Kantonsspital St.Gallen


Julia Walch

Brugger F, Walch J, Hägele-Link S, Abela E, galovic m, Kägi G. Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson's disease. Neuroimage Clin 2020; 28:102469.
Stark R S, Walch J, Kägi G. The Phenotypic Variation of a Family and the Role of Heterozygosity. Mov Disord Clin Pract 2019; 6:700-703.
Walch J. The phenotypic variation of a PARK-Parkin family and the role of heterozygosity. Movement Disorders Clinical Practice 2019; 2019 Sep:700-703.
Brugger F, Walch J. Dysphagie beim Mb. Parkinson. Leading Opinions Neurologie und Psychiatrie 2016;.
Hundsberger T, Weber J, Tettenborn B, Walch J. Radiation-induced cavernoma after total body irradiation and haematopoietic stem cell transplantation in an adult patient suffering from acute myeloid leukaemia. Case Reports in Neurology 2013; 5:91-97.
(2020). Deep brain stimulation in two patients with immunosuppressive therapy. In Dorin P, Walch J, Krüger M, Kägi G, Mittas S, Bohlhalter S, haegele-link s, & Brugger F (Eds.), (pp. 1): -.
Walch J (2019). Chorea-acanthocytosis: Challenges in early diagnosis and excellent treatment response to Deep Brain Stimulation (DBS) – a case report. In (pp. 1): kein.
Walch J (2019). Combined central and peripheral demyelination (CCPD)- a case report. In (pp. 1): kein.
Walch J (2018). STRAW-II „STRoke AWareness“ - Awareness of Stroke in a small region of Switzerland in comparison with international population based epidemiological studie. In (pp. 1): kein.
Walch J, prochnicki a, Zieglgänsberger D, haegele-link s, Tettenborn B, Hader C, Weber J, & heilbronner r (2016). Acute clinical deterioration of a patient with spinal dural arteriovenous malformation after lumbar puncture and steroid treatment – a case report and discussion of possible reasons. In .
Walch J, & Kägi G (2016). Cervical dystonia preceeding Parkinson`s disease – continuum – coincidence or epiphenomena. In .
Walch J, Kägi G, Tettenborn B, & Stark R (2015). The clinical spectrum of PARKIN disease (PARK 2) and heterozygous gene mutation carriers. In .
Walch J, siebel p, Tettenborn B, & Weber J (2011). Amnesia due to fornix infarction – a case report. In .
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