Gilda Porta

Hospital Samaritano de São Paulo — Brazil

Medicine · Health Sciences

41h-index9.6kcitations266works8.12yr avg
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Research Topics

Liver Disease Diagnosis and Treatment(71), Liver Diseases and Immunity(67), Pediatric Hepatobiliary Diseases and Treatments(53), Liver Disease and Transplantation(44), Organ Transplantation Techniques and Outcomes(37)

Publications265 total

High frequency of ABCB4 and ABCB11 gene variants in adult patients with idiopathic chronic or recurrent cholestasis
Hepatology Communications·2025· 1 citedOpen Access
Hepatopulmonary syndrome in children and adolescents with portal hypertension in Brazil: A multicenter study
Journal of Pediatric Gastroenterology and Nutrition·2025Open Access
Efficacy of ileal bile acid transport inhibitors in children with Alagille syndrome: a meta-analysis
European Journal of Pediatrics·2025
Double Versus Single Hepatic Artery Anastomosis in Pediatric Left Liver Grafts: A Reassessment of Outcomes
Pediatric Transplantation·2025Open Access
Evaluating and Monitoring Liver Disease Severity in Glycogen Storage Disease Type IX: Performance of Novel and Established Clinical Scores
Genetics in Medicine Open·2025Open Access
OC22 Long-term maintenance of response and improved liver heath with maralixibat in patients with progressive familial intrahepatic cholestasis (PFIC): 2-year data from the MARCH-ON study
2025· 1 cited
Portal Vein Obstruction in Pediatric Liver Transplant Patients: An Evaluation of Self‐Reported Management Practices
Health Science Reports·2025Open Access
FISPGHAN statement on the global public health impact of metabolic dysfunction‐associated steatotic liver disease
Journal of Pediatric Gastroenterology and Nutrition·2024· 9 citedOpen Access
OP-2 WILSON DISEASE (WD) DIAGNOSIS WITH NEXT-GENERATION SEQUENCING (NGS) IN CLINICAL PRACTICE: A PILOT STUDY
Annals of Hepatology·2024Open Access
OP- 15 OUTCOME OF PREGNANCIES IN A SERIES OF WILSON DISEASE PATIENTS
Annals of Hepatology·2024Open Access
Global burden of disease attributable to metabolic risk factors in adolescents and young adults aged 15–39, 1990–2021
Clinical Nutrition·2024· 38 citedOpen Access
Maple syrup urine disease diagnosis in Brazilian patients by massive parallel sequencing
Molecular Genetics and Metabolism·2024
WED-185 Frequency of ATP8B1, ABCB11 and ABCB4 gene mutations in adult patients with idiopathic chronic cholestasis
Journal of Hepatology·2024
Natural history study of hepatic glycogen storage disease type IV and comparison to Gbe1ys/ys model
JCI Insight·2024· 6 citedOpen Access
Maralixibat in progressive familial intrahepatic cholestasis (MARCH-PFIC): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
˜The œLancet. Gastroenterology & hepatology·2024· 41 citedOpen Access
Wilson disease: the diagnostic challenge and treatment outcomes in a series of 262 cases
Arquivos de Neuro-Psiquiatria·2024· 5 citedOpen Access
An international multidisciplinary consensus on pediatric metabolic dysfunction-associated fatty liver disease
Med·2024· 41 citedOpen Access
Dental Care for Pediatric Liver Transplantation: A Case Report.
Revista de Odontopediatría Latinoamericana·2024Open Access
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Pediatric Transplantation·2024Open Access
Maple Syrup Urine Disease Diagnosis in Brazilian Patients by Massive Parallel Sequencing
SSRN Electronic Journal·2024Open Access
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Frequent Co-authors

Irene Kazue Miura(15), Eduardo Luiz Rachid Cançado(12), Renata Pugliese(12), Paulo Lisboa Bittencourt(10), Eduardo A. Fonseca(10), João Seda Neto(10), Paulo Chapchap(9), Flair José Carrilho(8), Adriana Porta(8), Mário Kondo(8), Anna Carla Goldberg(7), Helry L. Cândido(7), Marcel R. Benavides(7), Jorge Kalil(6), Flávia Heinz Feier(6), André L. Godoy(5), Albert J. Czaja(4), Antônio Atílio Laudanna(4), Themis Reverbel da Silveira(4), Vera B. Danesi(4)