Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion von Capra, Anna Paola, Ferro, Elisa, La Rosa, Maria Angela, Briuglia, Silvana, Russo, Tiziana, Arena, Salvatore, Salpietro Damiano, Carmelo, Romeo, Carmelo, Impellizzeri, Pietro

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Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease von Rigoli, Luciana, Romano, Claudio, Caruso, Rosario Alberto, Lo Presti, Maria A, Di Bella, Chiara, Procopio, Vincenzo, Lo Giudice, Giuseppina, Amorini, Maria, Costantino, Giuseppe, Sergi, Maria D, Cuppari, Caterina, Calabro, Giovanna Elisa, Gallizzi, Romina, Salpietro, Carmelo Damiano, Fries, Walter

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Early Identification of Cardiovascular Involvement in Patients With β-Thalassemia Major von Cusmà Piccione, Maurizio, MD, Piraino, Basilia, MD, Zito, Concetta, MD, PhD, Khandheria, Bijoy K., MD, Di Bella, Gianluca, MD, PhD, De Gregorio, Cesare, MD, Oreto, Lilia, MD, Rigoli, Luciana, MD, Ferraù, Valeria, MD, Salpietro, Carmelo Damiano, MD, Carerj, Scipione, MD

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Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay von Colosimo, Alessia, Guida, Valentina, Rigoli, Luciana, Di Bella, Chiara, De Luca, Alessandro, Briuglia, Silvana, Stuppia, Liborio, Carmelo Salpietro, Damiano, Dallapiccola, Bruno

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Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children von Lo Giudice, Giuseppe, Nicita, Fabiana, Militi, Angela, Bertino, Rossella, Matarese, Marco, Currò, Monica, Damiano, Carmelo Salpietro, Mannucci, Carmen, Calapai, Gioacchino

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NGAL as an Early Biomarker of Kidney Disease in Joubert Syndrome: Three Brothers Compared von Lacquaniti, Antonio, Chirico, Valeria, Donato, Valentina, Briuglia, Silvana, Cernaro, Valeria, Gallizzi, Romina, Salpietro, Carmelo Damiano, Buemi, Michele

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Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia von Salpietro, Carmelo Damiano, Briuglia, Silvana, Cutrupi, Maria Concetta, Gallizzi, Romina, Rigoli, Luciana, Dallapiccola, Bruno

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A mitochondrial DNA mutation (A3243g mtDNA) in a family with cyclic vomiting von SALPIETRO, Carmelo Damiano, BRIUGLIA, Silvana, MERLINO, Maria Valeria, DI BELLA, Chiara, RIGOLI, Luciana

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Pain in neonatal intensive care: role of melatonin as an analgesic antioxidant von Gitto, Eloisa, Aversa, Salvatore, Salpietro, Carmelo Damiano, Barberi, Ignazio, Arrigo, Teresa, Trimarchi, Giuseppe, Reiter, Russel J., Pellegrino, Salvatore

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Age and sex prevalence estimate of Joubert syndrome in Italy von Nuovo, Sara, Bacigalupo, Ilaria, Ginevrino, Monia, Battini, Roberta, Bertini, Enrico, Borgatti, Renato, Casella, Antonella, Micalizzi, Alessia, Nardella, Marta, Romaniello, Romina, Serpieri, Valentina, Zanni, Ginevra, Valente, Enza Maria, Vanacore, Nicola

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Disomy of distal Xq in males: Case report and overview von Novelli, Antonio, Bernardini, Laura, Salpietro, Damiano Carmelo, Briuglia, Silvana, Merlino, Maria Valeria, Mingarelli, Rita, Dallapiccola, Bruno

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Hallerman-Streiff syndrome: Patient with decreased GH and insulin-like growth factor-1 von Damiano Salpietro, Carmelo, Briuglia, Silvana, Valeria Merlino, Maria, Piraino, Basilia, Valenzise, Mariella, Dallapiccola, Bruno

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Early Identification of Cardiovascular Involvement in Patients With ?-Thalassemia Major von Cusmà Piccione, Maurizio, Piraino, Basilia, Zito, Concetta, Khandheria, Bijoy K, Di Bella, Gianluca, De Gregorio, Cesare, Oreto, Lilia, Rigoli, Luciana, Ferraù, Valeria, Salpietro, Carmelo Damiano, Carerj, Scipione

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Description, Nomenclature, and Mapping of a Novel Cerebello-Renal Syndrome with the Molar Tooth Malformation von Valente, Enza Maria, Salpietro, Damiano Carmelo, Brancati, Francesco, Bertini, Enrico, Galluccio, Tiziana, Tortorella, Gaetano, Briuglia, Silvana, Dallapiccola, Bruno

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On the use of conventional and tissue Doppler echocardiography in patients with β-Thalassemia major and myocardial iron-overload: Preliminary data by a single centre study von de Gregorio, Cesare, Piraino, Basilia, Morabito, Gaetano, Salpietro, Carmelo Damiano, Coglitore, Sebastiano

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Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies von RIGOLI, Luciana, CHIMENZ, Roberto, DI BELLA, Chiara, CAVALLARO, Emanuela, CARUSO, Rosario, BRIUGLIA, Silvana, FEDE, Carmelo, SALPIETRO, Carmelo Damiano

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Increased protein carbonyl groups in the serum of patients affected by thalassemia major von Trombetta, Domenico, Gangemi, Sebastiano, Saija, Antonella, Minciullo, Paola Lucia, Cimino, Francesco, Cristani, Mariateresa, Briuglia, Silvana, Piraino, Basilia, Isola, Stefania, Salpietro, Carmelo Damiano

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Cutis laxa in Kabuki make-up syndrome von Vaccaro, Mario, Salpietro, Damiano Carmelo, Briuglia, Silvana, Merlino, Maria Valeria, Guarneri, Fabrizio, Dallapiccola, Bruno

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What Syndrome Is This? von Carmelo Salpietro, Damiano, Guarneri, Fabrizio, Rigoli, Luciana, Bruglia, Silvana, Guarneri, Claudio, Vaccaro, Mario

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What syndrome is this? Kabuki make-up syndrome von Salpietro, Damiano Carmelo, Guarneri, Fabrizio, Rigoli, Luciana, Bruglia, Silvana, Guarneri, Claudio, Vaccaro, Mario

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