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Differential
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acanthocytosis
accomodation, abnormal
acral sensory symptoms
alternating rapid movement
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anal wink response
anorexia
antecedent illness
anti GQ1b IgG antibody
antiganglioside antibodies
antioxidant
areflexia
arrhythmia, cardiac
ascending paralysis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atypical
autoantibodies
axonal degeneration
Babinski sign
botulism
brain atrophy
Brown-Vialetto-Van Laere syndrome
bulbar palsy
bulbar palsy, acute
burning paresthesia
campylobacter infection
cardiomyopathy
CAT scan
CAT scan, abnormal
caudate nucleus, atrophy
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellum, disease of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
Charcot-Marie-Tooth
children
chorea
chorein
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
congestive heart failure
consanguinity
constipation
contractures, joint
corneal reflex, abnormal
corpus callosum, hypoplastic
corpus callosum, lesion of
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
denervation of muscle
denervation potentials
developmental disability
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dopa responsive dystonia
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dystonia
dystonia, children
electromyogram
electromyogram, decremental response
encephalopathy
encephalopathy, progressive
enteritis
enzyme, defect
episodic neurologic deficits
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
Fisher's syndrome
flaccid paralysis
flu-like illness
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
F-wave response
gait disorder
galactorrhea
gaze palsy
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
glioma
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hammertoes
hand deformity
hearing loss
heel-knee-shin test
hoarseness
hydrocephalus
hyperreflexia
hypertonia
hypophosphatemia
hyporeflexia
hypotonia
imbalance
immunoelectrophoresis, serum
incoordination
intellectual deficit
L-dopa
leg weakness, bilateral
leg weakness, unilateral
lethargy
lid
lid abnormalities
lip, biting
liver disease
lymphadenopathy
malabsorption
meningismus
mental retardation
microcephaly
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, spinal cord
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
myelomalacia
nasal speech
nausea and vomiting
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, sensory
neurotoxin
next-generation sequencing
numbness, ascending
numbness, extremity
nystagmus
nystagmus, gaze-evoked
nystagmus, vertical
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
overlap syndrome
pain, abdominal
palatal myoclonus
papilledema
paralysis
paralysis, acute
paralysis, acute areflexic
parenteral alimentation
paresthesias
Parkinson disease
Parkinsonism syndrome
perioral numbness
pes cavus
philtrum, tented
POLG1 gene
positional head-hanging test
postoperative neurologic complications
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
prolactin, elevated
proprioception, abnormal
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
quadriparesis
quadriplegia
reading disorder, acquired
recurrent
renal tubular acidosis
ReNU syndrome
repetitive nerve stimulation
respiratory failure
respiratory tract infection
reversible neurologic disorder
review article
riboflavin transporter deficiency
Romberg's sign
saccadic eye movements, abnormal
scannig speech
scoliosis
seizure
sensory loss
sensory nerve action potentials
short stature
single photon emission computed tomography
slurred speech
spastic ataxia
spasticity
speech arrest
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, absence of
speech, loss of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spinopontine atrophy, dominant
spontaneous remission
stool culture
subdural hematoma
tandem gait, ataxic
tauopathy
telangiectases
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
tick bite
tick paralysis
tongue, biting
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, postural
trinucleotide repeats
tyrosine hydroxylase deficiency
upgaze, paralysis of
vestibulopathy
vibratory sensation, abnormal
vision, blurred
vital capacity
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
workup
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 700 to 750 of 845 << Previous Next >>

Aphasic Status Epilepticus:A Case Report
Neurol 31:888-890, Dinner,D.S., 1981

Isolated Fear in Complex Partial Status Epilepticus
Ann Neurol 8:639-641, McLachlan,R.S.,et al, 1980

Ocular Myasthenia:Diagnosis & Therapy
In Neuro-Ophthalmology, Vol X ed. by J. Glaser. CV Mosby Co, St. Louis, Daroff,R., 1980

The Acute Sensory Neuronopathy Syndrome:A Distinct Clinical Entity
Ann Neurol 7:354-358, Sterman,A.B.,et al, 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

The Aphasia Syndrome of Stroke in the Left Anterior Cerebral Artery Territory
Arch Neurol 37:97-l00, Alexander,M.P.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Aphasia After Left Hemispheric Intracerebral Hemorrhage
Neurol 30:1193-1202, Alexander,M.P.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Studies Of A Patient With Megaloblastic Anemia & An Abnormal Transcobalamin II
NEJM 303:1209-1212, Seligman,P.A.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Children's Language Disorders:Recent Research Advances
Ann Neurol 7:497-507, Ludlow,C.L., 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Complex Partial Status Epilepticus following Myelography with Metrizamide
Ann Neurol 8:325-327, Russel,D.,et al, 1980

Valproic Acid Therapy in Childhood Epilepsy
JAMA 244:785-788, Coulter,D.L.,et al, 1980

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

Tapia's Syndrome
Arch Neurol 36:257-260, Schoenberg,B.S.,et al, 1979

Cervical Myelopathy after Metrizamide Myelography
BMJ 2:1262-1263, Bastow,M.,et al, 1979

Aphasia Rehabilitation
Arch Neurol 36:187, Benson,D.F., 1979

Aphasia, The Sole Manifestation of Focal Status Epilepticus
Neurol 29:745-748, Hamilton,N.G.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Interaction Between Clonazepam & Sodium Valproate
NEJM 300:678-679, Watson,W.A., 1979

Electroencephalographic Absence Status with Minimal Behavior Change
Arch Neurol 36:176-178, Fincham,R.W.,et al, 1979

Language Deficits After Apparent Clinical Recovery from Childhood Aphasia
Ann Neurol 6:405-409, Woods,B.,et al, 1979

Aphemia with Hemiplegic Migraine
Neurol 29:1317-1318, Jenkyn,L.R., 1979

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Headaches After Lumbar Puncture & Insensitivity To Pain In Psychiatric Patients
NEJM 301:110, Torrey,E., 1979

Pain Sensitivity In Schizophrenics
NEJM 301:946-947, Hoo,J.J.,et al, 1979

Absence Status (Petit Mal Status) With Focal Characteristics
Arch Neurol 36:417-421, Niedermeyer,E.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Aphasia Following Infarction of the Left Supplementary Motor Area
Neurol 28:1220-1223, Masdeu,J.C.,et al, 1978

Identification of Speech Lateralization by Intracarotid Injection of Methohexital
Ann Neurol 4:86, Willmore,L.J.,et al, 1978

Changing Patterns of Childhood Aphasia
Ann Neurol 3:273, Woods,B.T.,et al, 1978

Speech Arrest in a Dextral with a Right MesialFfrontal Astrocytoma
Arch Neurol 35:252, Caplan,L.R.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Polyneuropathy in Waldenstrom's Macroglobulinemia
Arch Neurol 35:423, Julien,J.,et al, 1978

Neuropathy Following Abuse of Nitrous Oxide
. et al, Neurol 28:504978., Layzer,R.B., 1978

Prolonged Epileptic Twilight States:Continuous Recordings with Nasopharyngeal Electrodes & Videotape Analysis
Neurol 28:239, Belafsky,M.A.,et al, 1978

Complex Partial Status Epilepticus (Psychomotor Status)
Neurol 28:189, Markand,O.N.,et al, 1978

Drug Therapy, Clonazepam
NEJM 299:812-816, Brown,T.R., 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978



Showing articles 700 to 750 of 845 << Previous Next >>