Results 161 to 170 of about 11,223 (226)
Suspected hyperthyroidism‐associated myoclonus in a cat
Abstract A 10‐year‐old, male, neutered domestic shorthair cat presented with a 2‐week history of progressively worsening myoclonic jerks predominantly involving the head. Jerks were continuous and marked at rest, but became less intense during activity.
Magdalena Maria Dyrka +5 more
wiley +1 more source
Hypocortisolaemia with gastrointestinal haemorrhage in a young cat
Abstract An 8‐month‐old, female, spayed domestic shorthair presented with a 1‐week history of lethargy and anorexia. On admission, the cat had severe hypoglycaemia, and hypovolaemic and distributive shock were suspected. Mucosal defects identified by ultrasonography were suggestive of gastrointestinal ulceration.
Victoria J. Skinner +2 more
wiley +1 more source
ABSTRACT Cystitis is common during pregnancy and requires effective antibiotic treatment to prevent complications. Gastric bypass surgery alters gastrointestinal anatomy and may impair oral drug absorption, raising concerns about antibiotic effectiveness.
Mette Østergaard Thunbo +5 more
wiley +1 more source
Vitamin D: Physiology, Pharmacology and Clinical Evidence for Supplementation—A Narrative Review
ABSTRACT Vitamin D is a nutrient and prohormone obtained from diet and supplements and synthesized in the skin. It is essential for calcium and phosphate homeostasis and skeletal health and influences multiple extra‐skeletal processes, yet deficiency remains common worldwide.
Jyrki K. Virtanen
wiley +1 more source
Frequency and Timing of Specialized Formula Prescriptions for Children Under 2 Years
We analysed routinely collected primary care data from the United Kingdom for children aged under 2 years. We found prescriptions for specialized formulas such as extensively hydrolysed formula or amino‐acid formula increased five‐fold between 2009 and 2025.
Nikita Punjabi +8 more
wiley +1 more source
Outcomes of children with cerebral palsy receiving long‐term respiratory support. This systematic review is commented by Cooper on pages 1492–1493 of this issue. Abstract Aim To systematically review the current knowledge gap in, and impact of, long‐term respiratory support in children and young people (CYP) with cerebral palsy (CP). Method We searched
Rajkumar Dhandayuthapani +5 more
wiley +1 more source
Summary Background Equine squamous gastric disease (ESGD) and equine glandular gastric disease (EGGD) can be treated with oral omeprazole, combined with sucralfate or an extended‐release intramuscular omeprazole (ERIO). Objectives To evaluate these different treatments for ESGD and EGGD and assess the influence of inflammatory bowel disease (IBD) on ...
L. C. Kranenburg +6 more
wiley +1 more source
Rare Variants in PFIC‐Related Genes Among Adults With Intrahepatic Cholestasis
ABSTRACT Aim Biallelic pathogenic variants in progressive familial intrahepatic cholestasis (PFIC)‐related genes cause severe pediatric cholestasis. However, the clinical significance of heterozygous variants in adult intrahepatic cholestasis remains unclear.
Shunji Hirose +9 more
wiley +1 more source
There are may causes for the development of the malabsorption syndrome but in our opinion disturbances in the enzymatic digestion of fats, proteins and carbohydrates occupy a very important place. We have discussed how these enzyme deficiencies may cause
J R, ROSS, F W, NUGENT
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Current Treatment Options in Gastroenterology, 2008
Lactose malabsorption is a syndrome producing constellation of symptoms, including abdominal pain, bloating, flatulence, diarrhea, and sometimes nausea and/or vomiting. Primary causes of lactose malabsorption due to loss of intestinal lactase activity include genetic/racial lactase nonpersistence, congenital lactase deficiency, and developmental ...
Richard J, Grand, Robert K, Montgomery
openaire +2 more sources
Lactose malabsorption is a syndrome producing constellation of symptoms, including abdominal pain, bloating, flatulence, diarrhea, and sometimes nausea and/or vomiting. Primary causes of lactose malabsorption due to loss of intestinal lactase activity include genetic/racial lactase nonpersistence, congenital lactase deficiency, and developmental ...
Richard J, Grand, Robert K, Montgomery
openaire +2 more sources

