1-4 of 4
P Gasparini
Close
Sort by
Journal Articles

Familial Pseudohyperkalemia Maps to the Same Locus as Dehydrated Hereditary Stomatocytosis (Hereditary Xerocytosis)

A. Iolascon, G.W. Stewart, J.F. Ajetunmobi, S. Perrotta, J. Delaunay, M. Carella, L. Zelante, P. Gasparini
Journal: Blood
Blood (1999) 93 (9): 3120–3123.
https://doi.org/10.1182/blood.V93.9.3120
Published: 1999
Journal Articles

Molecular basis for the hereditary hyperferritinemia-cataract syndrome [letter]

D Girelli, O Olivieri, P Gasparini, R Corrocher
Journal: Blood
Blood (1996) 87 (11): 4912–4913.
https://doi.org/10.1182/blood.V87.11.4912.bloodjournal87114912
Published: 1996
Journal Articles

Molecular basis for the recently described hereditary hyperferritinemia- cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation") [see comments]

D Girelli, R Corrocher, L Bisceglia, O Olivieri, L De Franceschi, L Zelante, P Gasparini
Journal: Blood
Blood (1995) 86 (11): 4050–4053.
https://doi.org/10.1182/blood.V86.11.4050.bloodjournal86114050
Published: 1995
Journal Articles

BCR breakpoint subregions and blast crisis lineage in CML patients [letter; comment]

G Martinelli, A Chiamenti, P Gasparini, PF Pignatti, A Ambrosetti, A Zaccaria, M Buzzi, N Testoni, S Tura, A Guerrasio
Journal: Blood
Blood (1992) 79 (3): 838–839.
https://doi.org/10.1182/blood.V79.3.838.838
Published: 1992