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Differential
(Click to cross reference)
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 1450 to 1500 of 1673 << Previous Next >>

Dysaesthesias & Dysautonomia:A Self-limited Syndrome of Painful Dysaesthesias & Autonomic Dysfunction in Childhood
JNNP 45:162-165, Nass,R.,et al, 1982

The Neuroleptic Malignant Syndrome
Arch Int Med 142:1183-1185, Smego,R.A.,et al, 1982

Misdiagnosis of Stroke
Lancet 1:328-331, Norris,J.W.&Hachinski,V.C., 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Conjugate Deviation of Gaze in Hepatic Encephalopathy
JNNP 45:1168, Sandyk, R.et al, 1982

Idiopathic Inflammatory Orbital Pseudotumor in Childhood
Ophthalmology 88:565-574, Mottow-Lippa,L., et al, 1981

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

Emergencies in the Home, Neurological Rmergencies
BMJ 283:473-474, Lister,T.P., 1981

Clonazepam:Effective Treatment for Restless Legs Syndrome in Uraemia
BMJ 283:885-886, Matthews,W.B.,et al, 1981

Respiratory & Bulbar Paralysis with Relapsing Hyperthyroidism
BMJ 283:275-276, Edelman,J.,et al, 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Ocular Skew Deviation in Hepatic Coma
(Letter) , JNNP 44:45881., , 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Midodrine, A New Agent in the Management of Idiopathic Orthostatic Hypotension & Shy-Drager Syndrome
Mayo Clin Proc 56:429-433, Schirger,A.,et al, 1981

Respiratory Distress & Arnold-Chiari Malformation
Neurol 31:97-100, Papasozomenos,S.,et al, 1981

Autonomic Dysfunction in Subacute Spongiform Encephalopathy
Arch Neurol 38:114-117, Khurana,R.K.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Management of Hepatic Encephalopathy
Editorial, BMJ 282:171-1721981., , 1981

Cholesterol Embolism as a Cause of Transient Ischemic Attacks & Cerebral Infarction
Neurol 31:860-865, Beal,M.F.,et al, 1981

Neuroleptic Malignant Syndrome:A Pathogenetic Role for Dopamine Receptor Blockage
Neurol 31:132-137, Henderson,V.W.,et al, 1981

The Hot Bath Test in the Diagnosis of Multiple Sclerosis
JAMA 246:1113-1114, Malhotra,A.S.,et al, 1981

Transient Bilateral Visual Reduction & Mydriasis After Propranolol Treatment
Ann Neurol 10:583, Parrish,D.O.,et al, 1981

Kernicterus & Central Pontine Myelinolysis in a 14-year-old Boy with Fulminating Viral Hepatitis
Ann Neurol 8:633-636, Ho,K-C.,et al, 1980

Pathology of Autonomic Neuropathy in Diabetes Mellitus
Ann Int Med 92:301-303, Duchen,L.W.,et al, 1980

Assessment of Cardiovascular Effects in Diabetic Autonomic Neuropathy & Prognostic Implications
Ann Int Med 92:308-311, Ewing,D.J.,et al, 1980

Neuropathology of Diabetic Neurogenic Bladder
Ann Int Med 92:316-318, Mastri,A.R., 1980

Sexual Function in Diabetic Patients
Ann Int Med 92:331-333, Ellenberg,M., 1980

The Neurotoxicity of the Rat Poison Vacor, A Clinical Study of l2 Cases
NEJM 302:73-77, LeWitt,P.A., 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Child Abuse as a Cause of Post-Traumatic Hypopituitarism
NEJM 302:724-728, Miller,W.L.,et al, 1980

Protein Binding of Valproic Acid in Uremic Patient
Neurol 30:557-559, Bruni,J.,et al, 1980

Shy-Drager syndrome:Diagnosis & treatment of cholinergic dysfunction
Neurol 30:805-809, Khurana,R.K.,et al, 1980

Acute Autonomic & Sensory Neuropathy
Ann Neurol 8:441-444, Colan,R.V.,et al, 1980

Finger Wrinkling after Immersion in Water
BMJ 281:586-587, Alvarez,G.,et al, 1980

Abnormal Adrenergic & Cholinergic Sensitivity in Cystic Fibrosis
NEJM 302:1453-1456, Davis,P.B.,et al, 1980

The Not-So-Benign Miller Fisher Syndrome, A Variant of the Guillain-Barre Syndrome
Arch Neurol 37:384-385, Blau,I.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Apneic Spells in Progressive Dialysis Encephalopathy
Arch Neurol 37:594-596, Garcia-Buffuel,L.,et al, 1980

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Pseudotumor Cerebri, Clinical Profile & Visual Outcome in 63 Patients
Mayo Clin Proc 55:541-546, Rush,J.A., 1980

Dysconjugate Gaze in Hepatic Coma
Ann Neurol 8:328-329, Caplan,L.R.,et al, 1980

Fatal Myeloencephalopathy Caused by Intrathecal Vincristine
Neurol 30:867-871, Slyter,H.,et al, 1980

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Acute Ataxia Associated with Ciguatera-type (Grouper) Tropical Fish Poisoning, Letter
Ann Neurol 7:491, Jones,H.R.Jr., 1980

Postlaminectomy Arteriovenous Fistula, Suspected From Right-Side Heart Cath
Arch Int Med 140:1168-1169, Thompson,J.A.,et al, 1980

Congestive Heart Failure During Carbamazepine Therapy
Ann Neurol 8:200-201, Terrence,C.F.,et al, 1980

CNS Manifestations of the Hemolytic-Uremic Syndrome
Am J Dis Child 134:869-872, Bale,J.F.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Trichlorethylene
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 457, Feldman,R.G., 1979

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979



Showing articles 1450 to 1500 of 1673 << Previous Next >>