Testa D - Search Results

1

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.

Mantuano E, Romano S, Veneziano L, Gellera C, Castellotti B, Caimi S, Testa D, Estienne M, Zorzi G, Bugiani M, Rajabally YA, Barcina MJ, Servidei S, Panico A, Frontali M, Mariotti C. Mantuano E, et al. Among authors: testa d. J Neurol Sci. 2010 Apr 15;291(1-2):30-6. doi: 10.1016/j.jns.2010.01.010. Epub 2010 Feb 2. J Neurol Sci. 2010. PMID: 20129625

2

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.

Gellera C, Castellotti B, Riggio MC, Silani V, Morandi L, Testa D, Casali C, Taroni F, Di Donato S, Zeviani M, Mariotti C. Gellera C, et al. Among authors: testa d. Neuromuscul Disord. 2001 May;11(4):404-10. doi: 10.1016/s0960-8966(00)00215-7. Neuromuscul Disord. 2001. PMID: 11369193

3

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.

Mariotti C, Castellotti B, Pareyson D, Testa D, Eoli M, Antozzi C, Silani V, Marconi R, Tezzon F, Siciliano G, Marchini C, Gellera C, Donato SD. Mariotti C, et al. Among authors: testa d. Neuromuscul Disord. 2000 Aug;10(6):391-7. doi: 10.1016/s0960-8966(99)00132-7. Neuromuscul Disord. 2000. PMID: 10899444

4

Progressive myoclonic ataxia with intrathecal immune activation in six patients.

Testa D, Ambrosoni E, Franceschetti S, Salmaggi A, Soliveri P, Girotti F. Testa D, et al. Neurol Sci. 2007 Aug;28(4):199-204. doi: 10.1007/s10072-007-0821-1. Epub 2007 Aug 10. Neurol Sci. 2007. PMID: 17690852

5

Unusual association of sporadic olivopontocerebellar atrophy and motor neuron disease.

Testa D, Tiranti V, Girotti F. Testa D, et al. Neurol Sci. 2002 Dec;23(5):243-5. doi: 10.1007/s100720200049. Neurol Sci. 2002. PMID: 12522682

6

Magnetic resonance signal abnormalities along the pyramidal tracts in amyotrophic lateral sclerosis.

Carella F, Grisoli M, Savoiardo M, Testa D. Carella F, et al. Among authors: testa d. Ital J Neurol Sci. 1995 Nov;16(8):511-5. doi: 10.1007/BF02282908. Ital J Neurol Sci. 1995. PMID: 8613411

7

Progressive dysarthria: definition and clinical follow-up.

Soliveri P, Piacentini S, Carella F, Testa D, Ciano C, Girotti F. Soliveri P, et al. Among authors: testa d. Neurol Sci. 2003 Oct;24(3):211-2. doi: 10.1007/s10072-003-0135-X. Neurol Sci. 2003. PMID: 14598092

8

Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy.

Testa D, Monza D, Ferrarini M, Soliveri P, Girotti F, Filippini G. Testa D, et al. Neurol Sci. 2001 Jun;22(3):247-51. doi: 10.1007/s100720100021. Neurol Sci. 2001. PMID: 11731878

9

Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?

Pareyson D, Testa D, Morbin M, Erbetta A, Ciano C, Lauria G, Milani M, Taroni F. Pareyson D, et al. Among authors: testa d. Neurology. 2003 May 27;60(10):1721-2. doi: 10.1212/01.wnl.0000059262.34846.8a. Neurology. 2003. PMID: 12771282 Free article. No abstract available.

10

Branched-chain amino acids in the treatment of amyotrophic lateral sclerosis.

Testa D, Caraceni T, Fetoni V. Testa D, et al. J Neurol. 1989 Dec;236(8):445-7. doi: 10.1007/BF00328503. J Neurol. 1989. PMID: 2614487

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

254 results

Search Page

Filters