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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 1500 to 1550 of 1673 << Previous Next >>

Cauda Equina Compression Presenting as Spontaneous Priapism
JNNP 42:280-282, Ravindran,M., 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Reversal of Incipient Brain Death From Head-Injury Apnea At the Scene Of Accidents
NEJM 301:109, Levine,J.E.,et al, 1979

Skin Wrinkling on Immersion of Hands
Arch Neurol 36:113-114, Braham,J.,et al, 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Uraemic Myoclonus:An Example of Reticular Reflex Myoclonus
JNNP 42:52-55, Chadwick,D.,et al, 1979

Physostigmine in Reye Syndrome
Ann Neurol 5:105, Pettegrew,J.W.,et al, 1979

Nephrotoxic Effects of Computerized Tomographic Brain Scan
NEJM 300:45-46, 1979. (Letter), Theerman,M.R.,et al, 1979

Acute Hepatic Failure Associated with the Use of Sodium Valproate
NEJM 300:962-966, Suchy,F.J.,et al, 1979

Autonomic Neuropathy in Rheumatoid Arthritis
BMJ 2:173-175, Edmonds,M.E.,et al, 1979

Paraparesis in Hereditary Multiple Exostoses:Case Report
Neurol 29:973-977, Ferrari,G.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

Eosinophilic Polymyositis
Arch Neurol 36:721-722, 1979, Stark,R.J., 1979

Disorders of Neuromuscular Transmission Caused by Drugs
NEJM 301:409-413, Argov,Z.,et al, 1979

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Ocular Involvement in Whipple's Disease
Arch Ophthalmol 96:1431-1436, Font,R.L.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Prolactin-Secreting Tumors & Hypogonadism in 22 Men
NEJM 299:847-852, Carter,J.N.,et al, 1978

Malignant Optic Gliomas in Adults
Arch Neurol 35:731-735, Harper,C.G.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Autonomic Epilepsy:Clonidine Blockade of Paroxysmal Catecholamine Release & Flushing
Ann Int Med 88:189, Metz,S.A.,et al, 1978

Visceral Stimuli Inducing Epilepsy
(letter) , NEJM 298:16678., Jacome,D.E., 1978

Intracranial Arteriovenous Malformations in Childhood
Ann Neurol 3:338, Kelly,J.J.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Search for the Uremic Toxin
NEJM 298:1000, 1978, Avram,M.M.,et al, 1978

Parathyroid Hormone as a Uremic Neurotoxin
NEJM 299:362, Sauerwein,H.P.,et al, 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Amanita Mushroom Poisoning with Recovery from Coma:A Case Report
Ann Neurol 3:177, Teutsch,C.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978

Papillophlebitis:Benign Retinopathy Resembling Papilledema or Paillitis
Ann Neurol 3:438, Ellenberger,C.,et al, 1978

Neurologic Manifestations of Cogan Syndrome
Neurol 28:278, Bicknell,J.M.,et al, 1978

The Hypothalamus in Parkinson Sisease
Ann Neurol 3:129, Langston,J.W.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Myoglobinuria & Renal Failure after Status Epilepticus
Neurol 28:200, Singhal,P.C.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Hypertensive Encephalopathy:A Clinicopathologic Study of 20 Cases
Neurol 28:928-939, Chester,E.M.,et al, 1978

Obstructive Sleep Apnea in Family Members
NEJM 299:969-973, Strohl,K.P.,et al, 1978

Growth & Development in Children with Sickle-Cell Trait
NEJM 299:686-689, Kramer,M.S.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Periodic Lateralized Epileptiform Discharge in EEG:Etiology & Recurrence
Clin Electroenceph 8:116-124, Dauben,R.D.&Adams,A.H., 1977

Anatomic Considerations For Computed Tomography of the Optic Chiasm
Arch Neurol 34:713, Strother,C.M.,et al, 1977

Gustatory Phenomena After Upper Dorsal Sympathectomy
Arch Neurol 34:619, Kurchin,A.,et al, 1977

Chronic Hydrocephalus Associated with Short Stature & Growth Hormone Deficiency
Ann Neurol 2:246, Hier,D.B.,et al, 1977



Showing articles 1500 to 1550 of 1673 << Previous Next >>