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38篇 您的检索式：作者名="Clarke NF"

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	题名	作者	年代	出处	被引量
1	Relative deficiency in arginine vasopresin in children after cardiopulmonary bypass显示文摘	Mastropietro CW Rossi NF Clark JA	2010	Crit Care Med2010，38，：	1
2	DNA methylationchanges in ovarian cancer:implications for early diagno-sis,prognosis and treatment显示文摘	Barton CA Hacker NF Clark SJ	2008	Gynecol Oncol2008，109，1：	1
3	DNA methylation changes in ovarian cancer: Implications for early diagno- sis, prognosis and treatment显示文摘	Barton CA Hacker NF Clark SJ	2008	Gynecol Onco12008，109，1：	1
4	The effects of placental extracts from nomotensive antt preeclamptic women on vasoconstriction and oxidative metabolism显示文摘	Tuomson NF Thornton S Clark JF	2000	Am J Obstel Gynecol2000，183，1：	1
5	Dietary carbohydrate (amount and type) in the prevention and management of diabetes:a statement by the American Diabetes Association显示文摘	Sheard NF Clark NG Brand-Miller JC	2004	Diabetes Care2004，27，9：	1
6	Dietary carbohydrate(amount and type) in the prevention and management of diatebes:a statement by the American diabetes association显示文摘	Sheard NF Clark NG Brand-Miller JC	2004	Diabetes Care2004，27，9：	1
7	Recent advances in nemaline myopathy显示文摘	Romero NB Sandaradura SA Clarke NF	2013	Curr Opin Neurol2013，26，5：	1
8	DNA methylation changes in ovarian cancer:implications for early diagnosis,prognosis and treatment显示文摘	Barton CA Hacker NF Clark SJ	2008	Gynecol Oncol2008，109，1：	1
9	Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy 显示文摘	Makri S Clarke NF Richard P	2009	Neuromuscul Disord2009，19，1：	1
10	DNA methylation changes in ovarian cancer:implications for early diagnosis,prognosis and treatment显示文摘	Barton CA Hacker NF Clark SJ	2008	Gynecol Oncol2008，109，1：	1
11	DNA methylation changes in ovarian cancer: implications for early diagnosis, prognosis and treat- ment显示文摘	Barton CA Hacker NF Clark SJ	2008	Gyneeol Onco12008，109，1：	1
12	The challenges of bringing autologous HSP-based vaccines to commercial reality显示文摘	Clark BL	2004	Methods2004，32，1：	1
13	Congenital fiber type disproportion-30 years on显示文摘	Clarke NF North KN	2003	J Neuropathol Exp Neurol2003，62，：	1
14	Actin mutations are one cause of congenital fibre type disproportion显示文摘	Laing NG Clarke NF Dye DE	2004	Ann Neurol2004，56，5：	1
15	Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion 显示文摘	Clarke NF Waddell LB Cooper ST	2010	Hum Mutat2010，31，7：	1
16	Congenital fiber-type disproportion显示文摘	Clarke NF	2011	Semin Pediatr Neurol2011，18，：	1
17	Mutations in TPM3 are a common cause of congenital fiber type disproportion显示文摘	Clarke NF Kolski H Dye DE	2008	Ann Neurol2008，63，：	1
18	Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion显示文摘	Clarke NF Waddell LB Cooper ST	2010	Hum Mutat2010，31，：	1
19	Actin mutations are one cause of congenital fibre type disproportion显示文摘	Laing NG Clarke NF Dye DE	2004	Ann Neurol2004，56，：	1
20	Congenital fiber-type Disproportion 显示文摘	Clarke NF North KN	2011	Semin Pediatr Neurol2011，18，4：	1

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