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Items: 12

1.

The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway.

Greco E, Aita A, Galozzi P, Gava A, Sfriso P, Negm OH, Tighe P, Caso F, Navaglia F, Dazzo E, De Bortoli M, Rampazzo A, Obici L, Donadei S, Merlini G, Plebani M, Todd I, Basso D, Punzi L.

Arthritis Res Ther. 2015 Apr 3;17:93. doi: 10.1186/s13075-015-0604-7.

2.

The role of minor salivary gland biopsy in the diagnosis of systemic amyloidosis: results of a prospective study in 62 patients.

Foli A, Palladini G, Caporali R, Verga L, Morbini P, Obici L, Russo P, Sarais G, Donadei S, Montecucco C, Merlini G.

Amyloid. 2011 Jun;18 Suppl 1:80-2. doi: 10.3109/13506129.2011.574354029. No abstract available. Erratum in: Amyloid. 2011 Jun;18 Suppl 1:82.

PMID:
21838441
3.

Proteomic characterization of amyloid deposits in transthyretin amyloidosis associated with various mutations.

Valentini V, Lavatelli F, Obici L, Donadei S, Perlini S, Palladini G, Merlini G.

Amyloid. 2011 Jun;18 Suppl 1:61-3. doi: 10.3109/13506129.2011.574354022. No abstract available. Erratum in: Amyloid. 2011 Jun;18 Suppl 1:63.

PMID:
21838434
4.

Favourable and sustained response to anakinra in tumour necrosis factor receptor-associated periodic syndrome (TRAPS) with or without AA amyloidosis.

Obici L, Meini A, Cattalini M, Chicca S, Galliani M, Donadei S, Plebani A, Merlini G.

Ann Rheum Dis. 2011 Aug;70(8):1511-2. doi: 10.1136/ard.2010.143438. Epub 2010 Dec 20. No abstract available.

PMID:
21173015
5.

Embryonic stem and haematopoietic progenitor cells resist to Aβ oligomer toxicity and maintain the differentiation potency in culture.

Neri T, Bucciantini M, Rosti V, Raimondi S, Relini A, Massa M, Zuccotti M, Donadei S, Stefani M, Redi CA, Merlini G, Stoppini M, Garagna S, Bellotti V.

Amyloid. 2010 Sep;17(3-4):137-45. doi: 10.3109/13506129.2010.530138. Epub 2010 Nov 10.

PMID:
21067308
6.

The intracellular quality control system down-regulates the secretion of amyloidogenic apolipoprotein A-I variants: a possible impact on the natural history of the disease.

Marchesi M, Parolini C, Valetti C, Mangione P, Obici L, Giorgetti S, Raimondi S, Donadei S, Gregorini G, Merlini G, Stoppini M, Chiesa G, Bellotti V.

Biochim Biophys Acta. 2011 Jan;1812(1):87-93. doi: 10.1016/j.bbadis.2010.07.002. Epub 2010 Jul 15.

7.

Dysfunctional inflammasome in Schnitzler's syndrome.

Pizzirani C, Falzoni S, Govoni M, La Corte R, Donadei S, Di Virgilio F, Trotta F, Lo Monaco A.

Rheumatology (Oxford). 2009 Oct;48(10):1304-8. doi: 10.1093/rheumatology/kep222. Epub 2009 Aug 20.

PMID:
19696060
8.

Clinical, radiological, and biochemical features of a bilateral buttock amyloidoma emerging after 27 years of hemodialysis.

Montagna G, Raimondi S, Moro G, Uggetti C, Relini A, Magrini U, Esposito G, Giorgetti S, Congi L, Mosconi M, Galli G, Villa G, Segagni S, Donadei S, Obici L, Merlini G, Stoppini M, Bellotti V.

Amyloid. 2009;16(3):115-21. doi: 10.1080/13506120903090783.

PMID:
19626482
9.

Identification of amyloidogenic light chains requires the combination of serum-free light chain assay with immunofixation of serum and urine.

Palladini G, Russo P, Bosoni T, Verga L, Sarais G, Lavatelli F, Nuvolone M, Obici L, Casarini S, Donadei S, Albertini R, Righetti G, Marini M, Graziani MS, Melzi D'Eril GV, Moratti R, Merlini G.

Clin Chem. 2009 Mar;55(3):499-504. doi: 10.1373/clinchem.2008.117143. Epub 2009 Jan 8.

10.

Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.

Gregorini G, Izzi C, Obici L, Tardanico R, Röcken C, Viola BF, Capistrano M, Donadei S, Biasi L, Scalvini T, Merlini G, Scolari F.

J Am Soc Nephrol. 2005 Dec;16(12):3680-6. Epub 2005 Oct 12.

11.

A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy.

Obici L, Demarchi A, de Rosa G, Bellotti V, Marciano S, Donadei S, Arbustini E, Palladini G, Diegoli M, Genovese E, Ferrari G, Coverlizza S, Merlini G.

Ann Neurol. 2005 Oct;58(4):639-44.

PMID:
16178030
12.

Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families.

Obici L, Palladini G, Giorgetti S, Bellotti V, Gregorini G, Arbustini E, Verga L, Marciano S, Donadei S, Perfetti V, Calabresi L, Bergonzi C, Scolari F, Merlini G.

Gastroenterology. 2004 May;126(5):1416-22.

PMID:
15131802

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