R Parvari Selected Research

Antibodies

1/2000

Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency.

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!

R Parvari Research Topics

Disease

1	Hypohidrosis 07/2004
1	Congenital Pain Insensitivity 07/2004
1	Congenital Abnormalities (Deformity) 03/2002
1	Infections 03/2002
1	Cystinuria 10/2001
1	Renal Insufficiency (Renal Failure) 03/2001
1	Anemia 03/2001
1	Cysts 03/2001
1	Hypertension (High Blood Pressure) 03/2001
1	Inherited Thyroxine-Binding Globulin Deficiency 10/2000
1	Hyperthermia 06/2000
1	Hereditary Sensory and Autonomic Neuropathies (HSAN) 06/2000
1	Type IB Isolated Growth Hormone Deficiency 01/2000
1	Pituitary Dwarfism 01/2000

Drug/Important Bio-Agent (IBA)

2	3-(2-carboxyindol-3-yl)propionic acidIBA 07/2004 - 06/2000
1	Phosphoprotein Phosphatases (Phosphatases, Protein)IBA 10/2001
1	SaltsIBA 03/2001
1	Codon (Codons)IBA 10/2000
1	Peptides (Polypeptides)IBA 10/2000
1	Nerve Growth Factor Receptor (Nerve Growth Factor Receptor, Low Affinity)IBA 06/2000
1	AntibodiesIBA 01/2000
1	Growth Hormone (Somatotropin)IBA 01/2000

Therapy/Procedure

1	Osteotomy 03/2002
1	Debridement 03/2002