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zadetkov: 97
1.
  • Glioma progression is shape... Glioma progression is shaped by genetic evolution and microenvironment interactions
    Varn, Frederick S.; Johnson, Kevin C.; Martinek, Jan ... Cell, 06/2022, Letnik: 185, Številka: 12
    Journal Article
    Recenzirano
    Odprti dostop

    The factors driving therapy resistance in diffuse glioma remain poorly understood. To identify treatment-associated cellular and genetic changes, we analyzed RNA and/or DNA sequencing data from the ...
Celotno besedilo
Dostopno za: GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
2.
  • The ever wider clinical spe... The ever wider clinical spectrum of RMND1-related disorders and limitedness of phenotype-based classifications
    Rioux, Alexis V.; Bergeron, Nicolas AD; Riopel, Julie ... Journal of molecular medicine, 10/2023, Letnik: 101, Številka: 10
    Journal Article
    Recenzirano
    Odprti dostop

    RMND1 has been identified as a mitochondriopathy-associated gene less than 12 years ago. The most common phenotype related to this gene is an early onset, severe form of encephalomyopathy that leads ...
Celotno besedilo
Dostopno za: EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ
3.
  • Longitudinal molecular traj... Longitudinal molecular trajectories of diffuse glioma in adults
    Barthel, Floris P; Johnson, Kevin C; Varn, Frederick S ... Nature, 12/2019, Letnik: 576, Številka: 7785
    Journal Article
    Recenzirano
    Odprti dostop

    The evolutionary processes that drive universal therapeutic resistance in adult patients with diffuse glioma remain unclear . Here we analysed temporally separated DNA-sequencing data and matched ...
Celotno besedilo
Dostopno za: EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ

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4.
  • From animal models to human... From animal models to human disease: a genetic approach for personalized medicine in ALS
    Picher-Martel, Vincent; Valdmanis, Paul N; Gould, Peter V ... Acta neuropathologica communications, 07/2016, Letnik: 4, Številka: 1
    Journal Article
    Recenzirano
    Odprti dostop

    Amyotrophic Lateral Sclerosis (ALS) is the most frequent motor neuron disease in adults. Classical ALS is characterized by the death of upper and lower motor neurons leading to progressive paralysis. ...
Celotno besedilo
Dostopno za: NUK, UL, UM, UPUK

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5.
  • Neuropathological character... Neuropathological characterization of the cavitating leukoencephalopathy caused by COA8 cytochrome c oxidase deficiency: a case report
    Chapleau, Alexandra; Boucher, Renée-Myriam; Pastinen, Tomi ... Frontiers in cellular neuroscience, 08/2023, Letnik: 17
    Journal Article
    Recenzirano
    Odprti dostop

    COA8-related leukoencephalopathy is a recently described rare cavitating leukoencephalopathy caused by biallelic variants in the COA8 gene. Clinically, it presents heterogeneously and usually follows ...
Celotno besedilo
Dostopno za: NUK, UL, UM, UPUK
6.
  • Cholinergic and Nadph‐δ neu... Cholinergic and Nadph‐δ neurons in the pedunculopontine and laterodorsal tegmental nuclei of human and nonhuman primates
    Coulombe, Vincent; Goetz, Laurent; Bhattacharjee, Manik ... Journal of comparative neurology, February 2024, 2024-02-00, 20240201, Letnik: 532, Številka: 2
    Journal Article
    Recenzirano
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    The brainstem pedunculopontine (PPN) and laterodorsal tegmental (LDTg) nuclei are involved in multifarious activities, including motor control. Yet, their exact cytoarchitectural boundaries are still ...
Celotno besedilo
Dostopno za: BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
7.
  • Platelet abnormalities in H... Platelet abnormalities in Huntington's disease
    Denis, Hélèna L; Lamontagne-Proulx, Jérôme; St-Amour, Isabelle ... Journal of neurology, neurosurgery and psychiatry, 03/2019, Letnik: 90, Številka: 3
    Journal Article
    Recenzirano
    Odprti dostop

    Huntington's disease (HD) is a hereditary disorder that typically manifests in adulthood with a combination of motor, cognitive and psychiatric problems. The pathology is caused by a mutation in the ...
Celotno besedilo
Dostopno za: CMK

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8.
Celotno besedilo
Dostopno za: FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
9.
  • Bevacizumab in the Treatmen... Bevacizumab in the Treatment of Refractory Brain Edema in High-grade Glioma
    Alsahlawi, Aysha K; Michaud-Couture, Claudie; Lachance, Alexandre ... Journal of pediatric hematology/oncology, 2024-Jan-01, 2024-01-00, 20240101, Letnik: 46, Številka: 1
    Journal Article
    Recenzirano

    We report the case of a 14-year-old boy with a steroid-dependent refractory tumor whose longstanding dexamethasone treatment was successfully discontinued after a course of bevacizumab. The use of ...
Celotno besedilo
Dostopno za: CMK
10.
Celotno besedilo
Dostopno za: EMUNI, FIS, FZAB, GEOZS, GIS, IJS, IMTLJ, KILJ, KISLJ, MFDPS, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, SBMB, SBNM, UKNU, UL, UM, UPUK, VKSCE, ZAGLJ

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zadetkov: 97

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