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5. Correction to: Long-term safety, discontinuation and mortality in an Italian cohort with advanced Parkinson’s disease on levodopa/carbidopa intestinal gel infusion (Journal of Neurology, (2022), 269, 10, (5606-5614), 10.1007/s00415-022-11269-7)

6. A novel MRPS34 gene mutation with combined OXPHOS deficiency in an adult patient with Leigh syndrome

12. EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia

16. Adult diagnosis of Cockayne syndrome

17. Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study

18. De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

19. Encephalopathies with intracranial calcification in children: clinical and genetic characterization

20. Corrigendum to “Restless legs syndrome in NKX2-1-related chorea: An expansion of the disease spectrum” [Brain Dev. 41 (2019) 250–256]

21. The impact of Next Generation Sequencing in rare movement disorders diagnosis: results from a tertiary referral center.

22. A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations

23. ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients

25. De Novo Mutations in PDE1 0A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

26. De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

27. Revisiting the Molecular Mechanism of Neurological Manifestations in Antiphospholipid Syndrome: Beyond Vascular Damage

30. The syndrome of deafness-dystonia: Clinical and genetic heterogeneity

31. Movement disorders in adult patients with classical galactosemia

40. A missense mutation in the KCTD17 gene causes autosomal dominant myoclonus-dystonia

42. De novo mutations in PDE10A cause childhood-onset chorea with bilateral striatal lesions

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