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Differential
(Click to cross reference)
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
advances in neurology
agammaglobulinemia
akinesia of eyelid function
ANA
apraxia of eyelid opening
arrhythmia, cardiac
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atrial fibrillation
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blepharospasm
blindness
botulism
brainstem, lesion of
brainstem, tuberculoma of
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cause of death
celiac disease, childhood
cerebellar ataxia, primary
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot's sign
chemosis
children
chromosomal abnormality
chromosome 14
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cogwheel rigidty
collagen vascular disease
coma
conjunctival injection
consanguinity
cornea, abnormal
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
deafmute
deafness
dementia
diabetes mellitus
digitalis intoxication
diplopia
dwarfism
dysarthria
dysphagia
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystrophin
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, progressive
enzyme, muscle disease
epidemiology of neurology
exercise intolerance
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
familial
fasciculation
fatigue
fibrillations
Fisher C.M.
fistula, arterio-venous, carotid-cavernous
Friedreich's ataxia
gait disorder
gargoylism
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
glabellar sign
glaucoma
Graves ophthalmopathy
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
hemianopia, homonymous
hepatic failure
hippus
Hispanics
histochemistry of muscle
Hurler's syndrome
hyperthyroidism
hypoglycorrhachia
hypogonadism
hypotonia
imbalance
immunohistochemistry
intestinal pseudoobstruction
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
lid closure, weakness of
malformation, CNS, congenital
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
MERRF syndrome
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
movement disorder
MRI
MRI, abnormal
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
myoclonus
myopathy
myopathy, distal
myopathy, mitochondrial
myopia
myositis
myositis, ocular
myotonia dystrophica
neck weakness
negative
neuritis
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
normal
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic disc edema
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
pons, lesion of
prognosis
progressive infantile poliodystrophy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, bilateral
proptosis, unilateral
prostigmine
pseudobulbar palsy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
ptosis, familial
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
ragged-red fibers
Raynaud's phenomenon
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate
seizure
sensorineural hearing loss
seronegative
short stature
skin, tight
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
standing difficulty
Stephens syndrome
steroid therapy, CNS treatment and complications with
strokelike episodes
symmetric brain lesions
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
upgaze, paralysis of
Usher's syndrome
visual field defect
visual fields, constricted
visual loss
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
wheelchair
white matter disease
wide based gait
xanthopsia
Showing articles 600 to 650 of 2440 << Previous Next >>

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,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

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 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

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

Clinical Reasoning: A 66-year-old Woman with Seizures and Progressive Right-Sided Weakness
Neurol 90:e435-e439, St-Pierre, B.D.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

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

Clinicopathologic Conference, Human Herpesvirus 6-Related Meningoencephalitis
NEJM 378:659-669, Case 5-2018, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

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

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

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

Orbital Apex Syndrome
NEJM 378:18, Sacks. C.A., 2018

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

Progressive multifocal leukoencephalpathy after fingolimod treatment
Neurol 90:1815-e1821, Berger, J.R.,et al, 2018

Clinicopathologic Conference, Digitalis Toxicity
NEJM 378:1931-1938, Case 15-2018, 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Progressive Multifocal Leukoencephalopathy after Treatment with Nivolumab
Emerg Inf Dis 24:1594-1596, Martinot, M.,et al, 2018

Endoscopic Management of a Fourth Ventricular Cyst
Asian J Neurosurg 13:503-506, Jafarpour,S., et al, 2018

Ophthalmic Manifestations of Giant Cell Arteritis
Rheumatology 57:ii63-1172, Vodopivec, I. & Rizzo, J.F. III, 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

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

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

Ocrelizumab versus Placebo in Primary Progressive Multiple Sclerosis
NEJM 376:209-220,280, Montalban, X.,et al, 2017

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 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



Showing articles 600 to 650 of 2440 << Previous Next >>