Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M L, Manca"'
Autor:
Anna Neri, M. L. Manca Bitti, Fulvia Gloria-Bottini, Sift Desk, Egidio Bottini, Patrizia Saccucci, A Magrini, Gloria-Bottini F
Publikováno v:
Journal of Advances In Allergy & Immunologic Diseases. 3:1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27ccf61e38d89862fb3c774c55a8ecbe
https://doi.org/10.25177/jaaid.3.1.1
https://doi.org/10.25177/jaaid.3.1.1
Autor:
A, Scano, F, Ebau, M L, Manca, V, Cabras, F, Cesare Marincola, M, Manconi, M, Pilloni, A M, Fadda, G, Ennas
Publikováno v:
International journal of pharmaceutics. 551(1-2)
Ball Milling technique has been used to prepare for the first time Vitis Vinifera extract-silica nanocomposites (VV-SiO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52ff24b85ffc15bea77fd001467b318f
https://pubmed.ncbi.nlm.nih.gov/30194010
https://pubmed.ncbi.nlm.nih.gov/30194010
Autor:
M. L. Manca Bitti, Ottavia Porzio, Arianna Massimi, Marinella Malaponti, Marco Cappa, D. Vinciguerra, L. Federici, Lucia Ghizzoni, Mauro Maccarrone, Alessandra Vottero, Sergio Bernardini
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder mainly caused by defects in the 21-hydroxylase gene (CYP21A2), coding for the enzyme 21-hydroxylase (21-OH). About 95% of the mutations arise from gene conversion between CYP21A2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1548cad3f86b77457c544f2e176d2cc5
http://hdl.handle.net/11697/155804
http://hdl.handle.net/11697/155804
Autor:
M. L. Manca Bitti, Giovanni Ghirlanda, Concetta Suraci, A. Crinò, Carla Giordano, F. Ferrazzoli, Maria Gisella Cavallo, M. Cassone Faldetta, E. Sarugeri, Maria Stella Sbriglia, M. C. Matteoli, M. Cervoni, Paolo Pozzilli, Raffaella Buzzetti, G. Multari, G. Marietti, N. Visalli, Dario Pitocco, S. Spera
Publikováno v:
Diabetologia. 43:1000-1004
Aims/hypothesis. Induction of tolerance to insulin is achievable in animal models of Type I (insulin-dependent) Diabetes mellitus by oral treatment with this hormone, which can lead to prevention of the disease. In the Diabetes Prevention Trial of Ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fea1a407701d8eb52ac2f1ba9c406a4e
https://doi.org/10.1007/s001250051482
https://doi.org/10.1007/s001250051482
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43fdb7c4b6ee23caff60bb11c0fa6f6
https://doi.org/10.1515/jpem.2010.23.3.291
https://doi.org/10.1515/jpem.2010.23.3.291
Autor:
A. Nicolucci, A. Maione, M. Franciosi, R. Amoretti, E. Busetto, F. Capani, D. Bruttomesso, P. Di Bartolo, A. Girelli, F. Leonetti, L. Morviducci, P. Ponzi, E. Vitacolonna, L. V. Cassano, N. Tota, V. Cherubini, A. Iannilli A. Corsi, P. Ponzani, V. Montani, P. Di Berardino, M. Velussi, F. Giorgino, V. Gigantelli, G. Beltramello, A. Pianta, R. Trevisan, G. Lepore, G. Forlani, G. Marchesini, D. Crazzolara, M. Marchesi, E. Zarra, B. Agosti, G. Careddu, L. Tomaselli, R. Vigneri, M. Agrusta, V. Di Blasi, S. Tumini, M. T. Anzellotti, P. Ruggeri, P. Foglini, M. Rossana, A Murri, S. Toni, M. F. Reali, M. Nizzoli, S. Aquati, G. d’Annunzio, N. Minuto, L. Cataldi, C. Bordone, R. Iannarelli, F. Sciarretta, M. Tagliaferri, M. A. Lezzi, L. Sciangula, A. Ciucci, M. Bonomo, E. Meneghini, G. Mariani, P. Colapinto, G. Testori, P. Rampini, R. Bonfanti, F. Meschi, G. Galimberti, A. Laurenzi, A. Veronelli, C. Mauri, C. Tortul, A. M. Cernigoi, M. E. De Feo, M. Piscopo, G. Annuzzi, L. Bozzetto, A. Franzese, P. Buono, S. Turco, A. Turco, F. Prisco, D. Iafusco, M. Trovati, P. Massucco, S. Costa, M, V. Provenzano, L. Strazzera, G. Ridola, E. Torlone, M. Orsini Federici, A. Bertolotto, M. Aragona, F. Pellicano, V. Manicardi, M. Michelini, M. Parenti, A. C. Babini, P. Borboni, A. Di Flaviani, M. L. Manca Bitti, S. Piccinini, A. Clementi, C. Tubili, C. Suraci, S. Carletti, A. Moretti, M. Maiello, V. C. Iannucci, N. Sulli, B. Shashaj, D. Fava, F. Massimiani, P. Pozzilli, S. Manfrini, C. Landi, I. Tanganelli, G. Grassi, M. Tomelini, R. De Luca, L. Corgiat Mansin, R. Candido, E. Manca, L. Tonutti, C. Noacco, I. Franzetti, P. Marnini.
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 25(2)
Aims The aim of this case–control study was to compare quality of life (QoL) and treatment satisfaction in adults with Type 1 diabetes (T1DM) treated with either continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDI). Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd8c465d542f816a84b291a15cab758d
https://pubmed.ncbi.nlm.nih.gov/18201210
https://pubmed.ncbi.nlm.nih.gov/18201210
Autor:
Novella Rapini, E. Del Duca, A. Maccari, G. Canu, M. L. Manca Bitti, Luigi Fontana, Alberto Verrotti, F. Angelini, Patrizia Saccucci, Nunzio Bottini, F. Chiarelli, Simona Piccinini, Cosimo Giannini
The missense PTPN22 C1858T polymorphism recently emerged as an important population-independent risk factor for type 1 diabetes (T1D) and other autoimmune diseases. The PTPN22 gene encodes the lymphoid tyrosine phosphatase (LYP), a negative regulator
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9f92927faf7850fa9d4bfb13acb1ed6
http://hdl.handle.net/11391/1230181
http://hdl.handle.net/11391/1230181
Autor:
M. L. Manca Bitti, F. Angelini, Valentina Pacciani, Paolo Rossi, Simona Piccinini, E. Del Duca
SummaryThe importance of dendritic cells (DC) in the activation of T cells and in the maintenance of self-tolerance is well known. We investigated whether alterations in phenotype and function of DC may contribute to the pathogenesis of Type 1 diabet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27db651f4ab02580e7b8d30983364104
http://hdl.handle.net/2108/103014
http://hdl.handle.net/2108/103014
Bayesian approach to searching for susceptibility genes: Gc2 and EsD1 alleles and multiple sclerosis
Publikováno v:
Collegium antropologicum. 26(1)
Multiple sclerosis (MS) is one of the most common causes of neurological disability in early adulthood. The current literature is interested in identifying biological or DNA markers associated with genetic susceptibility to MS. The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9d5516883327bfd75a65171431d2f3d
https://pubmed.ncbi.nlm.nih.gov/12137326
https://pubmed.ncbi.nlm.nih.gov/12137326
Autor:
A, Tessa, M L, Manca, M, Mancuso, M R, Renna, L, Murri, B, Martini, F M, Santorelli, G, Siciliano
Publikováno v:
Functional neurology. 15(4)
We report on a patient suffering from a progressive mitochondrial disorder characterized by ocular myopathy, exercise intolerance, and muscle wasting. Morphological examination of muscle biopsy showed increased variability in fiber size and scattered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cbb5a52ad59fd30b61e09aaff4752a65
https://pubmed.ncbi.nlm.nih.gov/11213524
https://pubmed.ncbi.nlm.nih.gov/11213524