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76篇 您的检索式：作者名="VIELHABER"

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	题名	作者	年代	出处	被引量
1	27例乙型血友病患者Ⅸ因子基因突变研究显示文摘采用PCR(聚合酶链反应)及GAWTS(GenomicAmplificationwithTranscriptsSequencing)技术,研究了江苏、湖北、山东、广东、福建、宁夏六省区27例乙型血友病患者及其家系成员FⅨ(九因子)基因各2.2Kb DNA序列。在2l例中发现20种不同类型的突变。其中12种是未曾报道的新突变。38%的突变发生在CpG二核苷致序列上,进一步证实了CpG确系突变热点。同时检出6例女性为致病基因携带者。对开展基因产前诊断及优生优育等,具有重要意义。	刘敬忠陈怀华张纪平尹洪臣曾淑燕石奇珍王海燕 Erica Vielhaber Steve S.Sommer	1994	高技术通讯1994，4，8：	3
2	Primary carnltine deficiency: adult onset lipid storage myopathy with a mild clinical course显示文摘	Vielhaber S Feistner H Weis J	2004	J Clin Neurosci2004，11，8：	1
3	Mitochondrial com-plex I deficiency in the epileptic focus of patients withtemporal lobe epilepsy 显示文摘	Kunz WS Kudin AP Vielhaber S	2000	Ann Neurol2000，48，5：	1
4	Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy显示文摘	Kunz W S Kudin A P Vielhaber S	2000	Ann Neurol2000，48，5：	1
5	Tragschnabelwagen furden Transport schwerer und gro volumiger Lasten显示文摘	VON HARALD WALDEEK ALFONS VIELHABER		0，，11：	1
6	Infant methylenetetra - hydrofolat reductase 677TT genotype is a risk factor for congenital heart disease显示文摘	Junker R Kotthoff S Vielhaber H	2001	Cardiovasc Res2001，51，：	1
7	Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease显示文摘	Ralf Junker Stefan Kotthoff Heinrich Vielhaber	2001	Cardiovasc Res2001，51，：	1
8	PAF-mediated pulmonaxy edema: a new role for acid sphingomyetinase and ceramide显示文摘	G6ggel R Winoto-Morbach S Vielhaber G	2004	Nat Med2004，10，2：	1
9	Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complexⅠ activity显示文摘	Schwarz CS Evert BO Seyfried J Schaupp M Kunz WS Vielhaber S	2001	Biochem Biophys Res Commun2001，280，4：	1
10	The mechanism of neuroprotection by topiramate in an animal model of epilepsy 显示文摘	Kudin AP Debska-Vielhaber G Vielhaber S	2004	Epilepsia2004，45，12：	1
11	Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy显示文摘	Vielhaber S Von Oertsen JH Kudin AF	2003	Epilepsia2003，44，：	1
12	Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis显示文摘	Vielhaber S Kunz D Winkler K	2000	Brain2000，123，7：	1
13	Improved results on the probabilistic theory of the joint linear complexity of multisequences显示文摘We improve previous results on the asymptotic behavior and the expected value of the joint linear complexity of random multisequences over finite fields.These results are of interest for word-based stream ciphers in cryptology.	NIEDERREITER Harald VIELHABER Michael WANG LiPing	2012	Science China(Information Sciences)2012，55，1：	1
14	Advances in cancer pain management 显示文摘	Vielhaber A Ponenoy RK	2002	Hematol Oncol Clin North Am2002，16，：	1
15	Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis显示文摘	Kunxz D Winkler K	2002	Brain2002，123，7：	1
16	Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis 显示文摘	Vielhaber S Kunz D Winkler K	2000	Brain2000，123，7：	1
17	Cerebral venous sinus thrombosis in infancy and childhood:role of genetic and acquired risk factors of thrombophilia显示文摘	Vielhaber H Ehrenforth S Koch HG		0，，07：	1
18	Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis显示文摘	Vielhaber S Kunz D Winkler K	2000	Brain2000，123，7：	1
19	Subfield‐specific Loss of Hippocampal N‐acetyl Aspartate in Temporal Lobe Epilepsy显示文摘	StefanVielhaber Heiko G.Niessen GrazynaDebska‐Vielhaber Alexei P.Kudin J?rgWellmer J?rnKaufmann Mircea ArielSch?nfeld RobertFendrich WielandWillker DieterLeibfritz JohannesSchramm Christian E.Elger Hans‐JochenHeinze Wolfram S.Kunz	2007	Epilepsia2007，，1：	1
20	Primary camitine deficiency: adult onset lipid storage myopathy with a mild clinical course 显示文摘	Vielhaber S Feistner H Weis J	2004	J Clin Neurosci2004，11，8：	1

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