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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2022 | 6 |
2023 | 1 |
Search Results
6
results
Results by year
Page 1
Rare genetic causes of obesity: Diagnosis and management in clinical care.
Ann Endocrinol (Paris). 2022 Feb;83(1):63-72. doi: 10.1016/j.ando.2021.12.003. Epub 2021 Dec 23.
Ann Endocrinol (Paris). 2022.
PMID: 34953778
Review.
Genetic conditions of short stature: A review of three classic examples.
Butler MG, Miller BS, Romano A, Ross J, Abuzzahab MJ, Backeljauw P, Bamba V, Bhangoo A, Mauras N, Geffner M.
Butler MG, et al.
Front Endocrinol (Lausanne). 2022 Oct 21;13:1011960. doi: 10.3389/fendo.2022.1011960. eCollection 2022.
Front Endocrinol (Lausanne). 2022.
PMID: 36339399
Free PMC article.
Review.
Item in Clipboard
The transition from pediatric to adult care in individuals with Prader-Willi syndrome.
Poitou C, Holland A, Höybye C, de Graaff LCG, Bottius S, Otterlei B, Tauber M.
Poitou C, et al.
Endocr Connect. 2022 Dec 15;12(1):e220373. doi: 10.1530/EC-22-0373. Print 2023 Jan 1.
Endocr Connect. 2022.
PMID: 36347048
Free PMC article.
Review.
Item in Clipboard
Hypothalamic syndrome.
Müller HL, Tauber M, Lawson EA, Özyurt J, Bison B, Martinez-Barbera JP, Puget S, Merchant TE, van Santen HM.
Müller HL, et al.
Nat Rev Dis Primers. 2022 Apr 21;8(1):24. doi: 10.1038/s41572-022-00351-z.
Nat Rev Dis Primers. 2022.
PMID: 35449162
Review.
Item in Clipboard
Bone Health in Adults With Prader-Willi Syndrome: Clinical Recommendations Based on a Multicenter Cohort Study.
van Abswoude DH, Pellikaan K, Rosenberg AGW, Davidse K, Coupaye M, Høybye C, Markovic TP, Grugni G, Crinò A, Caixàs A, Poitou C, Mosbah H, Weir T, van Vlimmeren LA, Rutges JPHJ, De Klerk LWL, Zillikens MC, van der Lely AJ, de Graaff LCG.
van Abswoude DH, et al.
J Clin Endocrinol Metab. 2022 Dec 17;108(1):59-84. doi: 10.1210/clinem/dgac556.
J Clin Endocrinol Metab. 2022.
PMID: 36149817
Free PMC article.
Item in Clipboard
Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature.
Rosenberg AGW, Wellink CM, Tellez Garcia JM, Pellikaan K, Van Abswoude DH, Davidse K, Van Zutven LJCM, Brüggenwirth HT, Resnick JL, Van der Lely AJ, De Graaff LCG.
Rosenberg AGW, et al.
J Clin Med. 2022 Jul 12;11(14):4033. doi: 10.3390/jcm11144033.
J Clin Med. 2022.
PMID: 35887798
Free PMC article.
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