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Kamran Moradkhani

Showing results (1-10 of 32) with videos related to

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Annales De Biologie Clinique|October 23, 2015
Pitfalls in the biological diagnosis of common hemoglobin disordersHenri Wajcman, Kamran Moradkhani
The Indian Journal of Medical Research|November 18, 2011
Abnormal haemoglobins: detection & characterizationHenri Wajcman, Kamran Moradkhani
Clinical Biochemistry|September 22, 2012
Pitfalls in the genetic diagnosis of Hb SKamran Moradkhani, Jean Riou, Henri Wajcman
BMC Research Notes|October 25, 2011
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi ArabiaSoad K Al-Jaouni, Jummanah Jarullah, Essam Azhar, et al.
Hemoglobin|October 22, 2008
Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin geneKamran Moradkhani, Jean Riou, Alain Francina, et al.
Blood Cells, Molecules & Diseases|October 16, 2007
Disturbance in the HIF-1alpha pathway associated with erythrocytosis: further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) geneMaha Al-Sheikh, Kamran Moradkhani, Marc Lopez, et al.
Hemoglobin|July 26, 2008
An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) geneKamran Moradkhani, Elodie Mazurier, Piero C Giordano, et al.
Hemoglobin|November 13, 2007
Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the JapaneseKamran Moradkhani, Joan Henthorn, Jean Riou, et al.
Reproductive Biomedicine Online|December 24, 2018
Morphokinetic parameters in chromosomal translocation carriers undergoing preimplantation genetic testingJenna Lammers, Arnaud Reignier, Carole Splingart, et al.
Blood Cells, Molecules & Diseases|February 2, 2012
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutationsAngelo Minucci, Kamran Moradkhani, Ming Jing Hwang, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Annales De Biologie Clinique|October 23, 2015
Pitfalls in the biological diagnosis of common hemoglobin disordersHenri Wajcman, Kamran Moradkhani
The Indian Journal of Medical Research|November 18, 2011
Abnormal haemoglobins: detection & characterizationHenri Wajcman, Kamran Moradkhani
Clinical Biochemistry|September 22, 2012
Pitfalls in the genetic diagnosis of Hb SKamran Moradkhani, Jean Riou, Henri Wajcman
BMC Research Notes|October 25, 2011
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi ArabiaSoad K Al-Jaouni, Jummanah Jarullah, Essam Azhar, et al.
Hemoglobin|October 22, 2008
Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin geneKamran Moradkhani, Jean Riou, Alain Francina, et al.
Blood Cells, Molecules & Diseases|October 16, 2007
Disturbance in the HIF-1alpha pathway associated with erythrocytosis: further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) geneMaha Al-Sheikh, Kamran Moradkhani, Marc Lopez, et al.
Hemoglobin|July 26, 2008
An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) geneKamran Moradkhani, Elodie Mazurier, Piero C Giordano, et al.
Hemoglobin|November 13, 2007
Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the JapaneseKamran Moradkhani, Joan Henthorn, Jean Riou, et al.
Reproductive Biomedicine Online|December 24, 2018
Morphokinetic parameters in chromosomal translocation carriers undergoing preimplantation genetic testingJenna Lammers, Arnaud Reignier, Carole Splingart, et al.
Blood Cells, Molecules & Diseases|February 2, 2012
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutationsAngelo Minucci, Kamran Moradkhani, Ming Jing Hwang, et al.
Pageof 4