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Your search keyword '"Ferraris, Silvio"' showing total 12 results
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12 results on '"Ferraris, Silvio"'

1. Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment

Author

Palmieri, Viviana Valeria, Lonero, Antonella, Bocchini, Sarah, Cassano, Gilda, Convertino, Alessio, Corica, Domenico, Crinò, Antonio, Fattorusso, Valentina, Ferraris, Silvio, Fintini, Danilo, Franzese, Adriana, Grugni, Graziano, Iughetti, Lorenzo, Lia, Rosanna, Macchi, Francesca, Madeo, Simona Filomena, Matarazzo, Patrizia, Nosetti, Luana, Osimani, Sara, Pajno, Roberta, Patti, Giuseppa, Pellegrin, Maria Chiara, Perri, Annamaria, Ragusa, Letizia, Rutigliano, Irene, Sacco, Michele, Salvatoni, Alessandro, Scarano, Emanuela, Stagi, Stefano, Tornese, Gianluca, Trifirò, Giuliana, Wasniewska, Malgorzata, Fischetto, Rita, Giordano, Paola, Licenziati, Maria Rosaria, and Delvecchio, Maurizio

Published
2019
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2. Italian pediatric nutrition survey

Author

Abate, Rosaria, Accorsi, Paola, Aidala, Enrico, Amarri, Sergio, Ancora, Gina, Angelotti, Luisella, Annibali, Roberta, Antonini Monica, Antonietta, Banzato, Claudia, Barbaglia, Michelangelo, Bardasi, Giulia, Barrani, Monica, Basso, Tiziano, Brach del Prever, Adalberto, Belli, Fina, Bellomo Anna, Rita, Besenzon, Luigi, Biagioni, Martina, Bonaudo, Roberto, Bruni, Giulia, Brunori, Elena, Cagnoli, Giacomo, Campanozzi, Angelo, Casaccia, Germana, Castello, Mario, Chiaro, Andrea, Cimadore, Nicoletta, Cioni, Maddalena, Cortinovis, Francesca, De Cosmi, Valentina, De Giacomo, Costantino, Del Vecchio, Sergio, Diamanti, Antonella, Di Leo, Grazia, Di Scala, Carmen, Famiani, Annalisa, Felici, Enrico, Ferraris, Silvio, Fomasi, Martina, Fontanella, Giovanna, Frimaire, Alessia, Fusco, Patrizia, Galvagno, Graziana, Gandullia, Paolo, Gasparrini, Enrico, Guanà, Riccardo, Guerra, Azzurra, Lanari, Marcello, Lacitignola, Laura, Lezo, Antonella, Lizzoli, Francesca, Maggiore, Giuseppe, Magistà Anna, Maria, Malaventura, Cristina, Marmetucci, Luigi, Mazzocchi, Alessandra, Mazzoni, Elisa, Melli, Paola, Memmini, Graziano, Meneghini, Anna, Miglietti, Nunzia, Migliore, Giuseppina, Mistura, Laura, Monaci, Alessandro, Morganti, Alessia, Nesi, Francesca, Opinto, Vittoria, Pace, Mariella, Palamone, Gianluigi, Panceri, Roberto, Parisi, Giuseppe, Pastore, Maria, Penagini, Francesca, Perrone, Michela, Petitti, Patrizia, Pettinari, Chiara, Peverelli, Paola, Pinon, Michele, Russo, Carla, Sala, Alessandra, Salata, Michele, Salmaso, Mara, Sangerardi, Maria, Santangelo, Barbara, Savino, Francesco, Scatà, Donata, Siani, Paolo, Spagnuolo, Maria Immacolata, Sparano, Paola, Stamati Filomena, Andreina, Tulli, Monica, Uga, Elena, Urbano, Flavia, Verlato, Giovanna, Zoppo, Marisa, Zuin, Giovanna, Lezo, A., Diamanti, A., Capriati, T., Gandullia, P., Fiore, P., Lacitignola, L., Gatti, S., Spagnuolo, M.I., Cecchi, N., Verlato, G., Borodani, S., Forchielli, L., Panceri, R., Brunori, E., Pastore, M., and Amarri, S.

Published
2017
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8. Anthropometric characteristics of newborns with Prader–Willi syndrome.

Author

Salvatoni, Alessandro, Moretti, Alex, Grugni, Graziano, Agosti, Massimo, Azzolini, Sara, Bonaita, Valentina, Cianci, Paola, Corica, Domenico, Crinò, Antonino, Delvecchio, Maurizio, Ferraris, Silvio, Greggio, Nella A., Iughetti, Lorenzo, Licenziati, Maria R., Madeo, Simona F., Nosetti, Luana, Pajno, Roberta, Rutigliano, Irene, Sacco, Michele, and Salvatore, Silvia

Abstract

This is a retrospective multicenter nationwide Italian study collecting neonatal anthropometric data of Caucasian subjects with Prader–Willi syndrome (PWS) born from 1988 to 2018. The aim of the study is to provide percentile charts for weight and length of singletons with PWS born between 36 and 42 gestational weeks. We collected the birth weight and birth length of 252 male and 244 female singleton live born infants with both parents of Italian origin and PWS genetically confirmed. Percentile smoothed curves of birth weight and length for gestational age were built through Cole's lambda, mu, sigma method. The data were compared to normal Italian standards. Newborns with PWS showed a lower mean birth weight, by 1/2 kg, and a shorter mean birth length, by 1 cm, than healthy neonates. Females with a 15q11‐13 deletion were shorter than those with maternal uniparental maternal disomy of chromosome 15 (p < .0001). The present growth curves may be useful as further traits in supporting a suspicion of PWS in a newborn. Because impaired prenatal growth increases risk of health problems later in life, having neonatal anthropometric standards could be helpful to evaluate possible correlations between the presence or absence of small gestational age and some clinical and metabolic aspects of PWS. [ABSTRACT FROM AUTHOR]

Published
2019
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9. Transient Abnormal Myelopoiesis in Noonan Syndrome

Author

Lanza Carlo, Ferraris Silvio, Farinasso Daniela, Barisone Elena, Bertorello Nicoletta, and Miniero Roberto

Subjects
Male, Pediatrics, medicine.medical_specialty, Pathology, Myeloproliferative Disorders, business.industry, Noonan Syndrome, Transient abnormal myelopoiesis, Infant, Newborn, Hematology, medicine.disease, Hematologic Diseases, Osteochondrodysplasia, Leukemia, Oncology, Refractory, hemic and lymphatic diseases, Recien nacido, Pediatrics, Perinatology and Child Health, medicine, Humans, Noonan syndrome, Myelopoiesis, business
Abstract

An infant affected by Noonan syndrome and presenting with abnormal hemopoiesis is described. Cytogenetic analysis, molecular studies, and in vitro culture assays ruled out myelodysplasia or other hematologic malignancies but were consistent with transient abnormal myelopoiesis. At present, 3 years and 10 months after diagnosis, the patient shows a normal hematologic picture. Supportive treatment in such patients, unless refractory cytopenias or overt leukemia develops, is emphasized.

Published
2002
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11. Mental retardation, peculiar facial dysmorphism and HbH inclusions in a 4-year-old boy.

Author

Valenzise, Mariella, Ferrero, Battista, Tosi, Teresa, Ferraris, Silvio, Silengo, Margherita, Ferrero, Giovanni Battista, and Tosi, Maria Teresa

Subjects
INTELLECTUAL disabilities, FACIAL abnormalities, FRAGILE X syndrome, THALASSEMIA in children, ERYTHROCYTES, COMPARATIVE studies, FACIAL manifestations of general diseases, RESEARCH methodology, MEDICAL cooperation, RESEARCH, X-linked intellectual disabilities, EVALUATION research, ALPHA-Thalassemia
Abstract

Reports on a case of a four-year-old boy with mental retardation, peculiar dysmorphism and HbH inclusions. Medical record; Patient phenotype; X-linked recessive disorder; Thalassemia; Vomiting and rumination.

Published
2002
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