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15篇 您的检索式:作者名="Anheim M"
    题名 作者 年代 出处 被引量
1Pathophysiogical and therapeutic progress in Friedreich ataxia 显示文摘Puccio H Anheim M Tranchant C 2014Rev Neurol(Paris)2014,170,5:1
2The autosomal recessive cerebellar ataxias 显示文摘Anheim M Tranehant C Koenig M 2012N Engl J Med2012,366,7:1
3EpidemiologicaI, clini- cal, paraclinical and molecular study of a cohort of 102 patientsaffected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical manage-ment 显示文摘Anheim M Fleury M Monga B 2010Neurogenetics2010,11,1:1
4A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy显示文摘Echaniz-Laguna A Rousso E Anheim M 2005Neurology2005,64,8:1
5A family with earlyonset and rapidly progressive X-linked spinal and bulbar muscular atrophy显示文摘Echaniz-Laguna A Rousso E Anheim M 2005Neurology2005,64,8:1
6Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers显示文摘Anheim M Elbaz A Lesage S 2012Neurology2012,78,6:1
7Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease显示文摘Lesage S Anheim M Condroyer C 2011Hum Mol Genet2011,20,1:1
8A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy显示文摘Echaniz-Laguna A Rousso E Anheim M 2005Rev Neu- ral2005,161,4:1
9The autosomal recessive cerebellar ataxias 显示文摘Anheim M Tranehant C Koenig M 2012N Engl J Med2012,366,7:1
10Epiderniological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive eerebellar ataxia from Alsace, Eastern France: implications for clinical management 显示文摘Anheim M Fleury M Monga B 2010Neumgenetics2010,11,1:1
11G51D a-synuclein mutation causes a novel parkinsonian-pyramidal syndrome 显示文摘Lesage S Anheim M Letoumel F 2013Ann Neurol2013,73,45:1
12Pure trigeminal motor neuropathy presenting with temporo-mandibular joint dysfunction in a patient with HIV and HCV infections显示文摘 Echaniz-Laguna A Rey D 2006Rev Neurol (Paris)2006,162,1:1
13Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients显示文摘Anheim M Monga B Fleury M 2009Brain2009,132,10:1
14Pathophysiogical and therapeutic progress in Friedreich ataxia显示文摘Puccio H Anheim M Tranchant C 2014Rev Neurol (Paris)2014,170,:1
15G51D alpha-synu-clein mutation causes a novel parkinsonian-pyramidal syn- drome显示文摘Lesage S Anheim M Letournel F 2013Ann Neurol2013,73,4:1
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