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MARYAM TARIQ, M.D
M.D
Internal Medicine Physician
NPI: 1750693446IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD60229780(WA)
Education
OTHER
Class of 2004
Research & Publications (20)
Effect of foliar application of micronutrients on the yield and quality of sweet orange (Citrus Sinensis L.).
PMID 19086544·Pak J Biol Sci·2007
8-other
Penetrating neck injury: case report and evaluation of management.
PMID 10992945·J Laryngol Otol·2000
5-case
Trithorax requires Hsp90 for maintenance of active chromatin at sites of gene expression.
PMID 19144915·Proc Natl Acad Sci U S A·2009
7-preclinical
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
PMID 19471313·Eur J Hum Genet·2009
8-other
Chromium chloride administration causes a substantial reduction of coronary lipid deposits, aortic lipid deposits, and serum cholesterol concentration in rabbits.
PMID 19225722·Biol Trace Elem Res·2009
7-preclinical
Impact of prior antibiotic use in culture-negative endocarditis: review of 86 cases from southern Pakistan.
PMID 19131263·Int J Infect Dis·2009
8-other
Haplotype analysis of two X-chromosome STR clusters in the Pakistani population.
PMID 19011887·Int J Legal Med·2009
8-other
Outbreak of dengue fever in Karachi 2006: a clinical perspective.
PMID 19534364·J Pak Med Assoc·2009
8-other
Pentoxifylline attenuates iminodipropionitrile-induced behavioral abnormalities in rats.
PMID 19584713·Behav Pharmacol·2009
7-preclinical
Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
PMID 18805827·J Med Genet·2009
8-other
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
PMID 19221800·Hum Genet·2009
5-case
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
PMID 19551394·Arch Dermatol Res·2009
8-other
Relationship between anti-acetylcholine receptor antibody titres and severity of myasthenia gravis.
PMID 19438131·J Pak Med Assoc·2009
4-observational
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
Synthesis, characterization and hypoglycemic activity of Zn(II), Cd(II) and Hg(II) complexes with glibenclamide.
PMID 18239301·Chem Pharm Bull (Tokyo)·2008
7-preclinical
Effects of subchronic versus acute in utero exposure to dexmedetomidine on foetal developments in rats.
PMID 18816303·Basic Clin Pharmacol Toxicol·2008
7-preclinical
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia.
PMID 18688569·J Hum Genet·2008
8-other
Characteristics of superficial fungal infections in the Riyadh region of Saudi Arabia.
PMID 18289321·Int J Dermatol·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 21601 76TH AVE W
EDMONDS, WA 98026 - Phone
- (425) 640-4000
Quick Facts
- NPI
- 1750693446
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 22
- Publications
- 20
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