Search Results - "Aguennouz, M."

Association between osteocalcin and residual β-cell function in children and adolescents newly diagnosed with type 1 diabetes: a pivotal study by Valenzise, M, Bombaci, B, Lombardo, F, Passanisi, S, Lombardo, C, Lugarà, C, D'Amico, F, Grasso, L, Aguennouz, M, Catalano, A, Salzano, G

“…This pivotal study aimed to evaluate circulating levels of bone remodeling markers in children and adolescents at the onset of type 1 diabetes (T1D)…”
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Telomere length modulation in human astroglial brain tumors by La Torre, Domenico, Conti, Alfredo, Aguennouz, M Hammed, De Pasquale, Maria Grazia, Romeo, Sara, Angileri, Filippo Flavio, Cardali, Salvatore, Tomasello, Chiara, Alafaci, Concetta, Germanò, Antonino

“…Telomeres alteration during carcinogenesis and tumor progression has been described in several cancer types. Telomeres length is stabilized by telomerase…”
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MicroRNAs expression in pituitary tumors: differences related to functional status, pathological features, and clinical behavior by Vicchio, T. M., Aliquò, F., Ruggeri, R. M., Ragonese, M., Giuffrida, G., Cotta, O. R., Spagnolo, F., Torre, M. L., Alibrandi, A., Asmundo, A., Angileri, F. F., Esposito, F., Polito, F., Oteri, R., Aguennouz, M. H., Cannavò, S., Ferraù, F.

“…Background MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression at post-transcriptional level, having a role in many biological…”
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Activation of nuclear factor-κB in inflammatory myopathies and Duchenne muscular dystrophy by MONICI, M. C, AGUENNOUZ, M, MAZZEO, A, MESSINA, C, VITA, G

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P02 ARGININE DEPRIVATION INDUCES ACQUISITION OF A SENESCENT PHENOTYPE AND FAVORS GENOMIC INSTABILITY IN MULTIPLE MYELOMA PLASMACELLS by Romano, A., Scandura, G., Giallongo, C., La Spina, E., Giallongo, S., Longhitano, L., Zuppelli, T., Dulcamare, I., Parrinello, N. L., Polito, F., Oteri, R., Aguennouz, M., Vicario, N., Amorini, A. M., Del Fabro, V., Conticello, C., Li Volti, G., Palumbo, G. A., Tibullo, D., Di Raimondo, F.

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Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency by Corti, S, Bordoni, A, Ronchi, D, Musumeci, O, Aguennouz, M, Toscano, A, Lamperti, C, Bresolin, N, Comi, G.P

“…Abstract Carnitine palmitoyltransferase II (CPT II) deficiency is the most common inherited disorder of lipid metabolism characterized in its adult form by…”
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MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2B by Aguennouz, M., Lo Giudice, C., Licata, N., Rodolico, C., Musumeci, O., Fanin, M., Migliorato, A., Ragusa, M., Macaione, V., Di Giorgio, R. M., Angelini, C., Toscano, A.

“…miRNA expression profile and predicted pathways involved in selected limb‐girdle muscular dystrophy (LGMD)2A/2B patients were investigated. A total of 187…”
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ANT1 is reduced in sporadic inclusion body myositis by Barca, E., Aguennouz, M., Mazzeo, A., Messina, S., Toscano, A., Vita, G. L., Portaro, S., Parisi, D., Rodolico, C.

“…To investigate ANT1 and NF-κB expression in inclusion body myositis (IBM) muscle and to verify their possible roles in the pathogenesis of the disease, we…”
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T.P.16 by Montagnese, F, Musumeci, O, Barca, E, Romeo, S, Ciranni, A, Aguennouz, M, Rodolico, C, Toscano, A

“…Pompe disease is a rare metabolic myopathy due to mutations in the gene encoding acid alpha-glucosidase (GAA) involved in glycogen degradation. Two clinical…”
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MDR-1 polymorphisms (G2677T and C3435T) in B-chronic lymphocytic leukemia: an impact on susceptibility and prognosis by Penna, G., Allegra, A., Alonci, A., Aguennouz, M., Garufi, A., Cannavò, A., Gerace, D., Alibrandi, A., Musolino, C.

“…Patients with B-chronic lymphocytic leukemia present diverse clinical features, genetic abnormalities, variable response to treatment, and heterogeneous…”
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P.17.10 New ETFDH mutations in a group of Italian patients with Riboflavin-Responsive Multiple Acyl-CoA Dehydrogenase Deficiency (RR-MADD) by Toscano, A, Barca, E, Rodolico, C, Romeo, S, Ciranni, A, Aguennouz, M, Vita, G, Musumeci, O

“…Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) is a rare autosomal recessive disorder of the electron transfer flavoproteins. Three clinical forms have been…”
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G.P.100 by Messina, S, Vita, G.L, Licata, N, Sframeli, M, Bitto, A, Distefano, M.G, Barcellona, C, Rosa, M. La, Romeo, S, Ciranni, A, Aguennouz, M, Squadrito, F, Vita, G

“…Muscle degeneration in Duchenne muscular dystrophy (DMD) is exacerbated by the endogenous inflammatory response and increased oxidative stress. A key role is…”
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RAGE-NF-κB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy by Macaione, V., Aguennouz, M., Rodolico, C., Mazzeo, A., Patti, A., Cannistraci, E., Colantone, L., Di Giorgio, R. M., De Luca, G., Vita, G.

“…Objectives –  An increased expression of adenine nucleotide translocator (ANT1), found in facioscapulohumeral muscular dystrophy (FSHD), is known to lead to a…”
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T.P.52 Pilot study of flavocoxid in ambulant DMD patients by Messina, S, Vita, G.L, Sframeli, M, Licata, N, Cama, A, Ciranni, A, Romeo, S, Aguennouz, M, Vita, G

“…Abstract Muscle degeneration in Duchenne muscular dystrophy (DMD) is exacerbated by the endogenous inflammatory response and increased oxidative stress. A key…”
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New Mutations in TK2 Gene Associated With Mitochondrial DNA Depletion by Galbiati, Sara, Bordoni, Andreina, Papadimitriou, Dimitra, Toscano, Antonio, Rodolico, Carmelo, Katsarou, Efi, Sciacco, Monica, Garufi, Anastasia, Prelle, Alessandro, Aguennouz, M.’hammed, Bonsignore, Maria, Crimi, Marco, Martinuzzi, Andrea, Bresolin, Nereo, Papadimitriou, Alex, Comi, Giacomo P.

“…Mitochondrial deoxyribonucleic acid depletion syndromes are autosomal recessive disorders characterized by a reduction of the amount of mitochondrial…”
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T.P.40 Implication of SIRT1 and its downstream pathways in dystrophic process by Messina, S, Vita, G.L, De Pasquale, M.G, Cama, A, Licata, A, Romeo, S, Ciranni, A, Lo Giudice, C, Toscano, A, Aguennouz, M, Vita, G

“…Abstract Muscle necrosis and exhaustible muscle regeneration are key elements in Duchenne muscular dystrophy (DMD) pathogenesis. Our group has previously…”
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P3.49 The soy isoflavone genistein promotes muscle regeneration and function acting on cell cycle and apoptosis in mdx mice by Messina, S, Vita, G.L, Bitto, A, Aguennouz, M, Squadrito, F, Vita, G

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G.P.11.05 A life threatening case of α-enolase deficiency by Musumeci, O, Rodolico, C, Ciranni, A, Aguennouz, M, Lanzano, N, Toscano, A

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Immunolocalization and activation of nuclear factor-κB in the sciatic nerves of rats with experimental autoimmune neuritis by Laurà, M., Mazzeo, A., Aguennouz, M., Santoro, M., Catania, M.A., Migliorato, A., Calapai, G., Vita, G.

“…Recent data support an important role played by nuclear factor kappa B (NF-κB) in peripheral neuropathies. We investigated expression and activation of NF-κB…”
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P4.20 Telomere length in exercised wild type and mdx mice by Messina, S, Vita, G.L, Aguennouz, M, Romeo, S, Pontoriero, D, Cozzoli, A, Capogrosso, R, Sbendorio, V, De Luca, A, Vita, G

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