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15篇 您的检索式：作者名="Strauss AW"

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		题名	作者	年代	出处	被引量
	1	Inherited cardiomyopathies 显示文摘	Kelly DP Strauss AW	1994	N Engl J Med1994，330，13：	1
	2	Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase defi- ciency 显示文摘	Yoon HR Strauss AW Yoo HW	2001	J Inherit Metab Dis2001，24，3：	1
	3	Inborn errors of mitochondrial fatty acid oxidation显示文摘	Bennett MJ Rinaldo P Strauss AW	2000	Crit Rev Clin Lab Sci2000，37，：	1
	4	Developmental expression of sarcomeric ubiquitous mitochondrial creatine kinase is tissue-specific显示文摘	Payne RM Strauss AW	1994	Biochem Biophys Acta1994，1219，1：	1
	5	Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screen- ing on their diagnosis and management 显示文摘	Shekhawat PS Matern D Strauss AW	2005	Pediatr Res2005，57，：	1
	6	Inherited cardiomyopathies显示文摘	Kelly DP Strauss AW	1994	N Engl J Med1994，330，13：	1
	7	Tandem mass spectrometric analysis for amino,organic,and fatty acid disorders in newborn dried blood spots:a two-year summary from the New England Newborn Screening Program显示文摘	Zytkovicz TH Fitzgerald EF Marsden D Larson CA Shih VE Johnson DM Strauss AW Comeau AM Eaton RB Grady GF	2001	Clin Chem2001，47，：	1
	8	Early detection of myocardial infarction in conscious dogs by analysis of plasma MM creatin kinase isoforms显示文摘	Hashimoto H Abendschein DR Strauss AW	1985	Circulation1985，7，2：	1
	9	Inherited cardiomyopathies显示文摘	Strauss AW	1993	N Engl J Med1993，330，4：	1
	10	Fetal fatty acid oxida- tion disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management显示文摘	Shekhawat PS Matern D Strauss AW	2005	Pediatr Res2005，57，52：	1
	11	Inborn errors of mitochondrial fatty acid oxidation显示文摘	Bennett MJ Rinaldo P Strauss AW	2000	Crit Rev Clin Lab Sci2000，37，：	1
	12	Diagnosis of mitochondrial trifunctional protein deficiency in blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis显示文摘	Matern D Strauss AW Hillman SL	1999	Pediatr Res1999，46，：	1
	13	Inherited long-chain 3-hydroxyacyl-loA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications显示文摘	Strauss AW Bennett MJ Rinaldo P	1999	Semin Perinatol1999，23，：	1
	14	Inheritd long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease ang other pregnancy complications显示文摘	Strauss AW	1999	Semin Perinatol1999，23，：	1
	15	Safety of a new micronized formulation of isotretinoin in patients with severe recalcitrant nodular acne: A randomized trial comparing micronized isotretinoin with standard isotretinoin 显示文摘	Strauss JS Leyden JJ Lucky AW	2001	J Am Acad dermatol2001，45，：	1

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