Found: 27
Select item for more details and to access through your institution.
Identification of a novel GNAS mutation for pseudohypoparathyroidism in a Chinese family.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 25, doi. 10.1007/s12020-009-9193-z
- By:
- Publication type:
- Article
Increased renal Akt/mTOR and MAPK signaling in type I diabetes in the absence of IGF type 1 receptor activation.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 126, doi. 10.1007/s12020-009-9190-2
- By:
- Publication type:
- Article
A reverse postural test as a screening tool for aldosterone-producing adenoma: a pilot study.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 75, doi. 10.1007/s12020-009-9188-9
- By:
- Publication type:
- Article
4-Nitrophenol isolated from diesel exhaust particles disrupts regulation of reproductive hormones in immature male rats.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 98, doi. 10.1007/s12020-009-9192-0
- By:
- Publication type:
- Article
Increased TTS abrogates IDO-mediated CD4<sup>+</sup> T cells suppression in patients with Graves’ disease.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 119, doi. 10.1007/s12020-009-9184-0
- By:
- Publication type:
- Article
Clinical and genetic analysis for four Chinese families with Prader–Willi syndrome.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 37, doi. 10.1007/s12020-009-9203-1
- By:
- Publication type:
- Article
A novel variant in Serpina7 gene in a family with thyroxine-binding globulin deficiency.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 83, doi. 10.1007/s12020-009-9202-2
- By:
- Publication type:
- Article
Hypothyroid Graves’ disease complicated with elephantiasis nostras verrucosa (ENV): a case report and review of the literature.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 6, doi. 10.1007/s12020-009-9200-4
- By:
- Publication type:
- Article
Resistin induces insulin resistance by both AMPK-dependent and AMPK-independent mechanisms in HepG2 cells.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 60, doi. 10.1007/s12020-009-9198-7
- By:
- Publication type:
- Article
Hemangiopericytoma-associated hypoglycemia improved by glucocorticoid therapy: a case report.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 151, doi. 10.1007/s12020-009-9197-8
- By:
- Publication type:
- Article
Metformin in combination with structured lifestyle intervention improved body mass index in obese adolescents, but did not improve insulin resistance.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 141, doi. 10.1007/s12020-009-9196-9
- By:
- Publication type:
- Article
Possible role for ENPP1 polymorphism in obesity but not for INSIG2 and PLIN variants.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 103, doi. 10.1007/s12020-009-9194-y
- By:
- Publication type:
- Article
Influence of insulin treatment on the lacrimal gland and ocular surface of diabetic rats.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 161
- By:
- Publication type:
- Article
Co-existence of glucagonoma with recurrent insulinoma in a patient with multiple endocrine neoplasia-type 1 (MEN-1).
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 20, doi. 10.1007/s12020-009-9183-1
- By:
- Publication type:
- Article
Effects of estrogen receptor α and β gene deletion on estrogenic induction of progesterone receptors in the locus coeruleus in female mice.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 169
- By:
- Publication type:
- Article
Genetic copy number alterations and IL-13 expression differences in papillary thyroid cancers and benign nodules.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 155, doi. 10.1007/s12020-009-9206-y
- By:
- Publication type:
- Article
Severe osteomalacia presenting with multiple vertebral fractures: a case report and review of the literature.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 30, doi. 10.1007/s12020-009-9209-8
- By:
- Publication type:
- Article
Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 16
- By:
- Publication type:
- Article
Acute myeloid leukemia with infiltration of thyroid gland complicating Hashimoto’s thyroiditis.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 147, doi. 10.1007/s12020-009-9173-3
- By:
- Publication type:
- Article
Coagulation and fibrinolysis in thyroid dysfunction.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 110, doi. 10.1007/s12020-009-9185-z
- By:
- Publication type:
- Article
R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 10, doi. 10.1007/s12020-009-9204-0
- By:
- Publication type:
- Article
GnRH receptor expression in human prostate cancer cells is affected by hormones and growth factors.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 87, doi. 10.1007/s12020-009-9195-x
- By:
- Publication type:
- Article
Changes of serum and urine neutrophil gelatinase-associated lipocalin in type-2 diabetic patients with nephropathy: one year observational follow-up study.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 45, doi. 10.1007/s12020-009-9187-x
- By:
- Publication type:
- Article
FSHβ knockout mouse model: a decade ago and into the future.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 1, doi. 10.1007/s12020-009-9199-6
- By:
- Publication type:
- Article
Hypercoagulability in Cushing’s syndrome: the role of specific haemostatic and fibrinolytic markers.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 70, doi. 10.1007/s12020-009-9186-y
- By:
- Publication type:
- Article
Natural course of benign adrenal incidentalomas in subjects with extra-adrenal malignancy.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 135, doi. 10.1007/s12020-009-9191-1
- By:
- Publication type:
- Article
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesity.
- Published in:
- Endocrine (1355008X), 2009, v. 36, n. 1, p. 52, doi. 10.1007/s12020-009-9156-4
- By:
- Publication type:
- Article