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Differential
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abdominal distention
abdominal muscle paralysis
abdominal protrusion
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
adverse drug reaction
alcohol
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alpha glucosidase
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
anterior horn cell disease
anti signal recognition particle antibody
aphonia
areflexia
arm weakness
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
aspartate aminotransferase
asymptomatic
ataxia
ataxia, sensory
ataxic gait
atrioventricular block
autoantibodies
autoimmune disease
azidodeoxythymidine
bone biopsy
bone pain
bone scanning
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, children
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
bradycardia
bulbar palsy
burning feet
burning paresthesia
cachexia
CAG repeats
calcification, intracranial
calf atrophy
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carpal tunnel syndrome
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar edema
cerebellar lesion
cerebral cortical atrophy
cerebral edema
cerebral embolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chromosomal abnormality
chromosome 5
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cold temperature
coma
conduction block
congenital heart disease
congestive heart failure
consanguinity
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deafness
delay in diagnosis
dementia
dementia, frontotemporal
dermatomyositis
developmental milestones
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic amyotrophy
diarrhea
differential diagnosis
difficulty climbing stairs
diplopia
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
drug induced neurologic disorders
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysmorphic
dysphagia
dysphonia
dyspnea
dyspraxia
dystrophic calcification
dystrophin
echocardiogram
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalomyelitis
encephalomyelitis, parainfectious
encephalopathy
encephalopathy, progressive
entrapment neuropathy
enzyme treatment
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
extraocular muscle lesion
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
fever
fibrillations
finger flexor weakness
finger weakness
flu-like illness
foot drop
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
gray matter
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
gynecomastia
hallucination
hand weakness
headache
headache, severe
headache, worst of life
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hoarseness
Hoesch test
human immunodeficiency virus type 1
hypercalcemia
hyperparathyroidism
hyperreflexia
hypertension
hyperthyroidism
hypoglycemia
hyponatremia
hypophonia
hyporeflexia
hypotelorism
hypotonia
hypotonia, infants
immediate recall
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
klippel feil syndrome
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lactic acidemia
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
level of consciousness, decreased
lid closure, weakness of
life expectancy
lumbosacral plexopathy
lumbosacral plexus
lumbosacral plexus, neuritis
lymphadenopathy
lymphadenopathy, cervical
lysosomal storage disease
lysosomes, abnoral
malignant hyperpyrexia
McArdle's disease
medulla oblongata, lesion of
MELAS syndrome
meningeal enhancement
meningismus
meningoencephalomyelitis
mental retardation
mental status, abnormal
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
MNGIE syndrome
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
monoparesis
mortality
motor neuron disease
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, muscle
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
mycoplasma
mycoplasma pneumoniae
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, amyloid
myopathy, autoimmune
myopathy, carcinomatous
myopathy, drug-induced
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
myopathy, mitochondrial
myopathy, necrotizing
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myositis, focal
myotonia dystrophica
myotonic discharges
nausea and vomiting
neck stiffness
neck weakness
negative
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuroophthalmology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neurotoxin
next-generation sequencing
night sweats
normal
nusinersen
nystagmus
nystagmus, rotary
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
osteomalacia
pacemaker, cardiac-transvenous
Paget's disease
pain
pain, abdominal
pain, leg
pain, severe
pain, thigh
paranoia
paraparesis
paraplegia
paraproteinemia
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias
photophobia
plasma cell dyscrasia
plasmapheresis
pleocytosis of cerebrospinal fluid
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, variant form
polyneuropathy, chronic inflammatory demyelinating-pure motor syn
polyneuropathy, chronic inflammatory demyelinating-sens atax var
polyneuropathy, chronic inflammatory demyelinating-variant forms
polyradiculoneuropathy
Pompe's disease of glycogen storage
porphyria
positive sharp waves
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
puerperium
quadriceps atrophy
quadriceps weakness
radionuclide imaging, heart
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
renal stones
repetitive nerve stimulation
respiratory failure
respiratory tract infection
retina, abnormal
retinal lesion
review article
rhabdomyolysis
rheumatoid arthritis
sarcoidosis
sclerosis, bone
scoliosis
scoliosis, neurologic association with
screening
seizure
sensorineural hearing loss
sensory symptoms
serologic testing
short stature
shoulder, subluxation
SMN1 gene
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
survival motor neuron gene
systemic illness
tandem gait, ataxic
temporalis muscle wasting
toe walking
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
toxins, nervous system
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
upward deviation of eyes
urine, dark
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
winging of scapula
X-linked bulbospinal neuronopathy
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 100 to 150 of 4234 << Previous Next >>

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Dysphagia and a rash
BMJ 361:k1590, McFarlane, M. & Disney, B., 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017



Showing articles 100 to 150 of 4234 << Previous Next >>