M Aebi Selected Research

Congenital disorder of glycosylation type 1E

1/2000

Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.

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!

M Aebi Research Topics

Disease

1	Post-Traumatic Stress Disorders (Post Traumatic Stress Disorder) 01/2017
1	Lordosis 03/2013
1	Osteoporosis 10/2006
1	Hip Fractures (Intertrochanteric Fractures) 09/2005
1	Intervertebral Disc Degeneration 10/2002
1	Congenital Disorders of Glycosylation 12/2001
1	Congenital disorder of glycosylation type 1E 01/2000

Drug/Important Bio-Agent (IBA)

1	MetalsIBA 03/2013
1	ElementsIBA 03/2013
1	CalciumIBA 10/2006
1	Prednisone (Sone)FDA LinkGeneric 10/2006
1	Biological ProductsIBA 10/2002
1	Polysaccharides (Glycans)IBA 12/2001
1	DolicholsIBA 01/2000
1	Mannose (D-Mannose)IBA 01/2000
1	Phosphates (Orthophosphate)IBA 01/2000

Therapy/Procedure

1	Meditation 01/2017
1	Pedicle Screws 03/2013
1	Ovariectomy (Oophorectomy) 10/2006
1	Hemiarthroplasty 09/2005