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Showing 1 to 13 of 13 for “"leukoencephalopathy"”.

  1. Hereditary diffuse leukoencephalopathy with spheroids: Insights into an adult onset neurodegenerative disease

    … of adult-onset WM disorders. Hereditary diffuse leukoencephalopathy with spheroids (HDLS) is an adult-onset, invariably lethal, brain WM disorder with an autosomal dominant inheritance pattern. The clinical symptoms are characterized by a constellation of features that progress to a devastating …

    goteborg Repository record for Hereditary diffuse leukoencephalopathy with spheroids: Insights into an adult onset neurodegenerative disease (opens in a new tab)

  2. Möglichkeiten der computertomographischen und magnetresonanztomographischen Bildgebung des zentralen Nervensystems während der Behandlung von akut-lymphoblastischen Leukämien und lymphoblastischen Non-Hodgkin-Lymphomen

    … obviously caused by asparaginase, and 6 with leukoencephalopathy caused by intrathecal methotrexate. The clotting problems appeared between the 18th and 40th day of treatment and only in the group of children with first manifestation. The cases with leukoencephalopathy were found between the …

    aachen Repository record for Möglichkeiten der computertomographischen und magnetresonanztomographischen Bildgebung des zentralen Nervensystems während der Behandlung von akut-lymphoblastischen Leukämien und lymphoblastischen Non-Hodgkin-Lymphomen (opens in a new tab)

  3. Neurocognitive outcomes in children experiencing seizures during treatment for acute lymphoblastic leukemia

    … more significant early neurotoxicity (i.e., leukoencephalopathy) than non-seizure cohorts. Based on these preliminary findings, it appears that children who experience treatment-related seizures are at greater neurocognitive risk when compared to counterparts who do not. Findings point to a …

    mississippi Repository record for Neurocognitive outcomes in children experiencing seizures during treatment for acute lymphoblastic leukemia (opens in a new tab)

  4. Modelling neuronal mitochondrial aminoacyl-tRNA synthetase defects

    … deficiency type 8 (COXPD8), characterised by leukoencephalopathy with ovarian failure, or cardiomyopathy, leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL), and pontocerebellar hypoplasia type 6 (PCH6). Despite their significance, the underlying pathological …

    cambridge Repository record for Modelling neuronal mitochondrial aminoacyl-tRNA synthetase defects (opens in a new tab)

  5. A study of the john Cunningham virus (jcv) seroprevalence among Zambian adults presenting with “meningoencephalitis” to the university teaching hospital, Lusaka, Zambia

    … to the development of progressive multifocal leukoencephalopathy (PML). Infection with the JCV occurs in childhood and the virus remains quiescent in the body, activating during immunosuppression. Exposure to the virus can be detected by testing for JC virus specific antibodies in an ELISA …

    zimbabwe Repository record for A study of the john Cunningham virus (jcv) seroprevalence among Zambian adults presenting with “meningoencephalitis” to the university teaching hospital, Lusaka, Zambia (opens in a new tab)

  6. A study of the john Cunningham virus (jcv) seroprevalence among Zambian adults presenting with “meningoencephalitis” to the university teaching hospital, Lusaka, Zambia

    … to the development of progressive multifocal leukoencephalopathy (PML). Infection with the JCV occurs in childhood and the virus remains quiescent in the body, activating during immunosuppression. Exposure to the virus can be detected by testing for JC virus specific antibodies in an ELISA …

    zambia Repository record for A study of the john Cunningham virus (jcv) seroprevalence among Zambian adults presenting with “meningoencephalitis” to the university teaching hospital, Lusaka, Zambia (opens in a new tab)

  7. Unravelling the Genetics of Cerebral Small Vessel Disease

    … arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by NOTCH3 variants, and the second most frequent, CADASIL type 2, by autosomal dominant HTRA1 variants. COL4A1/2 variants can cause small vessel stroke and intracerebral haemorrhage. This thesis investigates …

    cambridge Repository record for Unravelling the Genetics of Cerebral Small Vessel Disease (opens in a new tab)

  8. Cloning of a putative human oncogenic virus, BK

    … cells of a patient with progressive multifocal leukoencephalopathy (PML) and was thus the first polyomavirus infection of humans to be discovered. (ZuRhein and Chou, 1965). In 1971, an immunologically distinct polyomavirus, BK, was isolated from the urine of an immunocompromised recipient of a …

    cape-town Repository record for Cloning of a putative human oncogenic virus, BK (opens in a new tab)

  9. Genetics of Cerebral Small Vessel Disease

    … Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), caused by mutations in the NOTCH3 gene. In recent years, other genes have also been found to cause familial SVD, such as COL4A1/A2, HTRA1, FOXC1 and TREX1. Genome wide association studies (GWAS) have also revealed loci …

    cambridge Repository record for Genetics of Cerebral Small Vessel Disease (opens in a new tab)

  10. REGULATION OF THE HUMAN NEUROTROPIC POLYOMAVIRUS, JCV, IN THE CENTRAL NERVOUS SYSTEM

    … central nervous system, progressive multifocal leukoencephalopathy (PML) that is seen primarily in immunodeficient individuals. Productive infection of JCV occurs only in glial cells and this restriction is to a great extent due to the activation of the viral promoter that has cell type-specific …

    temple Repository record for REGULATION OF THE HUMAN NEUROTROPIC POLYOMAVIRUS, JCV, IN THE CENTRAL NERVOUS SYSTEM (opens in a new tab)

  11. Towards a blood-based biomarker for remyelination: Glial cell death and associated byproducts in demyelinating disease

    … sclerosis (MS) and progressive multifocal leukoencephalopathy (PML). MS is a chronic neuroinflammatory and neurodegenerative disease affecting over two million people worldwide and is a major cause of neurological disability, particularly in young adults. PML is a rare, severe demyelinating …

    cambridge Repository record for Towards a blood-based biomarker for remyelination: Glial cell death and associated byproducts in demyelinating disease (opens in a new tab)

  12. NEUROFIBROMATOSIS TYPE 2 PROTEIN (NF2) AS A REGULATOR OF TUMOR SUPPRESSORS AND VIRAL ONCOPROTEINS IN HUMAN GLIOBLASTOMA

    … demyelinating disorder, Progressive Multifocal Leukoencephalopathy (PML), seen in severely immunocompromised patients. Infection of oligodendrocytes with JCV leads to their lytic destruction and the development of white matter lesions in PML patients. Its main regulatory protein, large tumor …

    temple Repository record for NEUROFIBROMATOSIS TYPE 2 PROTEIN (NF2) AS A REGULATOR OF TUMOR SUPPRESSORS AND VIRAL ONCOPROTEINS IN HUMAN GLIOBLASTOMA (opens in a new tab)

  13. Methotrexat-induzierte Leukenzephalopathie bei Patienten mit akuter lymphatischer Leukämie oder lymphoblastischem Non-Hodgkin-Lymphom in Abhängigkeit vom MTHFR-C677T-Status

    The antifolate Methotrexate and folate metabolism is central in therapy of pediatric Acute Lymphatic Leukemia (ALL). Methylenetetrahydrofolate reductase (MTHFR) is an important enzyme of folate metabolism, so that combination of MTX-therapy and mutation of the MTHFR gene (MTHFR C677T) might result …

    aachen Repository record for Methotrexat-induzierte Leukenzephalopathie bei Patienten mit akuter lymphatischer Leukämie oder lymphoblastischem Non-Hodgkin-Lymphom in Abhängigkeit vom MTHFR-C677T-Status (opens in a new tab)