Chaîma Sahli - Concepedia

Author

Chaîma Sahli

Also Known As

C. A. Sahli, C. Sahli, CHAIMA SAHLI, Chaima A. Sahli, Chaima Abdelhafidh Sahli, Chaima Sahli, Chaîma Sahli, Chaïma Abdelhafidh Sahli

Publications

187

Citations

H-Index

Concepts

All Affiliations

Chaîma Sahli is an author at Children's Hospital specializing in genetics, inherited metabolic disease, and medicine.

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	28
2	Health Sciences	1	1	15
3	Public Health	1	1	15
4	Biostatistics	1	1	15
5	Diabetes	1	1	14

Chaîma Sahli

Publications

115

Citations

H-Index

Page 1

	Year	Citations
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia Chaîma Sahli, Amina Bibi, Faida Ouali, Clinical Chemistry and Laboratory Medicine (CCLM)	2013	45
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia Chaîma Sahli, Amina Bibi, Faida Ouali, Clinical Chemistry and Laboratory Medicine (CCLM)	2013	27
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients Latifa Jouini, Chaîma Sahli, Naouel Laaouini, Molecular Biology Reports ImmunohematologyLaboratory HematologyClinical ExpressionGeneticsGenetic Epidemiology	2013	15
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association Naouel Laouini, Afsha Bibi, H. Ben Ammar, Molecular Biology Reports Glucose-6-phosphate Dehydrogenase DeficiencyMetabolic DisorderMetabolic DiseaseInherited Metabolic DiseaseGenetics	2012	14
A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del Rym Dabboubi, Yessine Amri, Salem Yahyaoui, European Journal of Medical Genetics Developmental AnomalyNew CaseGenetic DisorderGeneticsInherited Metabolic Disease	2020	14

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