Thomas Wieser
Publications by Year
Research Areas
Migraine and Headache Studies, Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Genetic Neurodegenerative Diseases, Biochemical and Molecular Research
Most-Cited Works
- → Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect(2003)139 cited
- → Muscle Carnitine Palmitoyltransferase II Deficiency(2005)131 cited
- → Use of Complementary and Alternative Medicine in Patients Suffering from Primary Headache Disorders(2009)106 cited
- → Carnitine palmitoyltransferase II deficiency(2003)71 cited
- → Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)(2006)62 cited
- → Absence of Known Familial Hemiplegic Migraine (FHM) Mutations in the CACNA1A Gene in Patients with common Migraine: Implications for Genetic Testing(2003)37 cited
- → A Novel Nonsense Mutation (515del4) in Muscle Carnitine Palmitoyltransferase II Deficiency(2002)21 cited
- → Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness(1999)21 cited
- → No Influence of 5‐HTTLPR Gene Polymorphism on Migraine Symptomatology, Comorbid Depression, and Chronification(2009)20 cited
- → Persistent ocular motor disturbances in migraine without aura(2004)19 cited