Joana Serra Caetano
Overview
Explore the profile of Joana Serra Caetano including associated specialties, affiliations and a list of published articles.
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10
Citations
22
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Recent Articles
1.
Puga F, Correia L, Vieira I, Caetano J, Cardoso R, Dinis I, et al.
J Clin Res Pediatr Endocrinol
. 2024 Apr;
16(3):314-322.
PMID: 38683018
Objective: Differentiated thyroid cancer (DTC) is the most common pediatric endocrine cancer but studies are scarce. Latest recommendations advocate for an individualized risk-based approach to select patients for additional therapy....
2.
Rosinha P, Ramalho D, Rodrigues O, Sousa S, Alves C, Lopes J, et al.
J Pediatr Endocrinol Metab
. 2022 Nov;
36(3):319-322.
PMID: 36351197
Objectives: We intend to describe a case of McCune-Albright Syndrome (MAS), a rare disease characterized by fibrous dysplasia (FD), cutaneous hyperpigmentation and hyperfunctioning endocrinopathies (HFE). Case Presentation: We report the...
3.
Vieira I, Mourinho Bala N, Ramos F, Dinis I, Cardoso R, Caetano J, et al.
Endocrinol Diabetes Metab Case Rep
. 2022 Sep;
2022.
PMID: 36070412
Summary: Congenital isolated adrenocorticotrophic hormone (ACTH) deficiency due to T-box transcription factor-19 (TBX19 mutation) (MIM 201400; ORPHA 199296) usually presents in the neonatal period with severe hypoglycemia, seizures, and sometimes...
4.
Mourinho Bala N, Goncalves R, Caetano J, Cardoso R, Dinis I, Mirante A
J Clin Res Pediatr Endocrinol
. 2022 May;
14(3):308-312.
PMID: 35633647
Objective: Primary adrenal insufficiency (PAI) is a rare condition in children, and is potentially life-threatening. The most common cause is congenital adrenal hyperplasia, and autoimmune etiology is the most frequent...
5.
Silva D, Lages A, Caetano J, Cardoso R, Dinis I, Gomes L, et al.
Endocrinol Diabetes Metab Case Rep
. 2021 Dec;
2021.
PMID: 34866060
Summary: Hypoparathyroidism is characterized by low or inappropriately normal parathormone production, hypocalcemia and hyperphosphatemia. Autosomal dominant hypocalcemia (ADH) type 1 is one of the genetic etiologies of hypoparathyroidism caused by...
6.
Romao Luz I, Martins J, Jeronimo M, Caetano J, Cardoso R, Dinis I, et al.
Acta Med Port
. 2020 Jul;
33(7-8):483-490.
PMID: 32669187
Introduction: Graves disease is characterized by the existence of autoantibodies directed to the thyrotropin receptor, which can have a stimulatory/inhibitory action, in women with the condition, their fetus or neonate....
7.
Grilo E, Pinto J, Caetano J, Pereira H, Cardoso P, Cardoso R, et al.
J Pediatr Endocrinol Metab
. 2016 Apr;
29(8):985-90.
PMID: 27115322
Limbic encephalitis is a rare neurological disorder that may be difficult to recognize. Clinical features include memory impairment, temporal lobe seizures and affective disturbance. We report the case of a...
8.
Martins L, Coutinho A, Jeronimo M, Caetano J, Cardoso R, Dinis I, et al.
Endocrinol Diabetes Metab Case Rep
. 2016 Mar;
2016:150131.
PMID: 26925233
Unlabelled: Alternating between hyper- and hypo-thyroidism may be explained by the simultaneous presence of both types of TSH receptor autoantibodies (TRAbs) - thyroid stimulating autoantibodies (TSAbs) and TSH blocking autoantibodies...
9.
Caetano J, Costa C, Baets J, Zimon Phd M, Venancio Phd M, Saraiva Phd J, et al.
Pediatr Neurol
. 2013 Oct;
50(1):104-7.
PMID: 24131582
Background: Autosomal recessive axonal neuropathy with neuromyotonia is a recently described entity associated to the HINT1 gene, encoding histidine triad nucleotide-binding protein 1. Patient: The authors report a Portuguese 16-year-old...
10.
Caetano J, Neto P, Alves M, Rodrigues F
Acta Med Port
. 2010 Jul;
23(3):385-90.
PMID: 20654256
Introduction: S. pyogenes is among the most common bacteria in Pediatrics, and is associated with a wide variety of infections and large range of severity. Aims: The aim was to...