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MUHAMMAD RAFIQ, M.D
M.D
Internal Medicine Physician
NPI: 1851316376Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
Research & Publications (20)
An unusual presentation of pedunculated thrombus in the distal arch of the aorta after splenectomy for B-cell lymphoma.
PMID 19118744·J Vasc Surg·2008
5-case
Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3.
PMID 19344874·Am J Hum Genet·2009
8-other
Design and development of a portable gamma radiation monitor.
PMID 19655937·Rev Sci Instrum·2009
8-other
Ameliorative effect of Partysmart in rat model of alcoholic liver disease.
PMID 18335812·Indian J Exp Biol·2008
7-preclinical
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
PMID 18070203·Br J Dermatol·2008
5-case
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations.
PMID 18025408·Diabetes Care·2008
8-other
Empowering the people: development of an HIV peer education model for low literacy rural communities in India.
PMID 18423006·Hum Resour Health·2008
8-other
Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
PMID 18353051·Pediatr Int·2008
8-other
Candida parapsilosis endocarditis 8 months after transient candidemia.
PMID 17395298·Int J Cardiol·2007
5-case
NCB-02 (standardized Curcumin preparation) protects dinitrochlorobenzene- induced colitis through down-regulation of NFkappa-B and iNOS.
PMID 17373747·World J Gastroenterol·2007
7-preclinical
Induction and evaluation of atherosclerosis in New Zealand white rabbits.
PMID 16538858·Indian J Exp Biol·2006
7-preclinical
Genome assembly comparison identifies structural variants in the human genome.
PMID 17115057·Nat Genet·2006
4-observational
Relationship of peritoneal transport rate and dialysis adequacy with inflammation in peritoneal dialysis patients.
PMID 16983929·Adv Perit Dial·2006
8-other
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM gene.
PMID 16673149·Neurogenetics·2006
8-other
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.
PMID 16261342·Hum Genet·2006
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
- 1901 W HARRISON ST
CHICAGO, IL 60612 - Phone
- (312) 864-6500
Quick Facts
- NPI
- 1851316376
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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