Found: 16
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Treating a patient with the Werner syndrome and osteoporosis using recombinant human insulin-like growth factor.
- Published in:
- 1994
- By:
- Publication type:
- journal article
Potential Pharmacological Interventions in Polycystic Kidney Disease.
- Published in:
- Drugs, 2007, v. 67, n. 17, p. 2495, doi. 10.2165/00003495-200767170-00004
- By:
- Publication type:
- Article
Serum uric acid, kidney volume and progression in autosomal-dominant polycystic kidney disease.
- Published in:
- Nephrology Dialysis Transplantation, 2013, v. 28, n. 2, p. 380, doi. 10.1093/ndt/gfs417
- By:
- Publication type:
- Article
The impact of type II diabetes mellitus in patients with autosomal dominant polycystic kidney disease.
- Published in:
- Nephrology Dialysis Transplantation, 2012, v. 27, n. 7, p. 2862, doi. 10.1093/ndt/gfr744
- By:
- Publication type:
- Article
The Authors Reply.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Angiogenic growth factors correlate with disease severity in young patients with autosomal dominant polycystic kidney disease.
- Published in:
- Kidney International, 2011, v. 79, n. 1, p. 128, doi. 10.1038/ki.2010.355
- By:
- Publication type:
- Article
Serum IGF 1 is low and correlated with osteoblastic surface in idiopathic osteoporosis.
- Published in:
- Journal of Bone & Mineral Research, 1995, v. 10, n. 8, p. 1218, doi. 10.1002/jbmr.5650100812
- By:
- Publication type:
- Article
Fluoride-stimulated [<sup>3</sup>H] thymidine uptake in a human osteoblastic osteosarcoma cell line is dependent on transforming growth factor β.
- Published in:
- Journal of Bone & Mineral Research, 1993, v. 8, n. 1, p. 19, doi. 10.1002/jbmr.5650080104
- By:
- Publication type:
- Article
Identification and Characterization of a Gene with Base Substitutions Associated with the Absorptive Hypercalciuria Phenotype and Low Spinal Bone Density.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1476, doi. 10.1210/jcem.87.4.8300
- By:
- Publication type:
- Article
Mapping a Gene Defect in Absorptive Hypercalciuria to Chromosome 1q23.3-q24.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 11, p. 3907, doi. 10.1210/jcem.84.11.6155
- By:
- Publication type:
- Article
Mutations in the Genomic Deoxyribonucleic Acid for SLC3A1 in Patients with Cystinuria.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 10, p. 3688, doi. 10.1210/jcem.83.10.5220
- By:
- Publication type:
- Article
Modifier genes play a significant role in the phenotypic expression of PKD1.
- Published in:
- Kidney International, 2005, v. 67, n. 4, p. 1256, doi. 10.1111/j.1523-1755.2005.00203.x
- By:
- Publication type:
- Article
Identification of two novel mutations [P122S (364C>T) and 1601delAC] in the SLC3A1 gene in type I cystinurics.
- Published in:
- Human Mutation, 2000, v. 15, n. 4, p. 390, doi. 10.1002/(SICI)1098-1004(200004)15:4<390::AID-HUMU33>3.0.CO;2-K
- By:
- Publication type:
- Article
335-base deletion in the mRNA coding for a dibasic amino acid transporter-like protein (SLC3A1) isolated from a patient with cystinuria.
- Published in:
- Human Mutation, 1998, v. 11, p. S69, doi. 10.1002/humu.1380110124
- By:
- Publication type:
- Article
Prevalence of Cardiovascular Events in Patients with Autosomal Dominant Polycystic Kidney Disease.
- Published in:
- American Journal of Nephrology, 2012, v. 36, n. 4, p. 362, doi. 10.1159/000343281
- By:
- Publication type:
- Article
Emergent Early Markers of Renal Progression in Autosomal-Dominant Polycystic Kidney Disease Patients: Implications for Prevention and Treatment.
- Published in:
- American Journal of Nephrology, 2012, v. 36, n. 2, p. 162, doi. 10.1159/000341263
- By:
- Publication type:
- Article