Corrado L - Search Results

1

NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes.

Riva P, Corrado L, Natacci F, Castorina P, Wu BL, Schneider GH, Clementi M, Tenconi R, Korf BR, Larizza L. Riva P, et al. Among authors: corrado l. Am J Hum Genet. 2000 Jan;66(1):100-9. doi: 10.1086/302709. Am J Hum Genet. 2000. PMID: 10631140 Free PMC article.

2

Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis.

Chiò A, Moglia C, Canosa A, Manera U, Grassano M, Vasta R, Palumbo F, Gallone S, Brunetti M, Barberis M, De Marchi F, Dalgard C, Chia R, Mora G, Iazzolino B, Peotta L, Traynor BJ, Corrado L, D'Alfonso S, Mazzini L, Calvo A. Chiò A, et al. Among authors: corrado l. Neurology. 2023 Jul 4;101(1):e83-e93. doi: 10.1212/WNL.0000000000207367. Epub 2023 May 18. Neurology. 2023. PMID: 37202167 Free PMC article.

3

Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review.

Lombardi M, Corrado L, Piola B, Comi C, Cantello R, D'Alfonso S, Mazzini L, De Marchi F. Lombardi M, et al. Among authors: corrado l. Genes (Basel). 2023 Nov 4;14(11):2039. doi: 10.3390/genes14112039. Genes (Basel). 2023. PMID: 38002982 Free PMC article.

4

Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations.

Gallo S, Vignaroli F, Contaldi E, Vecchio D, Corrado L, D'Alfonso S, Cantello R, Magistrelli L. Gallo S, et al. Among authors: corrado l. Parkinsonism Relat Disord. 2024 Jan;118:105953. doi: 10.1016/j.parkreldis.2023.105953. Epub 2023 Dec 7. Parkinsonism Relat Disord. 2024. PMID: 38086249 No abstract available.

5

Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation.

Contaldi E, Gallo S, Corrado L, D'Alfonso S, Magistrelli L. Contaldi E, et al. Among authors: corrado l. Cerebellum. 2024 Jun;23(3):1226-1230. doi: 10.1007/s12311-023-01619-0. Epub 2023 Oct 19. Cerebellum. 2024. PMID: 37857779

6

A case of early-onset Parkinson's disease in a patient with KBG syndrome.

Magistrelli L, Contaldi E, Caushi F, Spano A, Cantello R, D'Alfonso S, Corrado L. Magistrelli L, et al. Among authors: corrado l. Neurol Sci. 2023 Dec;44(12):4537-4539. doi: 10.1007/s10072-023-06988-2. Epub 2023 Aug 4. Neurol Sci. 2023. PMID: 37540342 No abstract available.

7

Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants.

De Marchi F, Tondo G, Corrado L, Menegon F, Aprile D, Anselmi M, D'Alfonso S, Comi C, Mazzini L. De Marchi F, et al. Among authors: corrado l. Genes (Basel). 2023 Aug 21;14(8):1658. doi: 10.3390/genes14081658. Genes (Basel). 2023. PMID: 37628709 Free PMC article. Review.

8

Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR.

Corrado L, Colapietro P, Larizza L, Riva P. Corrado L, et al. Mol Cell Probes. 1999 Jun;13(3):199-202. doi: 10.1006/mcpr.1999.0237. Mol Cell Probes. 1999. PMID: 10369745

9

Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population.

Natacci F, Colapietro P, Riva P, Corrado L, Rossi LN, Maninetti MM, Casciati MC, Zambrino Ca, Lanzi G, Larizza L. Natacci F, et al. Among authors: corrado l. Mol Cell Probes. 1999 Dec;13(6):415-20. doi: 10.1006/mcpr.1999.0268. Mol Cell Probes. 1999. PMID: 10657145

10

Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype.

Natacci F, Corrado L, Pierri M, Rossetti M, Zuccarini C, Riva P, Miozzo M, Larizza L. Natacci F, et al. Among authors: corrado l. Am J Med Genet. 2000 Dec 18;95(5):467-72. doi: 10.1002/1096-8628(20001218)95:5<467::aid-ajmg11>3.0.co;2-t. Am J Med Genet. 2000. PMID: 11146468

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