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A Giambona

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

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International Journal of Laboratory Hematology|September 30, 2015
Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermediaM Vinciguerra, C Passarello, F Cassarà, et al.
Human Genetics|May 1, 1995
The great heterogeneity of thalassemia molecular defects in SicilyA Giambona, P Lo Gioco, M Marino, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Beta-thalassemia mutations in SicilyA Maggio, R Di Marzo, A Giambona, et al.
Human Genetics|January 1, 1985
alpha alpha alpha anti-4.2 Haplotype and heterozygous beta null thalassemia in a Sicilian familyS Acuto, G Butticé, B Saitta, et al.
International Journal of Clinical Practice|March 3, 2015
Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosisA Giambona, G Damiani, M Vinciguerra, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 2, 2020
ReplyG Makrydimas, G Damiani, C Jakil, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 28, 2020
Celocentesis for early prenatal diagnosis of hemoglobinopathyG Makrydimas, G Damiani, C Jakil, et al.
Bone Marrow Transplantation|September 1, 1996
Evidence of induced non-tolerance in HLA-identical twins with hemoglobinopathy after in utero fetal transplantationF Orlandi, A Giambona, F Messana, et al.
Transplantation|April 27, 1996
Lack of evidence of permanent engraftment after in utero fetal stem cell transplantation in congenital hemoglobinopathiesM Westgren, O Ringden, S Eik-Nes, et al.
American Journal of Hematology|November 3, 1998
Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutationsL A Ugozzoli, J D Lowery, A A Reyes, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
International Journal of Laboratory Hematology|September 30, 2015
Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermediaM Vinciguerra, C Passarello, F Cassarà, et al.
Human Genetics|May 1, 1995
The great heterogeneity of thalassemia molecular defects in SicilyA Giambona, P Lo Gioco, M Marino, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Beta-thalassemia mutations in SicilyA Maggio, R Di Marzo, A Giambona, et al.
Human Genetics|January 1, 1985
alpha alpha alpha anti-4.2 Haplotype and heterozygous beta null thalassemia in a Sicilian familyS Acuto, G Butticé, B Saitta, et al.
International Journal of Clinical Practice|March 3, 2015
Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosisA Giambona, G Damiani, M Vinciguerra, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 2, 2020
ReplyG Makrydimas, G Damiani, C Jakil, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 28, 2020
Celocentesis for early prenatal diagnosis of hemoglobinopathyG Makrydimas, G Damiani, C Jakil, et al.
Bone Marrow Transplantation|September 1, 1996
Evidence of induced non-tolerance in HLA-identical twins with hemoglobinopathy after in utero fetal transplantationF Orlandi, A Giambona, F Messana, et al.
Transplantation|April 27, 1996
Lack of evidence of permanent engraftment after in utero fetal stem cell transplantation in congenital hemoglobinopathiesM Westgren, O Ringden, S Eik-Nes, et al.
American Journal of Hematology|November 3, 1998
Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutationsL A Ugozzoli, J D Lowery, A A Reyes, et al.
Pageof 2