Giuseppe Albeggiani
Palermo, Italy
Last Updated: 09/26/2026
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Found 9 publications
IL-33/s-ST2 ratio, systemic symptoms, and basophil activation in Pru p 3-sensitized allergic patients.
Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]
Published: March 21, 2018
Novel α-galactosidase A mutation in patients with severe cardiac manifestations of Fabry disease.
Journal: Gene
Published: April 15, 2013
De novo mutation in a male patient with Fabry disease: a case report.
Journal: BMC research notes
Published: March 29, 2013
Alteration of proteomic profiles in PBMC isolated from patients with Fabry disease: preliminary findings.
Journal: Molecular bioSystems
Published: February 07, 2013
Misdiagnosis of familial Mediterranean fever in patients with Anderson-Fabry disease.
Journal: Clinical genetics
Published: May 23, 2012
Novel alpha-galactosidase A mutation in a female with recurrent strokes.
Journal: Clinical biochemistry
Published: April 12, 2012
Identification of a novel mutation in the alpha-galactosidase A gene in patients with Fabry disease.
Identification of a novel mutation in the alpha-galactosidase A gene in patients with Fabry disease.
Journal: Clinical biochemistry
Published: January 13, 2012
A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report.
Journal: BMC cardiovascular disorders
Published: December 20, 2011
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Last Updated: 09/26/2026