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107篇 您的检索式：作者名="WILCKEN B"

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	题名	作者	年代	出处	被引量
1	The pathogenesis of coronary disease.A possible role for methionine metabolism显示文摘	Wilcken DE Wilcken B		0，，：	2
2	Clinical approach to inborn errors of metagolism presenting in the newborn period显示文摘	Ellaway CJ Wilcken B Christodoulou J	2002	J Paediatr Child Health2002，38，5：	1
3	The natural history of vascular disease in homocystinuria and the effects of treatment显示文摘	WILCKEN D E WILCKEN B	1997	J Inherit Metab Dis1997，20，2：	1
4	Tow-yearpilot study of newborn screening for congenital adrenal hyperplasia in New South Wales compared with nationwide case surveillance in Australia显示文摘	Gleen HK Wiley V Wilcken B	2008	J Paediatr Child Health2008，44，10：	1
5	Vascular complications of severe hyperhomocyste-inemia in patient with homocystinuria duo to CBS deficiency显示文摘	Yap S Eileen R Wilcken B	2000	Semin Thromb Haemost2000，26，：	1
6	Screening newboms for inborn errors of metabolism by tandem mass spectrometry显示文摘	Wilcken B Wiley V Hammond J	2003	N Engl J Med2003，348，23：	1
7	An introduction to nutritional treatment in inborn errors of disorders, different approaches 显示文摘	Wilcken B	2003	Southeast Asian J Trop Med Public Health2003，343，：	1
8	Two-year pilot study of newborn screening for congenital adrenal hyperplasia in New South Wales compared with nation wide case surveillance in Australia显示文摘	Gleeson HK Wiley V Wilcken B	2008	J Padiatr Child Health2008，44，10：	1
9	The pathogenesis of coronary artery disease:a possible role for methionine metabolism显示文摘	Wilcken DEL Wilcken B	1976	J Clin Invest1976，57，：	1
10	The natural history of vascular dis- ease in homecystinuria and the effects of treatment 显示文摘	Wilcken DE Wilcken B	1997	J In- herit Metab Dis1997，20，2：	1
11	Two-year pilot study of newborn screening for congenital adrenal hyperplasia in New South Walescompared with nationwide case surveillance in Australia显示文摘	Gleeson HK Wiley V Wilcken B	2008	J Paediatr Child Health2008，44，10：	1
12	The pathogenesis of wronary attery disease a possible role for methionine metavdism 显示文摘	Wilcken DE Wilcken B	1976	J Clin Invest1976，57，4：	1
13	Newborn screening for congeni- tal hypothyroidism in vmy-low-birth-weight babies: the need for a second test显示文摘	Bijarnia S Wilcken B Wiley VC	2011	J Inherit Metab Dis2011，54，3：	1
14	Two-year pilot study of newborn screening for congenital adrenal hyperplasia in New South Wales compared with nationwide case surveillance in Australia 显示文摘	Gleeson HK Wiley V Wilcken B	2008	J Paediatr Child Health2008，44，10：	1
15	Anorexia nervosa(restrictive subtype)is associated with a polymorphism in the novel norepinephrine transporter gene promoter polymorphic region显示文摘	Urwin RE Bennetts B Wilcken B	2002	Mol Psychiatry2002，7，：	1
16	Geographical and ethnic variation of the 677C > T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR) :findings from over 7000 newborns from 16 areas world wide 显示文摘	Wilcken B Bamforth F Li Z	2003	J Med Genet2003，40，8：	1
17	A possible role for methiomine metabolism显示文摘	Wilcken B	1976	J Clinl- nvest1976，157，：	1
18	Leukoencephalopathies associated with disorders of cobalamin and folate metabolism显示文摘	Wilcken B	2012	Semin Neurol2012，32，1：	1
19	Newborn screening for congeni- tal hypothyroidism in very-low-birth-weight babies: the need for a second test显示文摘	Bijarnia S Wilcken B Wiley VC	2011	J Inherit Metab Dis2011，34，3：	1
20	Hartnup disorder: polymorphisms identified in the neutral amino acid transporter SLC1A5 显示文摘	Potter SJ Lu A Wilcken B	2002	J Inherit Metab Dis2002，25，6：	1

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