Detalhe da pesquisa
1.
Severe Hemolytic Anemia: Atypical Presentation of Cobalamin Deficiency.
J Pediatr Hematol Oncol
; 46(3): 172-174, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408112
2.
Insights Into Pediatric Autoimmune Gastritis: Is There a Role for Helicobacter pylori Infection?
J Pediatr Gastroenterol Nutr
; 68(6): e99-e104, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30664567
3.
Severe anaemia with reticulocytopenia: When watchful waiting is the best attitude.
J Paediatr Child Health
; 55(3): 362-363, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30288829
4.
Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients.
Blood Cells Mol Dis
; 46(2): 166-70, 2011 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21138793
5.
Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
Br J Haematol
; 149(5): 785-94, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20346007
6.
Linkage of typically cytosolic peroxidases to erythrocyte membrane - A possible mechanism of protection in Hereditary Spherocytosis.
Biochim Biophys Acta Biomembr
; 1862(3): 183172, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31870655
7.
Fatty Liver and Autoimmune Hepatitis: Two Forms of Liver Involvement in Lipodystrophies.
GE Port J Gastroenterol
; 26(5): 362-369, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31559327
8.
A case of hepatopulmonary syndrome solved by mycophenolate mofetil (an inhibitor of angiogenesis and nitric oxide production).
J Hepatol
; 58(3): 630-3, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23104163
9.
Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis.
Blood Cells Mol Dis
; 41(1): 5-9, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18387321
10.
A case report of a 4-year-old child with glucose-6-phosphate dehydrogenase deficiency: An evidence based approach to nutritional management.
Turk J Pediatr
; 59(2): 189-192, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29276873
11.
Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesis.
Orphanet J Rare Dis
; 11(1): 102, 2016 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27456001
12.
Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.
Blood Cells Mol Dis
; 44(2): 117-9, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-19931474
13.
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]. / Défice de glicose-6-fosfato desidrogenase, ictericia neonatal e sindroma de Gilbert.
Acta Med Port
; 15(6): 409-12, 2002.
Artigo
em Português
| MEDLINE | ID: mdl-12680285
14.
Erythropoiesis versus inflammation in Hereditary Spherocytosis clinical outcome.
Clin Biochem
; 44(13): 1137-1143, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21704613