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Resultats globals: 4 registres trobats en 0.02 segons.
Articles, 4 registres trobats
Articles 4 registres trobats  
1.
8 p, 258.5 KB Hyponatremia in Children and Adults with Prader-Willi Syndrome : A Survey Involving Seven Countries / Coupaye, Muriel (European Reference Network on Rare Endocrine Conditions) ; Pellikaan, Karlijn (University Medical Centre Rotterdam) ; Goldstone, Anthony (Imperial College London) ; Crinò, Antonino (Bambino Gesù Hospital) ; Grugni, Graziano (Istituto Auxologico Italiano) ; Markovic, Tania (University of Sydney) ; Høybye, Charlotte (Karolinska University Hospital and Karolinska Institutet (Suecia)) ; Caixàs i Pedragós, Assumpta (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT)) ; Mosbah, Helena (European Reference Network on Rare Endocrine Conditions) ; De Graaff, Laura C. G. (University Medical Centre Rotterdam) ; Tauber, Maithé (Institut Toulousain des Maladies Infectieuses et Inflammatoires) ; Poitou, Christine (Sorbonne University) ; Universitat Autònoma de Barcelona
In Prader-Willi syndrome (PWS), conditions that are associated with hyponatremia are common, such as excessive fluid intake (EFI), desmopressin use and syndrome of inappropriate antidiuretic hormone (SIADH) caused by psychotropic medication. [...]
2021 - 10.3390/jcm10163555
Journal of clinical medicine, Vol. 10 (august 2021)  
Registre complet - Creative Commons
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)  
Registre complet - Creative Commons
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)  
Registre complet - Creative Commons
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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