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Maria Carla Sollaino

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Clinical Practice and Epidemiology in Mental Health : CP & EMH|November 4, 2021
Microcytic Anaemia as Susceptibility Factors in Bipolar Spectrum Disorders: Review of the Literature, Replication Survey, and Co-Segregation within FamiliesAlberto Bocchetta, Caterina Chillotti, Raffaella Ardau, et al.
Hemoglobin|January 6, 2012
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]Antonella Fais, Maria Carla Sollaino, Susanna Barella, et al.
Acta Haematologica|September 24, 2014
Investigating the alpha1(NcoI) mutationMaria Franca Desogus, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H diseaseMaria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, et al.
Haematologica|October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermediaMaria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Haematologica|July 14, 2011
Two atypical forms of HbH disease in SardiniaMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Hemoglobin|March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian childMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Biophysical Journal|July 18, 2006
Structure-function relationship in a variant hemoglobin: a combined computational-experimental approachMatteo Ceccarelli, Paolo Ruggerone, Roberto Anedda, et al.
Acta Haematologica|November 13, 2013
α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermediaRaffaella Origa, Maria Carla Sollaino, Caterina Borgna-Pignatti, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Clinical Practice and Epidemiology in Mental Health : CP & EMH|November 4, 2021
Microcytic Anaemia as Susceptibility Factors in Bipolar Spectrum Disorders: Review of the Literature, Replication Survey, and Co-Segregation within FamiliesAlberto Bocchetta, Caterina Chillotti, Raffaella Ardau, et al.
Hemoglobin|January 6, 2012
A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]Antonella Fais, Maria Carla Sollaino, Susanna Barella, et al.
Acta Haematologica|September 24, 2014
Investigating the alpha1(NcoI) mutationMaria Franca Desogus, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|September 25, 2010
Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H diseaseMaria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, et al.
Haematologica|October 2, 2009
Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermediaMaria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, et al.
Haematologica|July 14, 2011
Two atypical forms of HbH disease in SardiniaMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Hemoglobin|March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian childMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.
Biophysical Journal|July 18, 2006
Structure-function relationship in a variant hemoglobin: a combined computational-experimental approachMatteo Ceccarelli, Paolo Ruggerone, Roberto Anedda, et al.
Acta Haematologica|November 13, 2013
α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermediaRaffaella Origa, Maria Carla Sollaino, Caterina Borgna-Pignatti, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Pageof 2