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21篇 您的检索式：作者名="MacMullen C"

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	题名	作者	年代	出处	被引量
1	Disparities in maternal out- comes among four ethnic populations 显示文摘	Shen JJ Tymkow C MacMullen N	2005	Ethn Dis2005，15，3：	1
2	Congenital 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
3	Genotype-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
4	Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations 显示文摘	Pinney SE MacMullen C Becker S	2008	J Clin Invest2008，118，1：	1
5	Clinical 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
6	Familial 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
7	Clinical 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
8	Hyperinsulinism/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	2001	J Clin Endocrinol Metab2001，86，4：	1
9	Disparitiesinmaternal outcomes among four ethnic populations 显示文摘	SHEN J J TYMKOW C MACMULLEN N	2005	Ethn Dis2005，15，3：	1
10	Disparities in maternal outcomes among four ethnic populations 显示文摘	Shen JJ Tymkow C MacMullen N	2005	Ethn Dis2005，15，3：	1
11	Disparities in maternal out- comes among four ethnic populations显示文摘	Shen JJ Tymkow C MacMullen N	2005	Ethn Dis2005，15，3：	1
12	Hyperinsulin-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	2001	J Clin Endocrinol Metab2001，86，4：	1
13	Clinicalcharacteristics and biochemical mechanisms of congenitalhyperinsulinism associated with dominant KATP channelmutations 显示文摘	Pinney SE MacMullen C Becker S	2008	J Clin Invest2008，118，8：	1
14	Simultaneous 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	Opakla D Lachman C E MacMullen S A	2003	Clinical and Diagnostic Laboratory Immunology2003，10，：	1
15	Clinical 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
16	Clinical 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
17	Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes显示文摘	Henwood M J Kelly A Macmullen C		0，，：	1
18	Histopathology of congenital hyperinsulinism:retrospective study with genotype correlations显示文摘	SUCHI M MACMULLEN C THORNTON P S	2003	Pediatr Dev Pathol2003，6，4：	1
19	Hyperinsulinism/hyperammone- mia 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	2001	J Clin Endocrinol Metab2001，86，4：	1
20	Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations显示文摘	Pinney SE MacMullen C Becker S Lin YW Hanna C Thornton P	2008	J Clin Invest2008，118，8：	1

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