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35 results on '"Magariello A"'

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1. Crowdsensing for a sustainable comfort and for energy saving.

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3. Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia

4. A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2.

5. Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia

6. LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines.

7. Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum.

10. Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy.

11. Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity

12. Comparison of different techniques for detecting 17p12 duplication in CMT1A

13. Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy

14. 5-HTTLPR, anxiety and gender interaction moderates right amygdala volume in healthy subjects.

15. A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.

16. MAO A VNTR polymorphism and amygdala volume in healthy subjects

17. Morphological correlates of MAO A VNTR polymorphism: New evidence from cortical thickness measurement

18. Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population

19. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.

20. Genetically dependent modulation of serotonergic inactivation in the human prefrontal cortex

21. Ventro-lateral prefrontal activity during working memory is modulated by MAO A genetic variation

22. A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies

23. Lifestyle and late effects after poliomyelitis. A risk factor study of two populations.

24. Hb MOLFETTA [β126(H4)Val→Leu, GTG→CTG]: A NEW, SILENT, NEUTRAL β CHAIN VARIANT FOUND IN AN ITALIAN WOMAN.

25. A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness.

26. Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.

27. A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

28. First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL.

29. Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathy

30. A Simple Method for Diagnosis of Autosomal Recessive Spinal Muscular Atrophy by Denaturing High-Performance Liquid Chromatography.

31. TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis.

32. Case report Gene conversion events in adult-onset spinal muscular atrophy.

33. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene

34. FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis

35. A splice-junction mutation in SBF2 gene causes autosomal recessive charcot-marie-tooth disease (CMT4B2) in a family from southern italy.