Santoro L - Search Results

1

T2 relaxometry of brain in myotonic dystrophy.

Di Costanzo A, Di Salle F, Santoro L, Bonavita V, Tedeschi G. Di Costanzo A, et al. Among authors: santoro l. Neuroradiology. 2001 Mar;43(3):198-204. doi: 10.1007/s002340000459. Neuroradiology. 2001. PMID: 11305750

2

Dilated Virchow-Robin spaces in myotonic dystrophy: frequency, extent and significance.

Di Costanzo A, Di Salle F, Santoro L, Bonavita V, Tedeschi G. Di Costanzo A, et al. Among authors: santoro l. Eur Neurol. 2001;46(3):131-9. doi: 10.1159/000050786. Eur Neurol. 2001. PMID: 11598331

3

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene.

De Michele G, Filla A, Cavalcanti F, Tammaro A, Monticelli A, Pianese L, Di Salle F, Perreti A, Santoro L, Caruso G, Cocozza S. De Michele G, et al. Among authors: santoro l. Neurology. 2000 Jan 25;54(2):496-9. doi: 10.1212/wnl.54.2.496. Neurology. 2000. PMID: 10668723

4

Modifications of brain tissue volumes in facioscapulohumeral dystrophy.

Quarantelli M, Lanzillo R, Del Vecchio W, Mollica C, Prinster A, Iadicicco L, Iodice V, Santoro L, Salvatore M. Quarantelli M, et al. Among authors: santoro l. Neuroimage. 2006 Sep;32(3):1237-42. doi: 10.1016/j.neuroimage.2006.04.226. Epub 2006 Jun 27. Neuroimage. 2006. PMID: 16806975

5

CTG repeat number in the nonaffected allele of myotonic dystrophy patients is not critical for disease expression.

Cipollaro M, Galderisi U, Iacomino G, Galano G, Di Bernardo G, Lus G, Cotrufo R, Orsini A, Santoro L, Pastore L, Sarrantonio C, Salvatore F, Cascino A. Cipollaro M, et al. Among authors: santoro l. Hum Biol. 1997 Dec;69(6):887-90. Hum Biol. 1997. PMID: 9353981

6

Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy.

Barbieri F, Pellecchia MT, Esposito E, Di Stasio E, Castaldo I, Santorelli F, Perretti A, Santoro L, De Michele G. Barbieri F, et al. Among authors: santoro l. Neurology. 2001 May 22;56(10):1412-4. doi: 10.1212/wnl.56.10.1412. Neurology. 2001. PMID: 11376202

7

Early detection of biventricular involvement in myotonic dystrophy by tissue Doppler.

Parisi M, Galderisi M, Sidiropulos M, Fiorillo C, Lanzillo R, D'Errico A, Grieco M, Innelli P, Santoro L, de Divitiis O. Parisi M, et al. Among authors: santoro l. Int J Cardiol. 2007 May 31;118(2):227-32. doi: 10.1016/j.ijcard.2006.06.056. Epub 2006 Oct 12. Int J Cardiol. 2007. PMID: 17045670 Clinical Trial.

8

Upper gastrointestinal tract motility in children with progressive muscular dystrophy.

Staiano A, Del Giudice E, Romano A, Andreotti MR, Santoro L, Marsullo G, Rippa PG, Iovine A, Salvatore M. Staiano A, et al. Among authors: santoro l. J Pediatr. 1992 Nov;121(5 Pt 1):720-4. doi: 10.1016/s0022-3476(05)81899-2. J Pediatr. 1992. PMID: 1432420

9

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.

Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S. Filla A, et al. Among authors: santoro l. J Neurol Sci. 1996 Oct;142(1-2):140-7. doi: 10.1016/0022-510x(96)00177-3. J Neurol Sci. 1996. PMID: 8902734

10

Premature aging in Werner's syndrome spares the central nervous system.

Postiglione A, Soricelli A, Covelli EM, Iazzetta N, Ruocco A, Milan G, Santoro L, Alfano B, Brunetti A. Postiglione A, et al. Among authors: santoro l. Neurobiol Aging. 1996 May-Jun;17(3):325-30. doi: 10.1016/0197-4580(96)00033-4. Neurobiol Aging. 1996. PMID: 8725892

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