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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
ankle reflex, preserved
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
lead poisoning
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
neuropathy, short-fiber
neurotoxin
next-generation sequencing
night sweats
normal
nusinersen
nystagmus
nystagmus, rotary
occupational neurologic disorders
occupational neuropathies
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
paralysis
paralysis, use-related
paranoia
paraparesis
paraplegia
paraproteinemia
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias
photophobia
physical activity
plasma cell dyscrasia
plasmapheresis
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis, provocation
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
rabies, nervous system involvement with
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
retrograde axonal flow
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
tetanus
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
viral infection
viral infection, CNS
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 1550 to 1600 of 4643 << Previous Next >>

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

Ischemic Stroke after Use of the Synthetic Marijuana "Spice"
Neurol 81:2090-2093, Freeman, M.J.,et al, 2013

Clinical Features of MS Associated with Leber Hereditary Optic Neuropathy mtDNA Mutations
Neurol 81:2073-2081, Pfeffer, G.,et al, 2013

Dyspnea as a Presenting Manifestation of Amyloid Myopathy
Neurol 81:e184, Ghosh, P.S.,et al, 2013

Clinicopathologic Conference, Methcathinone (Bath Salts) Intoxication
NEJM 369:2536-2545, Case 40-2013, 2013

Isolated Bipallidal Lesions Caused by Extrapontine Myelinolysis
Neurol 81:1722-1723, Floris, G.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Headache and Focal Neurologic Deficits in a 37-Year-Old Woman
JAMA Neurol 70:1445-1449, Ayodele, M.O.,et al, 2013

Advanced MRI Morphologic Study Shows No Atrophy in Healthy Individuals with Hippocampal Hyperintensity
AJNR 34:1585-1588, Labate, A.,et al, 2013

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

Clinicopathologic Conference, Inflammatory Myopathy and Myasthenia Gravis Assoc. with Thymoma
NEJM 369:764-773, Case 26-2013, 2013

MRI-Identified Pathology in Adults with New-Onset Seizures
Neurol 81:920-927, Hakami, T.,et al, 2013

IgG4-Related Orbital Disease and Enlargement of the Trigeminal Nerve Branches
Neurol 81:e117-e118, Deschamps, R.,et al, 2013

Chiasmal Enlargement and Enhancement in Leber Hereditary Optic Neuropathy
Neurol 81:e126-e127, Ong, E.,et al, 2013

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

West Nile Virus: Review of the Literature
JAMA 310:308-315,267, Petersen, L.R.,et al, 2013

Teaching NeuroImages: Multiple Epidural Abscesses after Acupuncture
Neurol 80:e169, Yu, H.J.,et al, 2013

Teaching NeuroImages: Unilateral Upper Limb Muscular Hyperplasia
Neurol 80:e170-e171, Gilhuis, J.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

The Eye of the Beholder: Inter-rater Agreement among Experts on Psychogenic Jerky Movement Disorders
JNNP 84:742-747, Van de Salm, S.,et al, 2013

Ciguatera Fish Poisoning
JAMA 309:2608, Goodman, D., 2013

The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
Medicine 92:223-243, Rider, L.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

A 39-year-old Man with Abdominal Cramps
Neurol 81:e5-e9, Jaiser, S.,et al, 2013

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Transglutaminase 6 Antibodies in the Diagnosis of Gluten Ataxia
Neurol 80:1740-1745, Hadjivassilou, M.,et al, 2013

Association between Guillain-Barr� Syndrome and Influenza a (H1N1) 2009 Monovalent Inactivated Vaccines in the USA: A Meta-Analysis
Lancet 381:1461-1468, Salmon, D.,et al, 2013

Clinicopathologic Conference, West Nile Virus Infection, Case 15-2013
NEJM 368:1919-1927, Vyas, J.,et al, 2013

Clinical Reasoning: A 12-year-old Boy with Ascending Weakness
Neurol 80:e110-ee114, French, K.F.,et al, 2013

Clinicopatholic Conference, Acute Infection with Hepatitis B Virus
NEJM 368:1239-1245, Case 10-2013, 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Multifocal VZV Vasculopathy with Temporal Artery Infection Mimics Giant Cell Arteritis
Neurol 80:2017-2021, Nagel, M.,et al, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Summary of Evidence-Based Guideline: Periprocedural Management of Antithrombic Medications in Patients with Ischemic Cerebrovascular Disease
Neurol 80:2065-2069, Armstrong, M.,et al, 2013

VZV Ischemic Optic Neuropathy and Subclinical Temporal Artery Infection without Rash
Neurol 80:220-222, Nagel, M.,et al, 2013

The Thalamus and Multiple Sclerosis
Neurol 80:210-219, Minagar, A.,et al, 2013

Correlation of Clinicoserologic and Pathologic Classifications of Inflammatory Myopathies
Medicine 92:15-24, Fernandez, C.,et al, 2013

Polymyalgia Rheumatica
Lancet 381:63-72, Kermani, T. & Washington, K., 2013

Dropped Head Syndrome: Report of Three Cases During Treatment with a Mek Inhibitor
Neurol 79:1929-1932, Chen, X.,et al, 2012

Should we be nervous about coeliac disease? Brain abnormalities in patients with coeliac disease referred for neurologic opinion
JNNP 83:1216-1221, Currie, S.,et al, 2012

Case Report: A Man Who Vomited until he couldnt Walk
Lancet 380:1966, Williams, D.,et al, 2012

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
Neurol 79:2349-2354, Morita, M.,et al, 2012

Neurosyphilis presenting as mesial temporal encephalitis
Neurol 79:e206-e209, AbdeleRahman, K.,et al, 2012

Brain Atrophy is Related to Lacunar Lesions and Tissue Microstructural Changes in CADASIL
Stroke 38:1786-1790, Jouvent, E.,et al, 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Botulinum Toxin A for Prophylactic Treatment of Migraine and Tension Headaches in Adults
JAMA 307:1736-1745, Jackson,J.L.,et al, 2012



Showing articles 1550 to 1600 of 4643 << Previous Next >>