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Articles, 3 records found
Articles 3 records found  
1.
13 p, 1.4 MB Risk Factors, Radiological and Clinical Outcomes in Subclinical and Clinical Pituitary Apoplexy / Biagetti, Betina (Hospital Universitari Vall d'Hebron) ; Sarria-Estrada, Silvana (Hospital Universitari Vall d'Hebron) ; Cordero Asanza, Esteban (Hospital Universitari Vall d'Hebron) ; Chaachou-Charradi, Anas (Hospital Universitari Vall d'Hebron) ; Ng-Wong, Yiken Karelys (Hospital Universitari Vall d'Hebron) ; Cicuendez, Marta (Hospital Universitari Vall d'Hebron) ; Hernandez, Irene (Hospital Universitari Vall d'Hebron) ; Rojano-Toimil, Alba (Hospital Universitari Vall d'Hebron) ; Costa, Pilar (Hospital Universitari Vall d'Hebron) ; Martinez-Saez, Elena (Hospital Universitari Vall d'Hebron) ; Casteràs, Anna (Hospital Universitari Vall d'Hebron) ; Simó Canonge, Rafael (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona
Pituitary apoplexy (PA) can be symptomatic, namely acute apoplexy (APA), or asymptomatic or subclinical (SPA). To describe the clinical characteristics and evolution of the patients with APA compared to SPA Patients and methods: Retrospective, longitudinal database analysis. [...]
2022 - 10.3390/jcm11247288
Journal of clinical medicine, Vol. 11 (december 2022)  
Detailed record - Creative Commons
2.
6 p, 158.0 KB Clinical challenges in the management of isolated GH deficiency type IA in adulthood / Casteràs, Anna (Hospital Universitari Vall d'Hebron) ; Kratzsch, Jürgen (University of Leipzig) ; Ferrández, Ángel (Hospital Universitario Miguel Servet (Saragossa)) ; Zafón, Carles (Hospital Universitari Vall d'Hebron) ; Carrascosa Lezcano, Antonio 1949- (Hospital Universitari Vall d'Hebron) ; Mesa Manteca, Jordi (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona
Isolated GH deficiency type IA (IGHDIA) is an infrequent cause of severe congenital GHD, often managed by pediatric endocrinologists, and hence few cases in adulthood have been reported. Herein, we describe the clinical status of a 56-year-old male with IGHDIA due to a 6. [...]
2014 - 10.1530/EDM-13-0057
Endocrinology, Diabetes & Metabolism Case Reports, Vol. 2014 (february 2014)  
Detailed record - Creative Commons
3.
5 p, 1.5 MB Brown tumor of the jaw after pregnancy and lactation in a MEN1 patient / Casteràs, Anna (Hospital Universitari Vall d'Hebron) ; Darder, Lídia (Hospital Universitari Vall d'Hebron) ; Zafón, Carles (Hospital Universitari Vall d'Hebron) ; Hueto Madrid, Juan Antonio (Hospital Universitari Vall d'Hebron) ; Alberola Ferranti, Margarita (Hospital Universitari Vall d'Hebron) ; Caubet, Enric (Hospital Universitari Vall d'Hebron) ; Mesa Manteca, Jordi (Hospital Universitari Vall d'Hebron) ; Universitat Autònoma de Barcelona. Departament de Medicina ; Universitat Autònoma de Barcelona. Departament de Cirurgia ; Universitat Autònoma de Barcelona. Departament de Ciències Morfològiques
Skeletal manifestations of primary hyperparathyroidism (pHPT) include brown tumors (BT), which are osteoclastic focal lesions often localized in the jaws. Brown tumors are a rare manifestation of pHTP in Europe and USA; however, they are frequent in developing countries, probably related to vitamin D deficiency and longer duration and severity of disease. [...]
2016 - 10.1530/EDM-16-0111
Endocrinology, Diabetes & Metabolism Case Reports, (November 2016) , ID 16-0111  
Detailed record - Creative Commons

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