Search Results - "Cattoni, Alessandro"

Case report: Fluctuating tumor markers in a boy with gonadotropin-releasing hormone-independent precocious puberty induced by a pineal germ cell tumor by Cattoni, Alessandro, Albanese, Assunta

“…GnRH-independent precocious puberty (GIPP) can be the presenting clinical picture experienced by patients with secreting germ cell tumor (GCT). Indeed, as…”
Get full text

The bronchiolitis epidemic in 2021-2022 during the SARS-CoV-2 pandemic: experience of a third level centre in Northern Italy by Faraguna, Martha Caterina, Lepri, Irene, Clavenna, Antonio, Bonati, Maurizio, Vimercati, Chiara, Sala, Debora, Cattoni, Alessandro, Melzi, Maria Luisa, Biondi, Andrea

“…The aim of this study is to compare the 2021-2022 bronchiolitis season to the four previous years (2017-2018, 2018-2019, 2019-2020, 2020-2021) to see if there…”
Get full text

ABO incompatibile graft management in pediatric transplantation by Balduzzi, Adriana, Bönig, Halvard, Jarisch, Andrea, Nava, Tiago, Ansari, Marc, Cattoni, Alessandro, Prunotto, Giulia, Lucchini, Giovanna, Krivan, Gergely, Matic, Toni, Kalwak, Krzyzstof, Yesilipek, Akif, Ifversen, Marianne, Svec, Peter, Buechner, Jochen, Vettenranta, Kim, Meisel, Roland, Lawitschka, Anita, Peters, Christina, Gibson, Brenda, Dalissier, Arnaud, Corbacioglu, Selim, Willasch, André, Dalle, Jean-Hugues, Bader, Peter

“…Up to 40% of donor-recipient pairs in SCT have some degree of ABO incompatibility, which may cause severe complications. The aim of this study was to describe…”
Get full text

High levels of physical activity in female adolescents with anorexia nervosa: medical and psychopathological correlates by Riva, Anna, Falbo, Mariella, Passoni, Paolo, Polizzi, Serena, Cattoni, Alessandro, Nacinovich, Renata

“…Purpose While overexercise is commonly described in patients who experience anorexia nervosa (AN), it represents a condition still underestimated, especially…”
Get full text

A Novel Germline Mutation of ADA2 Gene in Two "Discordant" Homozygous Female Twins Affected by Adenosine Deaminase 2 Deficiency: Description of the Bone-Related Phenotype by Vai, Silvia, Marin, Erika, Cosso, Roberta, Saettini, Francesco, Bonanomi, Sonia, Cattoni, Alessandro, Chiodini, Iacopo, Persani, Luca, Falchetti, Alberto

“…Adenosine Deaminase 2 Deficiency (DADA2) syndrome is a rare monogenic disorder prevalently linked to recessive inherited loss of function mutations in the…”
Get full text

Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multi-center nation-wide cohort by Casale, Maddalena, Forni, Gian Luca, Cassinerio, Elena, Pasquali, Daniela, Origa, Raffaella, Serra, Marilena, Campisi, Saveria, Peluso, Angelo, Renni, Roberta, Cattoni, Alessandro, De Michele, Elisa, Allò, Massimo, Poggi, Maurizio, Ferrara, Francesca, Di Concilio, Rosanna, Sportelli, Filomena, Quarta, Antonella, Putti, Maria Caterina, Notarangelo, Lucia Dora, Sau, Antonella, Ladogana, Saverio, Tartaglione, Immacolata, Picariello, Stefania, Marcon, Alessia, Sturiale, Patrizia, Roberti, Domenico, Lazzarino, Antonio Ivan, Perrotta, Silverio

“…Transfusion-dependent patients typically develop iron-induced cardiomyopathy, liver disease, and endocrine complications. We aimed to estimate the incidence of…”
Get full text

Pubertal attainment and Leydig cell function following pediatric hematopoietic stem cell transplantation: a three-decade longitudinal assessment by Cattoni, Alessandro, Nicolosi, Maria Laura, Capitoli, Giulia, Gadda, Alberto, Molinari, Silvia, Louka, Sotiris, Buonsante, Andrea, Orlandi, Simona, Salierno, Gianluca, Bellani, Iacopo, Vendemini, Francesca, Ottaviano, Giorgio, Gaiero, Alberto, Fichera, Graziella, Biondi, Andrea, Balduzzi, Adriana

“…Impaired testosterone secretion is a frequent following hematopoietic stem cell transplantation (HSCT) in pediatrics, but long-term longitudinal trendlines of…”
Get full text

Thyroid function disorders and secondary cancer following haematopoietic stem cell transplantation in pediatrics: State of the art and practical recommendations for a risk-based follow-up by Cattoni, Alessandro, Molinari, Silvia, Riva, Benedetta, Di Marco, Santo, Adavastro, Marta, Faraguna, Martha Caterina, Garella, Vittoria, Medici, Francesco, Nicolosi, Maria Laura, Pellegrinelli, Claudia, Lattuada, Martina, Fraschini, Donatella, Pagni, Fabio, Biondi, Andrea, Balduzzi, Adriana

“…Thyroid disorders (TD) represent a remarkable share of all the late morbidities experienced following pediatric haematopoietic stem cell transplantation…”
Get full text

Late Effects After Haematopoietic Stem Cell Transplantation in ALL, Long-Term Follow-Up and Transition: A Step Into Adult Life by Diesch-Furlanetto, Tamara, Gabriel, Melissa, Zajac-Spychala, Olga, Cattoni, Alessandro, Hoeben, Bianca A W, Balduzzi, Adriana

“…Haematopoietic stem cell transplant (HSCT) can be a curative treatment for children and adolescents with very-high-risk acute lymphoblastic leukaemia (ALL)…”
Get full text

Endocrine, auxological and metabolic profile in children and adolescents with Down syndrome: from infancy to the first steps into adult life by Molinari, Silvia, Fossati, Chiara, Nicolosi, Maria Laura, Di Marco, Santo, Faraguna, Martha Caterina, Limido, Francesca, Ocello, Laura, Pellegrinelli, Claudia, Lattuada, Martina, Gazzarri, Alessandra, Lazzerotti, Alessandra, Sala, Debora, Vimercati, Chiara, Capitoli, Giulia, Daolio, Cecilia, Biondi, Andrea, Balduzzi, Adriana, Cattoni, Alessandro

“…Down syndrome (DS) is the most common chromosomal disorder worldwide. Along with intellectual disability, endocrine disorders represent a remarkable share of…”
Get full text

Growth patterns in children with mucopolysaccharidosis type I-Hurler after hematopoietic stem cell transplantation: Comparison with untreated patients by Cattoni, Alessandro, Chiaraluce, Sofia, Gasperini, Serena, Molinari, Silvia, Biondi, Andrea, Rovelli, Attilio, Parini, Rossella

“…The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mucopolysaccharidosis I Hurler (MPS-IH) has been historically…”
Get full text

Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child by Faraguna, Martha Caterina, Musto, Francesca, Crescitelli, Viola, Iascone, Maria, Spaccini, Luigina, Tonduti, Davide, Fedeli, Tiziana, Kullmann, Gaia, Canonico, Francesco, Cattoni, Alessandro, Dell'Acqua, Fabiola, Rizzari, Carmelo, Gasperini, Serena

“…Mucopolysaccharidosis-plus syndrome (MPS-PS) is a novel autosomal recessive disorder caused by a mutation in the gene. This syndrome presents with typical…”
Get full text

Pelvic ultrasound and pubertal attainment in girls with sexual precocity: the pivotal role of uterine volume in predicting the timing of menarche by Cattoni, Alessandro, Russo, Gianni, Capitoli, Giulia, Rodari, Giulia, Nicolosi, Maria Laura, Molinari, Silvia, Tondelli, Daniele, Pelliccia, Ciretta, Radaelli, Silvia, Arosio, Andrea Mario Luciano, Fontana, Katia, Tattesi, Giulia, Passoni, Paolo, Boneschi, Annalisa, Giavoli, Claudia, Meroni, Silvia Laura Carla, Stancampiano, Marianna Rita, Garuti, Elda, Biondi, Andrea, Balduzzi, Adriana, Bizzarri, Carla

“…Among girls assessed for pubertal precocity, pelvic ultrasound (pUS) may represent a pivotal tool to predict the time expected to elapse between sonographic…”
Get full text

Dexamethasone Stimulation Test in the Diagnostic Work-Up of Growth Hormone Deficiency in Childhood: Clinical Value and Comparison With Insulin-Induced Hypoglycemia by Cattoni, Alessandro, Molinari, Silvia, Medici, Francesco, De Lorenzo, Paola, Valsecchi, Maria Grazia, Masera, Nicoletta, Adavastro, Marta, Biondi, Andrea

“…dexamethasone has been demonstrated to elicit GH secretion in adults, but few data are available about its effectiveness as a provocative in the diagnostic…”
Get full text

Proposal of an Algorithm to Early Detect Attenuated Type I Mucopolysaccharidosis (MPS Ia) among Children with Growth Abnormalities by Baronio, Federico, Zucchini, Stefano, Zulian, Francesco, Salerno, Mariacarolina, Parini, Rossella, Cattoni, Alessandro, Deodato, Federica, Gaeta, Alberto, Bizzarri, Carla, Gasperini, Serena, Pession, Andrea

“…Diagnostic delay is common in attenuated Mucopolysaccharidosis Type I (MPS Ia) due to the rarity of the disease and the variability of clinical presentation…”
Get full text

Correction: ABO incompatibile graft management in pediatric transplantation by Balduzzi, Adriana, Bönig, Halvard, Jarisch, Andrea, Nava, Tiago, Ansari, Marc, Cattoni, Alessandro, Prunotto, Giulia, Lucchini, Giovanna, Krivan, Gergely, Matic, Toni, Kalwak, Krzyzstof, Yesilipek, Akif, Ifversen, Marianne, Svec, Peter, Buechner, Jochen, Vettenranta, Kim, Meisel, Roland, Lawitschka, Anita, Peters, Christina, Gibson, Brenda, Dalissier, Arnaud, Corbacioglu, Selim, Willasch, André, Dalle, Jean-Hugues, Bader, Peter

“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
Get full text

The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report by Cattoni, Alessandro, Spano, Alice, Tulone, Anna, Boneschi, Annalisa, Masera, Nicoletta, Maitz, Silvia, Di Blasio, Anna Maria, Persani, Luca, Guizzardi, Fabiana, Rossetti, Raffaella

“…Non-syndromic primary ovarian insufficiency due to ovarian dysgenesis in 46,XX patients is an uncommon finding in the general population, even though several…”
Get full text

An Attempt to Induce Transient Immunosuppression Pre-erythrocytapheresis in a Girl With Sickle Cell Disease, a History of Severe Delayed Hemolytic Transfusion Reactions and Need for Hip Prosthesis by Cattoni, Alessandro, Cazzaniga, Giovanni, Perseghin, Paolo, Zatti, Giovanni, Gaddi, Diego, Cossio, Andrea, Biondi, Andrea, Corti, Paola, Masera, Nicoletta

“…We report on a case of delayed hemolytic transfusion reaction (DHTR) occurred 7 days after an erythrocytapheresis or eritroexchange procedure (EEX) treated…”
Get full text

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation by Cattoni, Alessandro, Jackson, Charlotte, Bain, Murray, Houghton, Jayne, Wei, Christina

“…ABCC8 gene mutations with different inheritance patterns have been well described to cause transient and permanent forms of neonatal diabetes with onset of…”
Get full text

Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia by Saettini, Francesco, Cattoni, Alessandro, Redaelli, Martina, Silvestri, Daniela, Ferrari, Giulia Maria, Biondi, Andrea, Jankovic, Momcilo, Spinelli, Marco

“…Aim To evaluate the cumulative prevalence of coeliac disease, systemic lupus erythematosus, autoimmune hyperthyroidism and primary immunodeficiencies in…”
Get full text