Mr. Richard L Eddy MD
Endocrinology-Diabetes | Endocrinology, Diabetes & Metabolism
221 W Stewart Ave Suite 101 Medford OR, 97501About
Dr. Richard Eddy practices Endocrinology in Medford, OR. Dr. Eddy specializes in preventing, diagnosing, and treating diseases related to hormone imbalance, and the bodys glands in the endocrine system. Endocrinologists are trained and certified to treat a variety of conditions, including menopause, diabetes, infertility, and thyroid disorders, among many others. Dr. Eddy examines patients, determines means of testing, diagnoses, and decides the best treatment methods.
Education and Training
Jefferson Med Coll-Thos Jefferson Univ, Philadelphia Pa 1961
Sidney Kimmel Medical College at Thomas Jefferson University 1961
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Endocrinology and Metabolism
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Assignment of the gene for beta-glucuronidase (beta-GUS) to chromosome 7 in man.
- The complete derived amino acid sequence of human lysyl oxidase and assignment of the gene to chromosome 5 (extensive sequence homology with the murine ras recision gene).
- Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7.
- Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression.
- A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-gamma in myeloid cells.
- The human ribonuclease/angiogenin inhibitor is encoded by a gene mapped to chromosome 11p15.5, within 90 kb of the HRAS protooncogene.
- Human collagen gene COL5A1 maps to the q34.2----q34.3 region of chromosome 9, near the locus for nail-patella syndrome.
- Cloning of human lysyl hydroxylase: complete cDNA-derived amino acid sequence and assignment of the gene (PLOD) to chromosome 1p36.3----p36.2.
- Mapping of genes for the human C5a receptor (C5AR), human FMLP receptor (FPR), and two FMLP receptor homologue orphan receptors (FPRH1, FPRH2) to chromosome 19.
- The human connexin gene family of gap junction proteins: distinct chromosomal locations but similar structures.
- Identification of a new endothelial cell growth factor receptor tyrosine kinase.
- Epidermal type I transglutaminase (TGM1) is assigned to human chromosome 14.
- Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells.
- Three epidermal and one simple epithelial type II keratin genes map to human chromosome 12.
- Assignment of the gene for human intra-acrosomal protein SP-10 to the p12----q13 region of chromosome 11.
Treatments
- Diabetes
- Menopause
- High Cholesterol
- Osteoporosis
- Type 2 Diabetes
- Hashimoto's Thyroiditis
- Hypothyroidism
- Thyroiditis
- Vascular Disease
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