Familial Isolated Hyperparathyroidism
- 1 January 2002
- journal article
- review article
- Published by Wolters Kluwer Health in Medicine
- Vol. 81 (1) , 1-26
- https://doi.org/10.1097/00005792-200201000-00001
Abstract
No abstract availableThis publication has 84 references indexed in Scilit:
- Extracellular Calcium Sensing and Extracellular Calcium SignalingPhysiological Reviews, 2001
- Identification of MEN1 gene mutations in families with MEN 1 and related disordersBritish Journal of Cancer, 2000
- PRIMARY HYPERPARATHYROIDISMEndocrinology and Metabolism Clinics of North America, 2000
- Mutation analysis of the MEN1 tumour suppressor gene in malignant melanomaMelanoma Research, 1999
- The Outcome of Subtotal Parathyroidectomy for the Treatment of Hyperparathyroidism in Multiple Endocrine Neoplasia Type 1Archives of Surgery, 1998
- Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related statesHuman Molecular Genetics, 1997
- Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.Journal of Clinical Investigation, 1997
- Chromosome I alterations in breast cancer: Allelic loss on Ip and Iq Is related to lymphogenic metastases and poor prognosisGenes, Chromosomes and Cancer, 1992
- Benign schwannoma and parathyroid adenoma occurring in the nonradiated neck: Report of two casesJournal of Surgical Oncology, 1990
- Angiomyolipoma Characteristic images by ultrasound and computed tomographyUrology, 1979