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Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.
Clin Genet. 2024 Nov 25. doi: 10.1111/cge.14659. Online ahead of print.
Clin Genet. 2024.
PMID: 39586716
Response to Recombinant Human Growth Hormone Therapy in Short Children Born at Very Low Birth Weight.
Homma TK, Dantas NCB, Freire BL, Cellin LP, Santillán Vásconez AM, Arnhold IJP, Scalco RC, Malaquias AC, de Lima Jorge AA.
Homma TK, et al. Among authors: cellin lp.
Horm Res Paediatr. 2024 Nov 13:1-11. doi: 10.1159/000542570. Online ahead of print.
Horm Res Paediatr. 2024.
PMID: 39536728
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Clinical Characteristics of Children with THRA Mutations: Variable Phenotype and Good Response to Recombinant Human Growth Hormone Therapy.
Andrade NLM, Rezende RC, Crisostomo LG, Dantas NCB, Cellin LP, de Souza V, Quedas EPS, Lerario AM, Vasques GA, Jorge AAL.
Andrade NLM, et al. Among authors: cellin lp.
Horm Res Paediatr. 2024 May 14:1-8. doi: 10.1159/000539348. Online ahead of print.
Horm Res Paediatr. 2024.
PMID: 38744258
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Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability.
Dantas NCB, Funari MFA, Lerário AM, Andrade NLM, Rezende RC, Cellin LP, Alves C, Crisostomo LG, Arnhold IJP, Mendonca B, Scalco RC, Jorge AAL.
Dantas NCB, et al. Among authors: cellin lp.
Eur J Endocrinol. 2023 Sep 1;189(3):387-395. doi: 10.1093/ejendo/lvad128.
Eur J Endocrinol. 2023.
PMID: 37695807
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