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Susanna Barella
Observed names:
Barella Susanna,
S Barella,
S. Barella
Institution:
Ospedale Microcitemico
Observed institutions:
University of Cagliari,
University of Pavia,
Istituto Giannina Gaslini,
Ospedale Microcitemico,
Azienda Ospedaliera G. Brotzu,
Hacettepe University
show all 6
ORCID:
0000-0002-1952-7836
Observed ORCID:
0000-0002-1952-7836
OpenAlex ID:
A5061216949
A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron
2008
·
M. A. Melis
, M. Cau
, et al.
·
Haematologica
·
186
PDF
Amelioration of Sardinian 0 thalassemia by genetic modifiers
2009
·
R. Galanello
, S. Sanna
, et al.
·
Blood
·
143
A pilot trial of deferiprone for neurodegeneration with brain iron accumulation
2011
·
G. Abbruzzese
, G. Cossu
, et al.
·
Haematologica
·
133
PDF
Relationship between transfusion regimen and suppression of erythropoiesis in β‐thalassaemia major
1995
·
Mario Cazzola
, Piero De Stefano
, et al.
·
British Journal of Haematology
·
128
KLF1 gene mutations cause borderline HbA2
2011
·
Lucia Perseu
, Stefania Satta
, et al.
·
Blood
·
105
Efficacy and safety of deferiprone for the treatment of pantothenate kinase-associated neurodegeneration (PKAN) and neurodegeneration with brain iron accumulation (NBIA): Results from a four years follow-up
2014
·
Giovanni Cossu
, Giovanni Abbruzzese
, et al.
·
Parkinsonism & Related Disorders
·
93
Hepatocellular carcinoma in thalassaemia: an update of the Italian Registry
2014
·
Caterina Borgna‐Pignatti
, Maria Chiara Garani
, et al.
·
British Journal of Haematology
·
86
PDF
H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
2002
·
Maria Antonietta Melis
, Milena Cau
, et al.
·
PubMed
·
80
Cholelithiasis and Gilbert's syndrome in homozygous β‐thalassaemia
2001
·
R. Galanello
, S. Piras
, et al.
·
British Journal of Haematology
·
77
PDF
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
2015
·
Fabrice Danjou
, Magdalena Zoledziewska
, et al.
·
Nature Genetics
·
76
PDF
Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome
1997
·
R. Galanello
, L. Perseu
, et al.
·
British Journal of Haematology
·
71
No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia
2008
·
R. Origa
, S. Barella
, et al.
·
Haematologica
·
63
PDF
Genotype of subjects with borderline hemoglobin A2 levels: Implication for, β‐thalassemia carrier screening
1994
·
R. Galanello
, S. Barella
, et al.
·
American Journal of Hematology
·
60
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis
1999
·
Mario Cazzola
, Yves Beguin
, et al.
·
British Journal of Haematology
·
58
PDF
Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes
2006
·
R. Origa
, M. C. Sollaino
, et al.
·
British Journal of Haematology
·
55
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients
1994
·
R Galanello
, S Barella
, et al.
·
Blood
·
55
PDF
Pretransfusion hemoglobin level and mortality in adults with transfusion-dependent β-thalassemia
2023
·
Khaled M. Musallam
, Susanna Barella
, et al.
·
Blood
·
45
HbH Disease in Sardinia: Molecular, Hematological and Clinical Aspects
2009
·
R. Galanello
, B. Aru
, et al.
·
Acta Haematologica
·
44
α-thalassemia carrier identification by DNA analysis in the screening for thalassemia
1998
·
Renzo Galanello
, Carla Sollaino
, et al.
·
American Journal of Hematology
·
40
PDF
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
1999
·
R. Galanello
, M. D. Cipollina
, et al.
·
European Journal of Pediatrics
·
34
Somatic deletion of the normal β‐globin gene leading to thalassaemia intermedia in heterozygous β‐thalassaemic patients
2004
·
Renzo Galanello
, Lucia Perseu
, et al.
·
British Journal of Haematology
·
31
PDF
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and -thalassemia intermedia
2015
·
R. Origa
, M. Cazzola
, et al.
·
Haematologica
·
30
PDF
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
2019
·
Roberta Russo
, Roberta Marra
, et al.
·
Frontiers in Physiology
·
28
PDF
Incidence of cancer and related deaths in hemoglobinopathies: A follow‐up of 4631 patients between 1970 and 2021
2022
·
Raffaella Origa
, Barbara Gianesin
, et al.
·
Cancer
·
27
PDF
Safety and Efficacy of the New Combination Iron Chelation Regimens in Patients with Transfusion-Dependent Thalassemia and Severe Iron Overload
2022
·
Raffaella Origa
, Monia Cinus
, et al.
·
Journal of Clinical Medicine
·
27
PDF
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Works count:
101
Citation count:
2,209
H-index:
25
I10-index:
46
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