Servidei S - Search Results

1

P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.

Conte A, Lattante S, Zollino M, Marangi G, Luigetti M, Del Grande A, Servidei S, Trombetta F, Sabatelli M. Conte A, et al. Among authors: servidei s. Neuromuscul Disord. 2012 Jan;22(1):73-5. doi: 10.1016/j.nmd.2011.08.003. Epub 2011 Sep 9. Neuromuscul Disord. 2012. PMID: 21907581

2

Giant axonal neuropathy: report on a case with focal fiber loss.

Sabatelli M, Bertini E, Servidei S, Fernandez E, Magi S, Tonali P. Sabatelli M, et al. Among authors: servidei s. Acta Neuropathol. 1992;83(5):543-6. doi: 10.1007/BF00310034. Acta Neuropathol. 1992. PMID: 1621511

3

Late onset scleroatonic familial myopathy (Ullrich disease): a study of two sibs.

Ricci E, Bertini E, Boldrini R, Sabatelli M, Servidei S, Mazziotta MR, Bosman C, Tonali P. Ricci E, et al. Among authors: servidei s. Am J Med Genet. 1988 Dec;31(4):933-42. doi: 10.1002/ajmg.1320310428. Am J Med Genet. 1988. PMID: 3239582

4

Autosomal recessive hypermyelinating neuropathy.

Sabatelli M, Mignogna T, Lippi G, Servidei S, Manfredi G, Ricci E, Bertini E, Lo Monaco M, Tonali P. Sabatelli M, et al. Among authors: servidei s. Acta Neuropathol. 1994;87(4):337-42. doi: 10.1007/BF00313601. Acta Neuropathol. 1994. PMID: 8017168

5

Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Di Trapani G, Gregori B, Servidei S, Ricci E, Sabatelli M, Tonali P. Di Trapani G, et al. Among authors: servidei s. Clin Neuropathol. 1997 Jul-Aug;16(4):195-200. Clin Neuropathol. 1997. PMID: 9266144

6

Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.

Sabatelli M, Mignogna T, Lippi G, Servidei S, Zollino M, Padua L, Lo Monaco M, De Armas L, Mereu ML, Tonali P. Sabatelli M, et al. Among authors: servidei s. Am J Med Genet. 1998 Jan 23;75(3):309-13. Am J Med Genet. 1998. PMID: 9475604

7

A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene.

Silvestri G, Rana M, DiMuzio A, Uncini A, Tonali P, Servidei S. Silvestri G, et al. Among authors: servidei s. Neuromuscul Disord. 1998 Jun;8(5):291-5. doi: 10.1016/s0960-8966(98)00037-6. Neuromuscul Disord. 1998. PMID: 9673981

8

Mitochondrial encephalomyopathies: gene mutation.

Servidei S. Servidei S. Neuromuscul Disord. 2000 Jan;10(1):XVI-XXIV. Neuromuscul Disord. 2000. PMID: 10677871 No abstract available.

9

Mitochondrial encephalomyopathies: gene mutation. Vol. 10 No. 2, February 2000.

Servidei S. Servidei S. Neuromuscul Disord. 2000 Feb;10(2):IX-XIII. Neuromuscul Disord. 2000. PMID: 10714594 No abstract available.

10

Mitochondrial encephalomyopathies: gene mutation.

Servidei S. Servidei S. Neuromuscul Disord. 2001 Mar;11(2):230-5. doi: 10.1016/s0960-8966(01)00205-x. Neuromuscul Disord. 2001. PMID: 11360877 No abstract available.

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

296 results

Search Page

Filters