Galen Cortina

Summary

Affiliation: University of California
Country: USA

Publications

  1. ncbi request reprint Enteroendocrine cell dysgenesis and malabsorption, a histopathologic and immunohistochemical characterization
    Galen Cortina
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 38:570-80. 2007
  2. doi request reprint A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption
    Steven Ohsie
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 40:1006-14. 2009
  3. pmc Diagnosis of dysplasia in upper gastro-intestinal tract biopsies through digital microscopy
    Dorina Gui
    Department of Pathology and Laboratory Medicine, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA
    J Pathol Inform 3:27. 2012
  4. pmc Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort
    Martin G Martin
    Department of Pediatrics, Division of Gastroenterology and Nutrition, Mattel Children s Hospital, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
    Gastroenterology 145:138-48. 2013
  5. pmc Serum and colonic mucosal immune markers in irritable bowel syndrome
    Lin Chang
    Center for Neurobiology of Stress, University of California, Los Angeles, California 90095 7378, USA
    Am J Gastroenterol 107:262-72. 2012
  6. ncbi request reprint Mutant neurogenin-3 in congenital malabsorptive diarrhea
    Jiafang Wang
    Department of Pediatrics, Division of Gastroenterology and Nutrition, Mattel Children s Hospital, Los Angeles, Calif, USA
    N Engl J Med 355:270-80. 2006
  7. doi request reprint Congenital visceral myopathy with a predominantly hypertrophic pattern treated by multivisceral transplantation
    Stephen Koh
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 39:970-4. 2008

Collaborators

  • S Vincent Wu
  • William R Treem
  • D G Farmer
  • Faysal Gok
  • Yaron Avitzur
  • Odul Egritas
  • Pu Qing Yuan
  • YVETTE TACHE
  • Martin G Martin
  • Dorina Gui
  • Jiafang Wang
  • Lin Chang
  • Garrett Gerney
  • Steven Ohsie
  • Stephen Koh
  • Valeria Albornoz
  • Zijun Chen
  • Deniz Engin Gok
  • Abdulrahman Al-Hussaini
  • Robert Bandsma
  • Iris Lindberg
  • R Sergio Solorzano-Vargas
  • Sarah Lawrence
  • Jessie Hulst
  • Lindsay A Pickett
  • Buket Dalgic
  • Aysen Aydogan
  • Lissy de Ridder
  • Christiane Sokollik
  • Sara Stanford
  • Michael Yourshaw
  • Senta Georgia
  • Emeran A Mayer
  • Iordanis Karagiannidis
  • David Dawson
  • Arlene Licudine
  • Sarah Dry
  • Minou Mayer
  • Iordanis Karagiannides
  • Sharat Singh
  • Hua Gong
  • Wendy Shih
  • Steve Hart
  • Elizabeth J Videlock
  • Mopelola Adeyemo
  • Collin Bowe
  • Bita Naini
  • Charalabos Pothoulakis
  • Angela P Presson
  • Doron Kahana
  • Robert F Bradley
  • Samuel W French
  • George Gershman
  • Jorge H Vargas
  • Ming Jer Tsai
  • Robert Tran
  • Ivor D Hill
  • Travis J Bailey
  • Jang Hyeon Cho
  • Laurie Reyen
  • Milan Jamrich
  • Marvin E Ament

Detail Information

Publications7

  1. ncbi request reprint Enteroendocrine cell dysgenesis and malabsorption, a histopathologic and immunohistochemical characterization
    Galen Cortina
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 38:570-80. 2007
    ..The histopathology of disease is similar to what has been found transiently in a single patient with autoimmune polyglandular syndrome type I...
  2. doi request reprint A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption
    Steven Ohsie
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 40:1006-14. 2009
    ..However, no loss of enterochromaffin cells was detected in group B. Two methods of enumerating endocrine cells were used and demonstrated 67% agreement...
  3. pmc Diagnosis of dysplasia in upper gastro-intestinal tract biopsies through digital microscopy
    Dorina Gui
    Department of Pathology and Laboratory Medicine, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, California, USA
    J Pathol Inform 3:27. 2012
    ..The aim of this study is to study the accuracy and efficiency of WSDI in the diagnosis of upper GI tract dysplasia...
  4. pmc Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort
    Martin G Martin
    Department of Pediatrics, Division of Gastroenterology and Nutrition, Mattel Children s Hospital, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
    Gastroenterology 145:138-48. 2013
    ..PC1/3 is an endoprotease that processes many prohormones expressed in endocrine and neuronal cells. We investigated clinical and molecular features of PC1/3 deficiency...
  5. pmc Serum and colonic mucosal immune markers in irritable bowel syndrome
    Lin Chang
    Center for Neurobiology of Stress, University of California, Los Angeles, California 90095 7378, USA
    Am J Gastroenterol 107:262-72. 2012
    ....
  6. ncbi request reprint Mutant neurogenin-3 in congenital malabsorptive diarrhea
    Jiafang Wang
    Department of Pediatrics, Division of Gastroenterology and Nutrition, Mattel Children s Hospital, Los Angeles, Calif, USA
    N Engl J Med 355:270-80. 2006
    ..The NEUROG3 gene (NEUROG3) is therefore a candidate for the cause of a newly discovered autosomal recessive disorder characterized by generalized malabsorption and a paucity of enteroendocrine cells...
  7. doi request reprint Congenital visceral myopathy with a predominantly hypertrophic pattern treated by multivisceral transplantation
    Stephen Koh
    Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California at Los Angeles, Los Angeles, CA 90095, USA
    Hum Pathol 39:970-4. 2008
    ..The patient had intestinal failure and the complications induced cirrhosis, eventually treated by multivisceral transplantation to correct the intestinal failure and cirrhosis...