Adriana Maria Alves DE Tommaso
Overview
Explore the profile of Adriana Maria Alves DE Tommaso including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
57
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0
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Recent Articles
1.
Alvarenga L, Sandy N, Gomez G, Hessel G, DE Tommaso A, Bellomo-Brandao M
Arq Gastroenterol
. 2021 Jul;
58(2):227-233.
PMID: 34287532
Background: Primary sclerosing cholangitis (PSC) is a rare hepatobiliary disorder, whose etiology remains not fully elucidated. Given how rare PSC is in childhood, until the recent publication of a multicenter...
2.
Takao M, Sandy N, Riccetto A, DE Tommaso A
Arq Gastroenterol
. 2021 Apr;
58(1):87-92.
PMID: 33909803
Background: Glycogen storage disease (GSD) type 1b is a multisystemic disease in which immune and infectious complications are present, in addition to the well-known metabolic manifestations of GSD. Treatment with...
3.
Jorge N, DE Tommaso A, Hessel G
Rev Paul Pediatr
. 2021 Feb;
39:e2020046.
PMID: 33566881
Objective: To perform anthropometric and dietary evaluation of patients with glycogenosis type Ia and Ib. Methods: This cross-sectional study is composed of a sample of 11 patients with glycogenosis divided...
4.
DE Tommaso A, Hessel G, Riccetto A, Semenzati G, Gusmao R
Rev Paul Pediatr
. 2019 Jul;
37(4):516-519.
PMID: 31291441
Objective: To discuss aspects of pre and post-operative otorhinolaryngology surgery in patients with glycogen storage disease type 1b. Case Description: Description of three clinical cases with probable glycogen storage disease...
5.
DE Tommaso A, de Carvalho Barra F, Hessel G, Moreno C, Giugliani R, Escanhoela C
Rev Paul Pediatr
. 2017 Nov;
36(1):4.
PMID: 29091130
Objective: To describe a case of cholesteryl ester storage disease (CESD) and discuss the importance of liver biopsy for diagnosis. Case Description: A female patient, aged two years and ten...
6.
Carlin M, Scherrer D, DE Tommaso A, Bertuzzo C, Steiner C
Genet Mol Biol
. 2014 Jan;
36(4):502-6.
PMID: 24385852
Glycogen storage disease (GSD) comprises a group of autosomal recessive disorders characterized by deficiency of the enzymes that regulate the synthesis or degradation of glycogen. Types Ia and Ib are...
7.
de Carvalho E, Dos Santos J, Reverbel da Silveira T, Kieling C, Silva L, Porta G, et al.
J Pediatr (Rio J)
. 2010 Dec;
86(6):473-9.
PMID: 21140036
Objective: To evaluate epidemiological, clinical and prognostic characteristics of children with biliary atresia. Methods: Data regarding portoenterostomy, liver transplantation (LTx), age at last follow-up and survival were collected from the...
8.
Rosa M, Hessel G, DE Tommaso A
Acta Gastroenterol Latinoam
. 2008 Nov;
38(3):187-93.
PMID: 18979898
In Brazil, approximately 130 new cases of hepatitis A per 100,000 inhabitants occur annually and 15% of the population has been in contact with hepatitis B virus. Portal hypertension causes...
9.
Bustorff-Silva J, Sbraggia Neto L, Olimpio H, de Alcantara R, Matsushima E, DE Tommaso A, et al.
J Pediatr Surg
. 2007 Aug;
42(8):1337-40.
PMID: 17706492
Background/purpose: The purpose of the study was to describe the initial experience with a novel approach to the surgical treatment of progressive familial intrahepatic cholestasis (PFIC), avoiding the creation of...
10.
Bellomo-Brandao M, Costa-Pinto E, DE Tommaso A, Hessel G
Arq Gastroenterol
. 2006 May;
43(1):45-9.
PMID: 16699618
Background: Few studies on autoimmune hepatitis have enrolled non-Caucasian groups. Aims: To evaluate Brazilian children with type 1 and 2 autoimmune hepatitis regarding outcome and clinical and biochemical parameters. Patients...