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21篇 您的检索式：作者名="DARRAS BT"

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	题名	作者	年代	出处	被引量
1	Origin of mutations in two families with X-linked chronic granulomatous disease显示文摘	Francke U Ochs HD Darras BT	1990	Blood1990，76，3：	1
2	Spinal mt~scular atrophy: a clinical and research update显示文摘	Markowitz JA Singh P Darras BT	2012	Pediatr Neurol2012，46，：	1
3	Serum trans- aminase levels in boys with Duchenne and Becker muscular dystrophy显示文摘	MCMILLAN H J GREGAS M DARRAS BT	2011	Pediatrics2011，127，1：	1
4	Juvenile my- asthenia gravis 显示文摘	Chiang I M Darras BT Kang PB	2009	Muscle Nerve2009，39，4：	1
5	Serum transaminase levels in boys with Duchenne and Becker muscular dystrophy 显示文摘	McMillan H J Gregas M Darras BT	2011	Pediatrics2011，127，1：	1
6	Juvenile myasthenia gravis显示文摘	Chiang LM Darras BT Kang PB	2009	Muscle Nerve2009，39，4：	1
7	More can be less: SMN1 gene duplications are associated with sporadic ALS显示文摘	Darras BT	2012	Neurology2012，78，11：	1
8	Safety and efficacy of carvedilol therapy for patients with dilated cardiomyopathy secondary to muscular dystrophy显示文摘	Rhodes J Margossian R Darras BT		0，，02：	1
9	More can be less:SMN1 gene duplications are associated with sporadic ALS 显示文摘	Darras BT	2012	Neurology2012，78，11：	1
10	Spinal muscular atrophies 显示文摘	Darras BT	2015	Pediatr Clin North Am2015，62，3：	1
11	Loss of heterozygosity for alleles on chromosome 10 in human brain tumours显示文摘	Ye Z Wu JK Darras BT	1993	Neurol Res1993，15，：	1
12	Diagnostic challenges for Pompe disease:An under- recognized cause of floppy baby syndrome 显示文摘	Howell RR Byrne B Darras BT	2006	Genet Med2006，8，5：	1
13	Juvenile myasthenia gravis 显示文摘	Chiang LM Darras BT Kang PB	2009	Muscle Nerve2009，39，4：	1
14	Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions 显示文摘	Harper JF Darras BT	1987	Am J Hum Genet1987，40，3：	1
15	Serum Transaminase Levels in Boys With Duchenne and Becker Muscular Dystrophy显示文摘	McMillan HJ Gregas M Darras BT	2011	Pediatrics2011，127，1：	1
16	Intragenic deletions in 21 Duchenne muscular dystrophy(DMD)/Becker muscular dystrophy(BMD) families studied with the dystrophin cDNA:location of breakpoints on HindⅢ and BglⅡ exoncontaining fragment maps,meiotic and mitotic origin of the mutations显示文摘	Darras BT Blattner P Harper JF	1988	Am J Hum Genet1988，43，5：	1
17	Autoimmune neuromuscular disorders in childhood显示文摘	McMillan HJ Darras BT Kang PB	2011	Curr Treat Options Neurol2011，13，6：	1
18	Clinical trials in spinal muscular atrophy显示文摘	Darras BT Kang PB	2007	Curr Opin Pediatr2007，19，6：	1
19	Assignment of human genes for phosphorylase kinase subunits alpha(PHKA) to Xq12-q13 and beta(PHKB) to 16q12-q13显示文摘	Francke U Harper JF Darras BT	1989	Am J Hum Genet1989，45，2：	1
20	Clinical correlates of charcot-marie-tooth disease in patients with pes cavus deformities显示文摘	Karakis I Gregas M Darras BT		0，，04：	1

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