Zobrazeno 1 - 10
of 65
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:
Morten Bjerregaard-Andersen, Jessica Da Silva, Rui Diogo, Ana Raquel Claro, Inês Ferro, Andreia Romana, Patrícia Rocha, Beatriz Sá, Goreti Lobarinhas, Sara Rolim, Claus Bogh Juhl, Kurt Højlund, Isabel Fernandes, Sónia Antunes, Maria Manuela Félix Calha, Guida Gama, Sofia Amálio, Mariana Figueiras, Teresa Silva, Margarida Rosado, Estela Ferrão, Luísa Arez, Ana Baptista, Adriana Martins Ferreira, Diana Alba, Carlos Godinho, Ana Luísa Leite, Maria de Lurdes Afonso Lopes, Maria Lurdes Sampaio, Joana Serra-Caetano, Eugenia Carvalho
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Viral respiratory infections may precipitate type 1 diabetes (T1D). A possible association between the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for COVID-19, and the incidence of T1D is b
Externí odkaz:
https://doaj.org/article/ec20d08584ec48a38a6f3648ae32f0e7
Publikováno v:
JCRPE, Vol 15, Iss 1, Pp 86-89 (2023)
The coexistence of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and Turner syndrome (TS) is rare. We report on a 6-year-old Portuguese girl with mosaic TS [45,XO(39)/47,XXX(21)] presenting with premature pubarche at the age o
Externí odkaz:
https://doaj.org/article/5da0d6f8c59f46a38390e32bc8cbc531
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
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:
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
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