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62篇 您的检索式:作者名="Bressman"
    题名 作者 年代 出处 被引量
1Phenomenology and classification of dystonia: a consensus update显示文摘Albanese A Bhatia K Bressman SB 2013Mov Disord2013,28,7:1
2Exteroceptive and interoceptive stimuli in dystonia显示文摘Greene PE Bressman S 1998Mov Disord1998,13,3:1
3A novel mitochondrial12SrRNA point mutation in parkinsonism, deafness, and neuropathy显示文摘Thyagarajan D Bressman S Bruno C 2000Ann Neurol2000,48,:1
4The diagnosis of dystonia 显示文摘Geyer HL Bressman SB 2006Lancet Neurol2006,5,9:1
5Phenomenology and classification of dystonia:a consensus update显示文摘Albanses A Bhatia K Bressman S B 2013Mov Disord2013,28,7:1
6Pediatric movement disor- ders 显示文摘Saunders-Pullman R Braun I Bressman S 1999Child Adolesc Psychiatr Clin N Am1999,8,4:1
7The diagnosis of dystonia显示文摘Geyer H L Bressman S B 2006Lancet Neurol2006,5,9:1
8A novel mito- chondrial 12SrRNA point mutation in parkinsonism, deaf- ness, and neuropathy显示文摘Thyagarajan D Bressman S Bruno C 2000Ann Neurol2000,48,:1
9The DYT1 phenotype and guidelines for diagnostic testing显示文摘Bressman SB Sabatti C Raymond D 2000Neurology2000,54,9:1
10Pediatric mov- ment disorders 显示文摘Saunders - Pullman R Braun I Bressman S 1999Child Adolesc Psychiatr Clin N Am1999,8,4:1
11Intragenic cis and transmodification of genetic susceptibility in DYT1 torsion dystonia显示文摘Risch NJ Bressman SB Senthil G 2007Am J Hum Genet2007,80,6:1
12A novel mitochondrial 12SrRNA point mutation in parkinsonism,deafness,and neuropathy显示文摘Thyagarajan D Bressman S Bruno C 2000Ann Neurol2000,48,5:1
13Treatment of dysphagia显示文摘Howard L Geyer Susan B Bressman MD 2007Lifelong Learning Neurol2007,,:1
14Regional metabolism in primary torsion dystonia: Effects of penetrance and genotype显示文摘M. Carbon S. Su V. Dhawan D. Raymond S. Bressman D. Eidelberg 2004Neurology2004,,:1
15Genetics of dystonia显示文摘Bressman S 2006J Neural Transm Suppl2006,,70:1
16Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families 显示文摘Ahnasy L Bressman SB Raymond D 1997Ann Neurol1997,42,4:1
17Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families显示文摘Almasy L Bressman SB Raymond D 0,,:1
18Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation显示文摘K Asanuma Y Ma J Okulski V Dhawan T Chaly M Carbon S B. Bressman D Eidelberg 2005Neurology2005,,:1
19Pediatric movement disorders显示文摘Saunders Pullman R Braun I Bressman S 0,,04:1
20The diagnosis of dystonia显示文摘Geyer HL Bressman SB 2006Lancet Neurol2006,5,9:1
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