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25篇 您的检索式：作者名="Huppke"

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	题名	作者	年代	出处	被引量
1	Natalizumab use in pediatric multiple sclerosis 显示文摘	HUPPKE P STARK W ZURCHER C	2008	Arch Neurol2008，65，：	1
2	Mutations in SLC33A1 cause a lethalautosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin显示文摘	Huppke P Brendel C Kalscheuer V	2012	Am J Hum Genet2012，90，1：	1
3	Molecular diagnosis of Rett syndrome 显示文摘	Huppke P Gartner J	2005	J Child Neurol2005，20，9：	1
4	Equilibrium dehydrogenation of ethane,propane,and the butanes显示文摘	FREY F E HUPPKE W F	1933	Industrial&Engineering Chemistry1933，25，1：	1
5	Influence of mutation type and locaton on phenotype in 123 patients with Rett syndrome显示文摘	Huppke P Held M Hanefeld F	2002	Neuropediatrics2002，33，2：	1
6	MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Geuet2002，39，8：	1
7	Neuromyelitis optica and NMO-IgG in European pediatric patients显示文摘	Huppke P Blüthner M Bauer O		0，，：	1
8	Induction and Detection of Long-Lasting Peptide-Specific Antibody Responses in Pigs and Beef Cattle, A Powerful Technology for Tracing Meat Processing Chains from Stock Farmers to Sales Counters 显示文摘	Raschke A Strich S Huppke S	2006	Food Control2006，17，1：	1
9	MECP2 gene nucleotide changes and their pathogenicity in males:proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
10	Induction and detection of long-lasting peptide-specific antibody responses in pigs and beef cattle:a powerful technology for tracing meat processing chains from stock farmers to sales counters显示文摘	RASCHKE A STRICH S HUPPKE S	2006	Food Control2006，17，1：	1
11	MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution 显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
12	Altered methylation pattern of the G6PD prompter in Rett syndrome显示文摘	Huppke P Bohlander S Krmer N		0，，02：	1
13	Neuromyelitis optica and NMO IgG in European pediatric patients显示文摘	Huppke P Bluthner M Bauer O	2010	Neurology2010，75，：	1
14	Molecular and biochemical characterization of a unique mutation in CCS,the human copper chaperone to superoxide dismutase显示文摘	Huppke P Brendel C Korenke GC	2012	Hum Mutat2012，33，8：	1
15	Altered methylation pattern of the G6PD promoter in Rett syndrome显示文摘	Huppke P Bohlander S Kramer N	2002	Neuropediatrics2002，33，：	1
16	Influence of mutation type and location on phenotype in 123 patients with Rett syndrome显示文摘	Huppke P Held M Hanefeld F	2002	Neuropediatrics2002，33，2：	1
17	Apheresis in treatment of acute inflammatory demyelinating disorders 显示文摘	Mtthlhausen J Kitze B Huppke P	2015	Atheroscler Suppl2015，18，：	1
18	Perisylvian polymicrogyria in Landau-Kleffner syndrome显示文摘	Huppke P Kallenberg K Gartner J	2005	Neurology2005，64，：	1
19	MECP2 gene nucleotide changes and their pathogenicity in males:proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
20	The spectrum of phenotypes in females with Rett Syndrome显示文摘	Huppke P Held M Laccone F	2003	Brain Dev2003，25，3：	1

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