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2015
Callea M, Yavuz I, Clarich G, Cammarata-Scalisi F. [Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2015;113(6):e341-4.
Nicchia E, Benedicenti F, De Rocco D, Greco C, Bottega R, Inzana F, Faleschini M, Bonin S, Cappelli E, Mogni M, Stanzial F, Svahn J, Dufour C, Savoia A. Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Birth Defects Res A Clin Mol Teratol 2015;103(12):1003-1010.
Benelli E, Carrato V, Martelossi S, Ronfani L, Not T, Ventura A. Coeliac disease in the ERA of the new ESPGHAN and BSPGHAN guidelines: a prospective cohort study. Arch Dis Child 2015;
Santarelli L, Staffolani S, Strafella E, Nocchi L, Manzella N, Grossi P, Bracci M, Pignotti E, Alleva R, Borghi B, Pompili C, Sabbatini A, Rubini C, Zuccatosta L, Bichisecchi E, Valentino M, Horwood K, Comar M, Bovenzi M, Dong L-F, Neuzil J, Amati M, Tomasetti M. Combined circulating epigenetic markers to improve mesothelin performance in the diagnosis of malignant mesothelioma. Lung Cancer 2015;
Santos Rde Luna Al, Crovella S, Celsi F. Comment to Santos et al., "hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype". Gene 2015;559(1):99-101.
Santos Rde Luna Al, Crovella S, Celsi F. Comment to Santos et al., "hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype". Gene 2015;559(1):99-101.
Catamo E, Addobbati C, Segat L, T Fragoso S, A Dantas T, H Mariz deAtaíde, L Junior Fda Rocha, PintoDuarte ALBranco, Coelho AVC, de Moura RR, Polesello V, Crovella S, P Garcia S. Comprehensive analysis of polymorphisms in the HLA-G 5' upstream regulatory and 3' untranslated regions in Brazilian patients with systemic lupus erythematosus. Tissue Antigens 2015;85(6):458-65.
Catamo E, Addobbati C, Segat L, T Fragoso S, A Dantas T, H Mariz deAtaíde, L Junior Fda Rocha, PintoDuarte ALBranco, Coelho AVC, de Moura RR, Polesello V, Crovella S, P Garcia S. Comprehensive analysis of polymorphisms in the HLA-G 5' upstream regulatory and 3' untranslated regions in Brazilian patients with systemic lupus erythematosus. Tissue Antigens 2015;85(6):458-65.
Catamo E, Addobbati C, Segat L, T Fragoso S, A Dantas T, H Mariz deAtaíde, L Junior Fda Rocha, PintoDuarte ALBranco, Coelho AVC, de Moura RR, Polesello V, Crovella S, P Garcia S. Comprehensive analysis of polymorphisms in the HLA-G 5' upstream regulatory and 3' untranslated regions in Brazilian patients with systemic lupus erythematosus. Tissue Antigens 2015;85(6):458-65.
Trapella C, Voltan R, Melloni E, Tisato V, Celeghini C, Bianco S, Fantinati A, Salvadori S, Guerrini R, Secchiero P, Zauli G. Design, Synthesis, and Biological Characterization of Novel Mitochondria Targeted Dichloroacetate-Loaded Compounds with Antileukemic Activity. J Med Chem 2015;
Girardelli M, Arrigo S, Barabino A, Loganes C, Morreale G, Crovella S, Tommasini A, Bianco AMonica. The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency. BMC Pediatr 2015;15(1):208.
Parisi P, Verrotti A, Costa P, Striano P, Zanus C, Carrozzi M, Raucci U, Villa MPia, Belcastro V. Diagnostic criteria currently proposed for "ictal epileptic headache": Perspectives on strengths, weaknesses and pitfalls. Seizure 2015;31:56-63.

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