نتائج البحث - "Giancarlo Parenti"

1

Crohn disease-like enterocolitis remission after empagliflozin treatment in a child with glycogen storage disease type Ib: a case report

المؤلفون: Giancarlo Parenti, Simona Fecarotta, Maria D'Armiento, Pietro Strisciuglio, Carmine Mollica, Erasmo Miele, Maria Veiga-da-Cunha, Enza Mozzillo, Annamaria Staiano, Massimo Martinelli, Terry G J Derks, A. Rossi

المساهمون: Center for Liver, Digestive and Metabolic Diseases (CLDM), Rossi, Alessandro, Miele, Erasmo, Fecarotta, Simona, Veiga-da-Cunha, Maria, Martinelli, Massimo, Mollica, Carmine, D'Armiento, Maria, Mozzillo, Enza, Strisciuglio, Pietro, Derks, Terry G J, Staiano, Annamaria, Parenti, Giancarlo

المصدر: Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-9 (2021)
Italian journal of pediatrics, 47(1):149, 1-9. BMC
Italian Journal of Pediatrics

مصطلحات موضوعية: Male, 0301 basic medicine, AUTOIMMUNITY, Empagliflozin, Case Report, Glycogen Storage Disease Type I, GUIDELINES, Pediatrics, Gastroenterology, Inflammatory bowel disease, 0302 clinical medicine, Crohn Disease, Glucosides, Granulocyte Colony-Stimulating Factor, Glycogen Storage Disease Type Ib, Continuous glucose monitoring, Enterocolitis, Remission Induction, NEUTROPHIL DYSFUNCTION, Absolute neutrophil count, medicine.symptom, COLITIS, medicine.medical_specialty, Neutropenia, Adolescent, 5-anhydroglucitol, RJ1-570, 03 medical and health sciences, Glycogen storage disease type Ib, Internal medicine, MANAGEMENT, medicine, Humans, Benzhydryl Compounds, Adverse effect, Sodium-Glucose Transporter 2 Inhibitors, 1,5-anhydroglucitol, business.industry, medicine.disease, 030104 developmental biology, Calprotectin, business, 030217 neurology & neurosurgery, INFLAMMATORY-BOWEL-DISEASE, 1B

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b079e9435d3019f0277442f1ca33ba4eTest
https://doi.org/10.1186/s13052-021-01100-wTest

2

Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance

المؤلفون: Giancarlo Parenti, Maria Grazia Caprio, Gianfranco Vallone, Raffaele Iorio, M.G. Puoti, Gabriella Esposito, Simona Fecarotta, Severo Pagliardini, Claudia Zuppaldi, Simona Spadarella, Maria Immacolata Spagnuolo, Fabiola Di Dato

المساهمون: Di Dato, Fabiola, Spadarella, Simona, Puoti, Maria Giovanna, Caprio, Maria Grazia, Pagliardini, Severo, Zuppaldi, Claudia, Vallone, Gianfranco, Fecarotta, Simona, Esposito, Gabriella, Iorio, Raffaele, Parenti, Giancarlo, Spagnuolo, Maria Immacolata

المصدر: Nutrients
Volume 11
Issue 10
Nutrients 11 (2019). doi:10.3390/nu11102397
info:cnr-pdr/source/autori:Di Dato, Fabiola; Spadarella, Simona; Puoti, Maria Giovanna; Caprio, Maria Grazia; Pagliardini, Severo; Zuppaldi, Claudia; Vallone, Gianfranco; Fecarotta, Simona; Esposito, Gabriella; Iorio, Raffaele; Parenti, Giancarlo; Spagnuolo, Maria Immacolata/titolo:Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance/doi:10.3390%2Fnu11102397/rivista:Nutrients/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:11
Nutrients, Vol 11, Iss 10, p 2397 (2019)

مصطلحات موضوعية: 0301 basic medicine, Male, Sucrose, Hereditary fructose intolerance, Gastroenterology, Severity of Illness Index, fructose, chemistry.chemical_compound, Diet, Carbohydrate-Restricted, Fructose-Bisphosphate Aldolase, Child, chemistry.chemical_classification, Liver injury, Aldolase B, Fructose, Liver steatosis, Sialotransferrin profile, Sorbitol, Adolescent, Alanine Transaminase, Biomarkers, Fatty Liver, Female, Fructose Intolerance, Genetic Predisposition to Disease, Humans, Mutation, Phenotype, Retrospective Studies, Sialoglycoproteins, Transferrin, Nutrition and Dietetics, biology, sucrose, lcsh:Nutrition. Foods and food supply, medicine.medical_specialty, lcsh:TX341-641, Article, liver steatosis, liver steatosi, 03 medical and health sciences, Internal medicine, medicine, sorbitol, Carbohydrate-Restricted, 030102 biochemistry & molecular biology, sialotransferrin profile, business.industry, aldolase B, medicine.disease, Diet, 030104 developmental biology, chemistry, biology.protein, Steatosis, business, Food Science

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee330900e46ba7dc4871956870b6f875Test

3

Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report

المؤلفون: Enza Raiano, Vincenzo Nigro, Pietro Strisciuglio, R. Della Casa, Alfonso Romano, Marco Savarese, Annalaura Torella, V. Gragnaniello, Generoso Andria, Simona Fecarotta, Giancarlo Parenti

المساهمون: Fecarotta, S, Gragnaniello, Vincenza, Della Casa, R, Romano, A, Raiano, E, Torella, A, Savarese, M, Nigro, V, Strisciuglio, P, Andria, G, Parenti, G, Medicum, Department of Medical and Clinical Genetics, University of Helsinki, Fecarotta, S., Gragnaniello, V., Della Casa, R., Romano, A., Raiano, E., Torella, A., Savarese, M., Nigro, V., Strisciuglio, P., Andria, G., Parenti, G.

مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Glycosylation, Congenital muscular dystrophy, GMPPB gene, medicine.drug_class, Alpha (ethology), GMPPB, Gastroenterology, 3124 Neurology and psychiatry, 03 medical and health sciences, 0302 clinical medicine, Prednisone, Adrenal Cortex Hormones, Internal medicine, Congenital Bilateral Cataracts, medicine, Humans, Child, Dystroglycans, Alpha-dystroglycanopathy, Genetics (clinical), biology, business.industry, 3112 Neurosciences, Walker-Warburg Syndrome, medicine.disease, Nucleotidyltransferases, Corticosteroid therapy, 3. Good health, 030104 developmental biology, Steroid therapy, Treatment Outcome, Neurology, GIRDLE MUSCULAR-DYSTROPHY, Pediatrics, Perinatology and Child Health, Mutation, biology.protein, Corticosteroid, Creatine kinase, Neurology (clinical), business, 030217 neurology & neurosurgery, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0145b305959e010b2e6e1e48d9cdf4bTest
http://hdl.handle.net/11588/738377Test

4

P016 Impact of liver transplant on metabolic profiles in children with inborn errors of protein metabolism

المصدر: Digestive and Liver Disease. 50:e364

مصطلحات موضوعية: chemistry.chemical_compound, Hepatology, chemistry, business.industry, Gastroenterology, Protein metabolism, Medicine, Physiology, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1387bdca9d597cd07f1f28a9c3835343Test
https://doi.org/10.1016/s1590-8658Test(18)31015-6

5

P168 Iatrogenic protein malnutrition: acrodermatitis, hypoalbuminemia, pancytopenia in a child with newly diagnosed propionic acidemia

المؤلفون: C. Zuppaldi, R. Di Pinto, Giancarlo Parenti, Simona Fecarotta, Ida D'Acunzo, R. Della Casa

المصدر: Digestive and Liver Disease. 50:e416

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Hepatology, business.industry, Acrodermatitis, Gastroenterology, Newly diagnosed, medicine.disease, Pancytopenia, Protein malnutrition, medicine, Hypoalbuminemia, Propionic acidemia, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::299dd0bcb99b778c5c0acea783f83dcbTest
https://doi.org/10.1016/s1590-8658Test(18)31166-6

6

P143 Protein tolerance in patients with in-born error of protein metabolism after liver transplantation

المصدر: Digestive and Liver Disease. 50:e408

مصطلحات موضوعية: medicine.medical_specialty, Hepatology, business.industry, medicine.medical_treatment, Gastroenterology, Protein metabolism, Liver transplantation, chemistry.chemical_compound, chemistry, Internal medicine, medicine, In patient, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ec0a035857757e87ffa7e108adc776aaTest
https://doi.org/10.1016/s1590-8658Test(18)31141-1

7

Vitamin E improves clinical outcome of patients affected by glycogen storage disease type Ib

المؤلفون: Angelo Benedetti, F. Balivo, Roberto Della Casa, Carlo Dionisi-Vici, Paola Marcolongo, Giancarlo Parenti, Giorgia Minopoli, Rossella Parini, Generoso Andria, Daniela Melis, S. Paci

المساهمون: Melis, D., Minopoli, G., Balivo, F., Marcolongo, P., Parini, R., Paci, S., Dionisi-Vici, C., Della Casa, R., Benedetti, A., Andria, G., Parenti, G.

المصدر: JIMD Reports ISBN: 9783662496671

مصطلحات موضوعية: medicine.medical_specialty, Antioxidant, Neutropenia, business.industry, medicine.medical_treatment, Vitamin E, IBD, macromolecular substances, medicine.disease, Gastroenterology, Article, Infection severity score, Internal medicine, Immunology, Glycogen Storage Disease Type Ib, medicine, Absolute neutrophil count, Neutrophil dysfunction, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c54eaf505a04f1d41b85912d0f406a7dTest
http://hdl.handle.net/11386/4760505Test

8

Chronic Diarrhea in Mucopolysaccharidosis IIIB

المؤلفون: Gianfranco Pontarelli, Giancarlo Parenti, Michelina Sibilio, Annamaria Staiano, Rossella Turco, Generoso Andria, Raffaella Vecchione, Luca Astarita, Erasmo Miele, Carla Ungaro, Paola Di Natale

المصدر: Journal of Pediatric Gastroenterology & Nutrition. 49:477-480

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7668fd69a3f8be4649897f5146210debTest
https://doi.org/10.1097/mpg.0b013e31818a082aTest

9

Crohn's-like ileo-colitis in patients affected by glycogen storage disease Ib: two years’follow-up of patients with a wide spectrum of gastrointestinal signs

المؤلفون: G. Andria, Salvatore Cucchiara, Giancarlo Parenti, R. Berni Canani, Gianluca Terrin, Michelina Sibilio, R. Della Casa, Daniela Melis

المساهمون: Melis, D, Parenti, Giancarlo, DELLA CASA, Roberto, Sibilio, M, BERNI CANANI, Roberto, Terrin, G, Cucchiara, S, Andria, G., Parenti, G

المصدر: Acta Paediatrica. 92:1415-1421

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf8815813722ac33918c94b50ec8577Test
https://doi.org/10.1111/j.1651-2227.2003.tb00825.xTest

10

Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: Possible role of microsomal glucose 6-phosphate accumulation

المؤلفون: A. Rossi, Roberto Della Casa, Simona Spadarella, Giovanna Muscogiuri, F. Balivo, Daniela Melis, Giancarlo Parenti, Mariacarolina Salerno, Rosario Pivonello, Generoso Andria, Pietro Formisano, Annamaria Colao

المساهمون: Melis, Daniela, Rossi, A, Pivonello, R, Salerno, Mariacarolina, Balivo, Francesca, Spadarella, Simona, Muscogiuri, G, Casa, Rd, Formisano, Pietro, Andria, Generoso, Colao, Annamaria, Parenti, Giancarlo

المصدر: Orphanet Journal of Rare Diseases

مصطلحات موضوعية: Male, medicine.medical_specialty, Adolescent, 11BHSD1, GSDI, Insulin-resistance, Metabolic syndrome, Case-Control Studies, Child, Disease Susceptibility, Female, Glucose-6-Phosphate, Glycogen Storage Disease Type I, Humans, Metabolic Syndrome, Microsomes, Prospective Studies, Biology, Gastroenterology, chemistry.chemical_compound, Insulin resistance, Internal medicine, Glycogen Storage Disease Type Ib, medicine, Genetics(clinical), Pharmacology (medical), Prospective cohort study, Genetics (clinical), Medicine(all), Glycogen storage disease type I, Glycogen, Research, Case-control study, General Medicine, medicine.disease, Endocrinology, 11ΒHSD1, chemistry, Metabolic control analysis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a6cca84ba813493723558c7da098b68Test
http://hdl.handle.net/11386/4760504Test

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