Found: 10
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What's new in metabolic and genetic hypoglycaemias: diagnosis and management.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Mutations in UCP2 in Congenital Hyperinsulinism Reveal a Role for Regulation of Insulin Secretion.
- Published in:
- PLoS ONE, 2008, v. 3, n. 12, p. 1, doi. 10.1371/journal.pone.0003850
- By:
- Publication type:
- Article
Identification of Genes Associated with the Corticotroph Phenotype in Bronchial Carcinoid Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 11, p. 5015, doi. 10.1210/jc.2002-020598
- By:
- Publication type:
- Article
Variable Expression of the V1 Vasopressin Receptor Modulates the Phenotypic Response of Steroid-Secreting Adrenocortical Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 6, p. 2029, doi. 10.1210/jcem.83.6.4873
- By:
- Publication type:
- Article
High Expression of the POU Factor Brn3a in Aggressive Neuroendocrine Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 1, p. 89, doi. 10.1210/jcem.82.1.3670
- By:
- Publication type:
- Article
Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter ( SLC6A8) deficiency syndrome.
- Published in:
- Journal of Inherited Metabolic Disease, 2013, v. 36, n. 1, p. 103, doi. 10.1007/s10545-012-9495-9
- By:
- Publication type:
- Article
Treatment by oral creatine, L-arginine and L-glycine in six severely affected patients with creatine transporter defect.
- Published in:
- Journal of Inherited Metabolic Disease, 2012, v. 35, n. 1, p. 151, doi. 10.1007/s10545-011-9358-9
- By:
- Publication type:
- Article
Multiple sources of metabolic disturbance in ETHE1‐related ethylmalonic encephalopathy.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 443, doi. 10.1007/s10545-010-9227-y
- By:
- Publication type:
- Article
Clinical and biochemical heterogeneity associated with fumarase deficiency.
- Published in:
- Human Mutation, 2011, v. 32, n. 9, p. 1046, doi. 10.1002/humu.21534
- By:
- Publication type:
- Article
High precursor level in maternal blood results from the alternate mode of proopiomelanocortin processing in human placenta.
- Published in:
- Clinical Endocrinology, 1999, v. 50, n. 1, p. 85, doi. 10.1046/j.1365-2265.1999.00612.x
- By:
- Publication type:
- Article