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Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations.
J Clin Endocrinol Metab. 2021 Mar 25;106(4):1041-1050. doi: 10.1210/clinem/dgaa955.
J Clin Endocrinol Metab. 2021.
PMID: 33383582
Free PMC article.
Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels.
Montenegro L, Seraphim C, Tinano F, Piovesan M, Canton APM, McElreavey K, Brabant S, Boris NP, Magnuson M, Carroll RS, Kaiser UB, Argente J, Barrios V, Brito VN, Brauner R, Latronico AC.
Montenegro L, et al.
Eur J Endocrinol. 2023 Sep 1;189(3):422-428. doi: 10.1093/ejendo/lvad129.
Eur J Endocrinol. 2023.
PMID: 37703313
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Dementia and mild cognitive impairment in patients with Parkinson's disease.
Teive HA, Piovesan MR, Werneck LC.
Teive HA, et al. Among authors: piovesan mr.
Arq Neuropsiquiatr. 2009 Dec;67(4):1165; author reply 1165.
Arq Neuropsiquiatr. 2009.
PMID: 20073125
No abstract available.
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