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Publications by Nikos Voulgaris
Identification of a Novel Mutation of the PRKAR1A Gene in a Patient With Carney Complex With Significant Osteoporosis and Recurrent Fractures
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Defects of the Carney Complex Gene (PRKAR1A) in Odontogenic Tumors
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
A Novel Mutation in the NCF2 Gene in a CGD Patient With Chronic Recurrent Pneumopathy
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Recurrent Right Ventricular Cardiac Myxoma in a Patient With Carney Complex: A Case Report
Journal of Medical Case Reports
Medicine
A Novel APOC2 Gene Mutation Identified in a Chinese Patient With Severe Hypertriglyceridemia and Recurrent Pancreatitis
Lipids in Health and Disease
Biochemistry
Endocrinology
Clinical Biochemistry
Metabolism
Diabetes
A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Identification of a Novel Splicing Mutation in the SLC25A13 Gene From a Patient With NICCD: A Case Report
BMC Pediatrics
Child Health
Pediatrics
Perinatology
A Novel POLG Gene Mutation in a Patient With SANDO
Journal of Experimental and Integrative Medicine
Alternative Medicine
Complementary
Identification of a Novel MEN1 Gene Mutation in Saudi Arabian Patient With Multiple Endocrine Tumors
Endocrinology&Metabolism International Journal
Multiple Fusiform Myxomatous Cerebral Aneurysms in a Patient With Carney Complex
Journal of Neurosurgery
Surgery
Neurology