1-5 of 5
A. Iolascon
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

UGT1 Promoter Polymorphism Accounts for Increased Neonatal Appearance of Hereditary Spherocytosis

A. Iolascon, M.F. Faienza, A. Moretti, S. Perrotta, E. Miraglia del Giudice
Journal: Blood
Blood (1998) 91 (3): 1093–1094.
https://doi.org/10.1182/blood.V91.3.1093
Published: 1998
Journal Articles

Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia

L Baronciani, A Zanella, P Bianchi, M Zappa, F Alfinito, A Iolascon, N Tannoia, E Beutler, G Sirchia
Journal: Blood
Blood (1996) 88 (6): 2306–2310.
https://doi.org/10.1182/blood.V88.6.2306.bloodjournal8862306
Published: 1996
Journal Articles

The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum

N Alloisio, P Texier, L Denoroy, C Berger, E Miraglia del Giudice, S Perrotta, A Iolascon, F Gilsanz, G Berger, J Guichard
Journal: Blood
Blood (1996) 87 (10): 4433–4439.
https://doi.org/10.1182/blood.V87.10.4433.bloodjournal87104433
Published: 1996
Journal Articles

Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)

S Perrotta, E Miraglia del Giudice, N Alloisio, G Sciarratta, L Pinto, J Delaunay, S Cutillo, A Iolascon
Journal: Blood
Blood (1994) 83 (11): 3346–3349.
https://doi.org/10.1182/blood.V83.11.3346.3346
Published: 1994