Publications by authors named "Christian Rauscher"

Claim this Profile
D
Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland-part I-systematic literature review and existing evidence.
Claudia Weiß, Katharina Vill, Matthias Baumann, Günther Bernert, Astrid Blaschek, Christian Rauscher

J Neuromuscul Dis· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.
Oliver Schwartz, Katharina Vill, Michelle Pfaffenlehner, Max Behrens, Claudia Weiß, Christian Rauscher

JAMA Pediatr· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
5
5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2.
Katharina Vill, Moritz Tacke, Anna König, Matthias Baumann, Manuela Baumgartner, Christian Rauscher

J Neurol· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study.
René Günther, Claudia Diana Wurster, Svenja Brakemeier, Alma Osmanovic, Olivia Schreiber-Katz, Christian Rauscher

Lancet Reg Health Eur· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study.
Claudia Weiß, Andreas Ziegler, Lena-Luise Becker, Jessika Johannsen, Heiko Brennenstuhl, Christian Rauscher

Lancet Child Adolesc Health· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1B.
Martin Krenn, Monika Schloegl, Ekaterina Pataraia, Ellen Gelpi, Sebastian Schröder, Christian Rauscher

Seizure· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Effect of Additional Pain Neuroscience Education in Interdisciplinary Multimodal Pain Therapy on Current Pain. A Non-Randomized, Controlled Intervention Study.
Michael Richter, Christian Rauscher, Alexander Kluttig, Joachim Mallwitz, Karl-Stefan Delank

J Pain Res· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[German version of the Neurophysiology of Pain Questionnaire : Translation, cross-cultural adaptation, reliability and validity].
Michael Richter, Britta Maurus, Martina Egan Moog, Christian Rauscher, Katja Regenspurger

Schmerz· June 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion.
Raphael Johannes Morscher, Christian Rauscher, Wolfgang Sperl, Olaf Rittinger

Seizure· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CAD mutations and uridine-responsive epileptic encephalopathy.
Johannes Koch, Johannes A Mayr, Bader Alhaddad, Christian Rauscher, Jörgen Bierau

Brain· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
Johannes Koch, Peter Freisinger, René G Feichtinger, Franz A Zimmermann, Christian Rauscher

Orphanet J Rare Dis· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A 1.1 million base pair X-chromosomal deletion covering the PDHA1 and CDKL5 genes in a female patient with West syndrome and pyruvate oxidation deficiency.
Johannes A Mayr, Johannes Koch, Christine Fauth, Franz A Zimmermann, Christian Rauscher

Neuropediatrics· June 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.
Carina Fischer, Slave Trajanoski, Lea Papić, Christian Windpassinger, Günther Bernert, Christian Rauscher

J Neurol· March 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency.
Johannes A Mayr, Olaf Bodamer, Tobias B Haack, Franz A Zimmermann, Florence Madignier, Christian Rauscher

Mol Genet Metab· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Outcome of severe unilateral cerebellar hypoplasia.
Andrea Poretti, Catherine Limperopoulos, Eliane Roulet-Perez, Nicole I Wolf, Christian Rauscher

Dev Med Child Neurol· August 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Wilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, Maike Leferink, Tom Hofste, Christian Rauscher

Brain· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis