Jakob Rath

Medical University of Vienna

Austria

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Articles (20)

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2025

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2025

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2025

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2022

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2021

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2021

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2021

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2020

Collaborators (16)

Wolfgang Löscher

Medical University of Innsbruck

AUSTRIA

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Stefano Forlivesi

IRCCS Istituto Delle Scienze Neurologiche di Bologna

ITALY

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Omar Keritam

Medical University of Vienna

AUSTRIA

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Fritz Zimprich

Medical University of Vienna

AUSTRIA

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Ashkan Shoamanesh

CANADA

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Bernhard Moser

Associate Professor for Thoracic Surgery

Medical University of Vienna

AUSTRIA

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Ekaterina Pataraia

Associated Professor

Medical University of Vienna

AUSTRIA

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Fiona Jäger

Medical University of Vienna

AUSTRIA

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Leonhard Müllauer

Pathologist/Molecular Pathologist/Associate Professor

Medical University of Vienna

AUSTRIA

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Theresa Brunet

GERMANY

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Martin Krenn

Medical University of Vienna

AUSTRIA

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Matias Wagner

Technical University of Munich

GERMANY

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Hakan Cetin

AUSTRIA

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Norbert Embacher

AUSTRIA

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Elisabeth Graf

Klinikum rechts der Isar der Technischen Universität München

GERMANY

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Markus Ponleitner

Medical University of Vienna

AUSTRIA

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Jakob Rath

Research Interests

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Articles (20)

Screening for Congenital Myasthenic Syndromes in Adults With Seronegative Myasthenia Gravis Using Next-Generation Sequencing

AlphaMissense prediction for the evaluation of missense variants in the diagnostic setting of neuromuscular disorders

Efficacy and safety of risdiplam in adults with 5q-associated spinal muscular atrophy: a nationwide observational cohort study in Austria

Signs of Intracranial Hypertension in Chronic Inflammatory Polyradiculoneuropathies—A Cross Sectional Cohort Study

Holistic Exome-Based Genetic Testing in Adults With Epilepsy

Effect of the Factor XIa Inhibitor Asundexian According to Baseline Infarct Pattern and on MRI Covert Infarct Outcomes

Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation

Investigation of serum neurofilament light chain as a biomarker in Fabry disease

The diagnostic and prognostic utility of repetitive nerve stimulation in patients with myasthenia gravis

A Homozygous PTRHD1 Missense Variant (pArg122Gln) in an Individual with Intellectual Disability, Generalized Epilepsy, and Juvenile Parkinsonism

Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnoses.

Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multicentre cohort study.

The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study

Short‐term and sustained clinical response following thymectomy in patients with myasthenia gravis

Neuroradiological differentiation of white matter lesions in patients with multiple sclerosis and Fabry disease.

Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial.

Incidence and clinical spectrum of rhabdomyolysis in general neurology: a retrospective cohort study

Real-world treatment of adult patients with Guillain-Barré syndrome over the last two decades

Cerebrospinal fluid analysis in Guillain–Barré syndrome: value of albumin quotients

Nerve conduction studies in Guillain-Barré syndrome: Influence of timing and value of repeated measurements.

Collaborators (16)

Wolfgang Löscher

Stefano Forlivesi

Omar Keritam

Fritz Zimprich

Ashkan Shoamanesh

Bernhard Moser

Ekaterina Pataraia

Fiona Jäger

Leonhard Müllauer

Theresa Brunet

Martin Krenn

Matias Wagner

Hakan Cetin

Norbert Embacher

Elisabeth Graf

Markus Ponleitner

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