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Amsterdam Gastroenterology Endocrinology and Metabolism, Amsterdam, the Netherlands
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Office for Rare Conditions, Royal Hospital for Children & Queen Elizabeth University Hospital, Glasgow, UK
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, registries have the potential to facilitate surveillance, audit and research. Generally, rare disease registries tend to focus more on the collection of detailed natural history data than support epidemiological research. On the other hand, linked datasets
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Wallenberg Centre of Molecular and Translational Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden
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registries related to health insurance. Ideally, for use in research projects, a register should cover the entire country/region or a large, well-defined sub-population whereby it is representative, and the data should be of acceptable validity ( 2
Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital/ University Medical Center Utrecht, Utrecht, The Netherlands
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Developmental Endocrinology Research Group, Royal Hospital for Children, University of Glasgow, Glasgow, UK
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European network was started (initiative: T.P. Links). 2017: Dekker et al. conducted a survey on the care for pediatric DTC in different European countries and concluded that national registries for pediatric DTC are limited, and treatment is very
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epidemiological information regarding chronic hypoparathyroidism, particularly among the Russian population, we initiated an observational registry study of chronic hypoparathyroidism. This study aimed to evaluate the etiological structure, demographics
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St.Anna Kinderspital, Medical University of Vienna, Vienna, Austria
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were described in a large cohort of children with CAH from the AQUAPE CAH registry ( 4 ). Treatment in classic CAH is necessary to compensate for glucocorticoid and mineralocorticoid deficiencies and also to blunt the ACTH secretion, the major driver
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the REGMEN (the Spanish Registry of Multiple Endocrine Neoplasia, Pheochromocytmas and Paragangliomas (PPGL)). Patients and methods The REGMEN is a collaborative and multicentric project designed by the Spanish Group for the Study of MEN and
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some limitations as well. First, because it was a retrospective registry-based study, there were missing data of several clinical variables. Multivariable Cox-proportional hazard models for disease outcome were not constructed due to this shortage
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therapy are not standard of care. SwissNET is a prospective ongoing nationwide registry of patients with NET of all organs. Its goal is to collect data from NET cases in order to provide quality assessments, to advance knowledge and to establish standard
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series. The aim of this study was to evaluate frequency, diabetes care, and outcome of patients with LD and insulin receptoropathies in the large multicenter DPV Registry. Patients and methods Data source and study population The current
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number and statistical accuracy by aggregating data from national or international acromegaly data registries ( 5 , 12 , 16 ). Although the importance of these studies is without question, some have uncovered significant differences between countries