Malabsorption syndromes - Open Access .click

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Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes

Histochemistry and Cell Biology, 2007
We investigated, for the first time, the expression of I- and L-FABP in two very rare hereditary lipid malabsorption syndromes as compared with normal subjects.
Claude Besmond, V Petit, L P Aggerbeck
exaly +2 more sources

Some of the next articles are maybe not open access.

Malabsorption Syndromes and Food Intolerance

Clinics in Perinatology, 2022
exaly

Prevalence of Lactose Malabsorption in a Finnish Rural Population

Scandinavian Journal of Gastroenterology, 1970
M Isokoski, J Jussila
exaly

The D-Xylose Absorption Test in Malabsorption Syndromes

New England Journal of Medicine, 1957
J A Benson
exaly

Secondary Malabsorption Syndromes of Intestinal Origin

Postgraduate Medicine, 1959
Paul A Green, Harold H Scudamore
exaly

The Malabsorption Syndromes

Pediatric Clinics of North America, 1967
J W Gerrard
exaly

Absorption of Copper in Malabsorption Syndromes*

Journal of Clinical Investigation, 1964
Irmin Sternlieb, I Sternlieb, Henry D Janowitz +2 more
exaly

Malabsorption syndromes in the horse

Equine Veterinary Education, 2006
exaly

The Paraneoplastic Syndromes

Ca-A Cancer Journal for Clinicians, 1968
exaly

OSTEOPENIA IN CHILDREN WITH MALABSORPTION SYNDROM [PDF]

Romanian Journal of Pediatrics, 2016
Introduction. Malabsorption syndromes result in the disturbance of bone normal development and function. Objective. The assessment of bone density in children with malabsorption syndromes. The analysis of risk factors for osteopenia.
Tania Elena Rusu +5 more
doaj +3 more sources

celiac disease
medicine
gastroenterology

diseases of the digestive system
vitamin a deficiency
malabsorption

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