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Pathomechanisms and Clinical Implications of Myasthenic Syndromes Exacerbated and Induced by Medical Treatments.
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- Frontiers in Molecular Neuroscience, 2020, v. 13, p. N.PAG, doi. 10.3389/fnmol.2020.00156
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- Article
Conflictual Aesthetics. Artistic Activism and the Public Sphere.
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- Springerin, 2020, n. 1, p. 75
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- Article
Dewey for Artists.
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- Springerin, 2018, n. 4, p. 74
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- Article
Estimation of patent foramen ovale size using transcranial Doppler ultrasound in patients with ischemic stroke.
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- Journal of Neuroimaging, 2022, v. 32, n. 1, p. 97, doi. 10.1111/jon.12935
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- Article
Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98501-y
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- Article
The TGF‐b/SOX4 axis and ROS‐driven autophagy co‐mediate CD39 expression in regulatory T‐cells.
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- FASEB Journal, 2020, v. 34, n. 6, p. 8367, doi. 10.1096/fj.201902664
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- Article
Paleontological Aspects of Austrian Arctic Endeavors.
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- Collections: A Journal for Museum & Archives Professionals, 2023, v. 19, n. 3, p. 495, doi. 10.1177/15501906231159037
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- Article
A Sunken Ship of the Desert at the River Danube in Tulln, Austria.
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- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0121235
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- Article
Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders.
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- Human Molecular Genetics, 2022, v. 31, n. 14, p. 2386, doi. 10.1093/hmg/ddac034
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- Article
A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype.
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- Epilepsia (Series 4), 2022, v. 63, n. 4, p. e35, doi. 10.1111/epi.17188
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- Article
Testing association of rare genetic variants with resistance to three common antiseizure medications.
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- Epilepsia (Series 4), 2020, v. 61, n. 4, p. 657, doi. 10.1111/epi.16467
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- Article
Short‐term and sustained clinical response following thymectomy in patients with myasthenia gravis.
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- European Journal of Neurology, 2022, v. 29, n. 8, p. 2453, doi. 10.1111/ene.15362
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- Article
Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study.
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- European Journal of Neurology, 2022, v. 29, n. 6, p. 1815, doi. 10.1111/ene.15306
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- Article
Cell adhesion-dependent trafficking and targeting of TRPC4 channels in human vascular endothelium.
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- BMC Pharmacology, 2007, v. 7, p. 1, doi. 10.1186/1471-2210-7-S2-A17
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- Article
Tarcisius Georg Sztubitz: Der Ordensname, seine Entwicklung und Besonderheiten.
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- Analecta Cisterciensia, 2019, v. 69, n. 1/2, p. 464
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- Article
„aus einem Trümmerhaufen des ausgebombten Hauses Wien III" - one century provenance context of the geological-paleontological collections in the Natural History Museum Vienna (1919 to 2019).
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- Annalen des Naturhistorischen Museums in Wien. Serie A, 2023, n. 124 A, p. 101
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- Publication type:
- Article
The geological-paleontological collections of the Natural History Museum Vienna. An exhaustive evaluation of provenance context (1807 to 1918).
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- Annalen des Naturhistorischen Museums in Wien. Serie A, 2023, n. 124 A, p. 73
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- Article
Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnoses.
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- Journal of Neurology, 2024, v. 271, n. 4, p. 1937, doi. 10.1007/s00415-023-12101-6
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- Article
The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study.
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- Journal of Neurology, 2023, v. 270, n. 2, p. 909, doi. 10.1007/s00415-022-11440-0
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- Article
Cerebrospinal fluid analysis in Guillain–Barré syndrome: value of albumin quotients.
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- Journal of Neurology, 2021, v. 268, n. 9, p. 3294, doi. 10.1007/s00415-021-10479-9
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- Article
Frequency and clinical features of treatment-refractory myasthenia gravis.
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- Journal of Neurology, 2020, v. 267, n. 4, p. 1004, doi. 10.1007/s00415-019-09667-5
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- Publication type:
- Article
Mutations outside the N-terminal part of <italic>RBCK1</italic> may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum.
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- Journal of Neurology, 2018, v. 265, n. 2, p. 394, doi. 10.1007/s00415-017-8710-x
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- Article
GNAO1 Haploinsufficiency Associated with a Mild Delayed‐Onset Dystonia Phenotype.
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- Movement Disorders, 2022, v. 37, n. 12, p. 2464, doi. 10.1002/mds.29258
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- Article
Scoring Algorithm‐Based Genomic Testing in Dystonia: A Prospective Validation Study.
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- Movement Disorders, 2021, v. 36, n. 8, p. 1959, doi. 10.1002/mds.28614
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- Article
Childhood‐onset progressive dystonia associated with pathogenic truncating variants in CHD8.
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- 2021
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- Case Study
Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy.
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- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 7, p. 1376, doi. 10.1002/acn3.51374
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- Article
Phenotypic variability of GABRA1‐related epilepsy in monozygotic twins.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 11, p. 2317, doi. 10.1002/acn3.50895
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- Article
Biallelic mutations in PIGP cause developmental and epileptic encephalopathy.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 5, p. 968, doi. 10.1002/acn3.768
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- Article
Das Burgenländische Volksliedarchiv.
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- Scrinium: Zeitschrift des Verbandes Österreichischer Archivarinnen und Archivare, 2021, n. 75, p. 85
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- Article
Rare Human Missense Variants can affect the Function of Disease-Relevant Proteins by Loss and Gain of Peroxisomal Targeting Motifs.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 18, p. 4609, doi. 10.3390/ijms20184609
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- Article
Inclusive history politics in the arts: Intervention at the Peace Cross St. Lorenz.
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- Art & the Public Sphere, 2020, v. 9, n. 1-2, p. 119, doi. 10.1386/aps_00037_1
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- Article
Muscle involvement in T-cell large granular lymphocytic leukemia presenting with asymmetric limb-girdle weakness and scapular winging.
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- 2022
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- Publication type:
- Letter