Lower Frequency of HLA-DRB1 Type 1 Diabetes Risk Alleles in Pediatric Patients with MODY.
- Published in:
- PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0169389
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- Publication type:
- Article
Works by Bilbao, José Ramón
Results: 8
1
2
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2370, doi. 10.1210/jc.2006-2287
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- Publication type:
- Article
3
Familial hypercalcemia and hypercalciuria: no mutations in the Ca[sup 2+] -sensing receptor gene.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 9, p. 748
- By:
- Publication type:
- Article
4
Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 7, p. 550
- By:
- Publication type:
- Article
5
Identification of loci associated with susceptibility to bovine paratuberculosis and with the dysregulation of the MECOM, eEF1A2, and U1 spliceosomal RNA expression.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79619-x
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- Publication type:
- Article
6
Evidence that the COMT <sup>Val158Met</sup> polymorphism moderates subclinical psychotic and affective symptoms in unaffected first-degree relatives of patients with schizophrenia
- Published in:
- European Psychiatry, 2008, v. 23, n. 3, p. 219, doi. 10.1016/j.eurpsy.2007.12.002
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- Publication type:
- Article
7
Associations between COMTVal<sup>158</sup>Met polymorphism and cognition: direct or indirect effects?
- Published in:
- European Psychiatry, 2006, v. 21, n. 5, p. 338, doi. 10.1016/j.eurpsy.2006.03.007
- By:
- Publication type:
- Article
8
Author Correction: Identification of loci associated with susceptibility to bovine paratuberculosis and with the dysregulation of the MECOM, eEF1A2, and U1 spliceosomal RNA expression.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice