HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

M R Mahdavi Selected Research

autosomal recessive Spastic paraplegia 20

1/2020A novel missense mutation (c.1006C>T) of SPG20 gene associated with Troyer syndrome.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


M R Mahdavi Research Topics

Disease

1autosomal recessive Spastic paraplegia 20
01/2020
1Hereditary Spastic Paraplegia
01/2020
1Inflammation (Inflammations)
10/2011
1Renal Insufficiency (Renal Failure)
10/2011
1Iron Deficiencies
10/2011
1Iron-Deficiency Anemia (Anemia, Iron Deficiency)
10/2011
1Tuberculosis (Tuberculoses)
09/2005

Drug/Important Bio-Agent (IBA)

1Proteins (Proteins, Gene)FDA Link
01/2020
1DNA (Deoxyribonucleic Acid)IBA
01/2020
1Indicators and Reagents (Reagents)IBA
10/2011
1IronIBA
10/2011
1Transferrin Receptors (Transferrin Receptor)IBA
10/2011
1Ferritins (Ferritin)IBA
10/2011
1P-2 (P 2)IBA
09/2005

Therapy/Procedure

1Renal Dialysis (Hemodialysis)
10/2011
1Kidney Transplantation
09/2005