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Page 1
The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature.
Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG. Pellikaan K, et al. Among authors: rosenberg agw. Genes (Basel). 2021 Jun 7;12(6):875. doi: 10.3390/genes12060875. Genes (Basel). 2021. PMID: 34200226 Free PMC article. Review.
Central Adrenal Insufficiency Is Rare in Adults With Prader-Willi Syndrome.
Rosenberg AGW, Pellikaan K, Poitou C, Goldstone AP, Høybye C, Markovic T, Grugni G, Crinò A, Caixàs A, Coupaye M, Van Den Berg SAA, Van Der Lely AJ, De Graaff LCG. Rosenberg AGW, et al. J Clin Endocrinol Metab. 2020 Jul 1;105(7):e2563-71. doi: 10.1210/clinem/dgaa168. J Clin Endocrinol Metab. 2020. PMID: 32232324 Free PMC article.
Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment.
Pellikaan K, Rosenberg AGW, Kattentidt-Mouravieva AA, Kersseboom R, Bos-Roubos AG, Veen-Roelofs JMC, van Wieringen N, Hoekstra FME, van den Berg SAA, van der Lely AJ, de Graaff LCG. Pellikaan K, et al. Among authors: rosenberg agw. J Clin Endocrinol Metab. 2020 Dec 1;105(12):e4671-87. doi: 10.1210/clinem/dgaa621. J Clin Endocrinol Metab. 2020. PMID: 32877518 Free PMC article.
Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome.
Pellikaan K, Rosenberg AGW, Davidse K, Kattentidt-Mouravieva AA, Kersseboom R, Bos-Roubos AG, Grootjen LN, Damen L, van den Berg SAA, van der Lely AJ, Hokken-Koelega ACS, de Graaff LCG. Pellikaan K, et al. Among authors: rosenberg agw. J Clin Med. 2021 Jul 23;10(15):3250. doi: 10.3390/jcm10153250. J Clin Med. 2021. PMID: 34362034 Free PMC article.
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 K, Ben Brahim Y, Rosenberg AGW, Davidse K, Poitou C, Coupaye M, Goldstone AP, Høybye C, Markovic TP, Grugni G, Crinò A, Caixàs A, Eldar-Geva T, Hirsch HJ, Gross-Tsur V, Butler MG, Miller JL, van den Berg SAA, van der Lely AJ, de Graaff LCG. Pellikaan K, et al. Among authors: rosenberg agw. J Clin Med. 2021 Sep 24;10(19):4361. doi: 10.3390/jcm10194361. J Clin Med. 2021. PMID: 34640379 Free PMC article.
What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'Internal Medicine for Rare Genetic Syndromes'.
Rosenberg AGW, Pater MRA, Pellikaan K, Davidse K, Kattentidt-Mouravieva AA, Kersseboom R, Bos-Roubos AG, van Eeghen A, Veen JMC, van der Meulen JJ, van Aalst-van Wieringen N, Hoekstra FME, van der Lely AJ, de Graaff LCG. Rosenberg AGW, et al. J Clin Med. 2021 Nov 22;10(22):5457. doi: 10.3390/jcm10225457. J Clin Med. 2021. PMID: 34830739 Free PMC article.
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 K, Ben Brahim Y, Rosenberg AGW, Davidse K, Poitou C, Coupaye M, Goldstone AP, Høybye C, Markovic TP, Grugni G, Crinò A, Caixàs A, Eldar-Geva T, Hirsch HJ, Gross-Tsur V, Butler MG, Miller JL, van der Kuy PM, van den Berg SAA, Visser JA, van der Lely AJ, de Graaff LCG. Pellikaan K, et al. Among authors: rosenberg agw. J Clin Med. 2021 Dec 10;10(24):5781. doi: 10.3390/jcm10245781. J Clin Med. 2021. PMID: 34945077 Free PMC article.
18 results