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36篇 您的检索式:作者名="MacMullen"
    题名 作者 年代 出处 被引量
1Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations显示文摘Sara E.Pinney Courtney MacMullen Susan Becker 0,,:1
2Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylu rea receptor SUR1显示文摘Macmullen CM Zhou Q Snider KE 0,,06:1
3Disparities in maternal out- comes among four ethnic populations 显示文摘Shen JJ Tymkow C MacMullen N 2005Ethn Dis2005,15,3:1
4Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K~+ channels:identification and rescue显示文摘Yan FF Lin YW MacMullen C 0,,:1
5Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes显示文摘Henwood MJ Kelly A Macmullen C 0,,:1
6Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations 显示文摘Pinney SE MacMullen C Becker S 2008J Clin Invest2008,118,1:1
7Serial MRI to determine the effect of dexamethasone on the cerebral pathology of tuberculous meningitis : An observational study 显示文摘Thwaite E Macmullen - Price J Tran TH 2007Lancet Neurol2007,6,3:1
8Serial MRIto determine the effect of dexamethasone on the cerebralpathology of tuberculous meningitis: an observationalstudy 显示文摘Thwaites GF Macmullen Price J Tran TH 2007Lancet Neurol2007,6,3:1
9Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations显示文摘Pinney SE MacMullen C Becker S 0,,:1
10Familial leucinesensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor显示文摘Magge SN Shyng SL MacMullen C 0,,:1
11Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor显示文摘Thornton PS MacMullen C Ganguly A 0,,:1
12Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase显示文摘MacMullen C Fang J Hsu BY 2001J Clin Endocrinol Metab2001,86,4:1
13Simultaneous quantitation of antibodies to neutralizing epitopes on virus-like particles for human papillomavirus types 6,11,16,and 18 by a multiplexed luminex assay显示文摘Opalka D Lachman CE MacMullen SA 2003Clin Diagn Lab Immunol2003,10,1:1
14Simultaneous quantitation of antibodies to neutralizing epitopes on virus-like particles for human papillomavirus types6,11,16,and 18 by a multiplexed luminex assay显示文摘Opakla D Lachman CE MacMullen SA 2003Clinical and Diagnostic Laboratory Immunology2003,10,:1
15Simultaneous quantitation of types6antibodies to neutralizing epitopes on virus-like particles for human papillomavirus,11,16,and 18 by a multiplexed luminex assay显示文摘Opalka D Lachman CE MacMullen SA 2003Clin Diagn Lab Immunol2003,10,1:1
16Disparitiesinmaternal outcomes among four ethnic populations 显示文摘SHEN J J TYMKOW C MACMULLEN N 2005Ethn Dis2005,15,3:1
17Disparities in maternal outcomes among four ethnic populations 显示文摘Shen JJ Tymkow C MacMullen N 2005Ethn Dis2005,15,3:1
18Serial MRI to determine the effect of dexamethasone on the cerebral pathology of tuberculous meningitis: an observational study 显示文摘Thwaites GE Macmullen Price J Tram TH 2007Lancet Neurol2007,6,3:1
19Disparities in maternal out- comes among four ethnic populations显示文摘Shen JJ Tymkow C MacMullen N 2005Ethn Dis2005,15,3:1
20Hyperinsulin-ism/hyperammonemia syndrome in children with regula- tory mutations in the inhibitory GTP binding domain of glutamate dehydrogenase 显示文摘MacMullen C Fang J Hsu B Y 2001J Clin Endocrinol Metab2001,86,4:1
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