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Differential
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abdominal distention
acanthocytosis
adrenoleukodystrophy
adverse drug reaction
alopecia
Alzheimer's disease
anisocoria
anosmia
antiretinal antibodies
aphasia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Argyll Robertson pupil
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
autoantibodies
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
brain biopsy
brainstem, atrophy
brainstem, hypoplasia
bulbar palsy
cachexia
calcification, intracranial
calf hypertrophy
CAR syndrome
carcinoma
carcinoma of lung
cardiomyopathy
caries
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral palsy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 17
chromosome 20
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
color vision
color vision, impaired
cone-rod dystrophy
congenital heart disease
congenital infection, CNS
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, hypoplastic
cranial nerve palsies
craniopharyngioma
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
cyst
cyst, parenchymal
cyst, subcortical
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
developmental abnormality of brain
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
diplegia, spastic cerebral
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalocele
enzyme, defect
epidermal nevus syndrome
extraocular muscle lesion
eye injury
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
false negative VDRL
familial
fasciculation
fatty acid dehydrogenase deficiency
feeding disorder
fingerprint bodies
fluorescein angiography
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
fourth ventricle, enlargement of
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glare, light-induced
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
hand flapping
headache
hearing loss
hearing loss, bilateral
hearing loss, congenital
hearing problems in children
heart block
hepatomegaly
heralding manifestation
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperpigmentation of skin
hyperreflexia
hypocholesterolemia
hypogonadism
hypomagnesemia
hypoparathyroidism
hyposmia
hypotonia
imbalance
immunofluorescence
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
intestinal pseudoobstruction
intrauterine infection, viral of CNS
iris, abnormal
iris, atrophy of
iron, brain
Joubert syndrome
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
life expectancy
light-near dissociation, causes of
lissencephaly
lymphocyte fingerprint profiles
lysosomal storage disease
macular degeneration
malabsorption
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
marche a petits pas
Marcus Gunn pupil
medial longitudinal fasciculus(MLF)
MELAS syndrome
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
micropthalmia
misdiagnosis
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
MRS
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myelopathy
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
myotonia dystrophica
nausea and vomiting
neuraminidase deficiency
neuritis
neurocutaneous disease
neuroendocrinology
neurogenic vs.myopathic atrophy
neuroichthyosis
neurolipidosis IV
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neurosyphilis
nevus
night blindness
nystagmus
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic glioma
optic nerve
optic nerve, lesion of
optic nerve, neoplasm of
optic neuropathy
optic neuropathy, hereditary
optical coherence tomography
pain, abdominal
palilalia
pancytopenia
PANK2 mutation
paraparesis
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
PAS positive material in the brain
patent ductus arteriosus
peroxisomal disease
peroxisomes
pes cavus
photophobia
photosensitivity, eye
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
polymyositis
polyneuropathy
Poretti-Boltshauser syndrome
postural abnormality
progeria
prognosis
progressive neurologic disorder
pseudohypertrophy
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
quadriparesis
quadriplegia
ragged-red fibers
rash
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
retina, abnormal
retinal arteriole attenuation
retinal degeneration
retinal detachment
retinal dysplasia
retinal lesion
retinitis pigmentosa
retinoblastoma
retinopathy
retropulsion
review article
RFLPs
rigidity
Romberg's sign
roving eye movements
rubella syndrome
schizophrenia
scotoma
scotoma, central
scotoma, paracentral-homonymous
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
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
skull x-ray, abnormal
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
spongy degeneration of brain
steatorrhea
steroid
steroid therapy, CNS treatment and complications with
stooped posture
substantia nigra
sudden death
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
systemic illness
tabes dorsalis
Tangier's disease
tapetoretinal degeneration
telangiectases
telangiectases, retinal
testicular atrophy
third nerve palsy
titubation
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
Usher's syndrome
uveitis
ventricular enlargement
viral infection, CNS
vision loss, sequential
vision, blurred
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
visual loss, sudden
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitritis
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
white matter disease
wide based gait
Wolfram syndrome
workup
Showing articles 150 to 200 of 809 << Previous Next >>

Acute severe visual loss and a brainstem mass
Lancet 380:1790, Meleth, A.,et al, 2012

Spectrum of Neurologic Complications in Chronic Lymphocytic Leukemia
Clin Lymphoma Myeloma Leuk 12:164-179, Lopes da Silva, R., 2012

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Muscle Histology vs MRI in Duchenne Muscular Dystrophy
Neurol 76:346-353, Kinali,M.,et al, 2011

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
Neurol 77:62-66, Schade van Westrum, S.M.,et al, 2011

Efficacy of Intravenous Tissue-Type Plasminogen Activator in Central Retinal Artery Occlusion Report From a Randomized, Controlled Trial
Stroke 42:2229-2234, Chen, C.S.,et al, 2011

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

MR Imaging of Vogt-Koyanagi-Harada Syndrome with Leptomeningeal Enhancement
AJNR 32:E169-E171, Lohman, B.D.,et al, 2011

Cancer Risk Among Patients with Myotonic Muscular Dystrophy
JAMA 306:2480-2486, Gadalla, S.M.,et al, 2011

Epidemiology, Pathogenesis, Clinical Manifestations and Diagnosis of Waldenstrom Macroglobulinemia
UptoDate, May, Rajkumar, S.V., 2011

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Clinical Presentation, Pathologic Features, and Diagnosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Clinicopath Conference, Giant Cell Arteritis
NEJM 362:537-546, Case 4-2010, 2010

Middle Cerebral Artery Aneurysm Rupture Presenting as Pure Acute Subdural Hematoma
Neurol 74:e13, Field,T.S. &Heran,M.K.S., 2010

Mexiletine Is an Effective Antimyotonia Treatment in Myotonic Dystrophy Type 1
Neurol 74:1441-1448, Logigian,E.L., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Longitudinal Study of Vision and Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis
Ann Neurol 67:749-760, Talman,L.S., et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Clinical Features of Facioscapulohumeral Muscular Dystrophy 2
Neurol 75:1548-1554, Greef,J.C.,et al, 2010

Perioperative Visual Loss in Ocular and Nonocular Surgery
Clin Ophthalmol 4:531-546, Berg, K.T.,et al, 2010

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

A 28-Year-Old Pregnant Woman with Encephalopathy
Neurol 73:e74-e79, Grinspan,Z.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Case 38-2009: A 16-Year-Old Boy with Paroxysmal Headaches and Visual Changes
NEJM 361:2367-2378, Brass,S.,et al, 2009

Carotid Plaque Rupture
Lancet 374:1703, Keenan,N.,et al, 2009

Interferon �-Associated Retinopathy in Patients Treated for Multiple Sclerosis
Neurol 70:1153-1155, Folden,D.V.,et al, 2008

T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
Neurol 70:1614-1619, McNeill,A.,et al, 2008

Local Intraarterial Fibrinolysis Administered in Aliquots for the Treatment of Central Retinal Artery Occlusion: The Johns Hopkins Hospital Experience
Stroke 39:1746-1750, Aldrich,E.M.,et al, 2008

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
Arch Neurol 65:1196-1201, Sveen,M.-L.,et al., 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Primary CNS Lymphoma with Intraocular Involvement: International PCNSL Collaborative Group Report
Neurol 71:1355-1360, Grimm,S.A.,et al, 2008

Clinicopath Conference, Postpartum Renal Failure Due to Thrombotic Microangiopathy Associated With Antiphospholipid Antibodies
NEJM 358:275-289, Case 2-2008, 2008

Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
Neurol 70:1128-1133, Keegan,B.M.,et al, 2008

Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007

Orthopedic Outcomes of Long-Term Daily Corticosteroid Treatment in Duchenne Muscular Dystrophy
Neurol 68:1607-1613, King,W.M.,et al, 2007

What Do We Really See When We Look at Magnetic Resonance Images?
Ann Neurol 62:207-208, Filippi,M. &Hartung,H.-P., 2007

Visual Loss After Povidone-Iodine Pleurodesis
NEJM 357:1264-1265, Khuri,F.R., 2007

Gene Therapy for Duchenne Muscular Dystrophy: Expectations and Challenges
Arch Neurol 64:1236-1241, Rodino-Klapac,L.R.,et al, 2007

Sudden Visual Loss
Lancet 370:590, Khan,J. &Chang,V., 2007

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Ocular Ischaemic Syndrome: A Medical Emergency
Lancet 367:1370, Chuah,J.L.,et al, 2006



Showing articles 150 to 200 of 809 << Previous Next >>