P1537: HEREDITARY ANEMIA CAUSED BY MULTILOCUS INHERITANCE OF PIEZO1, SLC4A1 AND ABCB6 MUTATIONS: A DIAGNOSTIC AND THERAPEUTIC CHALLENGE.
Main Authors: | B. E. Rosato, S. L. Alper, G. Tomaiuolo, R. Russo, A. Iolascon, I. Andolfo |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2022-06-01
|
Series: | HemaSphere |
Online Access: | http://journals.lww.com/10.1097/01.HS9.0000849004.04269.ae |
Similar Items
-
Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients
by: Immacolata Andolfo, et al.
Published: (2021-06-01) -
Increased Red Cell KCNN4 Activity in Sporadic Hereditary Xerocytosis Associated With Enhanced Single Channel Pressure Sensitivity of PIEZO1 Mutant V598M
by: Radhakrishnan Gnanasambandam, et al.
Published: (2018-10-01) -
P1468: PIEZO1 GAIN-OF-FUNCTION VARIANTS ACCOUNT FOR STRESSED ERYTHROPOIESIS BY ALTERING APOPTOSIS, HYPOXIA CELL RESPONSE, AND GLYCOLYSIS
by: Barbara Eleni Rosato, et al.
Published: (2023-08-01) -
Recommendations for Pregnancy in Rare Inherited Anemias
by: Ali T. Taher, et al.
Published: (2020-08-01) -
Recommendations regarding splenectomy in hereditary hemolytic anemias
by: Iolascon, A, et al.
Published: (2017)