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Differential
(Click to cross reference)
abdominal protrusion
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
acridine orange-RNA fluorescence
Alzheimer's disease
amyloid
amyloid plaques
areflexia
arteritides
ataxia
autoantibodies
axonal degeneration
axonal spheroid
axonal transection
boxing
brain biopsy
brain biopsy, complications of
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calf hypertrophy
carcinoma
cardiomyopathy
CAT scan, abnormal
central nuclei, muscle
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
congenital myopathy
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
dementia
denervation of muscle
denervation potentials
desmin
developmental disability
developmental milestones
developmental retardation
difficulty climbing stairs
disability, neurological
distal muscle weakness
dysphagia
dyspnea
dystrophin
electromyogram
electron microscopy
emerin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
enzyme, defect
exercise intolerance
eye closure
face, elongated
facial appearance, abnormal
facial weakness
familial
fatigue
fetal movements, reduced
fetus
fibrillations
floppy infant
gadolinium
gait disorder
gene mutation
genetic counselling
genetic neurologic disorders
gliomatosis cerebri
glycogen storage disease
Gowers maneuver
head injury
headache
histochemistry
histochemistry of muscle
histopathology
human immunodeficiency virus type 1
hypertrophic intracranial pachymeningitis
hypertrophic intracranial pachymeningitis, etiology
hypertrophic pachymeningitis, IgG4 related disease
hypertrophic spinal pachymeningitis
hypotonia
hypotonia, infants
IgG4-related disease
immunohistochemistry
immunoperoxidase staining
intellectual deterioration
Kearns-Sayre syndrome
lactic acidemia
Leigh's disease
lid closure, weakness of
lumbar puncture
lumbar puncture, complications of
meningeal biopsy
mental retardation
merosin
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal gammopathy
MRI
MRI, abnormal
MRI, contrast enhanced
MRS
multicore myopathy
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle biopsy, needle
muscle cramp
muscle pain
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker, carrier
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, critically ill
myopathy, desmin
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, vacuolar
myotonia dystrophica
N-acetyl-L-aspartic acid
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, primary of CNS
neoplasm, primary of CNS-treatment of
nerve biopsy
neurofibrillary degeneration
neurogenic atrophy
neurogenic vs.myopathic atrophy
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
nucleotidase-5 activity
nystagmus
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
pain
paraspinal muscle
paraspinal muscle weakness
peripheral nerve, lesion of
pleocytosis of cerebrospinal fluid
poliomyelitis
polymyositis
polymyositis, infantile
polyneuropathy, critically ill
post polio syndrome
prognosis
progressive neurologic disorder
ptosis
ptosis, bilateral
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
review article
scoliosis
single-fiber electromyography
skin, biopsy
standing difficulty
stem cell transplantation
Stephens syndrome
stooped posture
suck, poor
treatment of neurologic disorder
type 1 muscle fiber
type 2 muscle fiber
undiagnosed
vasculitides
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weakness, proximal
Western immunoblot test
wheelchair
winging of scapula
X-linked myopathy
Showing articles 0 to 31 of 31

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

IgG4-Related Disease and Hypertrophic Pachymeningitis
Medicine 92:206-216, Wallace, Z.,et al, 2013

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Diagnosis and Management of Gliomatosis Cerebri:Recent Trends
Surg Neurol 36:431-440, Ross,I.B.,et al, 1991

BA4 Amyloid Protein Deposition in Brain After Head Trauma
Lancet 338:1422-1423, Roberts,G.W.,et al, 1991

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

Necrotizing Vasculitis and HIV Replication in Peripheral Nerves
NEJM 321:685-686, Gherardi,R.,et al, 1989

Antineural Autoantibodies in Patients with Paraneoplastic Cerebellar Degeneration
Arch Neurol 46:1225-1229, Tsukamoto,T.,et al, 1989

Immunocytochemistry of Neurofibrillary Tangles in Dementia Pugilistica and Alzheimer's Disease:Evidence for Common Genesis
Lancet 2:1456-1458, Roberts,G.W., 1988

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy
Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982

Needle Biopsy of Skeletal Muscle In The Diag of Myopathy & Clinical Study of Muscle Funct & Repair
NEJM 302:261-271, Edwards,R.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Acridine Orange-Nucleic Acid Fluorescence
Arch Neurol 37:641-644, Perl,D.P.,et al, 1980

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977



Showing articles 0 to 31 of 31