Results 31 to 40 of about 15,466 (254)
CLINICAL PATTERNS OF MALABSORPTION SYNDROMES IN CHILDREN
Malabsorption syndrome encompasses a variety of gastrointestinal disorders that impair nutrient absorption in children, presenting wide range of clinical manifestations.
Ginel Baciu+8 more
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Diagnosis and Treatment of Infectious Enteritis in Neonatal and Juvenile Ruminants. [PDF]
Common causes of infectious enteritis in neonate and juvenile ruminants include viral, bacterial, and protozoal pathogens. The most common presenting sign in ruminants with infectious enteritis is diarrhea.
Chigerwe, Munashe, Heller, Meera C
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Effect of Ferric Sodium EDTA administration, in combination with vitamin C, folic acid, copper gluconate, zinc gluconate and selenomethionine, on cardiovascular risk evaluation: exploration of the HRV frequency domain [PDF]
diseases. Using the Heart Rate Variability (HRV) analysis is possible to provide an evaluation of the safety and the effectiveness of intervention.
Curcio, A.+6 more
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A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity. [PDF]
Four siblings presented with congenital diarrhea and various endocrinopathies. Exome sequencing and homozygosity mapping identified five regions, comprising 337 protein-coding genes that were shared by three affected siblings. Exome sequencing identified
Abbasi, Montaser+11 more
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Autoimmune polyglandular syndromes
Autoimmune polyendocrine syndromes (APS) are a group of syndromes characterized by autoimmune damage of two or more endocrine glands, leading most often to their hypofunction.
V. V. Smirnov, I. D. Gurova
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A case of superior mesenteric artery syndrome
Superior mesenteric artery (SMA) syndrome, also known as Cast syndrome, Wilkie's syndrome, or duodenal ileus, is a rare condition involving compression of the duodenum between the aorta and the SMA, primarily attributed to loss of the intervening ...
Shiavax J Rao, MD+3 more
doaj
Neuroacanthocytosis (NA) syndromes are a group of genetically defined diseases characterized by the association of red blood cell acanthocytosis and progressive degeneration of the basal ganglia.
Walker Ruth H, Danek Adrian, Jung Hans H
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Outer retina changes on optical coherence tomography in vitamin A deficiency
Background Vitamin A deficiency is rare in the United States and can be missed in patients with malabsorption syndromes without a high dose of suspicion.
Meghan K. Berkenstock+2 more
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Pain in systemic connective tissue diseases [PDF]
Pain is frequent in patients with connective tissue diseases (CTDs), particularly those affected by systemic sclerosis (SSc) and systemic lupus erythematosus (SLE) in which it is virtually ubiquitous and can have different causes.
Atzeni, Fabiola+4 more
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