Izabella Obál

Aalborg Universitetshospital
Klinisk Lektor, Klinisk Institut
Det Sundhedsvidenskabelige Fakultet
Klinisk Lektor, Det Sundhedsvidenskabelige Fakultet
Klinik Hoved-Orto
Afdelingslæge, Neurologi

E-maili.obal@rn.dk, iobal@dcm.aau.dk

Hobrovej 18-22, Aalborg Universitetshospital, Syd
9000 Aalborg
Danmark

Publikationer pr. år

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2 Igangværende

Center for Rehabiliteringsrobotik
Struijk, L. N. S. A., Dremstrup, K., Jochumsen, M. R., Moeslund, T. B., Rasmussen, J., Gaihede, M., Obál, I., Bai, S., Bak, T., Kanstrup, A. M., Vinge, L., Mohammadi, M., Bengtson, S. H., Kobbelgaard, F. V., Kæseler, R. L., Thøgersen, M., Leerskov, K., Bentsen, B., Johansen, D., Pálsdóttir, Á. A. & Kirtas, O.
24/03/2021 → …
Projekter: Projekt › Forskning
Intelligent Hybrid Light Weight Tendon Based Exoskeleton for Severely Disabled Individuals
Struijk, L. N. S. A., Dremstrup, K., Mohammadi, M., Jochumsen, M. R., Moeslund, T. B., Rasmussen, J., Gaihede, M., Kanstrup, A. M., Bak, T., Bai, S., Obál, I. & Vinge, L.
24/03/2021 → …
Projekter: Projekt › Forskning

6 Tidsskriftartikel
1 Review (oversigtsartikel)

Passive transfer of sera from als patients with identified mutations evokes an increased synaptic vesicle number and elevation of calcium levels in motor axon terminals, similar to sera from sporadic patients
Meszlényi, V., Patai, R., Polgár, T. F., Nógrádi, B., Körmöczy, L., Kristóf, R., Spisák, K., Tripolszki, K., Széll, M., Obál, I., Engelhardt, J. I. & Siklós, L., 3 aug. 2020, I: International Journal of Molecular Sciences . 21, 15, s. 1-18 18 s., 5566.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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2 Downloads (Pure)
Experimental Motor Neuron Disease Induced in Mice with Long-Term Repeated Intraperitoneal Injections of Serum from ALS Patients
Obál, I., Nógrádi, B., Meszlényi, V., Patai, R., Ricken, G., Kovacs, G. G., Tripolszki, K., Széll, M., Siklós, L. & Engelhardt, J. I., 2 maj 2019, I: International Journal of Molecular Sciences . 20, 10, 2573.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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3 Citationer (Scopus)

30 Downloads (Pure)
Paraneoplastic neuromyelitis optica spectrum disorder: A case report and review of the literature
Annus, Á., Bencsik, K., Obál, I., Kincses, Z. T., Tiszlavicz, L., Höftberger, R. & Vécsei, L., 2018, I: Journal of Clinical Neuroscience. 48, s. 7-10 4 s.
Publikation: Bidrag til tidsskrift › Review (oversigtsartikel) › peer review
7 Citationer (Scopus)
Axotomy Leads to Reduced Calcium Increase and Earlier Termination of CCL2 Release in Spinal Motoneurons with Upregulated Parvalbumin Followed by Decreased Neighboring Microglial Activation
Paizs, M., Patai, R., Engelhardt, J. I., Katarova, Z., Obal, I. & Siklos, L., 2017, I: CNS & Neurological Disorders - Drug Targets. 16, 3, s. 356-367 12 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
4 Citationer (Scopus)
Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac Phenotype
Csányi, B., Hategan, L., Nagy, V., Obál, I., Varga, E. T., Borbás, J., Tringer, A., Eichler, S., Forster, T., Rolfs, A. & Sepp, R., 2017, I: International Heart Journal. 58, 3, s. 454-458 5 s.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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8 Citationer (Scopus)

Center for Rehabiliteringsrobotik

Intelligent Hybrid Light Weight Tendon Based Exoskeleton for Severely Disabled Individuals

Passive transfer of sera from als patients with identified mutations evokes an increased synaptic vesicle number and elevation of calcium levels in motor axon terminals, similar to sera from sporadic patients

Experimental Motor Neuron Disease Induced in Mice with Long-Term Repeated Intraperitoneal Injections of Serum from ALS Patients

Paraneoplastic neuromyelitis optica spectrum disorder: A case report and review of the literature

Axotomy Leads to Reduced Calcium Increase and Earlier Termination of CCL2 Release in Spinal Motoneurons with Upregulated Parvalbumin Followed by Decreased Neighboring Microglial Activation

Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac Phenotype