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Giusy Ranucci

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis
2018 · Elena V. Polishchuk, Assunta Merolla, et al. · Gastroenterology · 265
Re-evaluation of the Diagnostic Criteria for Wilson Disease in Children With Mild Liver Disease
2010 · Emanuele Nicastro, Giusy Ranucci, et al. · Hepatology · 214
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Systematic review of response criteria and endpoints in autoimmune hepatitis by the International Autoimmune Hepatitis Group
2022 · Simon Pape, Romée J.A.L.M. Snijders, et al. · Journal of Hepatology · 182
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Nutritional Deficiencies in Children with Celiac Disease Resulting from a Gluten-Free Diet: A Systematic Review
2019 · Giovanni Di Nardo, Maria Pia Villa, et al. · Nutrients · 156
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SCYL1 variants cause a syndrome with lowγ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN)
2018 · Dominic Lenz, Patricia McClean, et al. · Genetics in Medicine · 69
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Genotype–phenotype correlation in Italian children with Wilson’s disease
2008 · Emanuele Nicastro, Georgios Loudianos, et al. · Journal of Hepatology · 68
Zinc monotherapy is effective in Wilson’s disease patients with mild liver disease diagnosed in childhood: a retrospective study
2014 · Giusy Ranucci, Fabiola Di Dato, et al. · Orphanet Journal of Rare Diseases · 67
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Leptin: The Prototypic Adipocytokine and its Role in NAFLD
2010 · Claudio Procaccini, Mario Galgani, et al. · Current Pharmaceutical Design · 67
Galacto-Oligosaccharide/Polidextrose Enriched Formula Protects against Respiratory Infections in Infants at High Risk of Atopy: A Randomized Clinical Trial
2018 · Giusy Ranucci, Vittoria Buccigrossi, et al. · Nutrients · 64
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Argininosuccinic aciduria: Recent pathophysiological insights and therapeutic prospects
2019 · Julien Baruteau, Carmen Diez‐Fernandez, et al. · Journal of Inherited Metabolic Disease · 52
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Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells
2018 · Silvia Parisi, Elena V. Polishchuk, et al. · Scientific Reports · 48
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Early-Life Intestine Microbiota and Lung Health in Children
2017 · Giusy Ranucci, Vittoria Buccigrossi, et al. · Journal of Immunology Research · 48
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Diagnostic approach to neonatal and infantile cholestasis: A position paper by the SIGENP liver disease working group
2021 · Giusy Ranucci, Claudia Della Corte, et al. · Digestive and Liver Disease · 41
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Congenital syphilis in the twenty-first century: an area-based study
2022 · Serena Salomè, Maria Donata Cambriglia, et al. · European Journal of Pediatrics · 37
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Subclinical neurological involvement does not develop if Wilson's disease is treated early
2016 · Raffaele Dubbioso, Giusy Ranucci, et al. · Parkinsonism & Related Disorders · 36
Multisystem inflammatory syndrome in children. An emerging clinical challenge for pediatric surgeons in the COVID 19 era
2021 · Francesco Valitutti, Alessandra Verde, et al. · Journal of Pediatric Surgery Case Reports · 34
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Diagnostic Approach to Acute Liver Failure in Children: A Position Paper by the SIGENP Liver Disease Working Group
2021 · A. Di Giorgio, E. Bartolini, et al. · Digestive and Liver Disease · 29
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Diagnosis of fatty liver in children should occur in parallel to investigation for other causes of liver disease
2023 · Jake P Mann, Anita CE Vreugdenhil, et al. · ˜The œLancet. Gastroenterology & hepatology · 28
Chronic liver involvement in urea cycle disorders
2019 · Giusy Ranucci, Miriam Rigoldi, et al. · Journal of Inherited Metabolic Disease · 27
Wilson’s disease: Prospective developments towards new therapies
2017 · Giusy Ranucci, Roman Polishchuck, et al. · World Journal of Gastroenterology · 26
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Non Invasive Assessment of Lung Disease in Ataxia Telangiectasia by High-Field Magnetic Resonance Imaging
2013 · Silvia Montella, Carmine Mollica, et al. · Journal of Clinical Immunology · 23
Case Report: Add-on treatment with odevixibat in a new subtype of progressive familial intrahepatic cholestasis broadens the therapeutic horizon of genetic cholestasis
2023 · Angela Pepe, Angelo Colucci, et al. · Frontiers in Pediatrics · 21
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ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype
2021 · Shaul Lerner, Raya Eilam, et al. · Human Genetics · 21
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Telemedicine in Patients Affected by Chronic Liver Disease: A Scoping Review of Clinical Outcomes and the Devices Evaluated
2023 · Paolo Capuano, Bethany Hileman, et al. · Journal of Clinical Medicine · 19
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Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene
2015 · Eva Mameli, Maria Barbara Lepori, et al. · Gene · 17
Works count: 112
Citation count: 1,878
H-index: 21
I10-index: 36
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