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Differential
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agitation
aminoacidopathies
aminoacidurias
aneurysm
aneurysm, intracranial
anosognosia
antiviral agents
aphasia
aphasia, global
aphasia, transcortical
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
athetosis
atypical
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basilar artery stenosis
behavioral disorder
bilirubin encephalopathy
blindness, sudden
brain atrophy
brain damage
brainstem, lesion of
breast feeding
bulbar palsy
CAG repeats
CAT scan
CAT scan, abnormal
catalepsy
cataplexy
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrospinal fluid, glycine
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
choreoathetosis
chromosomal abnormality
chromosome 6
Clinical Pathologic Conference(C.P.C.)
congenital myasthenic syndromes
conjugate gaze, forced
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
developmental retardation
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
disease modifying agents
downward gaze, paralysis of
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
emtricitabine
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
epidemiology of neurology
executive dysfunction
exercise intolerance
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
false negative
familial
fever
floppy infant
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
Guillain Barre syndrome, infantile and childhood form
hallucination
hallucination, visual
head injury
headache
hearing loss
hemiparesis
hemorrhage, thalamic
hepatomegaly
hepatosplenomegaly
hoarseness
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypophonia
hyporeflexia
iatrogenic neurologic disorders
imbalance
impulsivity
inattention
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, location of
intracerebral hemorrhage, volume
intraventricular hemorrhage
jaundice
kernicterus
lactic acidemia
leucine
lid closure, weakness of
life expectancy
lipid storage disorder of CNS
lysosomal storage disease
maple syrup urine disease
MELAS syndrome
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
metabolic disorder, primary
miglustat
migraine
mimics
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
moro reflex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, muscle
MRI, negative
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myoclonus
myopathy
myopathy, drug-induced
myopathy, mitochondrial
nasal speech
nausea and vomiting
neglect
neoplasm, primary of CNS
nerve conduction studies
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neurotoxic
neurotoxin
Niemann-Pick disease
nystagmus
ocular motility, disorders of
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, head injury causing
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
ophthalmoplegia, total
ophthalmoplegic migraine
opisthotonus
organomegaly
paranoia
Parkinsonism syndrome
personality change
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
ragged-red fibers
rapidly progressing neurologic illness
renal failure
retinal degeneration
retropulsion
review article
salivation, excessive
schizophrenia
screening
seizure
seizure, children
seizure, laughing as manifestation
sensorimotor stroke
sensorineural hearing loss
setting sun phenomena
short stature
skew deviation
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
strokelike episodes
subthalamic nucleus
suck, poor
systemic illness
temporal lobe, lesion
term infant
thalamic aphasia
third nerve palsy
third nerve palsy, childhood
third nerve palsy, congenital
third nerve palsy, cyclic
transverse smile
treatment of neurologic disorder
tremor
trinucleotide repeats
upgaze, paralysis of
ventricular enlargement
vertical gaze
viral infection
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
visuospatial disturbance
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
wheelchair
whole genome sequencing
wide based gait
Showing articles 850 to 900 of 1791 << Previous Next >>

Expanded Spectrum of Herpes Simplex Encephalitis in Childhood
J Pediatr 126:234-241, Schlesinger,Y.,et al, 1995

Postvaricella Basal Ganglia Infarction in Children
AJNR 16:449-452, Silverstein,F.S.&Brunberg,J.A., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Cranial Ultrasound Predict of Disabling & Nondisabling Cerebral Palsy at Age Two in Low Birth Wt Population
Pediatrics 95:249-254, Pinto-Martin,J.A.,et al, 1995

Painful Oculomotor Palsy Caused by Posterior-Draining Dural Carotid Cavernous Fistulas
Arch Ophthalmol 113:1045-1049, Acierno,M.D.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Withdrawal of Antiepileptic Drug Treatment in Childhood Epilepsy:Factors Related to Age
JNNP 59:477-481, Murakami,M.,et al, 1995

Multiple Subpial Transection:A Review of 21 Cases
JNNP 58:344-349, Sawhney,I.M.S.,et al, 1995

Elevated Serum lactate Correlates with Intracranial Hemorrhage in Neonates Treated with Extracorporeal Life Support
Pediatrics 96:914-917, Grayck,E.N.,et al, 1995

Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995

Brainstem Ocular Motility Defects and AIDS
Am J Ophthalmol 106:437-442, Hamed,L.M.,et al, 1995

Eye Movement Abnormalities in Systemic Lupus Erythematosus
Arch Neurol 52:1145-1149, Keane,J.R., 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Lid Nystagmus as a Sign of Intrinsic Midbrain Disease
J Neuro-Ophthalmol 15:236-240, Brodsky,M.C.&Boop,F.A., 1995

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

Treatment for Children with Brain Tumours
BMJ 311:1213-1214, Stevens,M.C.G.,et al, 1995

Simultaneous, Multiple Cranial Neuropathies in Diabetes Mellitus
J Neuro-Ophthalmol 15:219-224, Eshbaugh,C.G.,et al, 1995

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995

Oval Pupil in Patients with Diabetes mellitus: Examination by Measurement of the Dark-Adapted Pupillary Area and Pupillary Light Reflex
Diabetes Res Clin Pract 29:43-48, Isotani,H.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Indication for Computed Tomography of the Brain in Patients with First Uncomplicated Generalised Seizure
BMJ 309:986-989, Schoenenberger,R.A.&Heim,S.M., 1994

Cervicomedullary Tumors in Children:A Distinct Subset of Brainstem Gliomas
Neurol 44:1798-1803, Robertson,P.L.,et al, 1994

Brain Tumors in Children
NEJM 331:1500-1507, Pollack,I.F., 1994

The Syndrome of'Cerebellar'Mutism and Subsequent Dysarthria
Neurol 44:2040-2046, vanDongen,H.R.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Surveillance Scanning of Children with Medulloblastoma
NEJM 330:892-895, Torres,C.F.,et al, 1994

Pure Midbrain Infarction:Clinical Syndromes, MRI, and Etiologic Patterns
Neurol 44:2032-2040, Bogousslavsky,J.,et al, 1994

Visual Morbidity in Giant Cell Arteritis:Clinical Characteristics and Prognosis for Vision
Ophthalmology 101:1779-1785, Liu,G.T.,et al, 1994

High Prevalence of Antiphospholipid Antibodies in Children with Idiopathic Cerebral Ischemia
Pediatrics 94:500-503, Angelini,L.,et al, 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994

Low-Dose Indomethacin and Prevention of Intraventricular Hemorrhage:A Multicenter Randomized Trial
Pediatrics 93:543-550, 643, 677994., Ment,L.R.,et al, 1994

Video Game-Related Seizures:A Report on 10 Patients and a Review of the Literature
Pediatrics 93:551-556, Graf,W.D.,et al, 1994

Spontaneous Dissections of Cervicocephalic Arteries in Childhood and Adolescence
Neurol 44:1607-1612, Schievink,W.I.,et al, 1994

A Pediatric Case of Carotid Rete Mirabile
Stroke 25:1268-1270, Fuwa,I., 1994

The Neurogenetic Genie:Testing for Huntington's Disease Mutation
Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994

CAG Repeat Size and Clinical Presentation in Huntington's Disease
Neurol 44:1137-1143, Ashizawa,T.,et al, 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Stroke and Cerebral Infarcts in Children Infected with Human Immunodeficiency Virus
Arch Pediatr Adolesc Med 148:965-970, Philippet,P.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Abducens Nerve Palsy in Spontaneous Intracranial Hypotension
Neurol 44:1552, Berlit,P.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Brief Report:Organic Osmolytes in the Brain of an Infant with Hypernatremia
NEJM 331:439-442, Lee,J.H.,et al, 1994

Focal Tectal Tumors:Management and Prognosis
Neurol 44:953-956, Squires,L.A.,et al, 1994

Brain Tumors in Patients with Fanconi's Anemia
Arch Pediatr Adolesc Med 148:661-663, Alter,B.P., 1994

Asking the Courts to Set the Standard of Emergency Care-The Case of Baby K
NEJM 330:1542-1545, Annas,G.J., 1994

Discontinuing Antiepileptic Drugs in Children with Epilepsy
NEJM 330:1407-1410, Tennison,M.,et al, 1994

Discontinuing Antiepileptic Drugs in Children with Epilepsy:A Prospective Study
Ann Neurol 35:534-545, 5091994., Shinnar,S.,et al, 1994



Showing articles 850 to 900 of 1791 << Previous Next >>