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Authors whose works are in public domain in at least one jurisdiction

List of works by Fritz Zimprich

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A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

scientific article
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

scientific article
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

scientific article
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

scientific article published on 11 August 2013
Genetic structure of Europeans: a view from the North-East

scientific article
The clinical impact of pharmacogenetics on the treatment of epilepsy

scientific article published on 08 July 2008
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article
Ancient and recent positive selection transformed opioid cis-regulation in humans

scientific article
Microglial cells are a component of the perivascular glia limitans

scientific article published in February 1991
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

scientific article
Pharmacoresistance in epilepsy: a pilot PET study with the P-glycoprotein substrate R-[(11)C]verapamil

scientific article
RBFOX1 and RBFOX3 mutations in rolandic epilepsy

scientific article
A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy

article
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

scientific article published on 06 September 2013
DEPDC5 mutations in genetic focal epilepsies of childhood

scientific article published on 14 April 2014
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies

scientific article
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia

scientific article published in March 2009
Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cells.

scientific article published on October 1991
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

scientific article
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

scientific article published on 16 June 2014
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy

scientific article published in June 2008
Analysis ofELP4,SRPX2, and interacting genes in typical and atypical rolandic epilepsy

article
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

scientific article
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

scientific article published on January 25, 2013
Expression of adhesion molecules and histocompatibility antigens at the blood-brain barrier.

scientific article
Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society

scientific article
Epidemiology of Amyotrophic Lateral Sclerosis and Effect of Riluzole on Disease Course

scholarly article by Hakan Cetin et al published 2015 in Neuroepidemiology
Clinical seizure lateralization in frontal lobe epilepsy.

scientific article published in March 2007
Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

scientific article
Real-time measurements of calcium dynamics in neurons developing in situ within zebrafish embryos

scientific article published in August 1998
Lack of Association Between ABCC2 Gene Variants and Treatment Response in Epilepsy

scientific article published on January 1, 2012
Role of LINGO1 polymorphisms in Parkinson's disease

scientific article
Coronavirus induced primary demyelination: indications for the involvement of a humoral immune response

article
Dynamic up-regulation of prodynorphin transcription in temporal lobe epilepsy

scientific article
Buffering intracellular calcium disrupts motoneuron development in intact zebrafish embryos

article
Epidemiology of myasthenia gravis in Austria: rising prevalence in an ageing society

scientific article published on 6 November 2012
The stigma of mental illness: anticipation and attitudes among patients with epileptic, dissociative or somatoform pain disorder

scientific article published in April 2007
Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features

scientific article
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures

scientific article
Andreas Rett and benign familial neonatal convulsions revisited

scientific article
Altered expression of voltage-dependent calcium channel alpha(1) subunits in temporal lobe epilepsy with Ammon's horn sclerosis

scientific article published in January 2002
Psychoses in epilepsy: A comparison of postictal and interictal psychoses

scientific article
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article
Calcium Channels in Neuroblastoma Cell Growth Cones

scientific article published on 01 March 1996
The effect of early prednisolone treatment on the generalization rate in ocular myasthenia gravis.

scientific article published on 25 December 2012
A genetic polymorphism of the endogenous opioid dynorphin modulates monetary reward anticipation in the corticostriatal loop

scientific article (publication date: 2014)
The receptor for advanced glycation endproducts and its ligands in patients with myasthenia gravis

scientific article published on 3 March 2012
Postictal psychosis in temporal lobe epilepsy: a case-control study

scientific article published on 16 March 2013
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

scientific article published on 29 July 2017
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

scientific article

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