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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 1600 to 1650 of 1673 << Previous Next >>

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Vincristine Neurotoxicity
Ann Int Med 80:733-737, Rosenthal,S.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Whipple'sDisease & the Nervous System-The Neurology of GI Disease
1974, Chapter 13, p. 207 Major Prob. In Neurology Vol. 3-Saunders., Pallis,C.A.&Lewis,P.D., 1974

Testicular Pain Sensationin Diabetic Autonomic Neuropathy
BMJ 2:638, Campbell,I.W.,et al, 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Autonomic Insufficiency in Uremia As a Cause of Hemodialysis-Induced Hypotension
NEJM 290:650, 6851974., Kersh,E., 1974

Postsympathectomy Neuralgia
Am J Surg 128:75, Raskin,N.,et al, 1974

Chronic Hepatic Encephalopathy Treated with Oral Lactose in a Patient with Lactose Malabsorption
NEJM 291:240, Welsh,J.D.,et al, 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Neurologic Changes in Liver Disease
Brain Dysfunction in Metabolic Disorders, ed. by F. Plum, Res. Publ. Assn. Nerv. Ment. Dis. , Vol. 5, , New York:RaVictor, M., 1974

Defect in Automatic Respiration in a Case of Multiple Sclerosis
Am J Med 56:433-436, Rizvi,S.S.,et al, 1974

Neonatal Seizures
NEJM 289:413, Volpe,J., 1973

Impaired Peripheral Chemosensitivity & Acute Respiratiory Failure in Arnold-Chiari Malfor & Syringomyelia
NEJM 288:947, Bokinsky,G.E.,et al, 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Congenital Anomalies & Herpesvirus Infection
Am J Dis Child 126:364, Montogomery,J.R.,et al, 1973

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

Acute Optic Neuropathy in Older Patients
Arch Neurol 28:182, Ellenberger,C., 1973

Placoid Pigment Epitheliopathy With Swelling of the Optic Disks
Arch Neurol 29:204-205, Jenkins,R.B.,et al, 1973

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

The Symptomatic Empty Sella Prevention & Correction via the Transsphenoidal Approach
J Neurosurg 37:533, Olson,E.,et al, 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Medical Approach to Ophthalmopathy of Graves'Disease
Mayo Clin Proc 47:980, Ivy,H., 1972

Optic Disc Vasculitis
Br J Ophthalmol 56:652, Hayreh,S., 1972

The Relationship of Motility Problems to Reading Problems
MCV Quart 8:298, McNeer,K., 1972

Depression of Growth in Hyperactive Children on Stimulant Drugs
NEJM 287:217, 1972; 287:249972., Safer,D.,et al, 1972

Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,et al, 1972

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

Case Record of MGH-NEJM Atheromatous Emboli to Brain
Kidney, 286:11461972., , 1972

The Radiology of Primary Orbital Meningioma
B J Rad 44:405, Lloyd,G., 1971

Diphenylhydantoin Metabolism in Uremia
NEJM 285:648, Letter,J.,et al, 1971

Hemifacial Atrophy
Brit J Oral Surg 9:102, Vickery,I.M., 1971

Cerebrospinal Fluid Glutamine as a Measure of Hepatic Encephalopathy
Arch Int Med 127:1033, Hourani,B.T.,et al, 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Hippus, In System of Ophthalmology
(Ed) , Vol 12 Neuro-ophthalmology C. V. Mosby Company 1971, p 637., Duke-Elder,W.S., 1971

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Electrical Lesions of the Nervous System
Handbook of Clinical Neurology, Vol. VII, p. 344, 1970, ed. Vinken & Bruyn., Panse,F., 1970

Nonbacterial Thrombotic Endocarditis
Arch Int Med 125:126, Wooley,C.F.,et al, 1970

Neurologic Disorders Seen In the Uremic Patient
Arch Int Med 126:781, Tyler,H.R., 1970

Acute Intermittent Porphyria
Medicine 49:1, Stein,J.,et al, 1970

Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969

Optic Glioma of Childhood
Br J Ophthalmol 53:793, Hoyt,W.&Baghdassarian,S., 1969

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Bell's Palsy
Arch Otolaryng 89:173-177, 1969, Drachman,D.A., 1969

Whipple's Disease Presenting with Ocular Inflammation & Minimal Intestinal Symptoms
John's Hopkin's Med Jour 123:175, Knox,D.L.,et al, 1968

Endocrine Function in Patients with Untreated Chromophobe Adenomas
Quart J Med 357, Neiman,E.A.,et al, 1968



Showing articles 1600 to 1650 of 1673 << Previous Next >>