1-4 of 4
Maria Carla Sollaino
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

KLF1 gene mutations cause borderline HbA 2

Lucia Perseu, Stefania Satta, Paolo Moi, Franca Rosa Demartis, Laura Manunza, Maria Carla Sollaino, Susanna Barella, Antonio Cao, Renzo Galanello
Journal: Blood
Blood (2011) 118 (16): 4454–4458.
https://doi.org/10.1182/blood-2011-04-345736
Published: 2011
Includes: Supplemental data
Journal Articles

Homozygous deletion of the major alpha-globin regulatory element (MCS-R2) responsible for a severe case of hemoglobin H disease

Maria Carla Sollaino, Maria Elisabetta Paglietti, Daniela Loi, Rita Congiu, Rosanna Podda, Renzo Galanello
Journal: Blood
Blood (2010) 116 (12): 2193–2194.
https://doi.org/10.1182/blood-2010-04-281345
Published: 2010
Journal Articles

Amelioration of Sardinian β 0 thalassemia by genetic modifiers

Brief Report
Renzo Galanello, Serena Sanna, Lucia Perseu, Maria Carla Sollaino, Stefania Satta, Maria Eliana Lai, Susanna Barella, Manuela Uda, Gianluca Usala, Goncalo R. Abecasis, Antonio Cao
Journal: Blood
Blood (2009) 114 (18): 3935–3937.
https://doi.org/10.1182/blood-2009-04-217901
Published: 2009
Journal Articles

Genetic Modifiers of Homozygous Beta Zero Thalassemia.

Renzo Galanello, MD, Serena Sanna, Lucia Perseu, Maria Carla Sollaino, Stefania Satta, Manuela Uda, Gianluca Usala, Goncalo Abecasis, David Schlessinger, Antonio Cao, MD
Journal: Blood
Blood (2008) 112 (11): 1874.
https://doi.org/10.1182/blood.V112.11.1874.1874
Published: 2008