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Resultats globals: 5 registres trobats en 0.02 segons.
Articles, 5 registres trobats
Articles 5 registres trobats  
1.
10 p, 988.4 KB Development of ACRODAT®, a new software medical device to assess disease activity in patients with acromegaly / van der Lely, Aart J. (Erasmus University Medical Center) ; Gomez, Roy (Pfizer Medical Affairs) ; Pleil, Andreas (Pfizer Inc) ; Badia, Xavier (Universitat de Barcelona) ; Brue, Thierry (Centre de Référence des Maladies Rares de l'hypophyse HYPO) ; Buchfelder, Michael (Universitatsklinikum Erlangen) ; Burman, Pia (University of Lund) ; Clemmons, David (UNC Hospitals Diabetes and Endocrinology Clinic) ; Ghigo, Ezio (University Hospital Città Salute e Scienza) ; Jorgensen, Jens Otto Lunde (Aarhus University) ; Luger, Anton (Medizinische Universität und Allgemeines Krankenhaus Wien) ; van der Lans-Bussemaker, Joli (Pfizer Medical Affairs) ; Webb, S. M 1952- (Institut d'Investigació Biomèdica Sant Pau) ; Strasburger, Christian J. (Charitė Universitätsmedizin Berlin) ; Universitat Autònoma de Barcelona
Despite availability of multimodal treatment options for acromegaly, achievement of long-term disease control is suboptimal in a significant number of patients. Furthermore, disease control as defined by biochemical normalization may not always show concordance with disease-related symptoms or patient's perceived quality of life. [...]
2017 - 10.1007/s11102-017-0835-5
Pituitary, Vol. 20 Núm. 6 (january 2017) , p. 692-701  
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2.
28 p, 2.7 MB Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion / Pellikaan, Karlijn (Erasmus University Medical Center Rotterdam) ; Ben Brahim, Yassine (Erasmus University Medical Center Rotterdam) ; Rosenberg, Anna G. W (Erasmus University Medical Center Rotterdam) ; Davidse, Kirsten (Erasmus University Medical Center Rotterdam) ; Poitou, Christine (European Reference Network) ; Coupaye, Muriel (European Reference Network) ; Goldstone, Anthony (Imperial College Healthcare NHS Trust) ; Høybye, Charlotte (Karolinska University Hospital and Karolinska Institutet (Suecia)) ; Markovic, Tania (University of Sydney, Sydney) ; Grugni, Graziano (Istituto Auxologico Italiano) ; Crinò, Antonino (Bambino Gesù Hospital) ; Caixàs i Pedragós, Assumpta (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT)) ; Eldar-Geva, Talia (Hebrew University School of Medicine) ; Hirsch, Harry (Shaare Zedek Medical Center) ; Gross-Tsur, Varda (Shaare Zedek Medical Center) ; Butler, Merlin (University of Kansas Medical Center) ; Miller, Jennifer L. (University of Florida) ; van den Berg, Sjoerd A. A. (University Medical Center Rotterdam) ; van der Lely, Aart J (Erasmus University Medical Center Rotterdam) ; de Graaff, Laura (European Reference Network) ; Universitat Autònoma de Barcelona
Prader-Willi syndrome (PWS) is a complex genetic syndrome characterized by hyperphagia, intellectual disability, hypotonia and hypothalamic dysfunction. Adults with PWS often have hormone deficiencies, hypogonadism being the most common. [...]
2021 - 10.3390/jcm10194361
Journal of clinical medicine, Vol. 10 (september 2021)  
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3.
22 p, 1.7 MB Hypogonadism in Women with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion / Pellikaan, Karlijn (Erasmus University Medical Center Rotterdam (Rotterdam, Països Baixos)) ; Ben Brahim, Yassine (Erasmus University Medical Center Rotterdam (Rotterdam, Països Baixos)) ; Rosenberg, Anna G. W. (Erasmus University Medical Center Rotterdam (Rotterdam, Països Baixos)) ; Davidse, Kirsten (Erasmus University Medical Center Rotterdam (Rotterdam, Països Baixos)) ; Poitou, Christine (ENDO-ERN (European Reference Network)) ; Coupaye, Muriel (ENDO-ERN (European Reference Network)) ; Goldstone, Anthony (Hammersmith Hospital (Londres)) ; Høybye, Charlotte (Karolinska University Hospital and Karolinska Institutet (Suecia)) ; Markovic, Tania (University of Sydney) ; Grugni, Graziano (Istituto Auxologico Italiano) ; Crinò, Antonino (Bambino Gesù Hospital) ; Caixàs i Pedragós, Assumpta (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT)) ; Eldar-Geva, Talia (Hebrew University School of Medicine) ; Hirsch, Harry (Shaare Zedek Medical Center) ; Gross-Tsur, Varda (Shaare Zedek Medical Center) ; Butler, Merlin (University of Kansas Medical Center) ; Miller, Jennifer L. (University of Florida) ; van der Kuy, Paul-Hugo M. (Erasmus University Medical Center Rotterdam) ; van den Berg, Sjoerd A. A. (Erasmus University Medical Center Rotterdam) ; Visser, Jenny A. (Erasmus University Medical Center Rotterdam) ; van der Lely, Aart J. (Erasmus University Medical Center Rotterdam) ; de Graaff, Laura (ENDO-ERN (European Reference Network)) ; Universitat Autònoma de Barcelona
Prader-Willi syndrome (PWS) is a rare neuroendocrine genetic syndrome. Characteristics of PWS include hyperphagia, hypotonia, and intellectual disability. Pituitary hormone deficiencies, caused by hypothalamic dysfunction, are common and hypogonadism is the most prevalent. [...]
2021 - 10.3390/jcm10245781
Journal of clinical medicine, Vol. 10 (december 2021)  
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4.
26 p, 1.2 MB Bone Health in Adults With Prader-Willi Syndrome : Clinical Recommendations Based on a Multicenter Cohort Study / van Abswoude, Denise H. ; Pellikaan, Karlijn ; Rosenberg, Anna G. W. ; Davidse, Kirsten ; Coupaye, Muriel ; Høybye, Charlotte ; Markovic, Tania ; Grugni, Graziano ; Crinò, Antonino ; Caixàs i Pedragós, Assumpta (Universitat Autònoma de Barcelona. Departament de Medicina) ; Poitou, Christine ; Mosbah, Helena ; Weir, Tessa ; van Vlimmeren, Leo A. ; Rutges, Joost P. H. J. ; De Klerk, Luuk W. L. ; Zillikens, M. Carola ; van der Lely, Aart J. ; de Graaff, Laura
Prader-Willi syndrome (PWS) is a rare complex genetic syndrome, characterized by delayed psychomotor development, hypotonia, and hyperphagia. Hormone deficiencies such as hypogonadism, hypothyroidism, and growth hormone deficiency are common. [...]
2022 - 10.1210/clinem/dgac556
The journal of clinical endocrinology & metabolism, Vol. 108 (september 2022) , p. 59-84  
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5.
8 p, 984.9 KB Hypertension in Acromegaly in Relationship to Biochemical Control and Mortality : Global ACROSTUDY Outcomes / Vila, Greisa (Medical University of Vienna) ; Luger, Anton (Medical University of Vienna) ; van der Lely, Aart Jan (Erasmus University Medical Centre) ; Neggers, Sebastian J. C. M. M. (Erasmus University Medical Centre) ; Webb, S. M 1952- (Institut d'Investigació Biomèdica Sant Pau) ; Biller, Beverly M. K. (Massachusetts General Hospital (Boston)) ; Valluri, Srinivas (Global Biometrics & Data Management, Pfizer Inc) ; Hey-Hadavi, Judith (Endocrine Care, Pfizer Inc) ; Universitat Autònoma de Barcelona
Hypertension is a major cardiovascular risk factor related to increased mortality in acromegaly. Surgical cure of acromegaly is associated with improvement in blood pressure levels, however little is known about the effect of pegvisomant (PEGV) treatment in patients with hypertension. [...]
2020 - 10.3389/fendo.2020.577173
Frontiers in endocrinology, Vol. 11 (november 2020)  
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