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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 1300 to 1350 of 4643 << Previous Next >>

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Rituximab as Treatment for anti-MuSK myasthenia gravis
Neurol 89:1069-1077, Hehir, M.K.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Neurologic Complications Associated with the Zika Virus in Brazilian Adults
JAMA Neurol 74:1190-1198,1164, Ferreira da Silva, I.R.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

A Case of Altered Mental Status, Not Otherwise Specified
Neurol 89:e154-e158, Swor, D.E.,et al, 2017

Alemtuzumab CARE-MS I 5-year follow-up
Neurol 89:1107-1116, Havrdova, E.,et al, 2017

Alemtuzumab CARE-MS II 5-year follow-up
Neurol 89:1117-1126, Coles, A.J.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

A Man with Rapidly Ascending Paralysis
Neurol 89:e25-e31, Rosenberg, J.,et al, 2017

Subarachnoid Hemorrhage
NEJM 377:257-266, Lawton, M.T. & Vates, G.E., 2017

Clinicopathologic Conference, Probable Acute Leptospirosis
NEJM 377:268-278, Case 22-2017, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

Acute Spinal Cord Compression
NEJM 376:1358-1369, Ropper, A.E. & Ropper, A.H., 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Posterior Ischemic Optic Neuropathy
UptoDate Aug, Tamhankar, M. & Volpe, N., 2017

Neuropsychiatric Involvement of Behcets Disease
www.SMGEbooks.com Dec, Soyak, M., 2017

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

A 35-year-old Woman with Hyperstartling Stiffness, and Accidental Falls
Neurol 88:e38-e41, Russo, S.P.,et al, 2017

Acute Hydrocephalus Caused by Radiographically Occult Fourth Ventricular Outlet Obstruction
Neurol 88:e36-e37, Duran, D.,et al, 2017

Rheumatoid Pannus of the Cervical Spine
Neurol 88:e51, Weerasinghe, D.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

MRI Findings in Collet-Sicard Syndrome
Neurol 88:811, , 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barre Syndrome
JAMA Neurol 74:26-33, Stevens, O.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Disseminated Cysticercosis
NEJM 375:e52, Baden, L.R., 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
, Griffiths, P.D.,et al, 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Tongue Fasciculations in Organophosphate Poisoning
NEJM 375:e47, Bande, L.R., 2016

Idiopathic Hypertrophic Pachymeningitis
Neurol 87:e270-e271, Wasilewski, A. & Samkoff L., 2016



Showing articles 1300 to 1350 of 4643 << Previous Next >>