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Adlette Inati

Showing results (31-40 of 68) with videos related to

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American Journal of Hematology|June 7, 2006
Pregnancy in patients with beta-thalassemia intermedia: outcome of mothers and newbornsAnwar H Nassar, Ihab M Usta, Johnny B Rechdan, et al.
Blood Cells, Molecules & Diseases|June 6, 2013
A rare case of Moyamoya syndrome in a β-thalassemia major patientAdlette Inati, Oulfat Tourjuman, Diana Bizri, et al.
Hemoglobin|May 13, 2021
Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated RegistryAdlette Inati, Chadi Al Alam, Cristel El Ojaimi, et al.
British Journal of Haematology|July 17, 2009
Levels of non-transferrin-bound iron as an index of iron overload in patients with thalassaemia intermediaAli Taher, Khaled M Musallam, Fouad El Rassi, et al.
Pediatric Blood & Cancer|March 5, 2014
A multicenter study on the Lebanese experience with hereditary spherocytosisAdlette Inati, Peter Noun, Nabil Kabbara, et al.
American Journal of Hematology|April 29, 2010
Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patientsChantal Farra, Laila Zahed, Paul J Nietert, et al.
Clinical Genetics|October 13, 2023
A homozygous frameshift variant expands the clinical spectrum of SAMD9 gene defectsCybel Mehawej, Maroun Ibrahim, Lynn Khalife, et al.
Acta Haematologica|October 18, 2005
Safety and effectiveness of 100 mg/kg/day deferiprone in patients with thalassemia major: a two-year studyAli Taher, Marwan Sheikh-Taha, Ala Sharara, et al.
Tissue Antigens|September 22, 2012
HLA population genetics: a Lebanese populationPedro Cano, Manuela Testi, Marco Andreani, et al.
The American Journal of Cardiology|July 22, 2008
Relation between iron-overload indices, cardiac echo-Doppler, and biochemical markers in thalassemia intermediaHussain Isma'eel, Abdul Hamid El Chafic, Fuad El Rassi, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
American Journal of Hematology|June 7, 2006
Pregnancy in patients with beta-thalassemia intermedia: outcome of mothers and newbornsAnwar H Nassar, Ihab M Usta, Johnny B Rechdan, et al.
Blood Cells, Molecules & Diseases|June 6, 2013
A rare case of Moyamoya syndrome in a β-thalassemia major patientAdlette Inati, Oulfat Tourjuman, Diana Bizri, et al.
Hemoglobin|May 13, 2021
Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated RegistryAdlette Inati, Chadi Al Alam, Cristel El Ojaimi, et al.
British Journal of Haematology|July 17, 2009
Levels of non-transferrin-bound iron as an index of iron overload in patients with thalassaemia intermediaAli Taher, Khaled M Musallam, Fouad El Rassi, et al.
Pediatric Blood & Cancer|March 5, 2014
A multicenter study on the Lebanese experience with hereditary spherocytosisAdlette Inati, Peter Noun, Nabil Kabbara, et al.
American Journal of Hematology|April 29, 2010
Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patientsChantal Farra, Laila Zahed, Paul J Nietert, et al.
Clinical Genetics|October 13, 2023
A homozygous frameshift variant expands the clinical spectrum of SAMD9 gene defectsCybel Mehawej, Maroun Ibrahim, Lynn Khalife, et al.
Acta Haematologica|October 18, 2005
Safety and effectiveness of 100 mg/kg/day deferiprone in patients with thalassemia major: a two-year studyAli Taher, Marwan Sheikh-Taha, Ala Sharara, et al.
Tissue Antigens|September 22, 2012
HLA population genetics: a Lebanese populationPedro Cano, Manuela Testi, Marco Andreani, et al.
The American Journal of Cardiology|July 22, 2008
Relation between iron-overload indices, cardiac echo-Doppler, and biochemical markers in thalassemia intermediaHussain Isma'eel, Abdul Hamid El Chafic, Fuad El Rassi, et al.
Pageof 7