High prevalence of sporadic late-onset nemaline myopathy in a cohort of whole-exome sequencing negative myopathy patients

Monoclonal gammopathy of undetermined significance (MGUS)

(2019) Tarek H Mouhieddine et al.   BLOOD

Sporadic late-onset nemaline myopathy

(2019) Elie Naddaf et al.   NEUROLOGY

Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort

(2018) Mauro Monforte et al.   JOURNAL OF NEUROLOGY

Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction

(2018) Heinz Jungbluth et al.   Nature Reviews Neurology

A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population

(2017) Stojan Perić et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

(2017) Lukas J. Schnitzler et al.   Orphanet Journal of Rare Diseases

A Clinical Approach to Muscle Diseases

(2008) Carlayne Jackson   SEMINARS IN NEUROLOGY