Zobrazeno 1 - 10
of 280
pro vyhledávání: '"Rita Cardoso"'
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
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
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:
Sónia Frota, Marisa Cruz, Rita Cardoso, Isabel Guimarães, Joaquim J. Ferreira, Serge Pinto, Marina Vigário
Publikováno v:
Brain Sciences, Vol 11, Iss 8, p 1100 (2021)
The phonology of prosody has received little attention in studies of motor speech disorders. The present study investigates the phonology of intonation (nuclear contours) and speech chunking (prosodic phrasing) in Parkinson’s disease (PD) as a func
Externí odkaz:
https://doaj.org/article/c47d1224613e436d92b2681e778b6105
Autor:
Margherita Fabbri, Isabel Guimarães, Rita Cardoso, Miguel Coelho, Leonor Correia Guedes, Mario M. Rosa, Catarina Godinho, Daisy Abreu, Nilza Gonçalves, Angelo Antonini, Joaquim J. Ferreira
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
BackgroundParkinson’s disease (PD) patients are affected by hypokinetic dysarthria, characterized by hypophonia and dysprosody, which worsens with disease progression. Levodopa’s (l-dopa) effect on quality of speech is inconclusive; no data are c
Externí odkaz:
https://doaj.org/article/fda216412fa44cd1beab1c7ea1ae3537