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HIBA DAGHER, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1609678937Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (18)
Rhinovirus 3C protease can localize in the nucleus and alter active and passive nucleocytoplasmic transport.
PMID 19403669·J Virol·2009
7-preclinical
T-cell cytokine profiles are altered in childhood asthma exacerbation.
PMID 19192232·Respirology·2009
8-other
Transforming growth factor-beta enhances rhinovirus infection by diminishing early innate responses.
PMID 19168696·Am J Respir Cell Mol Biol·2009
8-other
A prospective study of the volume of pleural fluid required for accurate diagnosis of malignant pleural effusion.
PMID 19017891·Chest·2009
8-other
Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
PMID 17071739·Nephrol Dial Transplant·2007
8-other
Prognostic outcomes after the initiation of an electronic telemedicine intensive care unit (eICU) in a rural health system.
PMID 17058472·S D Med·2006
4-observational
Vascular endothelial growth factor induction by rhinovirus infection.
PMID 16555282·J Med Virol·2006
4-observational
Delayed intracranial vasospasm following carotid endarterectomy.
PMID 16088117·Cerebrovasc Dis·2005
5-case
Rhinovirus infects primary human airway fibroblasts and induces a neutrophil chemokine and a permeability factor.
PMID 15714497·J Med Virol·2005
8-other
Rhinovirus detection: comparison of real-time and conventional PCR.
PMID 15041207·J Virol Methods·2004
4-observational
Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis.
PMID 12776268·Am J Kidney Dis·2003
8-other
Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome.
PMID 12325029·Hum Mutat·2002
8-other
A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome.
PMID 11728953·Am J Kidney Dis·2001
4-observational
COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.
PMID 11473630·Kidney Int·2001
8-other
Ocular clues to the nature of disease causing end-stage renal failure.
PMID 10692536·Nephrol Dial Transplant·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
- 17201 I 45 S
THE WOODLANDS, TX 77385 - Phone
- (936) 290-1322
Quick Facts
- NPI
- 1609678937
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 18
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