Sökning: "polycystic kidney disease"

Visar resultat 1 - 5 av 6 avhandlingar innehållade orden polycystic kidney disease.

  1. 1. Renal and extrarenal signs of autosomal dominant polycystic kidney disease

    Författare :Henrik Hadimeri; Göteborgs universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; autosomal dominant polycystic disease; extrarenal manifestations; arterial aneurysms; arterio-venous fistulas; continuous ambulatory peritoneal dialysis; echocardiography;

    Sammanfattning : The aim of the study was to evaluate the clinical impact of renal and extrarenal manifestations of ADPKD (Autosomal Dominant Polycystic Kidney Disease). For this purpose, prospective and retrospective analyses of patients with ADPKD in different populations were performed. LÄS MER

  3. 2. Dysregulation of the immune system in chronic kidney disease and the impact on disease manifestations and co-morbidity

    Författare :Senka Sendic; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Background: Chronic kidney disease (CKD) is associated with an increased risk of cardiovascular disease and infections. Both conditions share the same underlying cause comprising of changes in innate and adaptive immunity. LÄS MER

  4. 3. Development of benzoquinoquinoxaline derivatives as triplex-specific probes : Recognition of DNA structures at repeats sequences

    Författare :Helen Bergquist; Rula Zain; Keith Fox; Stockholms universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; Triplex; H-DNA; BQQ; BQQ-OP; BQQ-Bodipy; triplet repeat; DNA; non-B-DNA; pkd1; frataxin; Friedreich s ataxia; Molecular biology; Molekylärbiologi; Molecular Biology; molekylärbiologi;

    Sammanfattning : Repeat sequences are associated with several human diseases, such as Friedreich’s ataxia, polycystic kidney disease and cancer. These sequences can form non-B-DNA structures, including triplex (H-DNA) DNA, and are associated with genomic instability and altered gene expression. LÄS MER

  5. 4. Molecular mechanisms of tumor development in hyperparathyroidism

    Författare :Filip Farnebo; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :parathyroid; hyperparathyroidism; MEN 1; FIHP; loss of heterozygosity; comparative genomic hybridization; mutation analysis; in situ hybridization;

    Sammanfattning : Loss of heterozygosity (LOH) analysis and comparative genomic hybridization (CGH) were used in an attempt to identify recurrent chromosomal alterations in different types of parathyroid tumors. These included familial and sporadic, benign and malignant, as well as primary, irradiation associated and secondary tumors. LÄS MER

  7. 5. Factors affecting the physical characteristics of arterio-venous fistula in patients with renal failure

    Författare :Ursula Hadimeri; Sven Göran Fransson; Bernd Stegmayr; Elisabeth Kenne Sarenmalm; Anders Magnusson; Linköpings universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES;

    Sammanfattning : Background and PurposeA patent access is vital for a dialysis patient. The arterio-venous fistula (AVF), the most important access for haemodialysis (HD), is frequently affected by extensive complications such as stenosis and occlusions. LÄS MER