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Differential
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acanthocytosis
adrenoleukodystrophy
adverse drug reaction
alopecia
anisocoria
anosmia
aphasia
areflexia
Argyll Robertson pupil
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxic gait
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
bladder dysfunction
blepharospasm
blindness
bradykinesia
brain atrophy
brainstem, atrophy
bulbar palsy
cachexia
calcification, intracranial
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
craniopharyngioma
cry, weak
cryptorchidism
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
diplegia, spastic cerebral
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmorphic
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
enzyme, defect
eye injury
eyes, sunken
facial appearance, abnormal
falling
false negative
false negative VDRL
familial
fasciculation
feeding disorder
fingerprint bodies
fluorescein angiography
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
gait disorder
gargoylism
gastrointestinal motility
gene
gene mutation
genetic linkage
genetic neurologic disorders
glaucoma
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
headache
hearing loss
hearing loss, bilateral
hearing loss, congenital
heart block
Hurler's syndrome
hydrocephalus
hyperpigmentation of skin
hyperreflexia
hypocholesterolemia
hypogonadism
hypoparathyroidism
hyposmia
imbalance
immunofluorescence
inclusion bodies
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iris, atrophy of
iron, brain
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
lens, dislocation of
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
light-near dissociation, causes of
macular degeneration
malabsorption
malformation, CNS, congenital
marche a petits pas
Marcus Gunn pupil
MELAS syndrome
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
myelopathy
myoclonus
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
neuritis
neurocutaneous disease
neuroichthyosis
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neurosyphilis
night blindness
nystagmus
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic glioma
optic nerve
optic nerve, neoplasm of
optic neuropathy
optical coherence tomography
palilalia
pancytopenia
PANK2 mutation
paraparesis
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
PAS positive material in the brain
peroxisomal disease
pes cavus
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
polyneuropathy
postural abnormality
progeria
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pupil
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
ragged-red fibers
rash
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal detachment
retinal lesion
retinitis pigmentosa
retinoblastoma
retinopathy
review article
rigidity
roving eye movements
schizophrenia
scotoma
scotoma, central
sea-blue histiocytes
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
serologic test for syphilis
sheathing of retinal veins
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, lesions in neurologic disorders
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia type 1
spinocerebellar degeneration
steatorrhea
stooped posture
substantia nigra
sudden death
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
tabes dorsalis
Tangier's disease
tapetoretinal degeneration
trauma
treatment of neurologic disorder
tremor
Usher's syndrome
uveitis
vision loss, sequential
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field defect, altitudinal
visual fields, constricted
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitritis
walking, difficulty with
weakness
weight loss
white matter disease
Wolfram syndrome
workup
Showing articles 100 to 150 of 817 << Previous Next >>

Management of Acute Retinal Ischemia
Ophthalmol 125:1597-1607, Viousse, V.,et al, 2018

Clinicopathologic Conference, Susacs Syndrome
NEJM 379:2152-2159, Case 37-2018, 2018

A Case of Bilateral Orbital Mass Lesions Presenting with Acute Monocular Vision Loss
Neurol 91:e2192-e2196, Bhatt, N.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 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

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Clinicopathologic Conference, Intracranial Hypertension Associated with Systemic Lupus Erythematosus and Steroid Use
NEJM 378:282-289, Case 2-2018, 2018

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018

Wyburn-Mason Syndrome
BMJ 360:k639, Guo, H.P,.et al, 2018

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

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

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

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

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

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

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

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

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Subarachnoid Hemorrhage
Medscape Aug, Becske, T. & Lutsep, H.L., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Terson Syndrome on CT head
Neurol 87:e133-e134, George, J.S.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Retinal Artery Occlusion and the Risk of Stroke Development
Stroke 47:376-382, Hyungtaek, T.,et al, 2016

A Red Eye from Carotid Stenosis
BMJ 352:e364, Perera, S.,et al, 2016

Ocular Manifestations in Systemic Lupus Erythematosus
Br J Ophthalmol 100:135-144, Silpa-Archa,S.,et al, 2016

Risk of Stroke in Retinal Vein Occlusion
Neurol 85:1578-1584, Park, S.J.,et al, 2015

Central Retinal Vein Occlusion with Bilateral Stenosis of the Internal Carotid Arteries
Lancet 385:914, Baroon, R. & Carvounis, P.E., 2015

Efficacy of Idebenone on Respiratory Function in Patients with Duchenne Muscular Dystrophy not using Glucocorticoids (DELOS): A Double-Blind Randomised Placebo-Controlled Phase 3 Trial
Lancet 385:1748-1757,1704, Buyse, G.M.,et al, 2015

Intravenous Fibrinolytic Therapy in Central Retinal Artery Occlusion
JAMA Neurol 72:1148-1154, Schrag, M.,et al, 2015

Retrobulbar Spot Sign Predicts Thrombolytic Treatment Effects and Etiology in Central Retinal Artery Occlusion
Stroke 46:2322-2324, Nedelmann, M.,et al, 2015

Complex Regional Pain Syndrome
Neurol 84:89-96, Birklein, F.,et al, 2015

Acute Myopia and Angle Closure Glaucoma from Topiramate in a Seven-Year-Old: A Case Report and Review of the Literature
BMC Pediatrics 14:96, Rapoport, Y.,et al, 2014

Blurred Vision and Epistaxis
BMJ 348:g91, Shirley, K. & McNicholl, F.P., 2014

Snowball-like Lesions with Sudden Hearing Loss
Neurol 82:e100, Oliveira, P. & Mayeux, J., 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Sudden Unilateral Painless Loss of Vision
BMJ 349:g4117, Georgalas, I.,et al, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

A Woman with Subacute Progressive Confusion and Gait Instability
Neurol 83 ;e62-e67, Martinez-Thompson, J.M.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Opportunistic Infections of the Retina in Patients with Aquaporin-4 Antibody Disease
JAMA Neurol 71:1429-1432, George, J.S.,et al, 2014

Posterior Reversible Encephalopathy Syndrome with Spinal Cord Involvement
Neurol 83:2002-2006,1996, de Havenon, A.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Acute Visual Loss with Ophthalmoplegia after Spinal Surgery: Report of a Case and Review of the Literature
Indian J Ophthalmol 62:963-965, Mukherjee, B. & Alam, M.S., 2014

The Acquired Metabolic Disorders of the Nervous System, High-Altitude (mountain) sickness
Adams & Victors Principles of Neurology Chp 40, pg 1139, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
Adams & Victors Principles of Neurology, Chp 31, pg 668, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014



Showing articles 100 to 150 of 817 << Previous Next >>