Monica K Andersen M.A., FAAA
Audiologist
2500 Tanglewilde Suite 160 Houston TX, 77063About
Dr. Monica Andersen is an audiologist practicing in Houston, TX. Dr. Andersen evaluates, diagnoses and treats hearing loss, balance issues and tinnitus. Audiologists can care for patients of all ages and treat almost all types of hearing loss. As an audiologist, Dr. Andersen takes part in services like prescribing and fitting hearing aids, recommending assisted listening devices and providing hearing rehabilitation. Audiologists can work in a number of settings such as hospitals, schools, clinics, private practices as well as government, military and VA hospitals.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Ifosfamide in malignant mesothelioma: a phase II study.
- Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centrom
- Therapy-related acute myeloid leukemia and myelodysplasia after high-dose chemotherapy and autologous stem cell transplantation.
- Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognos
- Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents.
- Therapy-related acute lymphoblastic leukaemia with MLL rearrangements following DNA topoisomerase II inhibitors, an increasing problem: report on two new cases and review of the literature since 1992.
- Clonal Ph-negative hematopoiesis in CML after therapy with imatinib mesylate is frequently characterized by trisomy 8.
- Causality of myelodysplasia and acute myeloid leukemia and their genetic abnormalities.
- Methylation of p15INK4B is common, is associated with deletion of genes on chromosome arm 7q and predicts a poor prognosis in therapy-related myelodysplasia and acute myeloid leukemia.
- Amplification or duplication of chromosome band 21q22 with multiple copies of the AML1 gene and mutation of the TP53 gene in therapy-related MDS and AML.
- Chronic myeloid leukaemia with BCR-ABL fusion genes located to both chromosomes 9, cyclic leukocytosis and nodal T-lymphoblastic transformation--durable complete remission following imatinib therapy.
- Mutations of genes in the receptor tyrosine kinase (RTK)/RAS-BRAF signal transduction pathway in therapy-related myelodysplasia and acute myeloid leukemia.
- Activating mutations of JAK2V617F are uncommon in t-MDS and t-AML and are only observed in atypic cases.
- FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
- Alternative genetic pathways and cooperating genetic abnormalities in the pathogenesis of therapy-related myelodysplasia and acute myeloid leukemia.
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