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ROBERT WOLLMANN, MD
MD
Anatomic Pathology Physician
NPI: 1376695056Individual
Specialties, Licenses & Credentials
Anatomic Pathology PhysicianPrimary
Pathology — Anatomic Pathology
Code: 207ZP0101X
Research & Publications (20)
The interaction between cytoplasmic prion protein and the hydrophobic lipid core of membrane correlates with neurotoxicity.
PMID 16537534·J Biol Chem·2006
7-preclinical
Fingolimod and related compounds in a spontaneous autoimmune polyneuropathy.
PMID 19647880·J Neuroimmunol·2009
7-preclinical
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome.
PMID 19251977·J Med Genet·2009
5-case
Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS.
PMID 18987190·J Neurosci·2008
7-preclinical
Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection.
PMID 18947414·J Neuroinflammation·2008
7-preclinical
A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelination.
PMID 18400855·J Virol·2008
7-preclinical
Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene.
PMID 18160659·J Neurosci·2007
7-preclinical
Diminishing apoptosis by deletion of Bax or overexpression of Bcl-2 does not protect against infectious prion toxicity in vivo.
PMID 18032675·J Neurosci·2007
4-observational
Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome.
PMID 17853947·J Clin Invest·2007
7-preclinical
Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations.
PMID 17594401·Clin Genet·2007
5-case
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex.
PMID 17336067·Neuromuscul Disord·2007
8-other
Cytosolic prion protein toxicity is independent of cellular prion protein expression and prion propagation.
PMID 17182694·J Virol·2007
4-observational
Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model.
PMID 16815027·Neurobiol Dis·2006
7-preclinical
Degenerative spine disease : pathologic findings in 985 surgical specimens.
PMID 16393686·Am J Clin Pathol·2006
8-other
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice.
PMID 16380713·Nat Genet·2006
7-preclinical
Ganglioneuromatous paraganglioma of the cauda equina--a pathological case study.
PMID 15892009·Hum Pathol·2005
5-case
K+ channel blockade impairs remyelination in the cuprizone model.
PMID 15378653·Glia·2004
7-preclinical
Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
PMID 14991812·Ann Neurol·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 180 HARVESTER DR STE 110
BURR RIDGE, IL 60527 - Phone
- (773) 834-4064
Quick Facts
- NPI
- 1376695056
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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