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JOHN ROSELL, MD
MD
Family Medicine Physician
NPI: 1972814648IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine Physician
Emergency Medicine
Code: 207P00000X
Q4681(TX)
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
Q4681(TX)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
OTHER
Class of 2010
Research & Publications (20)
Combined use of MSWI bottom ash and fly ash as aggregate in concrete formulation: environmental and mechanical considerations.
PMID 19427118·J Hazard Mater·2009
8-other
Universal foliage-stem scaling across environments and species in dicot trees: plasticity, biomechanics and Corner's Rules.
PMID 19141123·Ecol Lett·2009
8-other
TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.
PMID 19458060·Nephrol Dial Transplant·2009
5-case
Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations.
PMID 17999439·Hum Mutat·2008
8-other
Risk factors for local recurrence in patients with pTa/pT1 urinary bladder cancer.
PMID 18609266·Scand J Urol Nephrol·2008
8-other
Reliability of death certificates in prostate cancer patients.
PMID 18609293·Scand J Urol Nephrol·2008
8-other
Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion.
PMID 18384142·Am J Med Genet A·2008
5-case
Dissection of the ascending aorta in a patient with HLA-B27 associated ankylosing spondylitis.
PMID 18381776·J Rheumatol·2008
5-case
A new early Pleistocene hominin mandible from Atapuerca-TD6, Spain.
PMID 18657300·J Hum Evol·2008
7-preclinical
Comparison of segmental with whole-body impedance measurements in peritoneal dialysis patients.
PMID 17977778·Med Eng Phys·2008
4-observational
MANBA polymorphism was related to increased risk of colorectal cancer in Swedish but not in Chinese populations.
PMID 17899454·Acta Oncol·2008
4-observational
dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
PMID 17509681·Leuk Res·2008
8-other
Long-term follow-up of conservatively managed incidental carcinoma of the prostate: a multivariate analysis of prognostic factors.
PMID 17454947·Scand J Urol Nephrol·2007
8-other
Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.
PMID 17331079·Ann Hum Genet·2007
8-other
Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.
PMID 17377518·Eur J Hum Genet·2007
8-other
Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications.
PMID 17397557·BMC Med Genet·2007
8-other
Whole-body and thoracic bioimpedance measurement: hypertension and hyperhydration in hemodialysis patients.
PMID 18002774·Annu Int Conf IEEE Eng Med Biol Soc·2007
3-trial
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).
PMID 16945536·Neuromuscul Disord·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 5201 HARRISBURG BLVD STE C
HOUSTON, TX 77011 - Phone
- (713) 558-3333
Quick Facts
- NPI
- 1972814648
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 16
- Publications
- 20
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