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40篇 您的检索式：作者名="De Fusco"

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	题名	作者	年代	出处	被引量
1	Haploinsufficiency of ATP1A2 encoding the Na+/K+pump alpha2 subunit associated with familial hemiplegic migraine type 2显示文摘	De Fusco M Marconi R Silvestri L	2003	Nat Genet2003，33，2：	1
2	The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy显示文摘	De Fusco M Becchetti A Patrignani A	2000	Nat Genet2000，26，3：	1
3	Hap- loinsufficiency of ATP1A2 encoding the Na ^+/ K^+ Pump alpha2 subunit associated with famil- ial hemiplegic migraine type 2 显示文摘	De Fusco M Marconi R Silvestri L et aI	2003	Nat Gen- et2003，33，2：	1
4	The α2B -adrenergic receptor is mutant in cortical myoclonus and epilepsy显示文摘	De Fusco M Vago R Striano P	2014	Ann Neurol2014，75，1：	1
5	ATP1A2 muta- tions in 11 families with familial hemiplegic migraine 显示文摘	Riant F De Fusco M Aridon P	2005	Hum Mutat2005，26，：	1
6	Insulin receptors during the menstrual cycle in normal women显示文摘	De Pirro R Fusco A Bertoli A	1978	Clin Endocrinol Metab1978，47，6：	1
7	Non-thermal effects of microwaves on proteins: thermophilic enzymes as model system显示文摘	Marina Porcelli Giovanna Cacciapuoti Stefania Fusco Rita Massa Guglielmo d’Ambrosio Costanzo Bertoldo Mario De Rosa Vincenzo Zappia	1997	FEBS Letters1997，，2：	1
8	Changes in doxorubicin distribution and toxicity in mice pretreated with the cyclosporin analogue SDZ PSC 833 显示文摘	Gonzalez O Colombo T De Fusco	1995	Cancer Chemother Pharmacol1995，36，4：	1
9	Haploinsufficiency of ATP1A2 encoding the Na+/Ka+ pump a2 subunit as- sociated with amilial hemiplegic migraine type2显示文摘	De Fusco M Marconi R Silvestri L	2003	Nat Genet2003，33，2：	1
10	Molecular Cloning, Expression Pattern, and Chromosomal Localization of the Human Na–Cl Thiazide-Sensitive Cotransporter (SLC12A3)显示文摘	Nadia Mastroianni Maurizio De Fusco Massimo Zollo Giulia Arrigo Orsetta Zuffardi Alberto Bettinelli Andrea Ballabio Giorgio Casari	1996	Genomics1996，，3：	1
11	Haploinsufficiency of ATP1A2 encoding the Na+/Ka+ pump a2 subunit as- sociated with amilial hemiplegic migraine type2 显示文摘	De Fusco M Marconi R Silvestri L	2003	Nat CJenet2003，33，2：	1
12	Spastic paraplegia and OXPHOS impairment caused by mutation in paraplegia,a nuclearencoded mitochondrial metalloprotease显示文摘	Casari A de Fusco M Ciarmatori S	1998	Cell1998，93，：	1
13	Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha 2 subunit associated with familial hemiplegic migraine type 2显示文摘	De Fusco M Marconi R Silvestri L		0，，02：	1
14	The nicotinic receptor beta2 subunit is mutant in nocturnal frontal lobe epilepsy显示文摘	De Fusco M Becchetti A	2000	Nat Genet2000，26，3：	1
15	Molecular identification of nontuberculous mycobacteria isolates in a Brazilian mycobacteria reference laboratory显示文摘	Ana Roberta Fusco da Costa Maria Luiza Lopes Ismari Perini Furlaneto Maísa Silva de Sousa Karla Valéria Batista Lima	2010	Diagnostic Microbiology & Infectious Disease2010，，4：	1
16	Familial hemophagocyticlymphohistiecytosi:how late can the onset be?显示文摘	Mien M De Fusco C Legrand F et a1	2001	Haenlatologica2001，86，5：	1
17	Further evidence of ge- netic heterogeneity in familial essential tremor 显示文摘	Aridon P Ragonese P De Fusco M	2008	Parkinsonism Relat Disord2008，14，1：	1
18	siRNA nanoformulation against the Ret/PTC1 junction oncogene is efficient in an in vivo model of papillary thyroid carcinoma显示文摘	De Martimprey H Bertrand JR Fusco A	2008	Nucleic Acids Res2008，36，21：	1
19	spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear- encoded mitochondrial metalloprotease 显示文摘	De Fusco M Ciarmatory S	1998	Cell1998，93，：	1
20	Haploinsufficiency ofATPIA2 encoding the Na+/K+ ATP subunit associated with familial herniplegic migraine type 2显示文摘	De Fusco M Marconi R Silvestri L l	2003	Nature genetics2003，33，2：	1

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