Back to Search
MARCIA RUBERG, PH.D.
PH.D.
School Psychologist
NPI: 1669684700Individual
Specialties, Licenses & Credentials
School PsychologistPrimary
Psychologist — School
Code: 103TS0200X
PS005685L(PA)
Research & Publications (20)
Atlastin-1, the dynamin-like GTPase responsible for spastic paraplegia SPG3A, remodels lipid membranes and may form tubules and vesicles in the endoplasmic reticulum.
PMID 19573020·J Neurochem·2009
4-observational
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.
PMID 18758830·Neurogenetics·2009
8-other
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.
PMID 19214208·PLoS Genet·2009
8-other
In vivo evidence for cerebral depletion in high-energy phosphates in progressive supranuclear palsy.
PMID 19190655·J Cereb Blood Flow Metab·2009
8-other
Recent advances in the genetics of spastic paraplegias.
PMID 18541115·Curr Neurol Neurosci Rep·2008
6-review
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.
PMID 18785640·Mov Disord·2008
8-other
Atypical parkinsonism in the Caribbean island of Guadeloupe: etiological role of the mitochondrial complex I inhibitor annonacin.
PMID 18816693·Mov Disord·2008
6-review
Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genes.
PMID 17992546·Neurogenetics·2008
8-other
Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.
PMID 18378516·Brain·2008
4-observational
Stimulation of subterritories of the subthalamic nucleus reveals its role in the integration of the emotional and motor aspects of behavior.
PMID 17556546·Proc Natl Acad Sci U S A·2007
8-other
Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.
PMID 17596714·Neurodegener Dis·2007
8-other
A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSP.
PMID 17597328·Neurogenetics·2007
5-case
Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis.
PMID 17321752·Mol Cell Neurosci·2007
8-other
New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.
PMID 17452582·Neurology·2007
8-other
Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells.
PMID 17336078·Neurobiol Dis·2007
7-preclinical
A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes.
PMID 17344386·J Neurosci·2007
7-preclinical
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
PMID 17347251·Brain·2007
8-other
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
PMID 17322883·Nat Genet·2007
7-preclinical
Annonacin, a natural mitochondrial complex I inhibitor, causes tau pathology in cultured neurons.
PMID 17634376·J Neurosci·2007
7-preclinical
REM sleep behavior disorder in patients with guadeloupean parkinsonism, a tauopathy.
PMID 17702273·Sleep·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1022 HARAL PL
CHERRY HILL, NJ 08034 - Phone
- (856) 427-6711
Quick Facts
- NPI
- 1669684700
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile