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Differential
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abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
Alexanders disease
Alexanders disease, adult onset
ammonia
amniocentesis
Angelman syndrome
anorexia
aspartate aminotransferase
astrogliopathy
ataxia
ataxic gait
auditory and vestibular pathways
autonomic dysfunction
B 12 deficiency
B 12 deficiency, infants
bacterial infection
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
biologic markers
bone age
brain biopsy
brainstem, lesion of
breast feeding
Brown-Vialetto-Van Laere syndrome
bulbar palsy
calcification, intracranial
carbonic anhydrase II deficiency
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
cataracts, congenital
celiac disease, childhood
cerebellar atrophy, secondary
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonarterial territory
cerebrovascular accident, recurrent
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 19
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clubbing of fingers
coma
complications
compression fracture
congenital infection, CNS
congenital infection, viral
congenital malformation
consanguinity
contractures, joint
Cornelia de Lange syndrome
cortical blindness
cortical infarction
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cultured skin fibroblasts
cystic fibrosis, neurologic complications with
cystinosis
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diarrhea
diencephalic syndrome
differential diagnosis
digits, abnormal
disability, neurological
drooling
dysarthria
dysmorphic
dysphagia
dystonia
eating disorder
electroencephalogram, abnormalities of
encephalomyelitis
encephalopathy
encephalopathy, neonatal
enzyme, defect
epileptic encephalopathy
evoked potentials
eye movement, disorders of
eyebrows, abnormal
facial appearance, abnormal
failure to thrive
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
floppy infant
fracture, pathologic
gait disorder
galactosemia
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genital hypoplasia
GFAP gene
glioma
gluten-free diet
growth hormone deficiency
growth retardation
hand deformity
hand flapping
head circumference
hearing loss
hemianopia
hemiparesis
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
hirsutism
human immunodeficiency virus type 1
hydrocephalus
hyperammonemic encephalopathy
hyperbilirubinemia
hyperphagia
hyperreflexia
hypogonadism
hypopigmentation of skin
hyporeflexia
hypothalamus, neoplasm of
hypothermia
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
incoordination
infantile bilateral striatal necrosis
infection
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
irritability
jaundice
Leigh's disease
lens, dislocation of
lenticular nucleus, lesion of, bilateral
lethargy
leukodystrophy
leukotrienes
life expectancy
liver disease
low birth weight
lymphadenopathy
lymphocytic interstitial pneumonitis
lymphoma
macrocephaly
malabsorption
MELAS syndrome
meningitis, CSF cell count-normal
mental retardation
metabolic acidosis
metabolic disorder, primary
microcephaly
micrognathia
micromelia
migratory lesion pattern
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
molybdenum cofactor deficiency
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, serial
muscle biopsy
myelination of nervous system
myoclonus
nasal bridge, wide
nausea and vomiting
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathy
nose, abnormal
nutritional deficiency
nystagmus
obesity
occipital lobe, infarction
occipital lobe, lesion of
oligodactyly
opisthotonus
opportunistic infection
optic atrophy
ornithine transcarbamylase deficiency
osteoporosis
pain, leg
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
parotitis
paroxysmal neurologic deficits
partial thromboplastin time, prolonged
patient information and support
peripheral blood smear
peroxisomal disease
personality change
phocomelia
photophobia
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prothrombin time, prolonged
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pulmonary infiltrates
pupil, ectopic-congenital
pyramidal tract dysfunction
quadriparesis
recurrent
renal failure
renal tubular acidosis
respiratory failure
review article
rhabdomyosarcoma
riboflavin transporter deficiency
Rosenthal fibers
saddle nose
screaming
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
seizure, neonatal
serum alanine aminotransferase
short stature
simian crease
skin, hematoma
skin, lesions in neurologic disorders
spastic diplegia
spasticity
spinal cord, compression of
strabismus
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuporous
suck, poor
symmetric brain lesions
syndactyly
synophrys
systemic illness
temper tantrums
thalamus, lesion of
thalamus, lesion of-bilateral
toe walking
tongue, protrusion of
transplacental virus infections
treatment of neurologic disorder
tremulousness
trichopoliodystrophy
urea-cycle enzymopathies
uric acid, low
urine test for metabolic disorders
vegetarianism
vertebral erosion
vitamin deficiency
vitamin K
vitamin K deficiency
weakness
weakness, generalized
weakness, progressive
white matter disease
wide based gait
Wolff-Parkinson-White syndrome
wrist drop
Showing articles 1400 to 1450 of 1673 << Previous Next >>

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Involvement of Upper-Airway Muscles in Extrapyramidal Disorders
NEJM 311:438-442, Vincken,W.G.,et al, 1984

Spasmodic Dysphonia
Lancet 2:1192, Gowers,W.R.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

Diabetic Neuropathy
Ann Neurol 15:2-12, Brown,M.J.,et al, 1984

Acute Ventilatory Failure & Myoglobinuria
Neurol 34:369-371, Taverner,D.,et al, 1984

Respiratory Failure in Myasthenia Gravis Due to Vocal Cord Paresis
Arch Neurol 41:567-568, Schmidt-Nowara,W.W.,et al, 1984

Living with Hydrocephalus
BMJ 288:813-814, Simpson,D., 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Substance P is Markedly Increased in Plasma of Patients with Hepatic Coma
Lancet 1:480-491, Hortnagl,H.,et al, 1984

Ventilatory Support by Pacing of the Conditioned Diaphragm in Quadriplegia
NEJM 310:1150-1155, Glenn,W.W.L.,et al, 1984

High-Dose Monotherapy in Treatment of Intractable Seizures
Neurol 34:707-711, Lesser,R.P.,et al, 1984

Acute Dysautonomia & Polyneuropathy
Arch Neurol 41:1100-1101, Taubner,R.W.,et al, 1984

Bilateral Hemorrhagic Infarction of the Pallidum
J Comput Assist Tomogr 8:125-127, Finelli,P.F., 1984

Sudden Unexpected Death Associated with Seizures:Analysis of 66 Cases
Epilepsia 24:84-88, Leestma,J.E.,et al, 1984

Indirect Injury of the Optic Nerve
Neurosurgery 14:756-764, Kline,L.B.,et al, 1984

Idiopathic Hemochromatosis (IHC) :Dementia & Ataxia as Presenting Signs
Neurol 33:1479-1483, Royden,H.,et al, 1983

Clinical Apnea & Brain-Stem Neural Function in Preterm Infants
NEJM 308:353-357, Henderson-Smart,D.J.,et al, 1983

CT Demonstration of Cerebral Subcortical Calcifications
J Comput Assist Tomogr 7:476-478, Swartz,J.D., 1983

Manifestations of Coronary Disease Predisposing to Stroke
JAMA 250:2942-2946, Kannel,W.B.,et al, 1983

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Acute Panautonomic Neuropathy
Ann Neurol 13:412-417, Low,P.A.,et al, 1983

Differential Changes of Autonomic Nervous System Function with Age in Man
Am J Med 75:249-258, Pfeifer,M.A.,et al, 1983

Paroxysmal Unilateral Hyperhidrosis & Malignant Mesothelioma
Arch Neurol 40:256, Pleet,D.L.,et al, 1983

Wilson's Disease:A Diagnostic Dilemma
BMJ 287:313-314, Nazer,H.,et al, 1983

Myositis of Chronic Graft Versus Host Disease
Neurol 33:1222-1224, Reyes,M.G.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Adult Inorganic Lead Intoxication:Presentation of 31 New Cases & a Review of Recent Advances in the Literature
Medicine 62:221-247, Cullen,M.R.,et al, 1983

Precipitation of Hepatic Encephalopathy by Propranolol in Cirrhosis
BMJ 287:585, Tarver,D.,et al, 1983

Valproate-Ethosuximide Combination Therapy for Refractory Absence Seizures
Arch Neurol 40:797-802, Rowan,A.J.,et al, 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

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

Neuropathologic Evaluation of 40 Confirmed Cases of Legionella Pneumonia
Neurol 33:1340-1344, Pendlebury,W.W.,et al, 1983

Mechanical Ventilation for Respiratory Failure in Myasthenia Gravis
Mayo Clin Proc 58:597-602, Gracey,D.R.,et al, 1983

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Postoperative Infection in Shunts for Hydrocephalus:Are Prophylactic Antibiotics Necessary
BMJ 284:1914-1915, Gardner,B.P.,et al, 1982

Pseudoseizures:Diagnostic Evaluation
Neurol 32:18-23, King,D.W.,et al, 1982

Pseudoseizures:Ictal Phenomena
Neurol 32:24-30, Gulick,T.A.,et al, 1982

Neurologic Manifestations of Podophyllin Toxicity
Neurol 32:308-311, Filley,C.M.,et al, 1982

Diagnosis & Management of Diabetic Autonomic Neuropathy
BMJ 285:916-918, Ewing,D.J.,et al, 1982

Ross Syndrome & Skin Changes
Neurol 32:1041-1042, Heath,P.D.,et al, 1982

Cerebral Embolism as the Initial Manifestation of Peripartum Cardiomyopathy
Neurol 32:668-671, Hodgman,M.T.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Ventilatory Failure in Myasthenia Gravis
JNNP 45:217-222, Ferguson,I.T.,et al, 1982

The Neuropathology of Glycine Encephalopathy:Five Cases with Immunohistochemical & Ultrastructural Observations
Neurol 32:975-985, Agamanolis,D.P.,et al, 1982

Neuro-ophthalmic Signs & Symptoms of Hysteria
Neurol 32:757-762, Keane,J.R., 1982



Showing articles 1400 to 1450 of 1673 << Previous Next >>