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CHARLES STROM, M.D.
M.D.
Surgery Physician
NPI: 1336378629Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
240846(MA)
Research & Publications (20)
[Perioperative antiarrhythmic drug management].
PMID 11573125·Anasthesiol Intensivmed Notfallmed Schmerzther·2001
6-review
Neonatal outcome of preimplantation genetic diagnosis by polar body removal: the first 109 infants.
PMID 11015504·Pediatrics·2000
8-other
Obstetric outcomes in 102 pregnancies after preimplantation genetic diagnosis.
PMID 10871489·Am J Obstet Gynecol·2000
8-other
Journals under threat: a joint response from history of science, technology and medicine editors.
PMID 19496523·Medizinhist J·2009
8-other
Plasma ghrelin and growth hormone regulation in response to metabolic state in hybrid striped bass: effects of feeding, ghrelin and insulin-like growth factor-I on in vivo and in vitro GH secretion.
PMID 19523371·Gen Comp Endocrinol·2009
7-preclinical
Apparent homozygosity of a novel frame shift mutation in the CFTR gene because of a large deletion.
PMID 19324987·J Mol Diagn·2009
5-case
Spherulitic networks: from structure to rheological property.
PMID 19292435·J Phys Chem B·2009
8-other
Leptin stimulates pituitary prolactin release through an extracellular signal-regulated kinase-dependent pathway.
PMID 18252950·J Endocrinol·2008
7-preclinical
Prevalence of known mutations in the familial Mediterranean fever gene (MEFV) in various carrier screening populations.
PMID 18496034·Genet Med·2008
8-other
Development of a novel, accurate, automated, rapid, high-throughput technique suitable for population-based carrier screening for Fragile X syndrome.
PMID 17438383·Genet Med·2007
4-observational
Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene.
PMID 17690208·J Mol Diagn·2007
8-other
Multiple property tolerance analysis for the evaluation of missense mutations.
PMID 19455225·Evol Bioinform Online·2007
8-other
Development of a web-based query tool for quality assurance of clinical molecular genetic test results.
PMID 17251341·J Mol Diagn·2007
8-other
Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.
PMID 17224689·Genet Med·2007
8-other
Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish population.
PMID 16645217·J Mol Diagn·2006
8-other
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype.
PMID 16778595·Genet Med·2006
8-other
Technical validation of a TM Biosciences Luminex-based multiplex assay for detecting the American College of Medical Genetics recommended cystic fibrosis mutation panel.
PMID 16825511·J Mol Diagn·2006
4-observational
Prenatal diagnosis for primary congenital glaucoma (bupthalmous).
PMID 16941518·Prenat Diagn·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
- Address
- 736 CAMBRIDGE ST
BRIGHTON, MA 02135 - Phone
- (617) 789-2990
Quick Facts
- NPI
- 1336378629
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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