Barbon G - Search Results

1

Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.

Pontara E, Gresele P, Cattini MG, Daidone V, Barbon G, Girolami A, Zanon E, Casonato A. Pontara E, et al. Among authors: barbon g. Blood Coagul Fibrinolysis. 2014 Jun;25(4):401-4. doi: 10.1097/MBC.0000000000000067. Blood Coagul Fibrinolysis. 2014. PMID: 24418945

2

Severe, recessive type 1 is a discrete form of von Willebrand disease: the lesson learned from the c.1534-3C>A von Willebrand factor mutation.

Casonato A, Cattini MG, Barbon G, Daidone V, Pontara E. Casonato A, et al. Among authors: barbon g. Thromb Res. 2015 Sep;136(3):682-6. doi: 10.1016/j.thromres.2015.07.014. Epub 2015 Jul 26. Thromb Res. 2015. PMID: 26251079

3

Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease.

Daidone V, Barbon G, Cattini MG, Pontara E, Romualdi C, Di Pasquale I, Hosokawa K, Casonato A. Daidone V, et al. Among authors: barbon g. Haemophilia. 2016 Nov;22(6):949-956. doi: 10.1111/hae.12971. Epub 2016 Jun 13. Haemophilia. 2016. PMID: 27293213

4

A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.

Casonato A, Daidone V, Barbon G, Pontara E, Di Pasquale I, Gallinaro L, Marullo L, Bertorelle G. Casonato A, et al. Among authors: barbon g. Haematologica. 2013 Jan;98(1):147-52. doi: 10.3324/haematol.2012.066019. Epub 2012 Aug 8. Haematologica. 2013. PMID: 22875612 Free PMC article.

5

The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity.

Daidone V, Saga G, Barbon G, Pontara E, Cattini MG, Morpurgo M, Zanotti G, Casonato A. Daidone V, et al. Among authors: barbon g. Br J Haematol. 2015 Aug;170(4):564-73. doi: 10.1111/bjh.13472. Epub 2015 Apr 23. Br J Haematol. 2015. PMID: 25904363 Free article. Clinical Trial.

6

Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis.

Casonato A, Galletta E, Cella G, Barbon G, Daidone V. Casonato A, et al. Among authors: barbon g. Arterioscler Thromb Vasc Biol. 2020 Sep;40(9):2187-2194. doi: 10.1161/ATVBAHA.120.314656. Epub 2020 Jul 9. Arterioscler Thromb Vasc Biol. 2020. PMID: 32640909 Free article.

7

Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor.

Daidone V, Barbon G, Pontara E, Cattini GM, Gallinaro L, Zampese E, Pizzo P, Casonato A. Daidone V, et al. Among authors: barbon g. Thromb Haemost. 2014 Dec;112(6):1159-66. doi: 10.1160/TH14-04-0391. Epub 2014 Sep 18. Thromb Haemost. 2014. PMID: 25230768

8

The homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature review.

Fusco C, Ucchino V, Barbon G, Bonini E, Mostacciuolo ML, Frattini D, Pisani F, Giustina ED. Fusco C, et al. Among authors: barbon g. J Child Neurol. 2011 Jan;26(1):49-57. doi: 10.1177/0883073810373142. J Child Neurol. 2011. PMID: 21212451 Review.

9

Novel mutations in the L1CAM gene support the complexity of L1 syndrome.

Bertolin C, Boaretto F, Barbon G, Salviati L, Lapi E, Divizia MT, Garavelli L, Occhi G, Vazza G, Mostacciuolo ML. Bertolin C, et al. Among authors: barbon g. J Neurol Sci. 2010 Jul 15;294(1-2):124-6. doi: 10.1016/j.jns.2010.03.030. Epub 2010 May 5. J Neurol Sci. 2010. PMID: 20447653

10

ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions.

Mulatero P, Schiavi F, Williams TA, Monticone S, Barbon G, Opocher G, Fallo F. Mulatero P, et al. Among authors: barbon g. J Hum Hypertens. 2016 Jun;30(6):374-8. doi: 10.1038/jhh.2015.98. Epub 2015 Oct 8. J Hum Hypertens. 2016. PMID: 26446392

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