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Research Output 1990 2020

2020

The Burden of Depression in Adolescents and the Importance of Early Recognition

Petito, A., Pop, T. L., Namazova-Baranova, L., Mestrovic, J., Nigri, L., Vural, M., Sacco, M., Giardino, I., Ferrara, P. & Pettoello-Mantovani, M., Jan 1 2020, (Accepted/In press) In : Journal of Pediatrics.

Research output: Contribution to journalEditorial

The Health Risks of Electronic Cigarettes Use in Adolescents

Ferrara, P., Franceschini, G., Corsello, G., Namazova-Baranova, L., Pop, T. L., Mestrovic, J., Giardino, I., Sacco, M., Vural, M., Nigri, L., Nagy, A., Szabo, L. & Pettoello-Mantovani, M., Jan 1 2020, (Accepted/In press) In : Journal of Pediatrics.

Research output: Contribution to journalEditorial

2019

A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway

Palumbo, P., Petracca, A., Maggi, R., Biagini, T., Nardella, G., Sacco, M. C., Di Schiavi, E., Carella, M., Micale, L. & Castori, M., Jan 1 2019, In : European Journal of Human Genetics.

Research output: Contribution to journalArticle

MAP Kinase Signaling System
Fibroblast Growth Factor 2
Holoprosencephaly
Exome
Autophagy

Anthropometric characteristics of newborns with Prader-Willi syndrome

Salvatoni, A., Moretti, A., Grugni, G., Agosti, M., Azzolini, S., Bonaita, V., Cianci, P., Corica, D., Crinò, A., Delvecchio, M., Ferraris, S., Greggio, N. A., Iughetti, L., Licenziati, M. R., Madeo, S. F., Nosetti, L., Pajno, R., Rutigliano, I., Sacco, M., Salvatore, S. & 3 others, Scarano, E., Trifirò, G. & Wasniewska, M., Oct 1 2019, In : American journal of medical genetics. Part A. 179, 10, p. 2067-2074 8 p.

Research output: Contribution to journalArticle

Prader-Willi Syndrome
Newborn Infant
Birth Weight
Gestational Age
Mothers

Complications and risk factors for severe outcome in children with measles

Group, SITIP. M. S., Lo Vecchio, A., Krzysztofiak, A., Montagnani, C., Valentini, P., Rossi, N., Garazzino, S., Raffaldi, I., Di Gangi, M., Esposito, S., Vecchi, B., Melzi, M. L., Lanari, M., Zavarise, G., Bosis, S., Valenzise, M., Cazzato, S., Sacco, M., Govoni, M. R., Mozzo, E. & 10 others, Cambriglia, M. D., Bruzzese, E., Di Camillo, C., Pata, D., Graziosi, A., Sala, D., Magurano, F., Villani, A., Guarino, A. & Galli, L., Jan 12 2019, In : Archives of Disease in Childhood.

Research output: Contribution to journalArticle

Measles
C-Reactive Protein
Genotype
Hospitalized Child
Encephalitis

Lifelong Negative Influence of School Violence on Children

Ferrara, P., Franceschini, G., Namazova-Baranova, L., Vural, M., Mestrovic, J., Nigri, L., Giardino, I., Pop, T. L., Sacco, M. & Pettoello-Mantovani, M., Dec 2019, In : Journal of Pediatrics. 215, p. 287-288.e2

Research output: Contribution to journalEditorial

Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

Di Stolfo, G., Accadia, M., Mastroianno, S., Leone, M. P., Palumbo, O., Palumbo, P., Potenza, D., Maccarone, P., Sacco, M., Russo, A. & Carella, M., Sep 1 2019, In : Molecular Genetics and Genomic Medicine. 7, 9, e855.

Research output: Contribution to journalArticle

Open Access
Chlorpheniramine
Genetic Databases
Long QT Syndrome
Chromosome Deletion
Prescriptions

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

Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology, Aug 28 2019, In : Endocrinology and Metabolism, Supplement. 48-49, p. 9-15 7 p.

Research output: Contribution to journalArticle

Uniparental Disomy
Insulin-Like Growth Factor I
Prader-Willi Syndrome
Therapeutics
Italy

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

On behalf of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology, Oct 1 2019, In : Growth Hormone and IGF Research. 48-49, p. 9-15 7 p.

Research output: Contribution to journalArticle

Uniparental Disomy
Insulin-Like Growth Factor I
Prader-Willi Syndrome
Therapeutics
Italy
2018

Complications and risk factors for severe outcome in children with measles

Lo Vecchio, A., Krzysztofiak, A., Montagnani, C., Valentini, P., Rossi, N., Garazzino, S., Raffaldi, I., Di Gangi, M., Esposito, S., Vecchi, B., Melzi, M. L., Lanari, M., Zavarise, G., Bosis, S., Valenzise, M., Cazzato, S., Sacco, M., Govoni, M. R., Mozzo, E., Cambriglia, M. D. & 9 others, Bruzzese, E., Di Camillo, C., Pata, D., Graziosi, A., Sala, D., Magurano, F., Villani, A., Guarino, A. & Galli, L., Jan 1 2018, (Accepted/In press) In : Archives of Disease in Childhood.

Research output: Contribution to journalArticle

Measles
C-Reactive Protein
Genotype
Hospitalized Child
Encephalitis

Food Insecurity and Children's Rights to Adequate Nutrition in Europe

Pettoello-Mantovani, M., Ehrich, J., Sacco, M., Ferrara, P., Giardino, I. & Pop, T. L., Jul 1 2018, In : Journal of Pediatrics. 198, p. 329-330.e1

Research output: Contribution to journalEditorial

Muscles
Lower Extremity
Congenital Hip Dislocation
Muscular Diseases
Bone Density

Urea Memory: Transient Cell Exposure to Urea Causes Persistent Mitochondrial ROS Production and Endothelial Dysfunction

d'Apolito, M., Colia, A. L., Manca, E., Pettoello-Mantovani, M., Sacco, M., Maffione, A. B., Brownlee, M. & Giardino, I., Oct 11 2018, In : Toxins. 10, 10

Research output: Contribution to journalArticle

Urea
Data storage equipment
Mitochondrial Dynamics
Dialysis
Mitochondrial Proteins
2017

Acute cerebellitis in children

Lancella, L., Esposito, S., Galli, M. L., Bozzola, E., Labalestra, V., Boccuzzi, E., Krzysztofiak, A., Cursi, L., Gattinara, G. C., Mirante, N., Buonsenso, D., Tagliabue, C., Castellazzi, L., Montagnani, C., Tersigni, C., Valentini, P., Capozza, M., Pata, D., Di Gangi, M., Dones, P. & 10 others, Garazzino, S., Baroero, L., Verrotti, A., Melzi, M. L., Sacco, M., Germano, M., Greco, F., Uga, E., Crichiutti, G. & Villani, A., Jun 12 2017, In : Italian Journal of Pediatrics. 43, 1

Research output: Contribution to journalArticle

Cerebellar Ataxia
Tomography
Magnetic Resonance Imaging
Signs and Symptoms
Length of Stay

Acute cerebellitis in children: An eleven year retrospective multicentric study in Italy

Lancella, L., Esposito, S., Galli, M. L., Bozzola, E., Labalestra, V., Boccuzzi, E., Krzysztofiak, A., Cursi, L., Gattinara, G. C., Mirante, N., Buonsenso, D., Tagliabue, C., Castellazzi, L., Montagnani, C., Tersigni, C., Valentini, P., Capozza, M., Pata, D., Di Gangi, M., Dones, P. & 10 others, Garazzino, S., Baroero, L., Verrotti, A., Melzi, M. L., Sacco, M., Germano, M., Greco, F., Uga, E., Crichiutti, G. & Villani, A., Jun 12 2017, In : Italian Journal of Pediatrics. 43, 1, 54.

Research output: Contribution to journalArticle

Cerebellar Ataxia
Italy
Retrospective Studies
Tomography
Magnetic Resonance Imaging

Effects on the incidence of cardiovascular events of the addition of pioglitazone versus sulfonylureas in patients with type 2 diabetes inadequately controlled with metformin (TOSCA.IT): a randomised, multicentre trial

Vaccaro, O., Masulli, M., Nicolucci, A., Bonora, E., Del Prato, S., Maggioni, A. P., Rivellese, A. A., Squatrito, S., Giorda, C. B., Sesti, G., Mocarelli, P., Lucisano, G., Sacco, M., Signorini, S., Cappellini, F., Perriello, G., Babini, A. C., Lapolla, A., Gregori, G., Giordano, C. & 31 others, Corsi, L., Buzzetti, R., Clemente, G., Di Cianni, G., Iannarelli, R., Cordera, R., La Macchia, O., Zamboni, C., Scaranna, C., Boemi, M., Iovine, C., Lauro, D., Leotta, S., Dall'Aglio, E., Cannarsa, E., Tonutti, L., Pugliese, G., Bossi, A. C., Anichini, R., Dotta, F., Di Benedetto, A., Citro, G., Antenucci, D., Ricci, L., Giorgino, F., Santini, C., Gnasso, A., De Cosmo, S., Zavaroni, D., Vedovato, M. & Thiazolidinediones Or Sulfonylureas Cardiovascular Accidents Intervention Trial (TOSCA.IT) study group, Sep 13 2017, In : The Lancet Diabetes and Endocrinology. 5, 11, p. 887-897 11 p.

Research output: Contribution to journalArticle

pioglitazone
Metformin
Type 2 Diabetes Mellitus
glimepiride
Multicenter Studies
2014

Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation

Delvecchio, M., Di Paola, R., Mangiacotti, D., Sacco, M., Menzaghi, C. & Trischitta, V., Jun 19 2014, In : Italian Journal of Pediatrics. 40, 1, 58.

Research output: Contribution to journalArticle

Lung ultrasound in pediatric pneumonia. the persistent need of chest X-rays

Catalano, D., Trovato, G., Sperandeo, M. & Sacco, M. C., 2014, In : Pediatric Pulmonology. 49, 6, p. 617-618 2 p.

Research output: Contribution to journalArticle

2013

MODY type 2 P59S GCK mutant: Founder effect in South of Italy

Delvecchio, M., Ludovico, O., Bellacchio, E., Stallone, R., Palladino, T., Mastroianno, S., Zelante, L., Sacco, M., Trischitta, V. & Carella, M., Jan 2013, In : Clinical Genetics. 83, 1, p. 83-87 5 p.

Research output: Contribution to journalArticle

Founder Effect
Glucokinase
Italy
Mutation
Maturity-Onset Diabetes of the Young, Type 2
2011

IL28B CC-genotype association with HLA-DQB1*0301 allele increases the prediction of spontaneous HCV RNA clearance in thalassaemic HCV-infected patients

Mangia, A., Santoro, R., Sarli, R., Mottola, L., Piazzolla, V., Petruzzellis, D., Bacca, D., Clemente, R., Copetti, M., Di Mauro, L., Lotti, G., Sacco, M. & Stefano, I., 2011, In : Antiviral Therapy. 16, 8, p. 1309-1316 8 p.

Research output: Contribution to journalArticle

Alleles
Genotype
RNA
Infection
Hepatitis C Antibodies

Metabolic syndrome in children with Prader-Willi syndrome: The effect of obesity

Brambilla, P., Crinò, A., Bedogni, G., Bosio, L., Cappa, M., Corrias, A., Delvecchio, M., Di Candia, S., Gargantini, L., Grechi, E., Iughetti, L., Mussa, A., Ragusa, L., Sacco, M., Salvatoni, A., Chiumello, G. & Grugni, G., Apr 2011, In : Nutrition, Metabolism and Cardiovascular Diseases. 21, 4, p. 269-276 8 p.

Research output: Contribution to journalArticle

Prader-Willi Syndrome
Obesity
Pediatrics
Morbidity
Mortality

Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: Patient-level meta-analysis of randomised trials

Early Breast Cancer Trialists' Collaborative Group (EBCTCG), Aug 27 2011, In : The Lancet. 378, 9793, p. 771-784 14 p.

Research output: Contribution to journalArticle

Tamoxifen
Meta-Analysis
Hormones
Breast Neoplasms
Mortality
2010

Calcium-Sensing Receptor (CASR) mutations in hypercalcemic states: Studies from a single endocrine clinic over three years

Guarnieri, V., Canaff, L., Yun, F. H. J., Scillitani, A., Battista, C., Muscarella, L. A., Wong, B. Y. L., Notarangelo, A., D'Agruma, L., Sacco, M., Cole, D. E. C. & Hendy, G. N., Apr 2010, In : Journal of Clinical Endocrinology and Metabolism. 95, 4, p. 1819-1829 11 p.

Research output: Contribution to journalArticle

Calcium-Sensing Receptors
Primary Hyperparathyroidism
Mutation
Assays
Functional analysis
2008

The Italian national survey for Prader-Willi syndrome: An epidemiologic study

Grugni, G., Crinò, A., Bosio, L., Corrias, A., Cuttini, M., De Toni, T., Di Battista, E., Franzese, A., Gargantini, L., Greggio, N., Iughetti, L., Livieri, C., Naselli, A., Pagano, C., Pozzan, G., Ragusa, L., Salvatoni, A., Trifirò, G., Beccaria, L., Bellizzi, M. & 19 others, Bellone, J., Brunani, A., Cappa, M., Caselli, G., Cerioni, V., Delvecchio, M., Giardino, D., Iannì, F., Memo, L., Pilotta, A., Pomara, C., Radetti, G., Sacco, M., Sanzari, A., Sartorio, A., Tonini, G., Vettor, R., Zaglia, F. & Chiumello, G., Apr 1 2008, In : American Journal of Medical Genetics, Part A. 146, 7, p. 861-872 12 p.

Research output: Contribution to journalArticle

Prader-Willi Syndrome
Epidemiologic Studies
Cause of Death
Therapeutics
Chromosomes, Human, Pair 15
2006

Recurrent intracranial hypertension induced by growth hormone therapy

Sacco, M. & Di Giorgio, G., Apr 2006, In : Journal of Pediatric Endocrinology and Metabolism. 19, 4, p. 545 1 p.

Research output: Contribution to journalArticle

Shprintzen-Goldberg omphalocele syndrome: A new patient with an expanded phenotype

Zelante, L., Germano, M., Sacco, M. & Calvano, S., Feb 15 2006, In : American Journal of Medical Genetics. 140 A, 4, p. 383-384 2 p.

Research output: Contribution to journalArticle

Umbilical Hernia
Scoliosis
Imperforate Anus
Phenotype
Learning Disorders
2005

Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: An overview of the randomised trials

Early Breast Cancer Trialists' Collaborative Group (EBCTCG), May 14 2005, In : Lancet. 365, 9472, p. 1687-1717 31 p.

Research output: Contribution to journalReview article

Tamoxifen
Fluorouracil
Cyclophosphamide
Breast Neoplasms
Recurrence

Sudden death in Prader-Willi syndrome during growth hormone therapy

Sacco, M. & Di Giorgio, G., 2005, In : Hormone Research. 63, 1, p. 29-32 4 p.

Research output: Contribution to journalArticle

Prader-Willi Syndrome
Sudden Death
Growth Hormone
Morbid Obesity
Epidemiologic Studies
2002

Effectiveness of GH therapy in a child with ulcerative colitis

Campanozzi, A., Spirito, F., Bisceglia, M. & Sacco, M., Jun 2002, In : Italian Journal of Pediatrics. 28, 3, p. 234-235 2 p.

Research output: Contribution to journalArticle

Turner Syndrome
Ulcerative Colitis
Therapeutics

Erratum: Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl co-transporter in Italian patients with Gitelman syndrome (Human mutation (2002) 20:78))

Syrén, M. L., Tedeschi, S., Cesareo, L., Bellantuono, R., Colussi, G., Procaccio, M., Alì, A., Domenici, R., Malberti, F., Sprocati, M., Sacco, M., Miglietti, N., Edefonti, A., Sereni, F., Casari, G., Coviello, D. A. & Bettinelli, A., 2002, In : Human Mutation. 20, 4, p. 321 1 p.

Research output: Contribution to journalArticle

Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndrome.

Syrén, M. L., Tedeschi, S., Cesareo, L., Bellantuono, R., Colussi, G., Procaccio, M., Alì, A., Domenici, R., Malberti, F., Sprocati, M., Sacco, M., Miglietti, N., Edefonti, A., Sereni, F., Casari, G., Coviello, D. A. & Bettinelli, A., Jul 2002, In : Human Mutation. 20, 1, p. 78 1 p.

Research output: Contribution to journalArticle

Gitelman Syndrome
Symporters
Mutation
Genes
Distal Kidney Tubule
2000

Phenotypic variability in Bartter syndrome type I

Bettinelli, A., Ciarmatori, S., Cesareo, L., Tedeschi, S., Ruffa, G., Appiani, A. C., Rosini, A., Grumieri, G., Mercuri, B., Sacco, M., Leozappa, G., Binda, S., Cecconi, M., Navone, C., Curcio, C., Syren, M. L. & Casari, G., Sep 2000, In : Pediatric Nephrology. 14, 10-11, p. 940-945 6 p.

Research output: Contribution to journalArticle

Bartter Syndrome
Alkalosis
Hypokalemia
Nephrocalcinosis
Hypercalciuria
1998

Skeletal age assessment in children and young adults: Comparison between a newly developed sonographic method and conventional methods

Castriota-Scanderbeg, A., Sacco, M. C., Emberti-Gialloreti, L. & Fraracci, L., May 1998, In : Skeletal Radiology. 27, 5, p. 271-277 7 p.

Research output: Contribution to journalArticle

Young Adult
Wrist
Age Determination by Skeleton
Pelvic Bones
Radiography
1997

Absence of mutations in the gene encoding thyroid transcription factor- 1 (TTF-1) in patients with thyroid dysgenesis

Perna, M. G., Civitareale, D., De Filippis, V., Sacco, M., Cisternino, C. & Tassi, V., 1997, In : Thyroid. 7, 3, p. 377-381 5 p.

Research output: Contribution to journalArticle

Thyroid Dysgenesis
Thyroid Gland
Mutation
Genes
Congenital Hypothyroidism

Agranulocytosis, arthritis and systemic vasculitis in a patient receiving the oral iron chelator L1 (deferiprone)

Castriota-Scanderbeg, A. & Sacco, M., 1997, In : British Journal of Haematology. 96, 2, p. 254-255 2 p.

Research output: Contribution to journalArticle

Systemic Vasculitis
Agranulocytosis
Chelating Agents
Arthritis
Iron

Il progetto per il registro italiano del Diabete Mellito insulino-dipendente (RIDI)

Translated title of the contribution: The Registry for Insulin-Dependent Diabetes Mellitus in Italy (RIDI) projectCherubini, V., Carle, F., Iannilli, A., Kantar, A., Coppa, G. V., Chiumello, G., Angius, E., Banin, P., Bellù, L., Berardi, R., Bernasconi, S., Mariani, S., Boscherini, B., Fonte, M. T., Cacciari, E., Salardi, S., Cadario, F., Calisti, N. V., Cardella, F., Cavallo, L. & 44 others, Cerasoli, G., Cerutti, F., Chiarelli, F., Verrotti, A., Cicchetti, M., Cotellessa, M., Picco, P., Crino, A., Dammacco, F., De Giorgi, G., De Luca, F., Falorni, A., Fifi, A., Franzese, A., Gargantini, G., Giorgetti, R., Guazzarotti, L., La Loggia, A., Lorini, R., D'Annunzio, G., Lucentini, L., Mannazzu, M. C., Marietti, G., Marsciani, A., Martinucci, M., Mastrangelo, C., Meossi, C., Meschi, F., Monciotti, C., Multari, G., Pinelli, L., Pocecco, M., Prisco, F., Jafusco, D., Reitano, G., Sacchini, P., Sacco, M., Salvatoni, A., Scaramuzza, A., Vanelli, M., Chiari, G., Vanini, R., Visentin, A. & Zanini, R., 1997, In : Rivista Italiana di Pediatria. 23, 5, p. 945-948 4 p.

Research output: Contribution to journalArticle

Type 1 Diabetes Mellitus
Italy
Registries
Epidemiology
Incidence

Splenic hemangioma in Turner syndrome: A case report

Castriota-Scanderbeg, A., Mingarelli, R., Sacco, M. & Dallapiccola, B., 1997, In : Pediatric Radiology. 27, 11, p. 894 1 p.

Research output: Contribution to journalArticle

1996

Hemorrhagic disease in an infant fed on a vitamin K-deficient soya formula

Pellegrino, M., Sacco, M., D'Altilia, M. R., Meleleo, D. & Giulia De Anseris, A., 1996, In : Journal of Pediatric Gastroenterology and Nutrition. 23, 4, p. 413-414 2 p.

Research output: Contribution to journalArticle

Hepatic iron overload in thalassemic patients: Proposal and validation of an MRI method of assessment

Bonetti, M. G., Castriota-Scanderbeg, A., Criconia, G. M., Mazza, P., Sacco, M., Amurri, B. & Masi, C., Sep 1996, In : Pediatric Radiology. 26, 9, p. 650-656 7 p.

Research output: Contribution to journalArticle

Iron Overload
Liver
Iron
Ferritins
Paraspinal Muscles

La polmonite da mycoplasma in età pediatrica: È possibile la diagnosi radiologica?

Translated title of the contribution: Mycoplasma pneumonia in childhood: Is the roentgenographic diagnosis possible?Castriota-Scanderbeg, A., Sacco, M. C. & Meleleo, D., Feb 1996, In : Rivista Italiana di Pediatria. 22, 1, p. 54-60 7 p.

Research output: Contribution to journalArticle

Mycoplasma Pneumonia
Pneumonia
Virus Diseases
Infection
Thorax

Sindrome di Bartter. Presentazione di un caso clinico con nefrocalcinosi

Translated title of the contribution: Bartter's syndrome. A case report with nephrocalcinosisSacco, M., Dell'olio, L. & Castriota Scanderbeg, A., Apr 1996, In : Minerva Pediatrica. 48, 4, p. 155-158 4 p.

Research output: Contribution to journalArticle

Bartter Syndrome
Nephrocalcinosis
Hypercalciuria
Indomethacin
Early Diagnosis
1995

Idrocele nella malattia di Kawasaki.

Translated title of the contribution: Hydrocele in Kawasaki diseaseSacco, M. C., Meleleo, D. & Castriota Scanderbeg, A., May 1995, In : Pediatria Medica e Chirurgica. 17, 3, p. 279-280 2 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome

La diagnosi di polmonite da mycoplasma nel bambino: quale il ruolo del radiogramma del torace?

Translated title of the contribution: Diagnosis of mycoplasma pneumonia in children: which is the role of thoracic radiography?Castriota-Scanderbeg, A., Popolizio, T., Sacco, M., Coppi, M., Scarale, M. G. & Cammisa, M., Jun 1995, In : Radiologia Medica. 89, 6, p. 782-786 5 p.

Research output: Contribution to journalArticle

Thoracic Radiography
Mycoplasma Pneumonia
Mycoplasma Infections
Pneumonia
Thorax

MALATTIA EMORRAGICA VITAMINA K-DIPENDENTE: UNA RARA MANIFESTAZIONE DELLA FIBROSI CISTICA

Translated title of the contribution: Vitamin K-dependent hemorragic disease: An unusual manifestation of cystic fibrosisD'Altilia, M. R., Meleleo, D., Gorgoglione, N., Pellegrino, M., Sacco, M. & Lotti, F., 1995, In : Rivista Italiana di Pediatria. 21, 3, p. 315-318 4 p.

Research output: Contribution to journalArticle

Vitamin K
Cystic Fibrosis
Vitamin K Deficiency
Malabsorption Syndromes
Blood Coagulation Factors
1994

VALUTAZIONE DELL'OTOTOSSICITA DELLA DESFERRIOXAMINA IN PAZIENTI TALASSEMICI. RISULTATI DI UN FOLLOW-UP DI 5 ANNI

Translated title of the contribution: Evaluation of desferrioxamine ototoxicity in thalassaemic patients. Follow-up over a 5-year period and resultsSacco, M., Meleleo, D., Tricarico, N., Greco Miani, A., Serra, E. & Parlatore, L., 1994, In : Minerva Pediatrica. 46, 5, p. 225-230 6 p.

Research output: Contribution to journalArticle

Deferoxamine
Audiometry
Ferritins
Poisons
Serum
1993

Pancreatite in corso di salmonellosi maggiore.

Translated title of the contribution: Pancreatitis associated with salmonellaPastore, M., Pellegrino, M., Maruzzi, M., Meleleo, D., D'Altilia, M. R. & Sacco, M., Nov 1993, In : Minerva Pediatrica. 45, 11, p. 471-473 3 p.

Research output: Contribution to journalArticle

Salmonella Infections
Salmonella
Pancreatitis
Abdominal Pain
Diarrhea
1991

Torsione dell'ovaio: una causa rara di addome acuto in età pediatrica. Presentazione di un caso.

Translated title of the contribution: Torsion of the ovary: an unusual cause of acute abdomen in childhood. Presentation of a caseSacco, M. & Scaramuzzi, G., May 1991, In : Pediatria Medica e Chirurgica. 13, 3, p. 319-320 2 p.

Research output: Contribution to journalArticle

Acute Abdomen
Infarction
Ovary
Necrosis
Therapeutics
1990

SINDROME EXTRAPIRAMIDALE DA MODERATO IPERDOSAGGIO DI DOMPERIDONE. DESCRIZIONE DI UN CASO

Translated title of the contribution: Extrapyramidal syndrome after moderate hyperdosage of domperidone: A case reportPellegrino, M., Sacco, M. & Lotti, F., 1990, In : Pediatria Medica e Chirurgica. 12, 2, p. 205-206 2 p.

Research output: Contribution to journalArticle