about
Differential elemental distribution of retained particles along the respiratory tract.Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumorTP53-Associated Pediatric Malignancies.Genomic landscape of paediatric adrenocortical tumours.Establishment and characterization of the first pediatric adrenocortical carcinoma xenograft model identifies topotecan as a potential chemotherapeutic agentInsulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age.Familial predisposition to adrenocortical tumors: clinical and biological features and management strategies.The International Pediatric Adrenocortical Tumor Registry initiative: contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors.Evaluating the roles of follicle-stimulating hormone receptor polymorphisms in gonadal hyperstimulation associated with severe juvenile primary hypothyroidism.Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of β cells.Population genetics of nine short tandem repeat loci: allele frequency distribution in a Brazilian population sample.Possible role of a radiation-induced p53 mutation in a Nelson's syndrome patient with a fatal outcome.Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect.Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment.Prognostic Significance of Major Histocompatibility Complex Class II Expression in Pediatric Adrenocortical Tumors: A St. Jude and Children's Oncology Group Study.Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg337His mutation of the p53 tumor suppressor protein.The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor genePathogenesis of Adrenocortical TumorsAspectos moleculares da tumorigênese hipofisáriaGermline Variants in Phosphodiesterase Genes and Genetic Predisposition to Pediatric Adrenocortical TumorsForty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Emilia Modolo Pinto
@ast
Emilia Modolo Pinto
@en
Emilia Modolo Pinto
@es
Emilia Modolo Pinto
@nl
type
label
Emilia Modolo Pinto
@ast
Emilia Modolo Pinto
@en
Emilia Modolo Pinto
@es
Emilia Modolo Pinto
@nl
prefLabel
Emilia Modolo Pinto
@ast
Emilia Modolo Pinto
@en
Emilia Modolo Pinto
@es
Emilia Modolo Pinto
@nl
P1053
K-3083-2017
P106
P21
P31
P3829
P496
0000-0001-5567-000X