Table of contents
General:books
Congenital myopathies:central core disease
centronuclear myopathy
congenital fiber type disproportion (pending)
multiminicore myopathy
nemaline myopathy
Inflammatory myopathies:antisynthetase syndrome associated myositis
dermatomyositis
immune mediated necrotizing myopathy
inclusion body myositis
polymyositis
Muscular dystrophies:Becker and Duchenne muscular dystrophy
congenital muscular dystrophies (pending)
facioscapulohumeral muscular dystrophy
limb girdle muscular dystrophy (pending)
myotonic dystrophy
oculopharyngeal muscular dystrophy
Metabolic myopathies:glycogen storage diseases
lipid storage diseases (pending)
mitochondrial myopathies (pending)
Myopathies with vacuoles or specific inclusions:Danon disease (pending)
myofibrillar myopathies (pending)
tubular aggregates myopathy (pending)
X linked myopathy with excessive autophagy (pending)
Toxin & drug induced myopathies:hydroxychloroqine myopathy (pending)
macrophagic myofasciitis
myosin heavy chain loss myopathy / critical illness myopathy (pending)
statin myopathy (pending)
steroid myopathy (pending)
zidovudine myopathy (pending)
Hereditary neuropathies:Charcot-Marie-Tooth disease (pending)
giant axon neuropathy (pending)
hereditary neuropathy with pressure palsies (pending)
Inflammatory demyelinating neuropathies:Guillain-Barre syndrome (pending)
chronic inflammatory demyelinating polyneuropathy (pending)
Other peripheral neuropathies:amyloid neuropathy
diabetic peripheral neuropathy (pending)
vasculitic neuropathy (pending)
Topics from other chapters:
histology-skeletal muscle
Muscle nontumor stains: acid phosphatase alkaline phosphatase ATPases (pending) COX Gomori trichrome (pending) myophosphorylase (pending) NADH-TR (pending) nonspecific esterase Oil Red O PAS phosphofructokinase (pending) SDH (pending)
Muscle nontumor stains: acid phosphatase alkaline phosphatase ATPases (pending) COX Gomori trichrome (pending) myophosphorylase (pending) NADH-TR (pending) nonspecific esterase Oil Red O PAS phosphofructokinase (pending) SDH (pending)
Index (Alphabetical table of contents)
A-E:amyloid neuropathy
antisynthetase syndrome associated myositis
Becker and Duchenne muscular dystrophy
central core disease
centronuclear myopathy
Charcot-Marie-Tooth disease (pending)
chronic inflammatory demyelinating polyneuropathy (pending)
congenital fiber type disproportion (pending)
congenital muscular dystrophies (pending)
Danon disease (pending)
dermatomyositis
diabetic peripheral neuropathy (pending)
F-N:facioscapulohumeral muscular dystrophy
giant axon neuropathy (pending)
glycogen storage diseases
Guillain-Barre syndrome (pending)
hereditary neuropathy with pressure palsies (pending)
hydroxychloroqine myopathy (pending)
immune mediated necrotizing myopathy
inclusion body myositis
limb girdle muscular dystrophy (pending)
lipid storage diseases (pending)
macrophagic myofasciitis
mitochondrial myopathies (pending)
multiminicore myopathy
myofibrillar myopathies (pending)
myosin heavy chain loss myopathy / critical illness myopathy (pending)
myotonic dystrophy
nemaline myopathy
neurogenic atrophy
O-Z:oculopharyngeal muscular dystrophy
polymyositis
spinal muscular atrophy (SMA) (pending)
statin myopathy (pending)
steroid myopathy (pending)
tubular aggregates myopathy (pending)
type II atrophy (pending)
vasculitic neuropathy (pending)
X linked myopathy with excessive autophagy (pending)
zidovudine myopathy (pending)
Find related Pathology books: muscle and peripheral nerve nontumor, pediatric, neuropathology