Sökning: "the infantile"
Visar resultat 16 - 20 av 29 avhandlingar innehållade orden the infantile.
16. Structural chromosomal aberrations and neuropsychiatric disorders
Sammanfattning : Infantile autism (IA) is a severe neurodevelopment disorder with a complex genetic predisposition. The underlying causes of autism are still not understood. LÄS MER
17. An exploratory journey into probiotic interactions : Bioactive properties of Limosilactobacillus reuteri and Bifidobacterium longum
Sammanfattning : Probiotics are defined as live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. The mechanisms by which probiotics affect the host are based on one of two principles: i) directly, by interacting with specific targets, or ii) indirectly, by contributing to the ecological niche constructions of the microbiota. LÄS MER
18. Enteric adenovirus type 41 : genome organization and specific detection procedures
Sammanfattning : Enteric adenoviruses (EAd) types 40 and 41 (Ad40 and Ad41) representing subgenus F, are primary pathogens of children being second only to rotaviruses as the most important cause of infantile diarrhea.The EAds differ from all other adenoviruses in their inability to grow in most conventional established cell lines and have been suggested to be deficient in some early gene functions since they could be complemented by Ad 5 early regions EIA and E1B. LÄS MER
19. Passive immunisation as therapy for gastrointestinal infections in children
Sammanfattning : Several prophylactic studies in animals and humans have shown potential efficacy of oral therapy with non-human antibodies against different pathogens. Passive immunisation with oral antibodies against different pathogens is an attractive way to treat different gastrointestinal infections caused by pathogens such as rotavirus or enteropathogenic and enterotoxigenic Escherichia coli (EPEC; ETEC). LÄS MER
20. Chorangiomas : histopthological, clinical and genetic studies
Sammanfattning : Chorangioma (CA), although, is the most common non-trophoblastic, vascular, tumor-likelesion of the placenta with incidence approximately 0.5-1% of all examined placentas, the specific etiology and genetic background of these lesions is still poorly understood. LÄS MER