Nemaline Myopathy Latest Advances

Find the Latest Research About Nemaline Myopathy

Last Updated: 02/24/2026

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Found 918 publications

Sporadic Late-Onset Nemaline Myopathy Presenting with Dropped Head Syndrome and Complicated with Sjögren's Syndrome: A Case Report.

Sporadic Late-Onset Nemaline Myopathy Presenting with Dropped Head Syndrome and Complicated with Sjögren's Syndrome: A Case Report.

Journal: Internal medicine (Tokyo, Japan)
Published: January 14, 2026

Sporadic Late-Onset Nemaline Myopathy Associated with Multiple Myeloma: A Case Report.

Sporadic Late-Onset Nemaline Myopathy Associated with Multiple Myeloma: A Case Report.

Journal: Internal medicine (Tokyo, Japan)
Published: December 03, 2025

Monoclonal Gammopathy - the common denominator of sporadic late-onset nemaline myopathy and paraproteinemic neuropathy.

Monoclonal Gammopathy - the common denominator of sporadic late-onset nemaline myopathy and paraproteinemic neuropathy.

Journal: Neuromuscular disorders : NMD
Published: September 29, 2025

Monoclonal Gammopathy of Clinical Significance-Associated Glycogen Storage Myopathy: A Novel Acquired Muscle Disease.

Monoclonal Gammopathy of Clinical Significance-Associated Glycogen Storage Myopathy: A Novel Acquired Muscle Disease.

Journal: Cureus
Published: September 01, 2025

Sporadic Late Onset Nemaline Myopathy

Sporadic Late Onset Nemaline Myopathy

Journal: Brain and nerve = Shinkei kenkyu no shinpo
Published: August 18, 2025

Sporadic late-onset nemaline myopathy (SLONM): Data from a case series and literature review of 144 patients.

Sporadic late-onset nemaline myopathy (SLONM): Data from a case series and literature review of 144 patients.

Journal: Autoimmunity reviews
Published: August 06, 2025

Proteomic analysis of nemaline myopathy in infants reveals distinct common dysregulated proteins and cellular pathways.

Proteomic analysis of nemaline myopathy in infants reveals distinct common dysregulated proteins and cellular pathways.

Journal: Frontiers in neurology
Published: July 08, 2025

CARE-compliant case report: Nemaline myopathy caused by the ACTA1 p.Q139H missense mutation.

CARE-compliant case report: Nemaline myopathy caused by the ACTA1 p.Q139H missense mutation.

Journal: Medicine
Published: June 25, 2025

KLHL41 orchestrates sarcomere assembly and size to drive skeletal muscle hypertrophy in vivo.

KLHL41 orchestrates sarcomere assembly and size to drive skeletal muscle hypertrophy in vivo.

Journal: bioRxiv : the preprint server for biology
Published: June 12, 2025

Sporadic late-onset nemaline myopathy with cardiomyopathy presenting as advanced heart failure despite autologous stem cell transplantation: a case report.

Sporadic late-onset nemaline myopathy with cardiomyopathy presenting as advanced heart failure despite autologous stem cell transplantation: a case report.

Journal: European heart journal. Case reports
Published: June 03, 2025

Parents as First Responders: Experiences of Emergency Care in Children with Nemaline Myopathy: A Qualitative Study.

Parents as First Responders: Experiences of Emergency Care in Children with Nemaline Myopathy: A Qualitative Study.

Journal: Nursing reports (Pavia, Italy)
Published: May 26, 2025

A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.

A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.

Journal: Journal of neuromuscular diseases
Published: May 21, 2025
Showing 1-12 of 918

Last Updated: 02/24/2026