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Topic:Abdominal

Research in the abdominal health and conditions category examines digestive physiology, gastrointestinal disorders, and treatment protocols in horses. This page compiles peer-reviewed studies and journal articles on the pathophysiology of common digestive issues, diagnostic techniques for conditions like colic and gastric ulcers, and evaluations of various treatment strategies.
An improved method for preparation of follicle stimulating and luteinizing hormones from horse pituitary glands.
Biochimica et biophysica acta    July 8, 1965   Volume 104, Issue 2 496-502 doi: 10.1016/0304-4165(65)90355-7
Saxena BB, Henneman PH.No abstract available
Immunological and Electrophoretic Properties of Equine Luteinizing Hormone.
Journal of animal science    May 1, 1965   Volume 24 347-354 doi: 10.2527/jas1965.242347x
DESJARDINS C, HAFS JD.No abstract available
PREPARATION OF EQUINE LUTEINIZING HORMONE.
Endocrinology    April 1, 1965   Volume 76 762-765 doi: 10.1210/endo-76-4-762
REICHERT LE, WILHELMI AE.No abstract available
The standing position for abdominal cryptorchidectomy in the horse.
Journal of the American Veterinary Medical Association    July 15, 1959   Volume 135, Issue 2 102-103 
BURGER CH.No abstract available
Gonadotropic activity of equine gonadotropin in combination with zinc.
The American journal of physiology    November 1, 1945   Volume 145 28-31 doi: 10.1152/ajplegacy.1945.145.1.28
LEATHEM JH.No abstract available
T-shaped malformation of the ventral colon in a Thoroughbred filly with colic.
   March 17, 2026  
A 4-month-old Thoroughbred filly presented for abdominal pain was diagnosed with a T-shaped malformation of the ventral colon at exploratory laparotomy. Following resection and anastomosis of the large colon, no further episodes of abdominal pain occurred during a 12-month follow-up. Acute dehiscence of the linea alba occurred as a complication of the initial laparotomy, but was successfully managed following additional surgical repair. T-shaped malformation of the ventral colon has not previously been reported and is considered a congenital malformation of mesocolon formation.
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