Tubular Aggregate Myopathy Latest Advances

Find the Latest Research About Tubular Aggregate Myopathy

Last Updated: 11/08/2026

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Found 2042 publications

Sporadic late-onset nemaline myopathy associated with monoclonal gammopathy: a case report with review of literature.

Sporadic late-onset nemaline myopathy associated with monoclonal gammopathy: a case report with review of literature.

Journal: The New Zealand medical journal

Published: October 08, 2026

X-linked myotubular myopathy, liver disease, and gene therapy.

X-linked myotubular myopathy, liver disease, and gene therapy.

Journal: Journal of neuromuscular diseases

Published: September 10, 2026

Clinical, histopathological, and biomarker characterization of XLMTM and ADCNM: Operational lessons, screening and baseline data of the Unite-CNM study.

Clinical, histopathological, and biomarker characterization of XLMTM and ADCNM: Operational lessons, screening and baseline data of the Unite-CNM study.

Journal: Journal of neuromuscular diseases

Published: August 14, 2026

294th ENMC international workshop: Diagnosis and management of paraproteinemic myopathies focusing on sporadic late-onset nemaline myopathy (SLONM) and light-chain (AL) amyloid myopathy. 27th -29th March 2026, Hoofddorp, The Netherlands.

294th ENMC international workshop: Diagnosis and management of paraproteinemic myopathies focusing on sporadic late-onset nemaline myopathy (SLONM) and light-chain (AL) amyloid myopathy. 27th -29th March 2026, Hoofddorp, The Netherlands.

Journal: Neuromuscular disorders : NMD

Published: August 05, 2026

READYCOM: protocol for a 2-year prospective natural history and cross-sectional muscle-fatigability study for improving trial readiness in congenital myopathies.

READYCOM: protocol for a 2-year prospective natural history and cross-sectional muscle-fatigability study for improving trial readiness in congenital myopathies.

Journal: BMJ open

Published: August 04, 2026

Co-existence of CLCN1 and DNM2 variants in a phenotype overlapping myotonia and myopathy.

Co-existence of CLCN1 and DNM2 variants in a phenotype overlapping myotonia and myopathy.

Journal: Molecular biology reports

Published: July 21, 2026

Nemaline myopathy patient and caregiver perspectives: a multinational cross-sectional study.

Nemaline myopathy patient and caregiver perspectives: a multinational cross-sectional study.

Journal: Neuromuscular disorders : NMD

Published: July 11, 2026

Myositis with nemaline rods: Clinical features and treatment outcomes.

Myositis with nemaline rods: Clinical features and treatment outcomes.

Journal: Journal of the neurological sciences

Published: July 04, 2026

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Journal: Human molecular genetics

Published: June 30, 2026

Kbtbd13 knockdown restores muscle function in a clinically relevant mouse model of nemaline myopathy type 6.

Kbtbd13 knockdown restores muscle function in a clinically relevant mouse model of nemaline myopathy type 6.

Journal: Science translational medicine

Published: June 24, 2026

MYOT-related myofibrillar myopathy presenting with normal creatine kinase and electromyography: importance of early genetic testing.

MYOT-related myofibrillar myopathy presenting with normal creatine kinase and electromyography: importance of early genetic testing.

Journal: BMJ case reports

Published: May 26, 2026

A case report of X-linked centronuclear myopathy in a neonate: clinical presentation, therapeutic process, and genetic insights.

A case report of X-linked centronuclear myopathy in a neonate: clinical presentation, therapeutic process, and genetic insights.

Journal: Frontiers in pediatrics

Published: May 24, 2026

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Last Updated: 11/08/2026