12
results
for author:"Liguori R."
in Literature Citations
| Axial myoclonus in paraproteinemic polyneuropathy. Vetrugno R., Liguori R., D'Alessandro R., D'Angelo R., Alessandria M., Montagna P. Muscle Nerve 38:1330-1335(2008) · Mapped (8) |
| Multiple sclerosis and hepatitis C virus infection are associated with single nucleotide polymorphisms in interferon pathway genes. Fortunato G., Calcagno G., Bresciamorra V., Salvatore E., Filla A., Capone S., Liguori R., Borelli S., Gentile I., Borrelli F. et al. J. Interferon Cytokine Res. 28:141-152(2008) · Mapped (27) |
| Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. La Morgia C., Achilli A., Iommarini L., Barboni P., Pala M., Olivieri A., Zanna C., Vidoni S., Tonon C., Lodi R. et al. Neurology 70:762-770(2008) · UniProtKB (18) |
| OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Amati-Bonneau P., Valentino M.L., Reynier P., Gallardo M.E., Bornstein B., Boissiere A., Campos Y., Rivera H., de la Aleja J.G., Carroccia R. et al. Brain 131:338-351(2008) · Mapped (2) |
| The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy. Liguori R., Mazzaccara C., Pasanisi F., Buono P., Oriani G., Finelli C., Contaldo F., Sacchetti L. Nutr Metab Cardiovasc Dis 16:466-470(2006) · Mapped (2) |
| Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy. Buono P., Pasanisi F., Nardelli C., Ieno L., Capone S., Liguori R., Finelli C., Oriani G., Contaldo F., Sacchetti L. Clin. Chem. 51:1358-1364(2005) · Mapped (8) |
| High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy. De Marco F., Liguori R., Giardina M.G., D'Armiento M., Angelucci E., Lucariello A., Morante R., Cimino L., Galeota-Lanza A., Tarantino G. et al. Clin. Chem. Lab. Med. 42:17-24(2004) · Mapped (20) |
| POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness. Mancuso M., Filosto M., Bellan M., Liguori R., Montagna P., Baruzzi A., DiMauro S., Carelli V. |
| Increased carotid artery intima-media thickness is associated with a novel mutation of low-density lipoprotein receptor independently of major cardiovascular risk factors. Pauciullo P., Giannino A., De Michele M., Gentile M., Liguori R., Argiriou A., Carlotto A., Faccenda F., Mancini M., Bond M.G. et al. Metab. Clin. Exp. 52:1433-1438(2003) · Mapped (11) |
| Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana. Salanoubat M., Lemcke K., Rieger M., Ansorge W., Unseld M., Fartmann B., Valle G., Bloecker H., Perez-Alonso M., Obermaier B. et al. Nature 408:820-822(2000) · UniProtKB (5,349) |
| Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability. Eunson L.H., Rea R., Zuberi S.M., Youroukos S., Panayiotopoulos C.P., Liguori R., Avoni P., McWilliam R.C., Stephenson J.B.P., Hanna M.G. et al. Ann. Neurol. 48:647-656(2000) · UniProtKB (1) |
| Sequence and analysis of chromosome 4 of the plant Arabidopsis thaliana. Mayer K.F.X., Schueller C., Wambutt R., Murphy G., Volckaert G., Pohl T., Duesterhoeft A., Stiekema W., Entian K.-D., Terryn N. et al. Nature 402:769-777(1999) · UniProtKB (4,588) |
