Salviati A - Search Results

1

Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy.

Gomez-Lira M, Marzari MG, Uziel G, Pignatti P, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. J Neuroimmunol. 2000 Nov 1;111(1-2):245-7. doi: 10.1016/s0165-5728(00)00367-2. J Neuroimmunol. 2000. PMID: 11063846

2

CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers.

Gomez-Lira M, Liguori M, Magnani C, Bonamini D, Salviati A, Leone M, Andreoli V, Trojano M, Valentino P, Savettieri G, Quattrone A, Pignatti PF, Momigliano-Richiardi P, Giordano M. Gomez-Lira M, et al. Among authors: salviati a. J Neuroimmunol. 2003 Jul;140(1-2):216-21. doi: 10.1016/s0165-5728(03)00208-x. J Neuroimmunol. 2003. PMID: 12864992

3

Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis.

Gomez-Lira M, Moretto G, Bonamini D, Benedetti MD, Pignatti PF, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. J Neuroimmunol. 2002 Dec;133(1-2):241-3. doi: 10.1016/s0165-5728(02)00361-2. J Neuroimmunol. 2002. PMID: 12446029

4

A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene.

Perusi C, Gomez-Lira M, Mottes M, Pignatti PF, Rizzuto N, Salviati A. Perusi C, et al. Among authors: salviati a. Mol Cell Probes. 1997 Dec;11(6):449-51. doi: 10.1006/mcpr.1997.0138. Mol Cell Probes. 1997. PMID: 9500813

5

Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutation.

Gomez-Lira M, Perusi C, Mottes M, Pignatti PF, Manfredi M, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. Hum Genet. 1998 Apr;102(4):459-63. doi: 10.1007/s004390050721. Hum Genet. 1998. PMID: 9600244

6

Two novel missense mutations causing adrenoleukodystrophy in Italian patients.

Perusi C, Gomez-Lira M, Mottes M, Pignatti PF, Bertini E, Cappa M, Vigliani MC, Schiffer D, Rizzuto N, Salviati A. Perusi C, et al. Among authors: salviati a. Mol Cell Probes. 1999 Jun;13(3):179-82. doi: 10.1006/mcpr.1999.0232. Mol Cell Probes. 1999. PMID: 10369742

7

Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients.

Gomez-Lira M, Perusi C, Mottes M, Pignatti PF, Uziel G, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. J Neurol Sci. 1999 May 1;165(1):62-5. doi: 10.1016/s0022-510x(99)00074-x. J Neurol Sci. 1999. PMID: 10426149

8

Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations.

Lira MG, Mottes M, Pignatti PF, Medica I, Uziel G, Cappa M, Bertini E, Rizzuto N, Salviati A. Lira MG, et al. Among authors: salviati a. Hum Mutat. 2000 Sep;16(3):271. doi: 10.1002/1098-1004(200009)16:3<271::AID-HUMU15>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10980539

9

A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease.

Gomez-Lira M, Perusi C, Brutti N, Farnetani MA, Margollicci MA, Rizzuto N, Pignatti PF, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. Hum Mutat. 1995;6(3):260-2. doi: 10.1002/humu.1380060313. Hum Mutat. 1995. PMID: 8535449 No abstract available.

10

Splicing mutation causes infantile Sandhoff disease.

Gomez-Lira M, Perusi C, Mottes M, Pignatti PF, Rizzuto N, Gatti R, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. Am J Med Genet. 1998 Jan 23;75(3):330-3. Am J Med Genet. 1998. PMID: 9475608 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

56 results

Search Page

Filters