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Differential
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acetazolamide
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
akinetic mute
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
anorexia
areflexia
arm swing, reduced
arrhythmia, cardiac
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
atrial fibrillation
attention deficit disorder with hyperactivity
attention span
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
bone marrow transplantation
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, syndrome
cardiomyopathy
CAT scan
CAT scan, abnormal
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congestive heart failure
consanguinity
corona radiata
cortical-basal ganglionic degeneration
cough
cranial neuropathy
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
depression
developmental milestones, loss of
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
electroencephalogram, abnormalities of
electromyogram
electrophoretic pattern, CSF
embolism
encephalitis
encephalopathy
epileptic encephalopathy
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial periodic ataxia
FARS2 deficiency
fatigue
fine motor function, impaired
finger nose finger test
finger numbness
foam cells
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glabellar sign
granular osmiphilic material
hammertoes
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
hormone replacement
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hypertonia
hypogonadism
hypogonadism, hypogonadotropic
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
Kayser-Fleischer ring
lacunar infarction
lacunar infarction, differential diagnosis of
lateropulsion
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
Lorenzo's oil
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
meningitis, CSF cell count-normal
microcephaly
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, spinal cord
MRI, spine
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
myelomalacia
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, sensory
next-generation sequencing
Niemann-Pick disease
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
olivary degeneration, hypertrophic
optic atrophy
ovarian dysgenesis
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
Perrault syndrome
personality change
pes cavus
pons, infarction of
pontine hemorrhage
positional head-hanging test
prevention of neurologic disorders
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
pure dysarthria
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
release phenomena
retropulsion
review article
rigidity
risk factors
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella virus
saccadic eye movements, abnormal
scoliosis
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
slit lamp examination
slurred speech
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
splenomegaly
spontaneous remission
square wave jerks
staggering
strokelike episodes
suck reflex
superior cerebellar artery infarction
superior cerebellar artery syndrome
symmetric brain lesions
tandem gait, ataxic
tau protein
tauopathy
thalamus, lesion of-bilateral
titubation
toe walking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vertigo, episodic
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, blurred
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
white matter disease
wide based gait
workup
 		Showing articles 100 to 150 of 1064 << Previous Next >>

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Clinicopath Conf
Acute & Chronic BActerial Osteomyelitis & Diskitis with Epidural Abscess, Case 16-1992, NEJM 326:107, -1076,, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Neurologic Syndrome in 25 Workers from an Aluminim Smelting Plant
Arch Int Med 152:1443-1448, White,D.M.,et al, 1992

"Numb, Clumsy Hands" and Tactile Agnosia Sescondary to High Cervical Spondylotic Myelopathy: A Clinical and Electrophysiological Correlation
Acta Neurol Scand 86:622-625, Chang,M.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Wilson Disease:Clinical Presentation, Treatment, and Survival
Ann Int Med 115:720-726, Stremmel,W.,et al, 1991

Parkinsonism and Defects of Praxis Following Methanol Poisoning
JNNP 54:843-844, Mozaz,M.J.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Neurologic Signs in Senescence
Arch Neurol 42:1154-1157, Jenkyn,L.R.,et al, 1985

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Asperger's Syndrome:A Clinical Account
Psychological Medicine 11:115-129, Wing,L., 1981

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Giant Axonal Neuropathy
Arch Neurol 36:107-108, Mizuno,Y.,et al, 1979

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Acute Bulbar Dysfunction & Hyperthyroidism
Am J Med 56:464, Kammer,G.M.,et al, 1974

Speech Defects in Children Aged 7 yrs, A National Study
BMJ 253, 1973 Feb., Butler,N.,et al, 1973

Specific Learning Disorders in Childhood
Psych Annals 2:, 1972 May., Gomez,M.R., 1972

Enlargement of the Sylvian Aqueduct:A Sequel of Head Injuries
JNNP 35:463-467, Boller,F.C.,et al, 1972

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024



Showing articles 100 to 150 of 1064 << Previous Next >>