Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Joana Serra Caetano"'
Autor:
Francisca Marques Puga, Laura Correia, Inês Vieira, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 314-322 (2024)
INTRODUCTION: 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. Lymphovascula
Externí odkaz:
https://doaj.org/article/b9e99953c1304889bf1315381bff8c27
Autor:
Nádia Mourinho Bala, Raquel S. Gonçalves, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 308-312 (2022)
INTRODUCTION: 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 acquired cause in this age g
Externí odkaz:
https://doaj.org/article/643ea4952d724ff1b972d8f7015f1bd2
Autor:
Inês Henriques Vieira, Nádia Mourinho Bala, Fabiana Ramos, Isabel Dinis, Rita Cardoso, Joana Serra Caetano, Dírcea Rodrigues, Isabel Paiva, Alice Mirante
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2022)
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 prolonged ch
Externí odkaz:
https://doaj.org/article/eddeb7a4645942389f32761ebb163cf9
Autor:
Diana Festas Silva, Adriana De Sousa Lages, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Leonor Gomes, Isabel Paiva, Alice Mirante
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
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 heterozygo
Externí odkaz:
https://doaj.org/article/3d72dd8f497c4b3e9acdd9e8bb105b34
Autor:
Inês Romão Luz, João Rio Martins, Mónica Jerónimo, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
Publikováno v:
Acta Médica Portuguesa, Vol 33, Iss 7-8 (2020)
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. Our aim was to review the case
Externí odkaz:
https://doaj.org/article/c388b8d903f44b61b0a89553859054f3
Autor:
Patrícia Sofia Ferreira Miranda, Ester Preciosa Maio Nunes Pereira, Joana Serra Caetano Baltazar Barreto, Margarida Maria Videira Henriques, Maria Alice Santos Cordeiro Mirante, Lina Maria Jesus Ferreira Cardoso Ramos
Publikováno v:
Revista Paulista de Pediatria, Vol 38 (2020)
ABSTRACT Objective: To present a case of bilateral gynecomastia in a prepubertal boy with autism spectrum disorder, diagnosed with myotonic dystrophy type 1. Case description: A 12-year-old boy with autism spectrum disorder presented at a follow-up v
Externí odkaz:
https://doaj.org/article/bd13b3fba9c04760953345558912abdc
Publikováno v:
Acta Médica Portuguesa, Vol 23, Iss 3 (2010)
S. pyogenes is among the most common bacteria in Pediatrics, and is associated with a wide variety of infections and large range of severity.The aim was to evaluate trends of Group A Streptococcal invasive disease in a paediatric tertiary hospital.Re
Externí odkaz:
https://doaj.org/article/71210ea460264c1e9f23baf79a4908f3
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:86-89
Coexistence of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and Turner Syndrome (TS) is rare. We report a 6-year-old Portuguese girl with mosaic TS [45,XO(39)/47,XXX(21)] presented with premature pubarche at the age of 5 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b4d47d9ed7136f8d93c124806997171
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0174
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0174
Autor:
Patrícia Rosinha, Diogo Ramalho, Orlando Rodrigues, Sérgio Sousa, Cristina Alves, Joana Lopes, Joana Serra Caetano, Alice Mirante
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 36:319-322
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 case of a 13-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d334a96ced76828c64451b6a159ee5a
https://doi.org/10.1515/jpem-2022-0357
https://doi.org/10.1515/jpem-2022-0357
Autor:
Cláudia Costa, Maria Inês Linhares, Filipa Bastos, Rita Cardoso, Isabel Dinis, Ana Paula Santos, Alice Mirante, Joana Serra-Caetano
Publikováno v:
Diabetology international
Background Postprandial hyperglycemia is one of the biggest challenges in children with type 1 diabetes (T1D). Ultra-fast-acting aspartic insulin (faster aspart) has a quicker onset of action and an earlier maximum activity. The aim of this study is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d19272d6dd2a6455b22ed87d38d3e7
https://doi.org/10.1007/s13340-021-00565-8
https://doi.org/10.1007/s13340-021-00565-8