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O. Hasselmann · SciRah

Researcher profile · Semantic Scholar

O. Hasselmann

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O. Hasselmann — researcher profile on SciRah

h-index: 10
Works: 26
Citations: 507

Most-cited papers

Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
T. Haack, Christopher B. Jackson, K. Murayama, L. Kremer +41 more
2015Annals of Clinical and Translational Neurology116 citations Open access
Semantic Scholar
Pyridoxine responsiveness in novel mutations of the PNPO gene
B. Plecko, K. Paul, P. Mills, P. Clayton +11 more
2014Neurology93 citations Open access
Semantic Scholar
Cerebral folate deficiency and CNS inflammatory markers in Alpers disease.
O. Hasselmann, N. Blau, V. Ramaekers, E. Quadros +2 more
2010Molecular Genetics and Metabolism83 citations Open access
Semantic Scholar
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome
E. O'Connor, A. Töpf, J. Müller, D. Cox +8 more
2016Brain : a journal of neurology54 citations Open access
Semantic Scholar
Treatment of spinal muscular atrophy with Onasemnogene Abeparvovec in Switzerland: a prospective observational case series study
G. Stettner, O. Hasselmann, A. Tscherter, Elea Galiart +2 more
2023BMC Neurology44 citations Open access
Semantic Scholar
Evaluation of real-life outcome data of patients with spinal muscular atrophy treated with nusinersen in Switzerland.
A. Tscherter, C. Rüsch, D. Baumann, C. Enzmann +14 more
2022Neuromuscular Disorders37 citations Open access
Semantic Scholar
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
C. Weiss, L. Becker, Johannes Friese, A. Blaschek +27 more
2024The Lancet Regional Health - Europe29 citations Open access
Semantic Scholar
Swiss paediatrician survey on complementary medicine.
Benedikt M. Huber, T. von Schoen-Angerer, O. Hasselmann, J. Wildhaber +1 more
2019Swiss medical weekly22 citations Open access
Semantic Scholar
Treatment with Nusinersen – Challenges Regarding the Indication for Children with SMA Type 1
A. Pechmann, M. Baumann, G. Bernert, M. Flotats-Bastardas +27 more
2019Journal of Neuromuscular Diseases13 citations
Semantic Scholar
Ethics in Child Health: Principles and Cases in Neurodisability
O. Hasselmann
2016Neuropediatrics12 citations
Semantic Scholar
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
C. Weiss, K. Vill, Matthias Baumann, G. Bernert +35 more
2025Journal of Neuromuscular Diseases4 citations Open access
Semantic Scholar
PNPO mutations in patients with pyridoxine dependent epilepsy
B. Plecko, K. Paul, E. Paschke, O. Maier +10 more
20131 citations
Semantic Scholar
P276 Folinic acid substitution in Alpers disease
O. Hasselmann, N. Blau, V. Ramaekers, E. Quadros
20091 citations
Semantic Scholar
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, C. Weiss, K. Vill, Matthias Baumann +36 more
2026Journal of Neuromuscular Diseases0 citations Open access
Semantic Scholar
Real-World Data on the Efficacy of Gene Replacement Therapy for Spinal Muscular Atrophy (SMA)
C. Weiß, L. Becker, J. Friese, A. Blaschek +26 more
2023Neuropediatrics0 citations
Semantic Scholar
Wie hätten Sie entschieden?
O. Hasselmann, T. Schmitt, B. Baertschi
2019Schweizerische Ärztezeitung0 citations Open access
Semantic Scholar
FV 113. Electrophysiological Diagnostic of Neuromuscular Diseases in Newborns, Infants, and Toddlers
P. Broser, O. Maier, O. Hasselmann, J. Lütschg
2018Neuropediatrics0 citations
Semantic Scholar
Recommendations of How Pediatric Palliative Care Can Be Reconciled with Autonomy
O. Hasselmann
20160 citations
Semantic Scholar
OP56 – 2339: Respecting “informed consent” in epileptic care
O. Hasselmann
20150 citations
Semantic Scholar
Crosstalk between Doctors, Ethicists, and Economist for the Good of Neuropediatrics
O. Hasselmann
20150 citations
Semantic Scholar
P95 – 1984 Treatment of epilepsy in 6 patients with MECP2 duplication syndrome
A. Hasse, C. Haberl, C. Betzler, O. Hasselmann +6 more
20130 citations
Semantic Scholar
Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report
K. Lengnick, O. Hasselmann, R. Horvath, B. Schoser +2 more
20100 citations
Semantic Scholar
Hemiconvulsion-hemiplegia-epilepsy (HHE) syndrome with neonatal onset-a rare and atypical occurrence
O. Maier, O. Hasselmann, P. Waibel, M. Weissert
20050 citations
Semantic Scholar
Myopathic sarcoidosis, an interdisciplinary challenge
O. Hasselmann, C. Künzle, J. Barben, C. Huemer
20050 citations
Semantic Scholar
Reversible posterior leucoencephalopathy (RPLS) in childhood – seldom reported, poorly understood
O. Hasselmann, P. Kolditz, M. Weissert
20040 citations
Semantic Scholar
On being a child and having children with the changing times
F. Aksu, U. Thyen, F. Hanefeld, G. Auerswald +29 more
20010 citations
Semantic Scholar

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