Wolfgang Sperl

Paracelsus Medical University — Austria

Biochemistry, Genetics and Molecular Biology · Life Sciences

64h-index11.0kcitations381works0.02yr avg
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Research Topics

Metabolism and Genetic Disorders(179), Mitochondrial Function and Pathology(159), ATP Synthase and ATPases Research(48), Diet and metabolism studies(32), Biochemical Acid Research Studies(22)

Publications376 total

Vom ersten Patienten zum nationalen Zentrum
Pädiatrie & Pädologie·2025Open Access
Alternativen zu Säuglingsnahrungen auf Kuhmilchproteinbasis
Monatsschrift Kinderheilkunde·2023· 4 citedOpen Access
Supplementary Figure S1 from Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma
2023Open Access
Data from Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma
2023Open Access
Data from Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma
2023Open Access
Supplementary Figure S1 from Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma
2023Open Access
Österreichische Beikostempfehlungen 2022
Monatsschrift Kinderheilkunde·2023· 1 cited
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy
Orphanet Journal of Rare Diseases·2022· 2 citedOpen Access
Role of Energy Metabolism and Mitochondrial Function in Inflammatory Bowel Disease
Inflammatory Bowel Diseases·2022· 29 cited
Expression of Oxidative Phosphorylation Complexes and Mitochondrial Mass in Pediatric and Adult Inflammatory Bowel Disease
Oxidative Medicine and Cellular Longevity·2022· 14 citedOpen Access
Correction: Spenger et al. Glutaric Aciduria Type I Missed by Newborn Screening: Report of Four Cases from Three Families. Int. J. Neonatal Screen. 2021, 7, 32
International Journal of Neonatal Screening·2021Open Access
Pädiatrische Fortbildung in Obergurgl 2022
Pädiatrie & Pädologie·2021Open Access
Mitteilungen der ÖGKJ
Monatsschrift Kinderheilkunde·2021Open Access
Clinical Experience of Neurological Mitochondrial Diseases in Children and Adults: A Single-Center Study
Balkan Journal of Medical Genetics·2021· 2 citedOpen Access
106 Diversity of clinical phenotype of patients with pyruvate dehydrogenase deficiency due to PDHA1 gene mutations
Abstracts·2021Open Access
Molekulare Pädiatrie
Monatsschrift Kinderheilkunde·2021· 1 citedOpen Access
Multidisziplinäre Diagnostik von Entwicklungsstörungen: Grundlage der „personalized precision medicine“
Monatsschrift Kinderheilkunde·2021· 1 citedOpen Access
Molekulare Medizin: Pathobiochemie als Schlüssel zur personalisierten Therapie vererbter Krankheiten
Monatsschrift Kinderheilkunde·2021Open Access
Rehabilitation for children and adolescents after cancer: importance and implementation in Austria
memo - Magazine of European Medical Oncology·2021· 4 citedOpen Access
Childhood Stroke: Long-Term Outcomes and Health-Related Quality of Life with a Special Focus on the Development of Epilepsy
Neuropediatrics·2021· 5 cited
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Frequent Co-authors

Johannes A. Mayr(29), Holger Prokisch(14), Peter Freisinger(13), Tobias B. Haack(12), Barbara Kofler(11), Franz Zimmermann(11), Thomas Meitinger(11), René G. Feichtinger(10), Johannes Koch(10), Uwe Ahting(6), Tim M. Strom(6), Boris Rolinski(6), Thomas Wieland(5), Massimo Zeviani(5), Markéta Tesařová(5), Daniela Karall(5), Jörn Oliver Sass(5), Saskia B. Wortmann(5), Elisabeth Graf(4), Birgit Haberberger(4)