PRKAR1A gene mutation in patients with cardiac myxoma
Authors:
Open Access
- 1 July 2005
- journal article
- research article
- Published by Elsevier in International Journal of Cardiology
- Vol. 102 (2) , 273-277
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Genetic and Histologic Studies of Somatomammotropic Pituitary Tumors in Patients with the "Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity and Schwannomas" (Carney Complex)The Journal of Clinical Endocrinology & Metabolism, 2000
- Prolactin Secretion Abnormalities in Patients with the "Syndrome of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity and Schwannomas" (Carney Complex)Journal of Pediatric Endocrinology and Metabolism, 2000
- A Concise Genetic and Clinical Guide to Multiple Endocrine Neoplasias and Related SyndromesJournal of Pediatric Endocrinology and Metabolism, 2000
- GENETICS OF CARNEY COMPLEX AND RELATED FAMILIAL LENTIGINOSES, AND OTHER MULTIPLE TUMOR SYNDROMESPediatric Pathology & Molecular Medicine, 2000
- Paradoxical Response to Dexamethasone in the Diagnosis of Primary Pigmented Nodular Adrenocortical DiseaseAnnals of Internal Medicine, 1999
- Carney complex: Diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomasAmerican Journal of Medical Genetics, 1998
- Thyroid Gland Abnormalities in Patients with the Syndrome of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity, and Schwannomas (Carney Complex)The Journal of Clinical Endocrinology & Metabolism, 1997
- Cardiac MyxomasNew England Journal of Medicine, 1995
- Dominant Inheritance of the Complex of Myxomas, Spotty Pigmentation, and Endocrine OveractivityMayo Clinic Proceedings, 1986
- The Complex of Myxomas, Spotty Pigmentation, and Endocrine OveractivityMedicine, 1985