Michelle Ignacio Manzano
Occupational Therapist
800 4TH ST SW APT N406 WASHINGTON DC, 20024About
Dr. Michelle Manzano practices Occupational Medicine in WASHINGTON, DC. Dr. Manzano evaluates the interaction between work and health. Occupational medicine physicians have general knowledge of worksite operations and are familiar with the toxic properties of materials used by employees and the potential hazards and stressors of work processes; in addition to being qualified to determine an employees physical and emotional fitness for work; diagnosing and treating occupational diseases; handling work related injuries; and having an understanding of rehabilitation methods, health education techniques, sanitation, and workers compensation laws.
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Expert Publications
Data provided by the National Library of Medicine- Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP.
- Differential response of human interferon-beta promoter elements to trans-activation by HSV VP16 and IRF-1.
- Detection of frequent BglII polymorphism by polymerase chain reaction and TaqI restriction fragment length polymorphism for 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4 isomerase at the human HSD beta 3 locus (1p11-p13).
- Synergism between distinct enhanson domains in viral induction of the human beta interferon gene.
- Induction of human interferon gene expression is associated with a nuclear factor that interacts with the NF-kappa B site of the human immunodeficiency virus enhancer.
- [Laryngeal pathology and occupational exposure to glass fibers. Does a cancerous risk exist?].
- Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21.
- Genetic linkage mapping of HSD3B1 and HSD3B2 encoding human types I and II 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase close to D1S514 and the centromeric D1Z5 locus.
- Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families.
- Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani origin.
- Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients.
- The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds.
- Genetic linkage mapping of the human steroid 5 alpha-reductase type 2 gene (SRD5A2) close to D2S352 on chromosome region 2p23-->p22.
- Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13.
- Recognition properties of a sequence-specific DNA binding antibody.
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2041 GEORGIA AVE NW WASHINGTON DC 20060