Found: 16
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Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 375, doi. 10.2350/08-12-0578.1
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- Article
CONGENITAL HYPERINSULINISM IN BRAZILIAN NEONATES: A STUDY OF HISTOLOGY, KATP CHANNEL GENES AND PROLIFERATION OF β-CELLS.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 3, p. 1
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- Article
Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma.
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 4, p. 1159, doi. 10.1210/clinem/dgab866
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- Article
The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 5, p. 1204, doi. 10.1002/ajmg.a.36444
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- Article
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43730-0
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- Article
Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2976, doi. 10.1210/jc.2004-0963
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- Article
Three novel mutations in CYP21 gene in Brazilian patients with the classical form of 21-hydroxylase deficiency due to a founder effect.
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- 2002
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- Publication type:
- journal article
Environmental Contaminants Modulate Breast Cancer Development and Outcome in TP53 p.R337H Carriers and Noncarriers.
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- Cancers, 2022, v. 14, n. 12, p. 3014, doi. 10.3390/cancers14123014
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- Article
TERT Expression in Wilms Tumor Is Regulated by Promoter Mutation or Hypermethylation, WT1, and N-MYC.
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- Cancers, 2022, v. 14, n. 7, p. 1655, doi. 10.3390/cancers14071655
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- Article
Genomic landscape of paediatric adrenocortical tumours.
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- Nature Communications, 2015, v. 6, n. 3, p. 6302, doi. 10.1038/ncomms7302
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- Article
A common polymorphism in the retinoic acid pathway modifies adrenocortical carcinoma age-dependent incidence.
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- 2020
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- Publication type:
- journal article
An update on the central nervous system manifestations of Li–Fraumeni syndrome.
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- Acta Neuropathologica, 2020, v. 139, n. 4, p. 669, doi. 10.1007/s00401-019-02055-3
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- Article
Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous.
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- Acta Neuropathologica, 2018, v. 136, n. 2, p. 315, doi. 10.1007/s00401-018-1814-2
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- Article
Pediatric Adrenocortical Carcinoma: The Nuts and Bolts of Diagnosis and Treatment and Avenues for Future Discovery.
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- Cancer Management & Research, 2024, v. 16, p. 1141, doi. 10.2147/CMAR.S348725
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- Article
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene.
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- Clinical Endocrinology, 2008, v. 68, n. 2, p. 226, doi. 10.1111/j.1365-2265.2007.03023.x
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- Article
Forty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-13646-9
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- Article