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ESRAA ISMAIL, MD
MD
Pediatrics Physician
NPI: 1346728227Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
4301116190(MI)
Research & Publications (20)
Characterization of temperate Lactobacillus gasseri phage LgaI and its impact as prophage on autolysis of its lysogenic host strains.
PMID 19296164·Curr Microbiol·2009
8-other
A case of non-O:1 Vibrio cholerae septicemia with meningitis, cerebral abscess and unilateral hydrocephalus in a preterm baby.
PMID 11681447·Eur J Clin Microbiol Infect Dis·2001
5-case
Kinetic evidence for the occurrence of independent ion-exchange processes in the cationic micellar-mediated reaction of piperidine with anionic phenyl salicylate.
PMID 19449852·J Phys Chem A·2009
8-other
Expression of recombinant human epidermal growth factor in Escherichia coli and characterization of its biological activity.
PMID 18556814·Appl Biochem Biotechnol·2008
8-other
Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
PMID 17365005·Hemoglobin·2007
8-other
Arthroscopy versus arthrocentesis. A retrospective study of disc displacement management without reduction.
PMID 17914517·Saudi Med J·2007
4-observational
HO-1 and VGEF gene expression in human arteries with advanced atherosclerosis.
PMID 16999951·Clin Biochem·2006
8-other
Working together to rebuild health care in post-conflict Somaliland.
PMID 16997666·Lancet·2006
8-other
Allgrove syndrome with features of familial dysautonomia: a novel mutation in the AAAS gene.
PMID 16938764·Acta Paediatr·2006
5-case
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
PMID 15738392·Proc Natl Acad Sci U S A·2005
8-other
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.
PMID 15024727·Hum Mutat·2004
8-other
Evaluation of blood units with isolated anti HBC for the presence of HBV DNA.
PMID 12515905·Dis Markers·2002
8-other
Chronic infantile neurological cutaneous articular syndrome in an Arab patient.
PMID 11737717·Pediatr Int·2001
5-case
Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency.
PMID 11668614·Hum Mutat·2001
5-case
Effects of Nonionic and Mixed Cationic-Nonionic Micelles on the Rate of Alkaline Hydrolysis of 4-Nitrophthalimide.
PMID 11482975·J Colloid Interface Sci·2001
8-other
Incomplete form of chronic infantile neurological cutaneous and articular syndrome.
PMID 11059560·Pediatr Int·2000
8-other
Carbonyl reductase: a novel metastasis-modulating function.
PMID 10728668·Cancer Res·2000
4-observational
A fatal small dose of phosphate enema in a young child with no renal or gastrointestinal abnormality.
PMID 10697146·J Pediatr Gastroenterol Nutr·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 5303 S CEDAR ST STE 205
LANSING, MI 48911 - Phone
- (517) 887-4305
Quick Facts
- NPI
- 1346728227
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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