Hereditary spherocytosis, elliptocytosis, and other red cell membrane disordersYBLRE-00309; No of Pages 12 Contents lists available at SciVerse ScienceDirect Blood Reviews
Diapositiva 1Naples – Italy September 24, 2020 Hereditary Stomatocytosis Classification of hereditary stomatocytosis (HSt): clinical and genetic aspects Diagnosis and
Anemia emolitica Difetti del trasporto di membrana (approccio diagnostico) Immacolata Andolfo, PhD Università degli Studi di Napoli, Federico II CEINGE, biotecnologie
2009by Immacolata Andolfo, Roberta Russo, Antonella Gambale, and Achille Iolascon Haematologica 2016 [Epub ahead of print] Citation: Andolfo I, Russo R, Gambale A, and Iolascon
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65SAndrew K. Stewart,1,5 Boris E. Shmukler,1,5 David H. Vandorpe,1,5 Alicia Rivera,2,7 John
193944_INT.pdfBlood Donor Selection WHO Library Cataloguing-in-Publication Data Blood donor selection: guidelines on assessing donor suitability for blood donation. 1.Blood
70619845Homozygous Southeast Asian Ovalocytosis in five live-born neonates by Amanda A. Lavinya, Ruzzieatul A. Razali, Munirah A. Razak, Rashidah Mohamed, Emmanuel J. Moses,
www.edoriumjournals.com International Journal of Case Reports and Images (IJCRI) International Journal of Case Reports and Images (IJCRI) is an international, peer reviewed,