VIICTR Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Results (43)
More Search Options
Match
Type
Why
Neurogenetics: advancing the "next-generation" of brain research.
Academic Article
Why?
Clinical neurogenetics: recent advances in the genetics of epilepsy.
Academic Article
Why?
CUDDAPAH, VISHNU
Person
Why?
MAHESHWARI, ATUL
Person
Why?
PREDICTIVE GENES, MECHANISMS, AND CLINICAL BIOMARKERS OF SUDEP
Grant
Why?
The Florida Learning Disabilities Research Center
Grant
Why?
ZOGHBI, HUDA
Person
Why?
COORG, ROHINI
Person
Why?
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia.
Academic Article
Why?
Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndrome.
Academic Article
Why?
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
Academic Article
Why?
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
Academic Article
Why?
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy.
Academic Article
Why?
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy.
Academic Article
Why?
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis.
Academic Article
Why?
Per Page
15
25
50
100
Page
of 3
Next
Prev
Search Criteria
Neurogenetics
Filter by Type
All
(43)
People
(17)
Research
(26)
_
Click "Why?" to see why an item matched the search.