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22 results on '"Frontali, M."'

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1. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

2. Riluzole in cerebellar ataxia

3. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

4. Family and molecular data for a fine analysis of age at onset in Huntington disease

6. CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci

7. Mating between two balanced translocation carriers in two unrelated families

8. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

9. The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates

10. Trinucleotide repeat length instability and age of onset in Huntington's disease

12. Predictive testing for Huntington’s disease: ten years’ experience in two Italian centres

13. Non-DYT1 dystonia in a large Italian family

14. Antenatal diagnosis of fetal skeletal malformations in 'at risk' cases

15. Primary torsion dystonia: the search for genes is not over

16. Spettroscopia protonica a risonanza magnetica del ponte e del cervelletto in una famiglia con atassia spinocerebellare tipo 1

18. AUTOSOMAL DOMINANT PURE CEREBELLAR ATAXIA: NEUROLOGICAL AND GENETIC STUDY

19. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): Clinical, neuroimaging, pathological and genetic study of a large Italian family

21. Erratum

22. The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias

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