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P I Salmela Selected Research

Hyperparathyroidism

6/2009Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition.

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P I Salmela Research Topics

Disease

1Hyperparathyroidism 2
06/2009
1Hyperparathyroidism
06/2009
1Neoplasms (Cancer)
06/2009
1Multiple Endocrine Neoplasia Type 1
06/2009
1medullary Thyroid cancer
05/2009
1Chronic Progressive External Ophthalmoplegia (Progressive External Ophthalmoplegia)
03/2005
1Kearns-Sayre Syndrome
03/2005
1VLCAD deficiency
03/2005
1MERRF Syndrome (Myoclonic Epilepsy and Ragged Red Fibers)
08/2003
1Myoclonic Epilepsies (Myoclonic Encephalopathy)
08/2003
1Type 1 Diabetes Mellitus (Autoimmune Diabetes)
09/2000
1Infections
09/2000
1Inborn Genetic Diseases (Disease, Hereditary)
09/2000
1Body Weight (Weight, Body)
09/2000
1Diabetes Mellitus
02/2000

Drug/Important Bio-Agent (IBA)

2aryl hydrocarbon receptor-interacting proteinIBA
06/2009 - 05/2009
2Mitochondrial DNA (mtDNA)IBA
03/2005 - 08/2003
1Cyclin-Dependent Kinase Inhibitor p27IBA
06/2009
1Calcium-Sensing ReceptorsIBA
06/2009
1Glycated Hemoglobin (Glycosylated Hemoglobin)IBA
09/2000
1Bicarbonates (Hydrogen Carbonate)IBA
09/2000
1AntigensIBA
09/2000
1Insulin (Novolin)FDA Link
02/2000