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WOJCIECH WISZNIEWSKI, M.D.
M.D.
NPI: 1700025681IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
P1153(TX)MD174854(OR)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
OTHER
Class of 2001
Research & Publications (15)
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14.
PMID 17265047·Hum Genet·2007
8-other
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies.
PMID 16103129·Hum Mol Genet·2005
7-preclinical
Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations.
PMID 17717711·Neurogenetics·2007
5-case
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.
PMID 17701891·Am J Hum Genet·2007
7-preclinical
GJB2 mutations and degree of hearing loss: a multicenter study.
PMID 16380907·Am J Hum Genet·2005
4-observational
Curcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutants.
PMID 16252242·Am J Hum Genet·2005
8-other
SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
PMID 15776429·Hum Mutat·2005
7-preclinical
Defective class II transactivator expression in a B lymphoma cell line.
PMID 14973505·Leukemia·2004
5-case
Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II.
PMID 12618906·Immunogenetics·2003
8-other
Three novel mutations of the CIITA gene in MHC class II-deficient patients with a severe immunodeficiency.
PMID 11862382·Immunogenetics·2002
8-other
High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.
PMID 11551103·Genet Test·2001
8-other
Mutation in the class II trans-activator leading to a mild immunodeficiency.
PMID 11466404·J Immunol·2001
5-case
In vitro expression analysis of R68G and R68S mutations in phenylalanine hydroxylase gene.
PMID 11051201·Acta Biochim Pol·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3181 SW SAM JACKSON PARK RD
PORTLAND, OR 97239 - Phone
- (503) 494-9300
Quick Facts
- NPI
- 1700025681
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 25
- Publications
- 15
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