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Differential
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absence
acrocyanosis
agitation
Aicardi-Goutieres syndrome
akathisia
alcohol
alcohol intolerance
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
amyloid angiopathy, cerebral
animal exposure
anticonvulsants
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, effectiveness
anticonvulsants, selection of
anxiety
aphasia
aphasia, progressive
apolipoprotein E
APP gene
apraxia
areflexia
arm weakness
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
beta adrenergic blocker
biologic markers
blindness
bone pain
bovine spongiform encephalopathy
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral vasculature
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
ceruloplasmin, serum
cherry red spot
cherry red spot-myoclonus syndrome
chewing movements
chilbran skin lesions
children
choking
chorea
chorea, familial
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 12
chromosome 2
chromosome 7
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
cognition
cognition, slowed
cogwheel rigidty
color vision, impaired
coma
confabulation
consanguinity
copper metabolism, abnormal
Creutzfeldt-Jakob disease, genetic
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dizziness
Dravet syndrome
drooling
dropped head syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyssynergia cerebellaris myoclonica
dystonia
dystonia, children
dystonia, face
dystonia, treatment of
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, video monitoring with
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
epsilon sarcoglycan gene
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial adult myoclonic epilepsy
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fundus, abnormality of
gait disorder
gangliosidosis GM2
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
granular osmiphilic material
growth hormone
growth retardation
Hallervorden Spatz disease
hallucination
hallucination, visual
handwriting
head lag
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
HLA
hyperekplexia
hyperhidrosis
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hyperthermia
hypertonia
hypertonia, congential
hypomyelination
hypothermia
hypotonia
iatrogenic neurologic disorders
imbalance
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
insight, loss
insomnia
intellectual deficit
intellectual deterioration
interferon alpha
intrauterine
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jewish
juvenile myoclonus epilepsy
Kayser-Fleischer ring
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
linear lesion
lipid storage disorder of CNS
liver biopsy
liver disease
lysosomal storage disease
macular degeneration
MELAS syndrome
memory, defect of recent
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
miglustat
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoparesis
mortality
motor cortex
movement disorder
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, hypointense signal foci on
MRI, negative
MRI, punctate pattern
MRI, susceptibility weighted
multiple sclerosis, misdiagnosis
muscle biopsy
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, essential
myoclonus, sleep
myoclonus, stimulus sensitive
myopathy, mitochondrial
mysoline
negative
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroendocrinology
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropsychiatry
next-generation sequencing
Niemann-Pick disease
normal
nystagmus
nystagmus, rotary
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
palatal myoclonus
paraparesis
paraparesis, spastic
paratonia
Parkinson disease
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pediatric neurology
penicillamine
pituitary, hormones of
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
pontocerebellar atrophy
prenatal
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
propranolol
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
Purkinje cell
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
rapidly progressing neurologic illness
real-time quaking-induced conversion
respiratory failure
retinal degeneration
review article
rigidity
Romberg's sign
Rosenthal fibers
SCN1A gene
screening
seizure
seizure, children
seizure, diagnosis of
seizure, drug resistance
seizure, familial
seizure, febrile
seizure, intractable
seizure, laughing as manifestation
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, prognosis in adults
seizure, stimulus sensitive
seizure, teenager
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
short stature
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sodium valproate
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
sphingolipodoses
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar ataxia type 7
spinopontine atrophy, dominant
spongy degeneration of brain
startle myoclonus
startle reaction
status epilepticus
stereotypy
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuporous
stuttering
systemic illness
tachycardia
tandem gait, ataxic
Tay-Sachs disease
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
titubation
tone, muscle, increased
topiramate
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, leg
tremor, treatment of
trichopoliodystrophy
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
visual acuity, decreased
visual loss
visuospatial disturbance
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
Wolfram syndrome
workup
Showing articles 1050 to 1100 of 2026 << Previous Next >>

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Acetylcholine Receptor Antibodies in Juvenile Myasthenia Gravis
Neurol 43:977-982, Andrews,P.I.,et al, 1993

Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Identical Twins with Similar Onset of Parkinson's Disease:A Case Report
Neurol 43:1159-1161, Pahwa,R.,et al, 1993

Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993

Juvenile Myoclonic Epilepsy
Arch Neurol 50:594-598, Grunewald,R.A.&Panayiotopoulos,C.P., 1993

Novel Brainstem Syndrome Associated with Prostate Carcinoma
Neurol 43:2591-2596, Baloh,R.W.,et al, 1993

Autosomal Dominant Parkinsoniam with Benign Course and Typical Lewy-Body Pathology
Neurol 43:2222-2227, Golbe,L.I.,et al, 1993

DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
JAMA 270:2316-2320, MacCollin,M.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Copper-Histidine Therapy for Menkes Disease
J Pediatr 123:828-830, Sarkar,B.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

Twinning and Cerebral Palsy:Experience in Four Northern California Counties, Births 1983 Through 1985
Pediatrics 92:854-858, Grether,J.K.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Twin Birth is Not a Risk Factor for Seizures
Neurol 43:2515-2519, Berkovic,S.F.,et al, 1993

Myoclonus Associated with Hyperthyroidism and Thymoma:A Case Report
Chin Med J 51:138-140, Liao,K-K.,et al, 1993

Familial Aggregation of Stroke
Stroke 24:1366-1371, Kiely,D.K.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
Lancet 341:1179-1181, Rose,J.,et al, 1993

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

Conjugal Alzheimer's Disease:Is There an Increased Risk in Offspring?
Ann Neurol 34:396-399, Bird,T.D.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Migraine Madness:Recurrent Psychosis after Migraine
JNNP 56:416-418, Fuller,G.N.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Sleep Paralysis
Lancet 341:406-407, Dahlitz,M.&Parkes,J.D., 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Antineuronal (anti-Ri) Antibodies in a Pt with Steroid-Responsive Opsoclonus-Myoclonus
Neurol 43:207-211, Dropcho,E.J.,et al, 1993

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

A Population-Based Study of Multiple Sclerosis in Twins:Update
Ann Neurol 33:281-285, Sadovnick,A.D.,et al, 1993

Use of Twin Cohorts for Research in Alzheimer's Disease
Neurol 43:261-267, Breitner,J.C.S.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993

Erythromelalgia:Association with Hereditary Sensory Neuropathy and Response to Amitriptyline
Neurol 43:621-622, Herskovitz,S.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Fatal Rabies Associated with Extensive Demyelination
Arch Neurol 50:317-323, Nelson,D.A.&Berry,R.G., 1993



Showing articles 1050 to 1100 of 2026 << Previous Next >>