Education

Fellowship
Pediatrics/Gastroenterology, UCLA School of Medicine, 1992
Residency
Pediatrics, Harbor - UCLA Medical Center, 1988
Internship
Pediatrics, Harbor - UCLA Medical Center, 1986
Degree
MD, Harvard Medical School, 1985

State License

G59974
  • About Me

    Links

  • Locations

    UCLA Children's Health Center

    (primary location)
    Address
    200 UCLA Medical Plaza
    Suite 265
    Los Angeles, California 90095
    Phone
    310-825-0867
    Address
    757 Westwood Plaza
    Los Angeles, California 90095
    Phone
    310-825-9111
  • Education

    Education

    Fellowship
    Pediatrics/Gastroenterology, UCLA School of Medicine, 1992
    Residency
    Pediatrics, Harbor - UCLA Medical Center, 1988
    Internship
    Pediatrics, Harbor - UCLA Medical Center, 1986
    Degree
    MD, Harvard Medical School, 1985
  • Clinical Interests
    • General Gastroenterology
    • Liver Transplantation
  • Research

    Research Interest

    Pediatric Diarrheal Disorders, Enteroendocrine Cell Development, Neurogenin-3, Intestinal Stem Cells

    Publications

    1. Kahana, D., Martín, M.G., 2008. Development of Gastrointestinal Function. Pediatric Nutrition Handbook, 6th Edition, Chapter 1. American Academy of Pediatrics.
    2. Martín, M.G. and Wright, E.M., 2008. Disorders of Epithelial Transport in the Small Intestine–Textbook of Gastroenterology, 5th edition. Editors: Yamada, T.; Alpers, D.H., Laine, L. Owyang, C., Powell, D.W.
    3. Martín, M.G. and Wright, E.M., 2008. Congenial intestinal transport defects – Pediatric Gastrointestinal Disease Textbook. 5th edition. Editors: Walker, W.A., Goulet, O., Kleinman, R.A., Sherman, P.M., Schneider, B.L., Sanderson, I.R.
    4. Kahana, D., Ulshen, M.H., Martín, M.G., 2007. Carbohydrate Absorption and Malabsorption. Nutrition in Pediatrics, 4th Edition, Chapter 61. Editors: Walker, W.A.
    5. Ohsie, S., Gerney, G., Gui, D., Kahana, D., Martín, M.G., Cortina, G. 2009 A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption. Hum Pathology. 40(7):1006-14.
    6. Cortina G., Burge, C.N., Farmer, D.G., Bhuta, S., Treem, W.R., Hill, I.D., Martín, M.G. 2007. Enteroendocrine cell dysgenesis and malabsorption, a histopathological and immunohistochemical characterization. Human Pathology. 38(4):570-80.
    7. Wang, J., Cortina, G., Wu, S.V., Tran, R., Cho, J.-H., Bailey, T. J., Jamrich, M., Tsai, M.-J., Ament, M.E., Treem, W.R., Hill, I.D., Vargas, J. H., Farmer, D.G., Reyen, L., Martín, M.G. 2006. Mutant Neurogenin-3 in Congenital Malabsorptive Diarrhea. New England Journal of Medicine. 355; 3: 270-280.
    8. Martín, M.G., Turk, E., Lostao, M.P., Kerner, C., Wright, E.M. 1996. Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption. Nature Genetics 12:216-220.
    9. Martín, M.G., Lostao, M.P., Turk, E., Lam, J.T., Kreman, M. Wright, E.M. 1997. Compound missense mutations in sodium/D-glucose cotransporter (SGLT1) results in trafficking defects. Gastroenterology 112:1206-1212.
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