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Research article

First published 2016-3

Rapid diagnosis of hypoglycin A intoxication in atypical myopathy of horses

Johannes Sander, Jessika-M. V. Cavalleri, Michael Terhardt [...]

Journal of Veterinary Diagnostic Investigation

Free access

Brief report

First published 2021-9

Atypical myopathy in 2 Bactrian camels

Manuela Hirz, Henrike A. Gregersen, Johannes Sander [...]

Journal of Veterinary Diagnostic Investigation

Open access

Case report

First published 2024

Atypical presentation of anti-small ubiquitin-like modifier 1 and melanoma differentiation-associated gene 5 antibody positive dermatomyositis presenting with significant inflammatory myopathy on biopsy and normal creatine kinase levels: A case report

Srikar Sama, Nidaa Rasheed, Kyle Shen [...]

Sage Open Medical Case Reports

Retricted access

Research article

First published 2006-02

Central Core Disease: Atypical Case With Respiratory Insufficiency in an Intensive Care Unit

Muzaffer Polat, Ayse Tosun, Yilmaz Ay [...]

Journal of Child Neurology

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Research article

First published 2006-12

Olanzapine overdose is associated with acute muscle toxicity

W S Waring, J Wrate, D N Bateman

Human & Experimental Toxicology

Open access

Case report

First published 2024

A Rare Case of Anti-TIF-1γ Antibody Positive Dermatomyositis in Adulthood

Upasana Agrawal, Manush Sondhi, Alexandra Zamora Smith [...]

Journal of Investigative Medicine High Impact Case Reports

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Research article

First published 2006-09

Clinical Approach to the Weak Patient in the Intensive Care Unit

Upinder K Dhand

Respiratory Care

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Research article

First published 2015-7

Analytical validation of a high-sensitivity cardiac troponin T assay in horses

Nicky Van Der Vekens, Marie-Astrid van Dievoet, Hendrik De Puydt [...]

Journal of Veterinary Diagnostic Investigation

Retricted access

Other

First published 1998-11

A Large-Scale Mitochondrial DNA Deletion Causing Progressive Ataxia

Shigeko Saitoh, Mariko Y. Momoi, Takehiro Ohki [...]

Journal of Child Neurology

Retricted access

Research article

First published 2015-3

A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene ( MTCYB ) in a Patient with Prader Willi Syndrome

Uluç Yiş, Fatih Süheyl Ezgü, Pakize Karakaya [...]

Journal of Child Neurology

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