Found: 8
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Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels.
- Published in:
- European Journal of Endocrinology, 2023, v. 189, n. 3, p. 422, doi. 10.1093/ejendo/lvad129
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- Publication type:
- Article
Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways.
- Published in:
- European Journal of Endocrinology, 2014, v. 171, n. 2, p. 253, doi. 10.1530/EJE-14-0232
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- Publication type:
- Article
Methylome profiling of healthy and central precocious puberty girls.
- Published in:
- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0581-1
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- Publication type:
- Article
Anthropometric, metabolic, and reproductive outcomes of patients with central precocious puberty treated with leuprorelin acetate 3-month depot (11.25 mg).
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 11, p. 1371, doi. 10.1515/jpem-2021-0142
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- Publication type:
- Article
Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
- Published in:
- 2020
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- Publication type:
- journal article
The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty.
- Published in:
- Endocrine Reviews, 2023, v. 44, n. 2, p. 193, doi. 10.1210/endrev/bnac020
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- Publication type:
- Article
Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment.
- Published in:
- Clinical Endocrinology, 2022, v. 97, n. 3, p. 284, doi. 10.1111/cen.14715
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- Publication type:
- Article
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.
- Published in:
- Clinical Endocrinology, 2018, v. 88, n. 3, p. 425, doi. 10.1111/cen.13535
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- Publication type:
- Article