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Abdullah Kutlar

Showing results (11-20 of 118) with videos related to

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American Journal of Hematology|May 28, 2025
Mean Corpuscular Hemoglobin Modulates HbF/F-Cell and Clinical Response to Gene Therapy and Hydroxyurea in Sickle Cell DiseaseMartin H Steinberg, Abdullah Kutlar, Paola Sebastiani
Expert Review of Hematology|December 23, 2021
A critical evaluation of crizanlizumab for the treatment of sickle cell diseaseNabin Raj Karki, Katherine Saunders, Abdullah Kutlar
Hemoglobin|December 3, 2003
Hb Setif [alpha94(G1)Asp --> Tyr (alpha2)] detected in a Turkish familyGunçag Dinçol, Dedrey Elam, Abdullah Kutlar, et al.
Expert Review of Hematology|January 26, 2012
Thalidomide and its analogs for hemoglobinopathies: two birds with one stone?Abdullah Kutlar, Steffen Meiler, Paul Swerdlow, et al.
British Journal of Haematology|January 20, 2021
Sickle cell disease: progress towards combination drug therapyBetty S Pace, Athena Starlard-Davenport, Abdullah Kutlar
Acta Haematologica|June 29, 2020
DIAPH1 Mutation as a Novel Cause of Autosomal Dominant Macrothrombocytopenia and Hearing LossNabin Raj Karki, Germame Ajebo, Natasha Savage, et al.
American Journal of Hematology|December 15, 2015
Intrapatient variability in fetal hemoglobin measurements over time in sickle cell patients not on fetal hemoglobin inducing agentsEsther Knapp, Hillel Cohen, Abdullah Kutlar, et al.
Hemoglobin|January 8, 2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian babyNiren Patel, Jason Fixler, Yoram Unguru, et al.
Acta Haematologica|November 24, 2021
Indolent T-Lymphoblastic Proliferation in Idiopathic Multicentric Castleman DiseaseNabin Raj Karki, Ahmed Samire Arfa, Natasha Savage, et al.
International Journal of Medical Sciences|April 1, 2006
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish maleGunçag Dinçol, Serkan Güvenç, Dedrey Elam, et al.
Pageof 12

Showing results (11-20 of 118) with videos related to

Sort By:
Pageof 12
American Journal of Hematology|May 28, 2025
Mean Corpuscular Hemoglobin Modulates HbF/F-Cell and Clinical Response to Gene Therapy and Hydroxyurea in Sickle Cell DiseaseMartin H Steinberg, Abdullah Kutlar, Paola Sebastiani
Expert Review of Hematology|December 23, 2021
A critical evaluation of crizanlizumab for the treatment of sickle cell diseaseNabin Raj Karki, Katherine Saunders, Abdullah Kutlar
Hemoglobin|December 3, 2003
Hb Setif [alpha94(G1)Asp --> Tyr (alpha2)] detected in a Turkish familyGunçag Dinçol, Dedrey Elam, Abdullah Kutlar, et al.
Expert Review of Hematology|January 26, 2012
Thalidomide and its analogs for hemoglobinopathies: two birds with one stone?Abdullah Kutlar, Steffen Meiler, Paul Swerdlow, et al.
British Journal of Haematology|January 20, 2021
Sickle cell disease: progress towards combination drug therapyBetty S Pace, Athena Starlard-Davenport, Abdullah Kutlar
Acta Haematologica|June 29, 2020
DIAPH1 Mutation as a Novel Cause of Autosomal Dominant Macrothrombocytopenia and Hearing LossNabin Raj Karki, Germame Ajebo, Natasha Savage, et al.
American Journal of Hematology|December 15, 2015
Intrapatient variability in fetal hemoglobin measurements over time in sickle cell patients not on fetal hemoglobin inducing agentsEsther Knapp, Hillel Cohen, Abdullah Kutlar, et al.
Hemoglobin|January 8, 2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian babyNiren Patel, Jason Fixler, Yoram Unguru, et al.
Acta Haematologica|November 24, 2021
Indolent T-Lymphoblastic Proliferation in Idiopathic Multicentric Castleman DiseaseNabin Raj Karki, Ahmed Samire Arfa, Natasha Savage, et al.
International Journal of Medical Sciences|April 1, 2006
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish maleGunçag Dinçol, Serkan Güvenç, Dedrey Elam, et al.
Pageof 12