Oral Isobutyramide Therapy in Patients with Thalassemia Intermedia: Results of a Phase II Open Study-Reference-Cited by-同舟云学术

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Oral Isobutyramide Therapy in Patients with Thalassemia Intermedia: Results of a Phase II Open Study

Published:2000-02 Issue:1 Volume:26 Page:105-111
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Domenica Cappellini Maria,Graziadei Giovanna,Ciceri Laura,Comino Alessia,Bianchi Paolo,Porcella Antonella,Fiorelli Gemino

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference30 articles.

1. Survival in Medically Treated Patients with Homozygous β-Thalassemia

2. The β-Thalassemias

3. Interaction between Homozygous β0Thalassaemia and the Swiss Type of Hereditary Persistence of Fetal Haemoglobin

4. Beta-thalassemia unlinked to the beta-globin gene in an English family

5. Pharmacological Manipulation of Fetal Hemoglobin Synthesis in Patients with Severe ?-Thalassemia

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1. High pressure Raman study of isobutyramide;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2024-04

2. Bach1 inhibitor HPP-D mediates γ-globin gene activation in sickle erythroid progenitors;Blood Cells, Molecules, and Diseases;2024-01

3. Kinetic Analysis of Consecutive/Parallel Transformation of Furfural to Biomass-Based Primary Amide by Using a “Concentration–Time” Integral;ACS Catalysis;2022-12-12

4. Solubility and solution thermodynamics of isobutyramide in 15 pure solvents at temperatures from 273.15 to 324.75 K;Journal of Molecular Liquids;2020-08

5. Reactivation of Fetal Hemoglobin for Treating β-Thalassemia and Sickle Cell Disease;Advances in Experimental Medicine and Biology;2017

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