HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Celeste Bento Selected Research

Hemoglobins (Hemoglobin)

11/2016Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations.
1/2014Genetic basis of congenital erythrocytosis: mutation update and online databases.
10/2013Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
3/2013Transient neonatal cyanosis associated with a new Hb F variant: Hb F viseu.
1/2012High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
11/2006The use of capillary blood samples in a large scale screening approach for the detection of beta-thalassemia and hemoglobin variants.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Celeste Bento Research Topics

Disease

4Polycythemia (Erythrocytosis)
01/2023 - 10/2013
4Thalassemia
05/2022 - 07/2011
4Anemia
03/2022 - 07/2011
4primary familial and congenital Polycythemia
06/2018 - 10/2013
3Hypoxia (Hypoxemia)
11/2023 - 01/2014
3Glucosephosphate Dehydrogenase Deficiency
02/2023 - 04/2011
3Hemolytic Anemia
01/2016 - 01/2010
2Hemoglobinopathies
01/2022 - 01/2012
2Cyanosis
11/2019 - 03/2013
2beta-Thalassemia (Cooley's Anemia)
04/2015 - 11/2006
2Pyruvate Kinase Deficiency of Red Cells
01/2010 - 09/2002
2Autistic Disorder (Autism)
04/2007 - 07/2004
1Congenital Heart Defects (Congenital Heart Defect)
01/2016
1Reperfusion Injury
12/2011
1Jaundice (Icterus)
07/2011
1Splenomegaly
07/2011
1Sickle Cell Anemia (Hemoglobin S Disease)
01/2010
1Rett Syndrome (Rett's Disorder)
06/2007

Drug/Important Bio-Agent (IBA)

6GlobinsIBA
05/2022 - 07/2011
6Hemoglobins (Hemoglobin)IBA
11/2016 - 11/2006
3Glucosephosphate Dehydrogenase (Glucose 6 Phosphate Dehydrogenase)IBA
02/2023 - 04/2011
3Oxygen (Dioxygen)IBA
11/2016 - 01/2014
3ErythropoietinFDA Link
01/2014 - 10/2013
2Prolyl Hydroxylases (Prolyl Hydroxylase)IBA
11/2023 - 01/2014
2EnzymesIBA
02/2023 - 01/2014
2Proteins (Proteins, Gene)FDA Link
06/2018 - 01/2014
2Ferritins (Ferritin)IBA
03/2015 - 01/2012
2IronIBA
01/2014 - 01/2012
2Messenger RNA (mRNA)IBA
04/2011 - 09/2002
1Proline (L-Proline)FDA Link
01/2023
1Nonsense Codon (Nonsense Mutation)IBA
03/2022
1Glycated Hemoglobin (Glycosylated Hemoglobin)IBA
01/2022
1Adenosine Monophosphate (AMP)IBA
01/2022
1hemoglobin M IwateIBA
11/2019
1Glucose-6-Phosphate Isomerase (Phosphoglucose Isomerase)IBA
01/2016
1Fetal Hemoglobin (Hemoglobin F)IBA
04/2015
1hemoglobin BethesdaIBA
01/2015
12,3-Diphosphoglycerate (2,3 Bisphosphoglycerate)IBA
01/2014
1OxygenasesIBA
01/2014
1Ketoglutaric Acids (Ketoglutaric Acid)IBA
01/2014
1Transcription Factors (Transcription Factor)IBA
01/2014
1Oxidoreductases (Dehydrogenase)IBA
03/2013
1Hemoglobin AIBA
03/2013
1MethemoglobinIBA
03/2013
1Cytochromes b5 (Cytochrome b5)IBA
03/2013
1hemoglobin PlasenciaIBA
01/2013
1Codon (Codons)IBA
01/2012
1Colloids (Colloid)IBA
12/2011
1Starch (Cornstarch)IBA
12/2011
1HES 130-0.4IBA
12/2011
1A 19IBA
07/2011
1Pyruvate KinaseIBA
01/2010
1Methyl-CpG-Binding Protein 2IBA
06/2007
1Serotonin (5 Hydroxytryptamine)IBA
04/2007
1AutoantibodiesIBA
07/2004

Therapy/Procedure

1Fluid Therapy (Oral Rehydration Therapy)
12/2011