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THOMAS ROSENBERG, MD
MD
Exclusive Provider Organization
NPI: 1235245853Individual
Specialties, Licenses & Credentials
Allergy & Immunology Physician
Allergy & Immunology
Code: 207K00000X
0414905(KS)
Exclusive Provider OrganizationPrimary
Exclusive Provider Organization
Code: 302F00000X
14905(KS)
Research & Publications (20)
Cell density of the lamina propria of neonatal vocal folds.
PMID 19326757·Ann Otol Rhinol Laryngol·2009
4-observational
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations.
PMID 15557429·Invest Ophthalmol Vis Sci·2004
5-case
A DNA vaccine targeting the receptor-binding domain of Clostridium difficile toxin A.
PMID 19464540·Vaccine·2009
7-preclinical
Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism.
PMID 19060277·Invest Ophthalmol Vis Sci·2009
8-other
A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe Islands.
PMID 18669544·Br J Ophthalmol·2009
8-other
Disparities in cesarean delivery rates and associated adverse neonatal outcomes in New York City hospitals.
PMID 19461418·Obstet Gynecol·2009
8-other
COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus.
PMID 19387081·Invest Ophthalmol Vis Sci·2009
8-other
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract.
PMID 19182255·Invest Ophthalmol Vis Sci·2009
8-other
An international collaborative family-based whole-genome linkage scan for high-grade myopia.
PMID 19324860·Invest Ophthalmol Vis Sci·2009
4-observational
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.
PMID 19098318·Invest Ophthalmol Vis Sci·2009
8-other
Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patients.
PMID 18203199·Am J Med Genet A·2008
8-other
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
PMID 18183041·Eur J Hum Genet·2008
5-case
Statistical modeling of global geogenic fluoride contamination in groundwaters.
PMID 18546705·Environ Sci Technol·2008
8-other
Coronary spasm after an adenosine stress test: an adverse effect of a vasodilator.
PMID 18664034·Acta Cardiol·2008
5-case
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
PMID 18235024·Invest Ophthalmol Vis Sci·2008
8-other
Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.
PMID 18273898·Hum Mutat·2008
8-other
Prevalence of age-related maculopathy and age-related macular degeneration among the inuit in Greenland. The Greenland Inuit Eye Study.
PMID 18267341·Ophthalmology·2008
8-other
Hepatitis C NS5B polymerase inhibitors: 4,4-Dialkyl-1-hydroxy-3-oxo-3,4-dihydronaphthalene-3-yl benzothiadiazine derivatives.
PMID 18599294·Bioorg Med Chem Lett·2008
7-preclinical
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
PMID 18552978·Mol Vis·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
- 8535 E 21ST ST N
WICHITA, KS 67206 - Phone
- (316) 609-2385
Quick Facts
- NPI
- 1235245853
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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