HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Max A Tischfield Selected Research

congenital fibrosis of the extraocular muscles

2/2016Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development.
12/2012An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.
9/2010Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations.

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:


Max A Tischfield Research Topics

Disease

3congenital fibrosis of the extraocular muscles
02/2016 - 09/2010
3Nervous System Diseases (Neurological Disorders)
06/2011 - 01/2010
1Craniosynostoses (Craniosynostosis)
01/2022
1Tourette Syndrome (Tourette's Syndrome)
01/2022
1Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
02/2017
1Malformations of Cortical Development
02/2016
1Polymicrogyria
12/2012

Drug/Important Bio-Agent (IBA)

5TubulinIBA
02/2016 - 01/2010
1Amyloid (Amyloid Fibrils)IBA
01/2022
1Cholinergic Agents (Cholinergics)IBA
01/2022
1Superoxide Dismutase-1IBA
02/2017
1Reactive Oxygen Species (Oxygen Radicals)IBA
02/2017
1KinesinsIBA
12/2012
1Microtubule-Associated Proteins (Microtubule-Associated Protein 2)IBA
04/2010
1Proteins (Proteins, Gene)FDA Link
04/2010