| Body na spoluautora | Body za publikaci pro MU | Odkaz ISVaV | | 1,01 | 4,03 | Analysis of SMN gene regions in patients with spinal muscular atrophy
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| 1,01 | 4,03 | Analysis of histopathologic and molecular genetic findings in Czech LGMD2A patients
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| 1,34 | 6,72 | Correlation between SMN2 copy-number, variations in expression of SMN2 mRNA and clinical outcome in SMA patients treated with phenylbutyrate and valproic acid
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| 0,40 | 2,77 | New Perspectives in the Treatment of Inherited Neuromuscular Disorders: Innovative Ideas for the Third Millenium
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| 2,24 | 6,72 | Analysis of point mutations in the SMN1 gene in Czech SMA patients
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| 4,06 | 20,32 | Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy
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| 2,81 | 19,70 | Quantitative analysis of CAPN3 transcripts in LGMD2A patients: involvement of nonsense-mediated mRNA decay
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| 1,58 | 9,50 | Analysis of histopathologic and molecular pathologic findings in czech LGMD2A patients
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(c) Michal Bulant, 2011