅
2007
🏛
Springer
🌐
English
⚖ 226 KB