Publications by authors named "Andreas Ferbert"

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Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.
Björn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, Tobias Reinberger, Lisa-Marie Nuxoll, Andreas Ferbert

Mov Disord· November 2024

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Chronic basilar artery occlusion: a retrospective monocentric study.
Christian Roth, Rosa Yavuz, Carolin Maschita, Andreas Ferbert, Johannes Matthaei

J Neurol· July 2024

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Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.
Mirja Thomsen, Katrin Marth, Sebastian Loens, Judith Everding, Johanna Junker, Andreas Ferbert

Mov Disord· March 2024

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Myelin protein zero mutation-related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort.
Juliane Bremer, Axel Meinhardt, Istvan Katona, Jan Senderek, Elke K Kämmerer-Gassler, Andreas Ferbert

Brain Pathol· January 2024

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Differential diagnosis of vacuolar myopathies in the NGS era.
Dorothea Mair, Saskia Biskup, Wolfram Kress, Angela Abicht, Wolfgang Brück, Andreas Ferbert

Brain Pathol· September 2020

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Factors influencing intracranial pressure (ICP) during percutaneous tracheostomy.
Jens Kleffmann, Roman Pahl, Andreas Ferbert, Christian Roth

Clin Neurol Neurosurg· August 2020

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De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient.
Christine Klein, Hauke Baumann, Luisa Olschewski, Henrike Hanssen, Alexander Münchau, Andreas Ferbert

Parkinsonism Relat Disord· July 2019

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Role of ANO3 mutations in dystonia: A large-scale mutational screening study.
Luisa Olschewski, Silvia Jesús, Han-Joon Kim, Sinem Tunc, Sebastian Löns, Andreas Ferbert

Parkinsonism Relat Disord· May 2019

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Progress of intracranial pressure and cerebral perfusion pressure in patients during the development of brain death.
Christian Roth, Andreas Ferbert, Johannes Matthaei, Stefanie Kaestner, Holger Engel

J Neurol Sci· March 2019

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Multimodal imaging findings during severe attacks of familial hemiplegic migraine type 2.
Christian Roth, Andreas Ferbert, Monika Huegens-Penzel, Ralf Siekmann, Tobias Freilinger

J Neurol Sci· September 2018

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Cerebral Fat Embolism: Clinical Presentation, Diagnostic Steps and Long-Term Follow-Up.
Juliane Dunkel, Christian Roth, Frank Erbguth, Wenke Dietrich, Monika Hügens-Penzel, Andreas Ferbert

Eur Neurol· May 2018

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Estimating the Quantitative Demand of NOAC Antidote Doses on Stroke Units.
Waltraud Pfeilschifter, Dana Farahmand, Daniela Niemann, Benno Ikenberg, Carina Hohmann, Andreas Ferbert

Cerebrovasc Dis· December 2017

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Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
Maike F Dohrn, Nicola Glöckle, Lejla Mulahasanovic, Corina Heller, Julia Mohr, Andreas Ferbert

J Neurochem· December 2017

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Leg Muscle Involvement in Facioscapulohumeral Muscular Dystrophy: Comparison between Facioscapulohumeral Muscular Dystrophy Types 1 and 2.
Dorothea Mair, Monika Huegens-Penzel, Wolfram Kress, Christian Roth, Andreas Ferbert

Eur Neurol· September 2017

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Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.
Markus Storbeck, Beate Horsberg Eriksen, Andreas Unger, Irmgard Hölker, Ingvild Aukrust, Andreas Ferbert

Eur J Hum Genet· September 2017

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Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
Lukas J Schnitzler, Tobias Schreckenbach, Aleksandra Nadaj-Pakleza, Werner Stenzel, Elisabeth J Rushing, Andreas Ferbert

Orphanet J Rare Dis· May 2017

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Early Physiotherapy by Passive Range of Motion Does Not Affect Partial Brain Tissue Oxygenation in Neurocritical Care Patients.
Christian Roth, Hubertus Stitz, Jens Kleffmann, Stefanie Kaestner, Wolfgang Deinsberger, Andreas Ferbert

J Neurol Surg A Cent Eur Neurosurg· January 2017

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Primary familial brain calcification in the 'IBGC2' kindred: All linkage roads lead to SLC20A2.
Karen Grütz, Claudia B Volpato, Aloysius Domingo, Daniel Alvarez-Fischer, Uwe Gebert, Andreas Ferbert

Mov Disord· December 2016

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Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement.
Andreas Unger, Gabriele Dekomien, Anne Güttsches, Thomas Dreps, Rudolf Kley, Andreas Ferbert

Neurology· November 2016

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Thomsen myotonia--A 4-generation family with a new mutation and a mild phenotype.
Adina-Ioana Derevenciuc, Angela Abicht, Suad Hamza, Christian Roth, Andreas Ferbert

Muscle Nerve· April 2016

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47 patients with FLNA associated periventricular nodular heterotopia.
Max Lange, Burkhard Kasper, Axel Bohring, Frank Rutsch, Gerhard Kluger, Andreas Ferbert

Orphanet J Rare Dis· October 2015

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Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies.
Dana Safka Brozkova, Tine Deconinck, Laurie Beth Griffin, Andreas Ferbert, Jana Haberlova

Brain· August 2015

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Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1.
Mirjam Larsen, Simone Rost, Nady El Hajj, Andreas Ferbert, Marcus Deschauer

Eur J Hum Genet· June 2015

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Extensive ischemic brainstem lesions and pneumocephalus after application of hydrogen peroxide (H2O2) during lumbar spinal surgery.
Jens Kleffmann, Andreas Ferbert, Wolfgang Deinsberger, Christian Roth

Spine J· April 2015

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Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies.
Anna-Lena Semmler, Sabrina Sacconi, J Elisa Bach, Claus Liebe, Jan Bürmann, Andreas Ferbert

Orphanet J Rare Dis· August 2014

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