Results 31 to 40 of about 21,572 (254)

Giardia intestinalis - atypical symptoms of infection in the daily practice of various specialists

open access: yesJournal of Education, Health and Sport, 2023
Giardia intestinalis infection is the most common parasitic infection in the world. The parasite's reservoir is mainly humans and many species of mammals. Giardiasis is a parasitic disease of the duodenum and small intestine.
Joanna Olszak   +9 more
doaj   +1 more source

A Case of Failure to Thrive- Investigation Beyond a Positive Sweat Test

open access: yesÇocuk Dergisi, 2021
Failure to thrive represents a difficult entity to define and can be associated with several diseases. Therefore, combining all the data (family history, perinatal and infancy information) with the physical examination and laboratory findings is a ...
Sara Maria Mosca Ferreira Da Silva   +5 more
doaj   +1 more source

Hashimoto's thyroiditis and autoimmune gastritis [PDF]

open access: yes, 2017
The term "thyrogastric syndrome" defines the association between autoimmune thyroid disease and chronic autoimmune gastritis (CAG), and it was first described in the early 1960s.
Brusca, Nunzia   +6 more
core   +3 more sources

Diagnosis and Treatment of Infectious Enteritis in Adult Ruminants. [PDF]

open access: yes, 2018
Infectious enteritis in adult ruminants is often a result of 1 or more viral, bacterial, or parasitic pathogens. Diagnosis of etiologic agents causing enteritis is important when considering herd implications and zoonotic potential of some etiologies ...
Chigerwe, Munashe, Heller, Meera C
core   +1 more source

Unusual manifestation of vitamin A deficiency presenting with generalized xerosis without night blindness

open access: yesClinical Case Reports, 2018
Key Clinical Message Vitamin A deficiency from malabsorption syndromes, including bariatric surgery, has become an emerging problem in developed countries. Early detection and prompt treatment lead to rapid and complete recovery.
Pariya Phanachet   +6 more
doaj   +1 more source

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]

open access: yes, 2014
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
core   +2 more sources

Time trend occurrence of duodenal intraepithelial lymphocytosis and celiac disease in an open access endoscopic population [PDF]

open access: yes, 2017
Background: Duodenal intraepithelial lymphocytosis (DIL) is a histological finding characterized by the increase of intraepithelial CD3T-lymphocytes over the normal value without villous atrophy, mostly associated to coeliac disease (CD), Helicobacter ...
Annibale, B.   +7 more
core   +2 more sources

A case of celiac disease with neurologic manifestations misdiagnosed as amyotrophic lateral sclerosis

open access: yesIntestinal Research, 2017
Celiac disease (CD) is an immune-mediated enteropathy and is a rare disease in Asia, including in Korea. However, the ingestion of wheat products, which can act as a precipitating factor of CD, has increased rapidly. CD is a common cause of malabsorption,
Hyoju Ham   +7 more
doaj   +1 more source

Central Retinal Vein Occlusion Revealing Coelic Disease

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2016
Introduction: Thrombosis has been widely reported in coeliac disease (CD) but central retinal vein occlusion (CRVO) is rarely described. Case presentation: A 27-year-old woman presented with acute visual loss and was diagnosed with CRVO.
Hana ZOUBEIDI   +3 more
doaj   +1 more source

Síndrome poliglandular autoimune tipo 1: descrição de caso e revisão da literatura [PDF]

open access: yes, 2012
Autoimmune polyendocrine syndrome type 1 (APECED) is a rare autosomal recessive disorder characterized by autoimmune multiorgan attack. The disease is caused by mutations in the autoimmune regulator gene (AIRE), resulting in defective AIRE protein, which
Dias-da-Silva, Magnus Régios   +2 more
core   +2 more sources

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