Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Maria Carla Sollaino"'
Autor:
Fabrice Danjou, Marcella Francavilla, Franco Anni, Stefania Satta, Franca-Rosa Demartis, Lucia Perseu, Matteo Manca, Maria Carla Sollaino, Laura Manunza, Elisabetta Mereu, Giuseppe Marceddu, Serge Pissard, Philippe Joly, Isabelle Thuret, Raffaella Origa, Joseph Borg, Gian Luca Forni, Antonio Piga, Maria Eliana Lai, Catherine Badens, Paolo Moi, Renzo Galanello
Publikováno v:
Haematologica, Vol 100, Iss 4 (2015)
Clinical and hematologic characteristics of beta(β)-thalassemia are determined by several factors resulting in a wide spectrum of severity. Phenotype modulators are: HBB mutations, HBA defects and fetal hemoglobin production modulators (HBG2:g.−15
Externí odkaz:
https://doaj.org/article/f1eabfc6af1f4b9fb60af40c26ea9568
Autor:
Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, Francesca Sarra, Eleonora Zaccheddu, Renzo Galanello
Publikováno v:
Haematologica, Vol 96, Iss 11 (2011)
Externí odkaz:
https://doaj.org/article/aa4c66c74fd7449d8a48976e95783560
Autor:
Maria Carla Sollaino, Maria Elisabetta Paglietti, Lucia Perseu, Nicolina Giagu, Daniela Loi, Renzo Galanello
Publikováno v:
Haematologica, Vol 94, Iss 10 (2009)
Ten patients with thalassemia intermedia with variable severity and apparent simple heterozygosis for β0 39 C>T nonsense mutation were submitted to clinical, hematologic and molecular studies. The presence of an unknown molecular defect (silent β-t
Externí odkaz:
https://doaj.org/article/5abc5df829474fc4bbe431b5ba2a8f7f
Publikováno v:
Clinical Practice and Epidemiology in Mental Health : CP & EMH
Background: Potential interactions between mood disorders and microcytic anaemias have been suggested by case reports, surveys of haematological parameters in psychiatric populations, and surveys of psychiatric morbidity in thalassaemic carriers. Obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e566d04b793ae4f42922cd2de6df13b
https://doi.org/10.2174/1745017902117010081
https://doi.org/10.2174/1745017902117010081
Autor:
Susanna Barella, Valeria Orecchia, Anna Rita Denotti, Raffaella Origa, Paolo Moi, Daniela Loi, Franco Anni, Maria Elisabetta Paglietti, Maria Franca Desogus, Fabrice Danjou, Maria Carla Sollaino
Publikováno v:
Blood Cells, Molecules, and Diseases. 69:102-106
Limited information is available on the hematological characterization of the α-thalassemia carrier in pediatric age. The objective of this report was to evaluate the red cell indices according to the α-globin genotype in a cohort of children evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0312da82da1a4bb69c09806f35f4dd1d
https://doi.org/10.1016/j.bcmd.2017.10.003
https://doi.org/10.1016/j.bcmd.2017.10.003
Autor:
Raffaella Origa, Maria Franca Desogus, Laura Manunza, Maria Elisabetta Paglietti, Franca Rosa Demartis, Maria Carla Sollaino, Arianna Ventrella, Susanna Barella, Stefania Satta
Publikováno v:
Acta Haematologica. 135:193-199
Background: The increase in HbA2 is the most important parameter for the identification of thalassemia carriers. However, in routine screening for hemoglobinopathies, some cases are difficult to classify because the level of HbA2 is not typically ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3c1d0727c3d1e2c572654b914faaca1
https://doi.org/10.1159/000442194
https://doi.org/10.1159/000442194
Autor:
Yunxiang Zhang, Ciprian Tomuleasa, Lihong Yang, Melissa Winfield, Maria Elisabetta Paglietti, Mounzer Agha, Dan Douer, Jianpin Zhou, Yanhui Jin, Alexandra Marculescu, Raffaella Origa, Xiaoli Cheng, Cheryl Tompkins, Arianna Ventrella, Giovanni Romanelli, Maria Carla Sollaino, Mingshan Wang, Sant-Rayn Pasricha, Jiong Hu, Müge Aydoğdu, Ruham Alshiekh-Nasany, Jing-Zhou Hou, Susanna Barella, Junmin Li, Rodolfo D. Cançado, Michael Boyiadzis, Ken Cheng, Paulo Caleb Junior Lima Santos, Anastasios Raptis, Xiaoyang Li, Edileide Correia, Ivana Gojo, Paula Fernanda Silva Fonseca, Stefania Satta, Alexandru Bardas, Claire Sheeran, Franca Rosa Demartis, Donald K. Bowden, Bhavana Bhatnagar, Anca Colita, Xiuping Hao, Druckerei Stückle, Jianqing Mi, Marly Maria Uellendahl Lopes, Laura Manunza, Hongming Zhu, C. Orban, Yingyu Wang, Kelly J. Norsworthy, Mary Guay, Antonio M. Esquinas, Weili Zhao, Maria Franca Desogus, Zeba N. Singh, Manuel Antonio Lescano, Roger E. Peverill, Haixiao Xie, Sidsel Christy Lindgaard, Stefan O. Ciurea, Annie Im, Satz Mengensatzproduktion, Alina Tanase
Publikováno v:
Acta Haematologica. 135:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf175a6e354a6bf1f87d1393a52444d2
https://doi.org/10.1159/000446059
https://doi.org/10.1159/000446059
Autor:
Franco Anni, Marcella Francavilla, Elisabetta Mereu, Joseph Borg, Philippe Joly, Gian Luca Forni, Isabelle Thuret, Serge Pissard, Franca Rosa Demartis, Catherine Badens, Matteo Manca, Stefania Satta, Laura Manunza, Paolo Moi, Renzo Galanello, A. Piga, Maria Carla Sollaino, Giuseppe Marceddu, Fabrice Danjou, Maria Eliana Lai, Raffaella Origa, Lucia Perseu
Publikováno v:
Haematologica
Haematologica, Ferrata Storti Foundation, 2015, 100 (4), pp.452-457. ⟨10.3324/haematol.2014.113886⟩
Haematologica, Ferrata Storti Foundation, 2015, 100 (4), pp.452-457. ⟨10.3324/haematol.2014.113886⟩
Clinical and hematologic characteristics of beta(β)-thalassemia are determined by several factors resulting in a wide spectrum of severity. Phenotype modulators are: HBB mutations, HBA defects and fetal hemoglobin production modulators (HBG2:g.-158C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26440b1fc1926b85a685df51e4e8d98a
https://doi.org/10.3324/haematol.2014.113886
https://doi.org/10.3324/haematol.2014.113886
Autor:
Susanna Barella, Maria Franca Desogus, Daniela Loi, Maria Carla Sollaino, Maria Elisabetta Paglietti, Raffaella Origa, Renzo Galanello
Publikováno v:
Blood Cells, Molecules, and Diseases. 52:46-49
α-Thalassemia commonly results from deletions or point mutations in one or both α-globin genes located on chromosome 16p13.3 giving rise to complex and variable genotypes and phenotypes. Rarely, unusual non-deletion defects or atypical deletions do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb21d5c3432e7e53fa402f6755c4549
https://doi.org/10.1016/j.bcmd.2013.06.004
https://doi.org/10.1016/j.bcmd.2013.06.004
Autor:
Maria Franca Desogus, Susanna Barella, Stefania Satta, Raffaella Origa, Laura Manunza, Paolo Moi, Franca Rosa Demartis, Maria Carla Sollaino, Maria Elisabetta Paglietti
Publikováno v:
Blood cells, moleculesdiseases. 64
α-thalassemia carriers are common in Mediterranean regions, particularly in the Sardinian population. Their haematological phenotype is characterized by reduced MCV and/or MCH with normal or slightly reduced HbA2 levels and normal HbF. Kruppel-like
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dea9f43231c77ac8dd79bc9e1a0edad9
https://pubmed.ncbi.nlm.nih.gov/28342932
https://pubmed.ncbi.nlm.nih.gov/28342932