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VALERIE OJI, PHARM.D., BCPP, PHD
PHARM.D., BCPP, PHD
Psychiatric Pharmacist
NPI: 1801891841Individual
Specialties, Licenses & Credentials
Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
Pharmacist — Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
Code: 1835P0018X
31996(NC)PD149165(AR)S015140(AZ)
Pharmacist
Pharmacist
Code: 183500000X
33415(TX)S015140(AZ)
Psychiatric PharmacistPrimary
Pharmacist — Psychiatric
Code: 1835P1300X
PD149165(AR)S015140(AZ)33415(TX)
Health & Wellness Coach
Health & Wellness Coach
Code: 171400000X
Research & Publications (19)
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
PMID 19183181·Br J Dermatol·2009
8-other
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.
PMID 16968736·Hum Mol Genet·2006
8-other
Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1.
PMID 16634887·Br J Dermatol·2006
8-other
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.
PMID 19536142·J Invest Dermatol·2009
7-preclinical
Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation.
PMID 19500103·Br J Dermatol·2009
5-case
Examination of MTM opportunities in pediatric behavioral health.
PMID 19496640·J Manag Care Pharm·2009
8-other
Transglutaminase-1 and bathing suit ichthyosis: molecular analysis of gene/environment interactions.
PMID 19212342·J Invest Dermatol·2009
8-other
Ichthyoses - Part 1: Differential diagnosis of vulgar ichthyoses and therapeutic options.
PMID 19192163·J Dtsch Dermatol Ges·2009
6-review
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.
PMID 19131948·J Invest Dermatol·2009
8-other
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubules.
PMID 18795921·Br J Dermatol·2009
8-other
A newly identified splice site mutation in ZMPSTE24 causes restrictive dermopathy in the Middle East.
PMID 18671782·Br J Dermatol·2008
5-case
Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis.
PMID 18355358·Clin Exp Dermatol·2008
5-case
Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia.
PMID 17546031·Nat Genet·2007
8-other
Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patients.
PMID 17255953·J Invest Dermatol·2007
8-other
The alpha and beta subunits of the metalloprotease meprin are expressed in separate layers of human epidermis, revealing different functions in keratinocyte proliferation and differentiation.
PMID 17195012·J Invest Dermatol·2007
8-other
Topical pimecrolimus: a novel therapeutic option for Netherton syndrome.
PMID 16225628·Br J Dermatol·2005
5-case
Detection of functionally active melanocortin receptors and evidence for an immunoregulatory activity of alpha-melanocyte-stimulating hormone in human dermal papilla cells.
PMID 16081629·Endocrinology·2005
8-other
SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases.
PMID 15304086·J Invest Dermatol·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 4 locations total
- Address
- 5325 W Butler Dr # D
Glendale, AZ 85302 - Phone
- (480) 383-9330
Quick Facts
- NPI
- 1801891841
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 9
- Locations
- 4
- Publications
- 19
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