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You searched for: Author/Creator Strautmanis, Jurgis

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2. Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study. (31st December 2022)

3. Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases. (December 2016)

4. Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy. (19th August 2013)

5. Kohlschütter–Tönz syndrome: Case report with novel feature and detailed review of features associated with ROGDI variants. Issue 4 (23rd December 2021)

6. Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia. (16th June 2022)

7. Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. Issue 1 (December 2016)

8. Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome. Issue 6 (13th November 2022)