| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 10834043 | 1065852 | 2005 | 5 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Tetrahydrobiopterin-responsive phenylketonuria: The New South Wales experience
												
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																																												کلمات کلیدی
												
											موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													 زیست شیمی
												
											پیش نمایش صفحه اول مقاله
												
												چکیده انگلیسی
												Recent studies have shown that a subgroup of phenylketonuric patients respond to high doses of BH4 (20 mg/kg) by a decrease of plasma phenylalanine. A clinically significant response has been defined as a decrease in phenylalanine by more than 30% within 24 h, after a BH4 challenge. We report our experience with 37 patients diagnosed with hyperphenylalaninemia, mild, moderate, or classical Phenylketonuria (PKU) using a seven day combined BH4 and phenylalanine load. Nine of the 37 patients responded with a 30% decrease in their phenylalanine levels in the first 8 h of treatment. A total of 17 patients (46%) had a decrease of at least 30% during the study period. This study confirms that a significant number of patients with mild to moderate PKU will respond to a BH4 load. Furthermore, it confirms that the seven-day phenylalanine test is more sensitive in detecting BH4 responsive patients.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Genetics and Metabolism - Volume 86, Supplement, December 2005, Pages 81-85
											Journal: Molecular Genetics and Metabolism - Volume 86, Supplement, December 2005, Pages 81-85
نویسندگان
												John J. Mitchell, Bridget Wilcken, Ian Alexander, Carolyn Ellaway, Helen O'Grady, Veronica Wiley, John Earl, John Christodoulou,