Stephan vom Dahl

Charles Darwin University — Australia

Medicine · Health Sciences

51h-index7.4kcitations892works1.92yr avg
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Research Topics

Lysosomal Storage Disorders Research(65), Metabolism and Genetic Disorders(59), Liver Disease Diagnosis and Treatment(30), Carbohydrate Chemistry and Synthesis(22), Pancreatic function and diabetes(20)

Publications890 total

Monozentrische retrospektive Analyse bei Alkaptonurie, einer ultraseltenen Aminoacidopathie: Diagnostischer Time lag, GI-Manifestationen und Therapie
Zeitschrift für Gastroenterologie·2025
Measuring sustainability in social enterprises: Development and validation of a multi-dimensional framework
Acta Psychologica·2025· 2 citedOpen Access
Evaluation of Lyso-Gb1 as a biomarker for Gaucher disease treatment outcomes using data from the Gaucher Outcome Survey
Orphanet Journal of Rare Diseases·2025· 5 citedOpen Access
ASMD (acid sphingomyelinase deficiency), formerly Morbus Niemann-Pick type A/B: four adult cases with idiopathic hepatosplenomegaly and first results from enzyme replacement therapy (ERT) with olipudase alfa
Zeitschrift für Gastroenterologie·2025
First successful pregnancies in patients with cerebrotendinous xanthomatosis treated with chenodeoxycholic acid in Germany
Zeitschrift für Gastroenterologie·2025
Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German‐speaking countries
Journal of Inherited Metabolic Disease·2024· 5 citedOpen Access
P.33 Novel dietary management strategies for classical homocystinuria (HCU) in HARMONY/ENSEMBLE phase 3 studies of pegtibatinase, an investigational enzyme replacement therapy
Molecular Genetics and Metabolism·2024· 1 cited
Primary amoebic meningoencephalitis in an infant
The American Journal of the Medical Sciences·2024· 1 cited
Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders
Annals of Clinical and Translational Neurology·2024· 7 citedOpen Access
Queer vulnerability and disaster situations
AIMS Geosciences·2024· 2 citedOpen Access
Morbus Gaucher
Elsevier eBooks·2024
Neurological Outcome in Screened Individuals with LCHAD/MTP Deficiency
Neuropediatrics·2023
Seltene und genetisch bedingte Lebererkrankungen
Die Gastroenterologie·2023Open Access
Transition seltener Leberkrankheiten im Kindesalter – was kommt auf die Hepatologie zu?
Die Gastroenterologie·2023
A Rapid Review of the Impacts of Climate Change on the Queer Community
Environmental Justice·2023· 16 cited
Distribution patterns in Tc-99m-DPD bone scintigraphies in patients with alkaptonuria
Nuklearmedizin - NuclearMedicine·2023
Lyso-Gb1 as a biomarker of the real-world situation in Gaucher disease: Comparative data from the Gaucher Outcome Survey (GOS) in ERT-treated and untreated patients
Molecular Genetics and Metabolism·2023
Management, vaccination status and COVID-19 morbidity of patients with Gaucher disease in Germany during the COVID-19 pandemic
Zeitschrift für Gastroenterologie·2023· 1 cited
Incidence of hepatic adenomas in adult glycogen storage disease type Ia/b
Zeitschrift für Gastroenterologie·2023· 1 cited
Radiofrequency Pulmonary Vein Isolation without Esophageal Temperature Monitoring: Contact-Force Characteristics and Incidence of Esophageal Thermal Damage
Journal of Clinical Medicine·2022· 2 citedOpen Access
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Frequent Co-authors

Dieter Häussinger(24), Carla E. M. Hollak(11), Nadia Belmatoug(9), Freimut Schliess(8), Neal J. Weinreb(8), Timothy M. Cox(7), Johannes M. F. G. Aerts(7), Ari Zimran(7), Pramod K. Mistry(7), Florian Läng(7), W. Gerok(6), Gregory M. Pastores(6), C Hallbrucker(6), Maja Di Rocco(5), Pilar Giraldo(4), Anna Tylki‐Szymańska(4), Dirk Graf(4), Derralynn Hughes(4), Eugen Mengel(4), Bruno Bembi(3)