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Nemaline myopathy (also
called rod
myopathy or
nemaline rod myopathy) is a congenital,
often hereditary neuromuscular disorder with many
symptoms that...
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Sporadic late-onset
nemaline myopathy, or SLONM, is a very rare disease, one of the
nemaline myopathies,
causing loss of
muscle bulk and
weakness in the...
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syndrome Nemaline myopathy Nemaline myopathy, type 1
Nemaline myopathy, type 2
Nemaline myopathy, type 3
Nemaline myopathy, type 4
Nemaline myopathy,...
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congenital myopathies that fall
within this
group are well understood, such as
nemaline myopathy (see below). Typically, the
development error in this category...
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myopathies include, but are not
limited to: (G71.2)
nemaline myopathy (characterized by
presence of "
nemaline rods" in the muscle), (G71.2) multi/minicore myopathy...
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autonomous region of
China (Guobiao
abbreviation and ISO-3166-2:CN code NM)
Nemaline myopathy, a
neuromuscular disorder Neuromelanin, a dark
pigment found in...
- similar, in
addition to
typical nemaline myopathy some
specialists distinguish another type of
myopathy called actinic nemaline myopathy. In the former, clumps...
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Neuromuscular disease Congenital nemaline myopathy (neuromuscular disorder)
Specialty Neurology,
neuromuscular medicine,
physical medicine and rehabilitation...
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Mutations in
nebulin cause some
cases of the
autosomal recessive disorder nemaline myopathy. A
smaller member of the
nebulin protein family,
termed nebulette...
- pathologist. In 1958, he
discovered a
muscular disease that was
later named nemaline myopathy. A
brain disease he and his
colleagues described in 1963 is eponymously...
