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  1. Article ; Online: Intracranial Subdural Fluid Accumulation Associated with a Choroid Plexus Carcinoma in a Dog.

    Schneider, Nina / Blutke, Andreas / Matiasek, Kaspar / Parzefall, Birgit

    Veterinary sciences

    2022  Volume 10, Issue 1

    Abstract: Choroid plexus tumors are commonly described as intraventricular mass lesions and account for 7-10% of intracranial, primary tumors in dogs. A 3-year-old Shetland sheepdog was presented with a history of slowly progressive lethargy, vision impairment and ...

    Abstract Choroid plexus tumors are commonly described as intraventricular mass lesions and account for 7-10% of intracranial, primary tumors in dogs. A 3-year-old Shetland sheepdog was presented with a history of slowly progressive lethargy, vision impairment and cognitive deficits. On magnetic resonance imaging, a subdural fluid accumulation (SFA) overlying and compressing the left parietotemporal lobe as well as multifocal changes consisting of cyst-like lesions, supposed intra-axial brain lesions and mild, multifocal meningeal thickening and generalized contrast enhancement were identified. Cerebrospinal fluid (CSF) analysis showed a mononuclear pleocytosis with negative results for infectious agents. The dog was treated with prednisolone followed by burr hole craniotomy with puncture of the SFA, which macroscopically appeared to be CSF-like fluid. After initial improvement, the dog deteriorated despite continuation of prednisolone and cytarabine therapy and was euthanized four weeks after surgery. Histopathology was consistent with a disseminated, neuroinvasive choroid plexus carcinoma (CPC) that involved the entire neuroaxis including the meninges of the brain and spinal cord. Immunohistochemical examination showed a strong Kir7.1 and a heterogenous cytokeratin-immunoreactivity in neoplastic cells. In conclusion, a CPC should be considered as a possible cause of a SFA even in the absence of an intraventricular mass lesion.
    Language English
    Publishing date 2022-12-30
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2768971-2
    ISSN 2306-7381 ; 2306-7381
    ISSN (online) 2306-7381
    ISSN 2306-7381
    DOI 10.3390/vetsci10010024
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Book ; Online ; Thesis: Die Rolle unterschiedlicher Mastzellsubtypen im Rahmen der intestinalen Karzinogenese

    Groll, Tanja Maria [Verfasser] / Matiasek, Kaspar [Akademischer Betreuer]

    2023  

    Author's details Tanja Maria Groll ; Betreuer: Kaspar Matiasek
    Keywords Tiere (Zoologie) ; Animals (Zoology)
    Subject code sg590
    Language German
    Publisher Universitätsbibliothek der Ludwig-Maximilians-Universität
    Publishing place München
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  3. Book ; Online ; Thesis: Korrelative histopathologische Charakterisierung immun-mediierter Polyneuropathien in einer europäischen Katzenpopulation

    Kolb, Ninja [Verfasser] / Matiasek, Kaspar [Akademischer Betreuer]

    2023  

    Author's details Ninja Kolb ; Betreuer: Kaspar Matiasek
    Keywords Tiere (Zoologie) ; Animals (Zoology)
    Subject code sg590
    Language German
    Publisher Universitätsbibliothek der Ludwig-Maximilians-Universität
    Publishing place München
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  4. Article ; Online: Olivopontocerebellar degeneration associated with 3-hydroxy-3-methylglutaric aciduria in a domestic shorthair cat.

    West, Natalie / Matiasek, Kaspar / Rusbridge, Clare

    JFMS open reports

    2021  Volume 7, Issue 2, Page(s) 20551169211037899

    Abstract: Case summary: A rescue charity-owned 6-month-old neutered female domestic shorthair cat was presented with progressive tetraparesis, increased extensor muscle tone and signs of spinocerebellar ataxia, including hypermetria. The cat's male sibling, with ... ...

    Abstract Case summary: A rescue charity-owned 6-month-old neutered female domestic shorthair cat was presented with progressive tetraparesis, increased extensor muscle tone and signs of spinocerebellar ataxia, including hypermetria. The cat's male sibling, with similar progressive neurological signs, had been euthanased 2 months previously. An inherited metabolic disorder was suspected. Urine for determination of organic acid concentration was obtained and the cat was prescribed carnitine and taurine supplementation. The cat was euthanased 3 months later following progressive neurological signs, including ataxia, tetraparesis, tendency to fall, bilateral absent menace response and intention tremor. A selective post-mortem examination was obtained, taking samples from the brain, cervical spinal cord, tibial branch of the sciatic nerve, muscle, liver and kidneys. Organic acid analysis results received after euthanasia revealed a marked elevation of 3-hydroxy-3-methylglutaric acid (45 mmol/mol creatine [normal range 0-2]) and isovalerylglycine (27 mmol/mol creatinine [normal range 0-2]). 3-Hydroxy-3-methylglutaric acid was deemed clinically relevant as it is a metabolite of 3-hydroxy-3-methylglutaryl-CoA lyase, the enzyme involved in the final step of leucine degradation. Post-mortem examination revealed diffuse, chronic-active, severe olivoponto-(spino)-cerebellar degeneration.
    Relevance and novel information: This is the first report of 3-hydroxy-3-methylglutaric aciduria in the veterinary literature and the first description of the neuropathology of this disorder in any species. 3-Hydroxy-3-methylglutaric aciduria in humans occurs rarely and is due to a deficiency in 3-hydroxy-3-methylglutaryl-coenzyme A lyase.
    Language English
    Publishing date 2021-10-06
    Publishing country England
    Document type Case Reports
    ZDB-ID 2822177-1
    ISSN 2055-1169 ; 2055-1169
    ISSN (online) 2055-1169
    ISSN 2055-1169
    DOI 10.1177/20551169211037899
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Novel association of gluten sensitivity with immune-mediated neuromuscular syndrome in a dog.

    Kolb, Ninja / Alf, Vanessa / Cappello, Rodolfo / Matiasek, Kaspar / Rosati, Marco

    Neuromuscular disorders : NMD

    2022  

    Abstract: Gluten-related disorders in humans comprise different entities, including coeliac disease. Patients typically have measurable titers of anti-gliadin IgG or IgA (AGAs) and anti-transglutaminase-2 IgA (TG2). In addition to intestinal symptoms, human ... ...

    Abstract Gluten-related disorders in humans comprise different entities, including coeliac disease. Patients typically have measurable titers of anti-gliadin IgG or IgA (AGAs) and anti-transglutaminase-2 IgA (TG2). In addition to intestinal symptoms, human patients often show various neurological complications. In dogs, the neurological manifestation is rarely reported. Here we describe the muscle and nerve biopsies of an 11-year-old, male Border Terrier presenting with lower motor neuron signs submitted for histological examination. Examination of the biopsies showed an oligofocal lymphohistiocytic and plasmocytic myositis and a diffuse neuropathy of mixed nodo-paranodal and demyelinating type. Suspecting a neuromuscular form of breed-related gluten hypersensitivity, measurements of AGAs and TG2 antibodies were performed. Both titers ranged above control values. Hence, a gluten-related neuromyopathy was diagnosed. A gluten-free diet was prescribed and a complete disappearance of clinical signs was observed. Gluten-related disorders should be considered as a differential diagnosis in dogs with intestinal and neuromuscular signs.
    Language English
    Publishing date 2022-06-26
    Publishing country England
    Document type Case Reports
    ZDB-ID 1077681-3
    ISSN 1873-2364 ; 0960-8966
    ISSN (online) 1873-2364
    ISSN 0960-8966
    DOI 10.1016/j.nmd.2022.06.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Olivopontocerebellar degeneration associated with 3-hydroxy-3-methylglutaric aciduria in a domestic shorthair cat

    West, Natalie / Matiasek, Kaspar / Rusbridge, Clare

    Journal of feline medicine and surgery open reports. 2021 Sept., v. 7, no. 2

    2021  

    Abstract: A rescue charity-owned 6-month-old neutered female domestic shorthair cat was presented with progressive tetraparesis, increased extensor muscle tone and signs of spinocerebellar ataxia, including hypermetria. The cat’s male sibling, with similar ... ...

    Abstract A rescue charity-owned 6-month-old neutered female domestic shorthair cat was presented with progressive tetraparesis, increased extensor muscle tone and signs of spinocerebellar ataxia, including hypermetria. The cat’s male sibling, with similar progressive neurological signs, had been euthanased 2 months previously. An inherited metabolic disorder was suspected. Urine for determination of organic acid concentration was obtained and the cat was prescribed carnitine and taurine supplementation. The cat was euthanased 3 months later following progressive neurological signs, including ataxia, tetraparesis, tendency to fall, bilateral absent menace response and intention tremor. A selective post-mortem examination was obtained, taking samples from the brain, cervical spinal cord, tibial branch of the sciatic nerve, muscle, liver and kidneys. Organic acid analysis results received after euthanasia revealed a marked elevation of 3-hydroxy-3-methylglutaric acid (45 mmol/mol creatine [normal range 0–2]) and isovalerylglycine (27 mmol/mol creatinine [normal range 0–2]). 3-Hydroxy-3-methylglutaric acid was deemed clinically relevant as it is a metabolite of 3-hydroxy-3-methylglutaryl-CoA lyase, the enzyme involved in the final step of leucine degradation. Post-mortem examination revealed diffuse, chronic-active, severe olivoponto-(spino)-cerebellar degeneration. This is the first report of 3-hydroxy-3-methylglutaric aciduria in the veterinary literature and the first description of the neuropathology of this disorder in any species. 3-Hydroxy-3-methylglutaric aciduria in humans occurs rarely and is due to a deficiency in 3-hydroxy-3-methylglutaryl-coenzyme A lyase.
    Keywords brain ; carnitine ; cats ; creatine ; creatinine ; enzymes ; euthanasia ; females ; inherited metabolic diseases ; leucine ; liver ; males ; medicine ; meglutol ; metabolites ; muscles ; necropsy ; nerve tissue ; neuropathology ; spinal cord ; surgery ; taurine ; tibia ; urine
    Language English
    Dates of publication 2021-09
    Publishing place SAGE Publications
    Document type Article
    ZDB-ID 2822177-1
    ISSN 2055-1169
    ISSN 2055-1169
    DOI 10.1177/20551169211037899
    Database NAL-Catalogue (AGRICOLA)

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  7. Book ; Online ; Thesis: Vergleichende Neuropathologie der Bornavirus-Enzephalitis in Mensch und Tier und Korrelation mit dem klinischen Verlauf

    Vollmuth, Yannik Verfasser] / [Liesche-Starnecker, Friederike [Akademischer Betreuer] / Matiasek, Kaspar Gutachter] / [Liesche-Starnecker, Friederike [Gutachter]

    2024  

    Author's details Yannik Vollmuth ; Gutachter: Kaspar Matiasek, Friederike Liesche-Starnecker ; Betreuer: Friederike Liesche-Starnecker
    Keywords Medizin, Gesundheit ; Medicine, Health
    Subject code sg610
    Language German
    Publisher Universitätsbibliothek der TU München
    Publishing place München
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  8. Book ; Online ; Thesis: Vergleich von SISPA und random-PCR als sequenzunabhängige Amplifikationsmethoden zum schnellen und einfachen Nachweis unbekannter DNA-Viren

    Dittberner, Eva / Matiasek, Kaspar

    2015  

    Author's details von Eva Dittberner
    Language German
    Size Online-Ressource
    Publisher Universitätsbibliothek der Ludwig-Maximilians-Universität
    Publishing place München
    Document type Book ; Online ; Thesis
    Thesis / German Habilitation thesis Ludwig-Maximilians-Univ., Diss.--München, 2015
    Database Special collection on veterinary medicine and general parasitology

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  9. Book ; Online ; Thesis: Vergleich von SISPA und random-PCR als sequenzunabhängige Amplifikationsmethoden zum schnellen und einfachen Nachweis unbekannter DNA-Viren

    Dittberner, Eva / Matiasek, Kaspar

    2015  

    Author's details von Eva Dittberner
    Language German
    Size Online-Ressource
    Publisher Universitätsbibliothek der Ludwig-Maximilians-Universität
    Publishing place München
    Document type Book ; Online ; Thesis
    Thesis / German Habilitation thesis Ludwig-Maximilians-Univ., Diss.--München, 2015
    Database Former special subject collection: coastal and deep sea fishing

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  10. Article: Evaluation and Utility of Submaximal Stimulation Intensity in Transcranial Magnetic Stimulation in the Standing Horse☆

    Walendy, Lara / Goehring, Lutz Steffen / Zablotski, Yuri / Weyh, Thomas / Matiasek, Kaspar / May, Anna

    Journal of equine veterinary science. 2022 May, v. 112

    2022  

    Abstract: Transcranial magnetic stimulation (TMS) has been successfully used in horses to evaluate function and integrity of descending motor pathways in patients affected by neurological gait abnormalities. In preceding studies, lengthening latency times (LT) of ... ...

    Abstract Transcranial magnetic stimulation (TMS) has been successfully used in horses to evaluate function and integrity of descending motor pathways in patients affected by neurological gait abnormalities. In preceding studies, lengthening latency times (LT) of cranially evoked limb muscle potentials have been considered a reliable diagnostic parameter. Standardized settings use device output signal intensities of 100%. The aim of this study was to determine the effect of submaximal stimulation intensities (SI) and to determine the minimum coil output necessary to evoke motor unit potentials. As an additional effect, lower stimulation intensities are supposed to decrease sensory irritation of the equine patient. Altogether, 36 neurologically healthy horses underwent TMS under sedation with a dome coil at stimulation intensities varying from 40% to 100% of device output intensity. Motor potentials were recorded by surface electrodes from all four limbs and LT was calculated in milliseconds. To further refine the stimulation settings, cortical motor thresholds (CMT) were assessed in triplets, using IFCN recommendations. The electromyographic recordings were evaluated in 30 horses. Increasing stimulation intensities resulted in significant (P < .05) LT shortening until application of 80% of maximal output intensity. Further increase to maximal SI of 100%, brought up no significant differences (P > .05). Gating effects were excluded as there was no difference of LT upon ascending and descending SI changes (P > .05). CMT revealed a large inter-individual variability amongst horses independent of their body size. There was a strong linearity in between CMT and LT even within submaximal SI ranges (P < .001). The inverse impact of SI on LT may be explained by deeper penetration of the magnetic field, circumvention of interposed neurons and subsequent activation of fast acting motor pathways. However, in warmblood horses a stimulation intensity of 80% coil output already appeared sufficient for reproducible activation of lower motor neurons in all limbs. Furthermore, due to the strong linear correlation of CMT and LT, the tested CMT algorithms may be used to estimate the normal LT on submaximal stimulation for equine myelopathy patients in future.
    Keywords body size ; electromyography ; gait ; horses ; magnetic fields ; muscles ; patients ; sedation ; transcranial magnetic stimulation ; veterinary medicine
    Language English
    Dates of publication 2022-05
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 2102631-2
    ISSN 1542-7412 ; 0737-0806
    ISSN (online) 1542-7412
    ISSN 0737-0806
    DOI 10.1016/j.jevs.2022.103912
    Database NAL-Catalogue (AGRICOLA)

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