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JESSICA GARBERN, M.D.
M.D.
Pediatric Cardiology Physician
NPI: 1770882359Individual
Specialties, Licenses & Credentials
Pediatric Cardiology PhysicianPrimary
Pediatrics — Pediatric Cardiology
Code: 2080P0202X
258400(MA)
Research & Publications (20)
Pelizaeus-Merzbacher disease: pathogenic mechanisms and insights into the roles of proteolipid protein 1 in the nervous system.
PMID 15694206·J Neurol Sci·2005
6-review
Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
PMID 19151366·J Child Neurol·2009
5-case
Characterizing iron deposition in multiple sclerosis lesions using susceptibility weighted imaging.
PMID 19243035·J Magn Reson Imaging·2009
8-other
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.
PMID 19562355·Acta Neuropathol·2009
5-case
An intergenerational contraction of a fully penetrant Huntington disease allele to a reduced penetrance allele: interpretation of results and significance for risk assessment and genetic counseling.
PMID 19267413·Am J Med Genet A·2009
5-case
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
PMID 19153371·Neurology·2009
8-other
Cerebellar leukoencephalopathy: most likely histiocytosis-related.
PMID 18936429·Neurology·2008
4-observational
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia.
PMID 19016590·J Bone Miner Res·2008
8-other
17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
PMID 17594399·Clin Genet·2007
5-case
Pelizaeus-Merzbacher disease: Genetic and cellular pathogenesis.
PMID 17115121·Cell Mol Life Sci·2007
6-review
Plexiform-like neurofibromas develop in the mouse by intraneural xenograft of an NF1 tumor-derived Schwann cell line.
PMID 17335073·J Neurosci Res·2007
7-preclinical
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation.
PMID 17438221·Neurology·2007
5-case
Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.
PMID 16856127·J Comp Neurol·2006
7-preclinical
Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect.
PMID 16374829·Ann Neurol·2006
5-case
Alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-mediated excitotoxic axonal damage is attenuated in the absence of myelin proteolipid protein.
PMID 16625661·J Neurosci Res·2006
4-observational
Quantifying the carrier female phenotype in Pelizaeus-Merzbacher disease.
PMID 16778599·Genet Med·2006
8-other
Glia-specific activation of all pathways of the unfolded protein response in vanishing white matter disease.
PMID 16825957·J Neuropathol Exp Neurol·2006
7-preclinical
Splice-site contribution in alternative splicing of PLP1 and DM20: molecular studies in oligodendrocytes.
PMID 16287154·Hum Mutat·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 300 LONGWOOD AVE
BOSTON, MA 02115 - Phone
- (617) 355-6000
Quick Facts
- NPI
- 1770882359
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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