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KATHARINE WALZ, M.D.
M.D.
Pediatrics Physician
NPI: 1487048377Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
A156113(CA)ML60561485(WA)MD213339(OR)
Research & Publications (15)
Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).
PMID 17024248·J Clin Invest·2006
7-preclinical
Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2).
PMID 14709593·Hum Mol Genet·2004
7-preclinical
Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.
PMID 12724422·Mol Cell Biol·2003
7-preclinical
Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.
PMID 18469339·Hum Mol Genet·2008
7-preclinical
Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)].
PMID 16566870·J Child Neurol·2006
8-other
Emergency Nursing Pediatric Course (ENPC): the new 3rd Edition.
PMID 15834392·J Emerg Nurs·2005
8-other
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.
PMID 15565467·Hum Genet·2004
7-preclinical
Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.
PMID 15459175·Hum Mol Genet·2004
4-observational
Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits.
PMID 15338647·Cold Spring Harb Symp Quant Biol·2003
6-review
COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast.
PMID 12972600·Mol Cell Biol·2003
4-observational
cDNA cloning, biochemical and phylogenetic characterization of beta- and beta'-subunits of Candida albicans protein kinase CK2.
PMID 12722181·Yeast·2003
8-other
Frontal lobe activation during object permanence: data from near-infrared spectroscopy.
PMID 12202098·Neuroimage·2002
8-other
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse.
PMID 11997338·Genome Res·2002
4-observational
[Liposuction for "body contouring" in gynecology].
PMID 11340956·Zentralbl Gynakol·2001
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
- 2825 E BARNETT RD
MEDFORD, OR 97504 - Phone
- (541) 789-7000
Quick Facts
- NPI
- 1487048377
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 15
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