O. Danielsson

发表

Expression of Thioredoxins and Glutaredoxins in Human Hepatocellular Carcinoma: Correlation to Cell Proliferation, Tumor Size and Metabolic Syndrome

A. Mollbrink, A. Vlamis-Gardikas, A. Fernandes, 2014, International journal of immunopathology and pharmacology.

Morphological alterations and redox changes associated with hepatic warm ischemia-reperfusion injury

B. Isaksson, G. Nowak, M. Björnstedt, 2017, World journal of hepatology.

Hepcidin levels correlate to liver iron content, but not steatohepatitis, in non-alcoholic fatty liver disease

R. Hultcrantz, N. Albiin, P. Stål, 2018, BMC Gastroenterology.

Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies.

M. Bottai, R. Zubarev, L. Padyukov, 2015, The Journal of clinical investigation.

Classification and Diagnostic Investigation in Inflammatory Myopathies: A Study of 99 Patients

J. Ernerudh, B. Lindvall, I. Gáti, 2013, The Journal of Rheumatology.

Associations between subcutaneous adipocyte hypertrophy and nonalcoholic fatty liver disease

M. Aouadi, M. Rydén, H. Hagström, 2022, Scientific Reports.

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients

Berg, S. Newhouse, A. Al-Chalabi, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

The Clinical and Pathological Spectrum of Idiopathic Inflammatory Myopathies : Implications for pathogenesis, classification and diagnosis

O. Danielsson, 2016 .

Bent Spine Syndrome: A Phenotype of Dysferlinopathy or a Symptomatic DYSF Gene Mutation Carrier

A. Landtblom, C. Gunnarsson, M. Vrethem, 2012, European Neurology.

Extracellular thiol-assisted selenium uptake dependent on the xc− cystine transporter explains the cancer-specific cytotoxicity of selenite

A. Fernandes, E. Larsen, M. Björnstedt, 2009, Proceedings of the National Academy of Sciences.

The Cell Culture Medium Affects Growth, Phenotype Expression and the Response to Selenium Cytotoxicity in A549 and HepG2 Cells

M. Björnstedt, R. Jawad, O. Danielsson, 2019, Antioxidants.

Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24

Marcela Dávila López, H. Zetterberg, R. Maroofian, 2019, Human molecular genetics.

Expression of apoptosis related proteins in normal and diseased muscle: A possible role for Bcl-2 in protection of striated muscle

J. Ernerudh, B. Lindvall, C. Nilsson, 2009, Neuromuscular Disorders.

Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin.

B. Brådvik, B. Udd, C. Hedberg, 2012, Brain : a journal of neurology.

Apoptosis in idiopathic inflammatory myopathies with partial invasion; a role for CD8+ cytotoxic T cells?

J. Ernerudh, K. Öllinger, B. Häggqvist, 2020, PloS one.

Luminescent Conjugated Oligothiophenes for Sensitive Fluorescent Assignment of Protein Inclusion Bodies

F. Heppner, W. Engel, K. Nilsson, 2013, Chembiochem : a European journal of chemical biology.

Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression

C. Weihl, B. Udd, J. Palmio, 2019, Neurology: Genetics.

A.O.9 Hypertrophic cardiomyopathy and abnormal glycogen storage in heart and skeletal muscle associated with inactivation of KLHL24

A. Abramsson, A. Oldfors, I. Nennesmo, 2016, Neuromuscular Disorders.

Increased prevalence of celiac disease in idiopathic inflammatory myopathies

B. Lindvall, C. Dahle, C. Hallert, 2017, Brain and behavior.

Skeletal muscle immunohistochemistry of acquired and hereditary myopathies

B. Häggqvist, O. Danielsson, 2021, Current opinion in rheumatology.

Immunohistochemical Typing of Adenocarcinomas of the Pancreatobiliary System Improves Diagnosis and Prognostic Stratification

B. Bozóky, B. Isaksson, M. Del Chiaro, 2016, PloS one.

No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland

P. Andersen, A. Birve, M. de Carvalho, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

July 2017 ENCALS statement on edaravone

A. Al-Chalabi, P. Andersen, A. Chiò, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Screening for Anti-HMGCR Antibodies in a Large Single Myositis Center Reveals Infrequent Exposure to Statins and Diversiform Presentation of the Disease

M. Dastmalchi, I. Nennesmo, P. Szczęsny, 2022, Frontiers in Immunology.

Liver Transplantation for Liver Metastasis of a Pseudopapillary Pancreatic Neoplasm in a Male Patient

J. Joneberg, C. Jorns, A. Romano, 2023, The American journal of case reports.

Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (SANDO). Two case reports

A. Landtblom, J. Jonasson, I. Gáti, 2011, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Chronic symptoms are common in patients with neuroborreliosis – a questionnaire follow‐up study

J. Ernerudh, P. Forsberg, M. Vrethem, 2002, Acta neurologica Scandinavica.

Designing administrative support systems for healthcare organizations

Eric Berglund, Olof Danielsson, O. Danielsson, 2015 .

Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

C. Lewis, J. Powell, A. Al-Chalabi, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Redefining resection margins and dissection planes in perihilar cholangiocarcinoma—radical resection is a rare event

C. Sturesson, E. Sparrelid, C. Fernández Moro, 2021, Virchows Archiv.