A pediatric case of pheochromocytoma without apparent hypertension associated with von Hippel-Lindau disease.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Works matching IS 09185739 AND DT 2018 AND VI 27 AND IP 2
Results: 8
1
2
Thyroid nodules and long-term follow-up among childhood cancer survivors who underwent hematopoietic stem cell transplantation.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
3
Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
4
Decrement in bone mineral density after parathyroidectomy in a pediatric patient with primary hyperparathyroidism.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
5
Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially?
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
6
Chromosome 6q24-related diabetes mellitus.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 2, p. 59, doi. 10.1297/cpe.27.59
- By:
- Publication type:
- Article
7
Recombinant human growth hormone in neonatalonset multisystem inflammatory disease.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
8
Thyroid hormone status in patients with severe selenium deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2018, v. 27, n. 2, p. 67, doi. 10.1297/cpe.27.67
- By:
- Publication type:
- Article