SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations
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Published in Human mutation (01.07.2011)
Published in Human mutation (01.07.2011)
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Can Anti-Thyroid Antibodies Influence the Outcome of Primary Chronic Immune Thrombocytopenia in Children?
Giordano, Paola, Delvecchio, Maurizio, Lassandro, Giuseppe, Valente, Federica, Palladino, Valentina, Chiarito, Mariangela, Wasniewska, Malgorzata, Faienza, Maria F
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2020)
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2020)
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SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development
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Published in The journal of clinical endocrinology and metabolism (01.05.2008)
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Thrombopoietin Receptor Agonists in Children with Immune Thrombocytopenia: A New Therapeutic Era
Lassandro, Giuseppe, Palladino, Valentina, Vecchio, Giovanni C D, Palmieri, Viviana V, Corallo, Paola C, Faienza, Maria F, Giordano, Paola
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2021)
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2021)
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Mechanisms of Enhanced Osteoclastogenesis in Alkaptonuria
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Published in The American journal of pathology (01.04.2018)
Published in The American journal of pathology (01.04.2018)
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Irisin serum levels are positively correlated with bone mineral status in a population of healthy children
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Published in Pediatric research (01.03.2019)
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LIGHT/TNFSF14 Promotes Osteolytic Bone Metastases in Non‐small Cell Lung Cancer Patients
Brunetti, Giacomina, Belisario, Dimas C, Bortolotti, Sara, Storlino, Giuseppina, Colaianni, Graziana, Faienza, Maria F, Sanesi, Lorenzo, Alliod, Valentina, Buffoni, Lucio, Centini, Elisa, Voena, Claudia, Pulito, Roberta, Novello, Silvia, Ingravallo, Giuseppe, Rizzi, Rita, Mori, Giorgio, Reseland, Janne E, Ware, Carl F, Colucci, Silvia, Ferracini, Riccardo, Grano, Maria, Roato, Ilaria
Published in Journal of bone and mineral research (01.04.2020)
Published in Journal of bone and mineral research (01.04.2020)
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LIGHT/TNFSF14 regulates estrogen deficiency‐induced bone loss
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Published in The Journal of pathology (01.04.2020)
Published in The Journal of pathology (01.04.2020)
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Unusual ultrasonographic finding of ovarian hyperstimulation syndrome in a preterm newborn with severe intra‐uterine growth retardation
D'Amato, Gabriele, D'Amato, Elena, Natale, Maria P, Brunetti, Giacomina, Faienza, Maria F
Published in Journal of paediatrics and child health (01.09.2019)
Published in Journal of paediatrics and child health (01.09.2019)
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High serum sclerostin levels in children with haemophilia A
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Published in British journal of haematology (01.01.2016)
Published in British journal of haematology (01.01.2016)
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Red blood cell transfusions and potentially related morbidities in neonates under 32 weeks' gestation
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Published in Blood transfusion = Trasfusione del sangue (01.03.2021)
Published in Blood transfusion = Trasfusione del sangue (01.03.2021)
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NR5A1 Gene Variants: Variable Phenotypes, New Variants, Different Outcomes
Faienza, Maria F., Chiarito, Mariangela, Baldinotti, Fulvia, Canale, Domenico, Savino, Carmela, Paradies, Guglielmo, Corica, Domenico, Romeo, Carmelo, Tyutyusheva, Nina, Caligo, Maria A., Wasniewska, Malgorzata G., Bertelloni, Silvano
Published in Sexual development (01.10.2020)
Published in Sexual development (01.10.2020)
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Evidence that fibrinolytic changes in paediatric obesity translate into a hypofibrinolytic state: relative contribution of TAFI and PAI-1
Semeraro, Fabrizio, Giordano, Paola, Faienza, Maria F, Cavallo, Luciano, Semeraro, Nicola, Colucci, Mario
Published in Thrombosis and haemostasis (01.08.2012)
Published in Thrombosis and haemostasis (01.08.2012)
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Linear growth and puberty in childhood obesity: what is new?
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Published in Minerva pediatrics (01.12.2021)
Published in Minerva pediatrics (01.12.2021)
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Analysis of Endothelial Protein C Receptor Gene and Metabolic Profile in Prader‐Willi Syndrome and Obese Subjects
Faienza, Maria F., Ventura, Annamaria, Lauciello, Rosaria, Crinò, Antonino, Ragusa, Letizia, Cavallo, Luciano, Spera, Sabrina, Grugni, Graziano
Published in Obesity (Silver Spring, Md.) (01.09.2012)
Published in Obesity (Silver Spring, Md.) (01.09.2012)
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IGF2 Gene Variants and Risk of Hypertension in Obese Children and Adolescents
Faienza, Maria F, Santoro, Nicola, Lauciello, Rosaria, Calabrò, Raffaele, Giordani, Lucia, Di Salvo, Giovanni, Ventura, Annamaria, Delvecchio, Maurizio, Perrone, Laura, Del Giudice, Emanuele M, Cavallo, Luciano
Published in Pediatric research (01.04.2010)
Published in Pediatric research (01.04.2010)
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Stories of experiences of care for growth hormone deficiency: the CRESCERE project
Marini, Maria G, Chesi, Paola, Mazzanti, Laura, Guazzarotti, Laura, Toni, Teresa D, Salerno, Maria C, Officioso, Annunziata, Parpagnoli, Maria, Angeletti, Cristina, Faienza, Maria F, Iezzi, Maria L, Aversa, Tommaso, Sacchetti, Cinzia
Published in Future science OA (01.03.2016)
Published in Future science OA (01.03.2016)
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Bone Remodeling in an Mps-1h Girl after Hematopoietic Stem Cell Transplantation along with Enzymatic Replacement Therapy
Tummolo, Albina, Brunetti, Giacomina, Piacente, Laura, Marzollo, Antonio, Biffi, Alessandra, Burlina, Alberto, Faienza, Maria Felicia
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2022)
Published in Endocrine, metabolic & immune disorders drug targets (01.01.2022)
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SOS1 MUTATIONS IN NOONAN SYNDROME: AN UPDATE ON MOLECULAR SPECTRUM, STRUCTURAL INSIGHTS ON PATHOGENIC EFFECTS, AND GENOTYPE-PHENOTYPE CORRELATIONS
Lepri, Francesca, de Luca, Alessandro, Stella, Lorenzo, Rossi, Cesare, Baldassarre, Giuseppina, Pantaleoni, Francesca, Cordeddu, Viviana, Williams, Bradley J, Dentici, Maria L, Caputo, Viviana, Venanzi, Serenella, Bonaguro, Michela, Kavamura, Maria Ines, Faienza, Maria F, Pilotta, Alba, Stanzial, Franco, Faravelli, Francesca, Gabrielli, Orazio, Marino, Bruno, Neri, Giovanni, Silengo, Margherita, Ferrero, Giovanni B, Torrente, Isabella, Selicorni, Angelo, Mazzanti, Laura, Digilio, Maria Cristina, Zampino, Giuseppe, Dallapiccola, Bruno, Gelb, Bruce D., Tartaglia, Marco
Published in Human mutation (28.04.2011)
Published in Human mutation (28.04.2011)
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Unusual ultrasonographic finding of ovarian hyperstimulation syndrome in a preterm newborn with severe intra-uterine growth retardation
D'Amato, Gabriele, D'Amato, Elena, Natale, Maria P, Brunetti, Giacomina, Faienza, Maria F
Published in Journal of paediatrics and child health (01.09.2019)
Published in Journal of paediatrics and child health (01.09.2019)
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