Cardoso R - Search Results

1

Type 1 diabetes and GAD65 limbic encephalitis: a case report of a 10-year-old girl.

Grilo E, Pinto J, Caetano JS, Pereira H, Cardoso P, Cardoso R, Dinis I, Pereira C, Fineza I, Mirante A. Grilo E, et al. Among authors: cardoso r, cardoso p. J Pediatr Endocrinol Metab. 2016 Aug 1;29(8):985-90. doi: 10.1515/jpem-2016-0016. J Pediatr Endocrinol Metab. 2016. PMID: 27115322

2

Clinical characteristics of polyglandular autoimmune syndromes in pediatric age: an observational study.

Bouça B, Nogueira A, Caetano J, Cardoso R, Dinis I, Mirante A. Bouça B, et al. Among authors: cardoso r. J Pediatr Endocrinol Metab. 2022 Feb 16;35(4):477-480. doi: 10.1515/jpem-2022-0050. Print 2022 Apr 26. J Pediatr Endocrinol Metab. 2022. PMID: 35170268

3

Ketoacidosis in new-onset type 1 diabetes: did the severity increase during the COVID-19 pandemic?

Botelho TA, Santos JMN, Pinho CMS, Martins AIBR, Formiga AIS, Serra-Caetano J, Cardoso RCF, Dinis ICAD, Mirante ASR. Botelho TA, et al. Among authors: cardoso rcf. J Pediatr Endocrinol Metab. 2021 Nov 12;35(1):73-77. doi: 10.1515/jpem-2021-0449. Print 2022 Jan 27. J Pediatr Endocrinol Metab. 2021. PMID: 34766743

4

The spectrum of pediatric adrenal insufficiency: insights from 34 years of experience.

Ventura M, Serra-Caetano J, Cardoso R, Dinis I, Melo M, Carrilho F, Mirante A. Ventura M, et al. Among authors: cardoso r. J Pediatr Endocrinol Metab. 2019 Jul 26;32(7):721-726. doi: 10.1515/jpem-2019-0030. J Pediatr Endocrinol Metab. 2019. PMID: 31194685

5

Autoimmune alternating hyper- and hypo-thyroidism: a rare condition in pediatrics.

Martins LC, Coutinho AR, Jerónimo M, Caetano JS, Cardoso R, Dinis I, Mirante A. Martins LC, et al. Among authors: cardoso r. Endocrinol Diabetes Metab Case Rep. 2016;2016:150131. doi: 10.1530/EDM-15-0131. Epub 2016 Feb 9. Endocrinol Diabetes Metab Case Rep. 2016. PMID: 26925233 Free PMC article.

6

Congenital hyperreninemic hypoaldosteronism due to aldosterone synthase deficiency type I in a Portuguese patient - Case report and review of literature.

Lages AS, Vale B, Oliveira P, Cardoso R, Dinis I, Carrilho F, Mirante A. Lages AS, et al. Among authors: cardoso r. Arch Endocrinol Metab. 2019 Feb;63(1):84-88. doi: 10.20945/2359-3997000000107. Arch Endocrinol Metab. 2019. PMID: 30864636 Free PMC article.

7

Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review.

Inácio I, Serra-Caetano J, Cardoso R, Dinis I, Mirante A. Inácio I, et al. Among authors: cardoso r. J Clin Res Pediatr Endocrinol. 2023 Feb 27;15(1):86-89. doi: 10.4274/jcrpe.galenos.2021.2021.0174. Epub 2021 Aug 6. J Clin Res Pediatr Endocrinol. 2023. PMID: 34355878 Free PMC article.

8

A variant in the CASR gene (c.368T>C) causing hypocalcemia refractory to standard medical therapy.

Festas Silva D, De Sousa Lages A, Caetano JS, Cardoso R, Dinis I, Gomes L, Paiva I, Mirante A. Festas Silva D, et al. Among authors: cardoso r. Endocrinol Diabetes Metab Case Rep. 2021 Dec 1;2021:21-0005. doi: 10.1530/EDM-21-0005. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2021. PMID: 34866060 Free PMC article.

9

Autoimmune Primary Adrenal Insufficiency in Children.

Mourinho Bala N, Gonçalves RS, Serra Caetano J, Cardoso R, Dinis I, Mirante A. Mourinho Bala N, et al. Among authors: cardoso r. J Clin Res Pediatr Endocrinol. 2022 Aug 25;14(3):308-312. doi: 10.4274/jcrpe.galenos.2022.2021-11-9. Epub 2022 May 31. J Clin Res Pediatr Endocrinol. 2022. PMID: 35633647 Free PMC article.

10

A serious and unusual presentation of congenital isolated ACTH deficiency due to TBX19 mutation, beyond the neonatal period.

Vieira IH, Mourinho Bala N, Ramos F, Dinis I, Cardoso R, Caetano JS, Rodrigues D, Paiva I, Mirante A. Vieira IH, et al. Among authors: cardoso r. Endocrinol Diabetes Metab Case Rep. 2022 Sep 1;2022:22-0277. doi: 10.1530/EDM-22-0277. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 36070412 Free PMC article.

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