Search Results - "De Pellegrin, Maurizio"

Transinguinal Ultrasound versus Magnetic Resonance in Spica Cast after Closed Reduction of Unstable Hips in DDH by Guindani, Nicola, Chiodini, Federico, De Pellegrin, Maurizio

“…During the treatment of unstable hips in developmental hip dysplasia (DDH), the position of the femoral head must be assessed in spica cast (SC) after…”
Get full text

Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome by Consiglieri, Giulia, Tucci, Francesca, De Pellegrin, Maurizio, Guerrini, Barbara, Cattoni, Alessandro, Risca, Giulia, Scarparo, Stefano, Sarzana, Marina, Pontesilli, Silvia, Mellone, Renata, Gasperini, Serena, Galimberti, Stefania, Silvani, Paolo, Filisetti, Chiara, Darin, Silvia, Forni, Giulia, Miglietta, Simona, Santi, Ludovica, Facchini, Marcella, Corti, Ambra, Fumagalli, Francesca, Cicalese, Maria Pia, Calbi, Valeria, Migliavacca, Maddalena, Barzaghi, Federica, Ferrua, Francesca, Gallo, Vera, Recupero, Salvatore, Canarutto, Daniele, Doglio, Matteo, Tedesco, Lucia, Volpi, Nicola, Rovelli, Attilio, la Marca, Giancarlo, Valsecchi, Maria Grazia, Zancan, Stefano, Ciceri, Fabio, Naldini, Luigi, Baldoli, Cristina, Parini, Rossella, Gentner, Bernhard, Aiuti, Alessandro, Bernardo, Maria Ester

“…Mucopolysaccharidosis type I Hurler (MPSIH) is characterized by severe and progressive skeletal dysplasia that is not fully addressed by allogeneic…”
Get more information

Recommendations for early diagnosis of Developmental Dysplasia of the Hip (DDH): working group intersociety consensus document by Agostiniani, Rino, Atti, Giuseppe, Bonforte, Salvatore, Casini, Carolina, Cirillo, Marco, De Pellegrin, Maurizio, Di Bello, Daniela, Esposito, Francesco, Galla, Ambra, Marrè Brunenghi, Giorgio, Romeo, Nicola, Tomà, Paolo, Vezzali, Norberto

“…Abstract This consensus document has been prepared by a multidisciplinary group of experts (Paediatricians, Radiologists, Paediatric Orthopaedics) and it is…”
Get full text

A Prevalent CXCR3+ Phenotype of Circulating Follicular Helper T Cells Indicates Humoral Dysregulation in Children with Down Syndrome by Ottaviano, Giorgio, Gerosa, Jolanda, Santini, Micaela, De Leo, Pasqualina, Vecchione, Andrea, Jofra, Tatiana, Trimarchi, Cristiana, De Pellegrin, Maurizio, Agosti, Massimo, Aiuti, Alessandro, Marinoni, Maddalena, Cicalese, Maria Pia, Fousteri, Georgia

“…Patients with Down syndrome (DS) are characterized by increased susceptibility to autoimmunity and respiratory tract infections that are suggestive of humoral…”
Get full text

Altered Frequency and Phenotype of HLA-G-Expressing DC-10 in Type 1 Diabetes Patients at Onset and in Subjects at Risk to Develop the Disease by Amodio, Giada, Mandelli, Alessandra, Curto, Rosalia, Rancoita, Paola M V, Stabilini, Angela, Bonfanti, Riccardo, de Pellegrin, Maurizio, Bosi, Emanuele, Di Serio, Clelia, Battaglia, Manuela, Gregori, Silvia

“…Type 1 diabetes (T1D) is a chronic autoimmune disease resulting in progressive destruction of β-cells. Several factors affecting lymphocyte and…”
Get full text

Exocrine pancreas function is impaired in adult relatives of patients with type 1 diabetes by Giovenzana, Anna, Vecchio, Federica, Cugnata, Federica, Nonis, Alessandro, Mandelli, Alessandra, Stabilini, Angela, Mazzi, Benedetta Allegra, De Pellegrin, Maurizio, Laurenzi, Andrea, Bonfanti, Riccardo, Battaglia, Manuela, Bosi, Emanuele, Petrelli, Alessandra

“…Aims Alterations of the exocrine pancreas have been reported in type 1 diabetes, but their contribution to the pathogenesis of the disease is poorly…”
Get full text

Ultrasound Diagnosis of Clavicle Fractures in Newborns: A Systematic Review by Galimberti, Luca, Garbetta, Gisella, Poloniato, Antonella, Rovelli, Rosanna, Barera, Graziano, Guindani, Nicola, De Pellegrin, Maurizio

“…Fractures of the clavicle are the most common birth injury among newborns. Aim of this systematic review was to provide a comprehensive analysis of the role of…”
Get full text

Double Diapering Ineffectiveness in Avoiding Adduction and Extension in Newborns Hips by De Pellegrin, Maurizio, Damia, Chiara Maria, Marcucci, Lorenzo, Moharamzadeh, Desiree

“…Hip flexion and abduction is fundamental for developmental dysplasia of the hip (DDH) treatment. At present, double diaper treatment has been inappropriately…”
Get full text

Dysplasia Epiphysealis Hemimelica (Trevor Disease) of the Talus in a Toddler: A Case Report With a Long Follow-up by De Pellegrin, Maurizio, Fracassetti, Dario, Bartolucci, Alessandra, Artioli, Elena, Mazzotti, Antonio

“…Visual Abstract This is a visual representation of the abstract…”
Get full text

Combined unsupervised and semi-automated supervised analysis of flow cytometry data reveals cellular fingerprint associated with newly diagnosed pediatric type 1 diabetes by Bechi Genzano, Camillo, Bezzecchi, Eugenia, Carnovale, Debora, Mandelli, Alessandra, Morotti, Elisa, Castorani, Valeria, Favalli, Valeria, Stabilini, Angela, Insalaco, Vittoria, Ragogna, Francesca, Codazzi, Valentina, Scotti, Giulia Maria, Del Rosso, Stefania, Mazzi, Benedetta Allegra, De Pellegrin, Maurizio, Giustina, Andrea, Piemonti, Lorenzo, Bosi, Emanuele, Battaglia, Manuela, Morelli, Marco J., Bonfanti, Riccardo, Petrelli, Alessandra

“…An unbiased and replicable profiling of type 1 diabetes (T1D)-specific circulating immunome at disease onset has yet to be identified due to experimental and…”
Get full text

Resection of Calcaneonavicular and Talocalcaneal Coalitions With Surgical Correction of the Hindfoot Valgus Deformity in One Step by De Pellegrin, Maurizio, Marcucci, Lorenzo, Brogioni, Lorenzo, Fracassetti, Dario

“…Background: Calcaneonavicular (CNC) and talocalcaneal (TCC) coalitions are the most common cause of rigid flatfoot in children. After resection, correction of…”
Get full text

Surgical Treatment of Clubfoot in Children with Moebius Syndrome by De Pellegrin, Maurizio, Marcucci, Lorenzo, Brogioni, Lorenzo, Prati, Giovanni

“…Moebius syndrome (MS) is a rare disease, with paralysis of the VI and VII cranial nerves, frequently associated with clubfoot (CF). The aim of this study was…”
Get full text

Guided Growth in Leg Length Discrepancy in Beckwith-Wiedemann Syndrome: A Consecutive Case Series by De Pellegrin, Maurizio, Brogioni, Lorenzo, Laskow, Guy, Barera, Graziano, Pajno, Roberta, Osimani, Sara, Russo, Silvia, Marcucci, Lorenzo

“…Beckwith-Wiedemann Syndrome (BWS) is a rare genetic disorder characterized by overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycemia,…”
Get full text

P1392: INTERIM ANALYSIS OF FIRST IN HUMAN PHASE I‐II CLINICAL TRIAL OF EX‐VIVO GENE THERAPY FOR HURLER SYNDROME: AN UPDATE AT 3 YEAR FOLLOW‐UP by Tucci, Francesca, Consiglieri, Giulia, Filisetti, Chiara, De Pellegrin, Maurizio, Mellone, Renata, Fumagalli, Francesca, Darin, Silvia, Sarzana, Marina, Scarparo, Stefano, Ciotti, Francesca, Silvani, Paolo, Baldoli, Cristina, Pontesilli, Silvia, Parini, Rossella, Marca, Giancarlo, Ciceri, Fabio, Naldini, Luigi, Aiuti, Alessandro, Gentner, Bernhard, Ester Bernardo, Maria

Get full text

Preface by De Pellegrin, Maurizio

Get full text

Foot Ankle Deformity in the Child by Pellegrin, Maurizio De

Get full text

Preface by De Pellegrin, Maurizio

Get full text

Developmental dysplasia of the hip screening during the lockdown for COVID-19: Experience from Northern Italy by Guindani, Nicola, De Pellegrin, Maurizio

“…Abstract Purpose Developmental dysplasia of the hip (DDH) ultrasound screening (USS), which is usually performed in Italy as an outpatient, was halted for an…”
Get full text

Subtalar Arthroereisis for Surgical Treatment of Flexible Flatfoot by De Pellegrin, Maurizio, Moharamzadeh, Désirée

“…Various surgical techniques are known for the treatment of flexible flatfoot in children after failure of nonsurgical attempts. Data collected in a review of…”
Get full text

Surgical Treatment of Calcaneonavicular and Talocalcaneal Coalitions by Moharamzadeh, Désirée, De Pellegrin, Maurizio

“…Tarsal coalition is determined by an absence of segmentation between one or more foot bones. The main symptom is activity-related foot pain, usually…”
Get full text