Isabel Couto Guerra
Overview
Explore the profile of Isabel Couto Guerra including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
8
Citations
15
Followers
0
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Recent Articles
1.
Vieira P, Da Silva Cardoso J, Teixeira C, Guerra I
An Pediatr (Engl Ed)
. 2024 Apr;
100(5):e12-e13.
PMID: 38582646
No abstract available.
2.
Fraga C, Losa A, Cascais I, Garrido C, Lachado A, Guerra I, et al.
J Pediatr Hematol Oncol
. 2024 Feb;
46(3):172-174.
PMID: 38408112
Two severe cases of hemolytic anemia are described in different pediatric age groups, both linked to severe cobalamin deficiency from distinct causes. The first case refers to an exclusively breastfed...
3.
Teixeira B, Losa A, Meireles A, Lachado A, Guerra I, Machado S, et al.
Cureus
. 2024 Feb;
16(1):e52869.
PMID: 38406084
Blueberry muffin syndrome (BMS) in neonates, characterized by widespread nodular lesions, presents diagnostic challenges due to its diverse etiologies. Hyperleukocytosis, with leukocyte counts exceeding 100,000/μL, is a rare phenomenon associated...
4.
Ashworth J, Abreu V, Guerra I, Almeida S, Cunha C, Moreira Silva H, et al.
Am J Med Genet A
. 2023 May;
191(7):1963-1967.
PMID: 37134188
Neurofibromatosis type 1 (NF-1) is a multisystem genetic disorder affecting the NF1 tumor suppressor gene. Patients typically develop superficial (cutaneous) and internal (plexiform) neurofibromas. The latter may rarely involve the...
5.
Popik E, Branco M, Guerra I, Costa E, Cleto E
J Paediatr Child Health
. 2018 Oct;
55(3):362-363.
PMID: 30288829
No abstract available.
6.
Vaz S, Guerra I, Freitas M, Marques L
BMJ Case Rep
. 2018 Apr;
2018.
PMID: 29680800
No abstract available.
7.
Sousa R, Goncalves C, Guerra I, Costa E, Fernandes A, Sucesso M, et al.
Orphanet J Rare Dis
. 2016 Jul;
11(1):102.
PMID: 27456001
Background: Red cell distribution width (RDW), a classical parameter used in the differential diagnosis of anemia, has recently been recognized as a marker of chronic inflammation and high levels of...
8.
Novo A, Guerra I, Rocha F, Gama-de-Sousa S, Borges T, Cerqueira R, et al.
BMJ Case Rep
. 2012 Jul;
2012.
PMID: 22751423
The Kallmann syndrome is characterised by the association of hypogonadotropic hypogonadism and hypo/anosmia. It represents a phenotypically and genotypically heterogeneous clinical entity, with six genes identified so far in the...