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GHOUSIA ALI, MD
MD
Adolescent Medicine (Family Medicine) Physician
NPI: 1518969518Individual
Specialties, Licenses & Credentials
Adolescent Medicine (Family Medicine) PhysicianPrimary
Family Medicine — Adolescent Medicine
Code: 207QA0000X
036084980(IL)
Research & Publications (20)
How to establish a successful revolving drug fund: the experience of Khartoum state in the Sudan.
PMID 19274366·Bull World Health Organ·2009
8-other
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·2009
8-other
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·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
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
First report of chikungunya from the Maldives.
PMID 18930301·Trans R Soc Trop Med Hyg·2009
7-preclinical
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum Genet·2008
8-other
Spatiotemporal organization of pre-mRNA splicing proteins in plants.
PMID 18630749·Curr Top Microbiol Immunol·2008
6-review
Regulation of alternative splicing of pre-mRNAs by stresses.
PMID 18630757·Curr Top Microbiol Immunol·2008
6-review
The SARS-CoV ferret model in an infection-challenge study.
PMID 18234270·Virology·2008
4-observational
Callus induction and in vitro plant regeneration of rice (Oryza sativa L.) under various conditions.
PMID 18817199·Pak J Biol Sci·2008
8-other
A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
PMID 18445047·Clin Genet·2008
8-other
Analyses of in vivo interaction and mobility of two spliceosomal proteins using FRAP and BiFC.
PMID 18414657·PLoS One·2008
8-other
Alternative splicing at NAGNAG acceptors in Arabidopsis thaliana SR and SR-related protein-coding genes.
PMID 18402682·BMC Genomics·2008
8-other
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family.
PMID 19038017·BMC Med Genet·2008
8-other
Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
PMID 18353051·Pediatr Int·2008
8-other
Serum retinol binding protein as an indicator of vitamin A status in cirrhotic patients with night blindness.
PMID 19568486·Saudi J Gastroenterol·2008
8-other
A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
PMID 18184143·Ann Hum Genet·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
- 2136 W DEVON AVE
CHICAGO, IL 60659 - Phone
- (773) 274-3060
Quick Facts
- NPI
- 1518969518
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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