Oliver Schwartz

Rudolf Buchheim Str. 8
Giessen, HE 35392, Germany

Last Updated: 09/26/2026

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Found 32 publications

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.

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.

Journal: Journal of neuromuscular diseases

Published: August 27, 2026

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.

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.

Journal: Journal of neuromuscular diseases

Published: November 24, 2025

Concerns About Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy-Reply.

Concerns About Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy-Reply.

Journal: JAMA pediatrics

Published: July 29, 2024

Efficacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study.

Efficacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study.

Journal: The Lancet regional health. Europe

Published: June 28, 2024

Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.

Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.

Journal: JAMA pediatrics

Published: April 08, 2024

Impaired Neurodevelopment in Children with 5q-SMA - 2 Years After Newborn Screening.

Impaired Neurodevelopment in Children with 5q-SMA - 2 Years After Newborn Screening.

Journal: Journal of neuromuscular diseases

Published: November 06, 2023

5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2.

5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2.

Journal: Journal of neurology

Published: October 30, 2023

Newbornscreening SMA - From Pilot Project to Nationwide Screening in Germany.

Newbornscreening SMA - From Pilot Project to Nationwide Screening in Germany.

Journal: Journal of neuromuscular diseases

Published: December 04, 2022

Correction to: Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany.

Correction to: Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany.

Journal: Orphanet journal of rare diseases

Published: October 26, 2022

Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.

Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 20, 2022

Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening.

Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening.

Journal: Children (Basel, Switzerland)

Published: October 16, 2022

Newborn Screening for SMA - Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?

Newborn Screening for SMA - Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?

Journal: Journal of neuromuscular diseases

Published: July 18, 2022

Showing 1-12 of 32

Last Updated: 09/26/2026