Pitfalls in the electron microscopic examination of skeletal muscle

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

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Oppenheim's myatonia congenita.

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Age-related morphological changes of the deltoid muscle from 50 to 79 years of age.

Acta neuropathologica·2001

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Neurology·2000

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA.

Human molecular genetics·2000

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

Human molecular genetics·2000

Whole Body Phase Angle as a Promising Marker of Disease Severity in Facioscapulohumeral Muscular Dystrophy.

Muscle & nerve·2026

Priorities for Advancing Palliative Care for Amyotrophic Lateral Sclerosis: A Consensus Report From a Palliative Care for ALS Working Group in the United States.

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Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011-2023.

Muscle & nerve·2026

Postural Torticollis and Early-Onset Scoliosis in Infants With SMA Identified Through Newborn Screening: Single Institution Experience.

Muscle & nerve·2026

Factors Affecting Disease Progression, Survival, and Caregiver Burden in United States Veterans at a Multidisciplinary Veterans Affairs ALS Center.

Muscle & nerve·2026

It's Virtually Here: Telemedicine, Virtual Care, and Neuromuscular Disease.

Muscle & nerve·2026

MRI Proton Density Fat Fraction as a Biomarker of Marrow Recovery Following Organ-Sparing Total Marrow Irradiation in Sickle Cell Disease.

Journal of magnetic resonance imaging : JMRI·2026

Delayed Diagnosis of Primary Sinonasal Mucosal Melanoma.

Cureus·2026

Spinal Mucormycosis Following a Traditional Cupping Procedure in a Diabetic Patient: A Rare Case Report from Somalia.

International medical case reports journal·2026

Atypical MRI presentation of symmetrical thalamic and basal ganglia lesions in adult-onset MOG-IgG-associated disease: a case report.

Frontiers in human neuroscience·2026

Metastatic Melanoma Presenting As Small Bowel Obstruction.

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Beyond Adenosine Deaminase (ADA) and Mycobacterial Growth Indicator Tube (MGIT): The Utility of Xpert MTB/RIF Ultra for Diagnosis and Resistance Determination in Suspected Tubercular Pleural Effusion in a High-Burden State.

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Pitfalls in the electron microscopic examination of skeletal muscle

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Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

Oppenheim's myatonia congenita.

Age-related morphological changes of the deltoid muscle from 50 to 79 years of age.

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA.

Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.

Whole Body Phase Angle as a Promising Marker of Disease Severity in Facioscapulohumeral Muscular Dystrophy.

Priorities for Advancing Palliative Care for Amyotrophic Lateral Sclerosis: A Consensus Report From a Palliative Care for ALS Working Group in the United States.

Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011-2023.

Postural Torticollis and Early-Onset Scoliosis in Infants With SMA Identified Through Newborn Screening: Single Institution Experience.

Factors Affecting Disease Progression, Survival, and Caregiver Burden in United States Veterans at a Multidisciplinary Veterans Affairs ALS Center.

It's Virtually Here: Telemedicine, Virtual Care, and Neuromuscular Disease.

MRI Proton Density Fat Fraction as a Biomarker of Marrow Recovery Following Organ-Sparing Total Marrow Irradiation in Sickle Cell Disease.

Delayed Diagnosis of Primary Sinonasal Mucosal Melanoma.

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Atypical MRI presentation of symmetrical thalamic and basal ganglia lesions in adult-onset MOG-IgG-associated disease: a case report.

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