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158 results on '"Lerario, Antonio M."'

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1. Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population

4. Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma

8. Idiopathic collapsing glomerulopathy is associated with APOL1high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population

11. Abstract 1501: Epigenetic dedifferentiation as a therapeutic strategy in adrenal cancer

14. Targeting Oncogenic Wnt/β-Catenin Signaling in Adrenocortical Carcinoma Disrupts ECM Expression and Impairs Tumor Growth.

17. Additional file 2 of Epigenetic regulation of innate immune memory in microglia

18. Additional file 1 of Epigenetic regulation of innate immune memory in microglia

19. Additional file 4 of Epigenetic regulation of innate immune memory in microglia

20. Additional file 3 of Epigenetic regulation of innate immune memory in microglia

21. Targeted massively parallel sequencing panel to diagnose genetic endocrine disorders in a tertiary hospital

24. Phosphodiesterase 2A and 3B variants are associated with primary aldosteronism

25. Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency

26. Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis

27. Statins Reduce Intratumor Cholesterol Affecting Adrenocortical Cancer Growth

30. Urinary Sediment Transcriptomic and Longitudinal Data to Investigate Renal Function Decline in Type 1 Diabetes

34. Evaluation of SHOX defects in the era of next‐generation sequencing

35. New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

36. Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR

39. A ZNRF3-dependent Wnt/β-catenin signaling gradient is required for adrenal homeostasis

40. Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein

41. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

42. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

43. Correlation between molecular features and genetic subtypes of Glioblastoma: critical analysis in 109 cases

47. Novel SUZ12 mutations in Weaver‐like syndrome

49. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

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