Profil bibliographique

Georg M. Stettner

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

85Publications signalées

1413Citations signalées

1Affiliations récentes

Institutions déclarées

Domaines associés

Neurogenetic and Muscular Disorders ResearchNeuroscience of respiration and sleepSleep and Wakefulness ResearchMuscle Physiology and DisordersHereditary Neurological Disorders

Publications récentes

Accès ouvert 2026 articleOpenAlex

Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland – part II – expert based recommendations for surveillance and management of side-effects

Andreas Ziegler, Claudia Weiß, Katharina Vill, Matthias Baumann et autres

0 citationsJournal of Neuromuscular Diseases

Accès ouvert 2026 articleOpenAlex

Safety and efficacy of fordadistrogene movaparvovec in ambulatory participants with Duchenne muscular dystrophy (CIFFREO): a phase 3, double-blind, randomised, placebo-controlled study

Francesco Muntoni, Andres Nascimento, Jinhong Shin, Michela Guglieri et autres

0 citationsZurich Open Repository and Archive (University of Zurich)

Accès ouvert 2026 articleOpenAlex

Developing, Implementing, and Evaluating a Care Management Model for Patients With Neuromuscular Diseases: Protocol for a Participatory Mixed Methods Study

Veronika Waldboth, Christina Schuler, Raffaella Willmann, Heidi Petry et autres

0 citationsZurich Open Repository and Archive (University of Zurich)

2026 articleOpenAlex

Safety and efficacy of fordadistrogene movaparvovec in ambulatory participants with Duchenne muscular dystrophy (CIFFREO): a phase 3, double-blind, randomised, placebo-controlled study

Francesco Muntoni, Andres Nascimento, Jinhong Shin, Michela Guglieri et autres

2 citationsThe Lancet Neurology

Accès ouvert 2026 articleOpenAlex

Genotype–phenotype correlations in 18 European patients with heterozygous KIF1A variants: key considerations for assessing KIF1A variant causality

Anna Uhrova Meszarosova, Elea Galiart, Petra Lassuthova, Konstantinos Kolokotronis et autres

3 citationsFrontiers in Medicine

Accès ouvert 2026 articleOpenAlex

Genotype–phenotype correlations in 18 European patients with heterozygous KIF1A variants: key considerations for assessing KIF1A variant causality

Anna Uhrova Meszarosova, Elea Galiart, Petra Lassuthova, Konstantinos Kolokotronis et autres

0 citationsZurich Open Repository and Archive (University of Zurich)

Accès ouvert 2025 reviewOpenAlex

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 et autres

4 citationsJournal of Neuromuscular Diseases

2025 articleOpenAlex

456PDefining the CIAO1-related disease spectrum: clinical and molecular insights into a novel defect in cytoplasmic iron-sulfur cluster assembly

R. Orbach, Reza Maroofian, Georg M. Stettner, J. Herwig et autres

0 citationsNeuromuscular Disorders

2025 articleOpenAlex

516PNewborn screening for spinal muscular atrophy: first anniversary in Switzerland

David Jacquier, André Klein, Georg M. Stettner, Philip J. Broser et autres

0 citationsNeuromuscular Disorders

Accès ouvert 2025 articleOpenAlex

Hearing rehabilitation in SERAC1 related MEGD(H)EL syndrome - implications from a multi-center retrospective cohort study

Sebastian Roesch, Anna O'Sullivan, Stefan Tschani, Anna Baghdasaryan et autres

0 citationsZurich Open Repository and Archive (University of Zurich)

Accès ouvert 2025 articleOpenAlex

Hearing rehabilitation in SERAC1 related MEGD(H)EL syndrome - implications from a multi-center retrospective cohort study

Sebastian Roesch, Anna O'Sullivan, Stefan Tschani, Anna; https://orcid.org/0000-0003-1026-706X Baghdasaryan et autres

0 citationsZurich Open Repository and Archive (University of Zurich)

Accès ouvert 2025 preprintOpenAlex

Developing, Implementing, and Evaluating a Care Management Model for Patients With Neuromuscular Diseases: Protocol for a Participatory Mixed Methods Study (Preprint)

Veronika Waldboth, Christina Schuler, Raffaella Willmann, Heidi Petry et autres

0 citations

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