Ms. Denyse B Herrmann PT
Physical Therapist
Us Hwy 491 N Shiprock NM, 87420About
Denyse Herrmann is a physical therapist practicing in Shiprock, NM. Denyse Herrmann specializes in physical treatment to help a patient reduce pain, restore mobility, rehabilitate an injury, or increase movement and overall function. As a physical therapist, Denyse Herrmann can treat multiple conditions with exercises, ultrasound, electrical stimulation, joint mobilization, heat, ice, massage, laser or light therapy and more. Denyse Herrmann will create a treatment plan based on the patients specific injury or condition, and might target a specific body part or body system based on the individual.
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Expert Publications
Data provided by the National Library of Medicine- Single dose, dose-escalating trial with fozivudine tidoxil (BM 21.1290).
- Phase I/II trial with fozivudine tidoxil (BM 21.1290): a 7 day randomized,
- Preparative continuous separation of biological particles by means of free-flow magnetophoresis in a free-flow electrophoresis chamber.
- Antitumor activity of Ilmofosine (BM 41.440) in the 3Lewis-lung carcinoma model.
- Drugs in autoimmune diseases.
- In vivo antitumor activity of ilmofosine.
- Treatment of human clonogenic tumor cells and bone marrow progenitor cells with bleomycin and peplomycin under 40.5 degrees C hyperthermia in vitro.
- Synergistic enhancement of the antiproliferative activity of cis-diamminedichloroplatinum(II) by the ether lipid analogue BM41440, an inhibitor of protein kinase C.
- Phase I trial of the thioether phospholipid analogue BM 41.440 in cancer patients.
- Synthesis of thioether phosphocholine analogues.
- Pharmacokinetics of the thioether phospholipid analogue BM 41.440 in rats.
- Cytotoxic activity of the thioether phospholipid analogue BM 41.440 in primary human tumor cultures.
- Inhibition of human tumor colony formation by the new alkyl lysophospholipid ilmofosine.
- BM 41.440: a new antineoplastic, antimetastatic, and immune-stimulating drug.
- Cytotoxic ether phospholipids. Different affinities to lysophosphocholine acyltransferases in sensitive and resistant cells.
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