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Differential
(Click to cross reference)
abdominal distention
abdominal muscle paralysis
abducens nerve paralysis
abscess, intracerebral
acetazolamide
acid maltase deficiency
acid maltase deficiency, adult
acoustic nerve
acquired immunodeficiency syndrome
activities of daily living scale
acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
alcohol
alcohol intolerance
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alkylating agents
alpha glucosidase
altered states of consciousness
aminoacidopathies
amiodarone
amitriptyline
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anemia
aneurysm
aneurysm, intracranial
ankle, swelling of
anterior horn cell disease
anterior tibial muscle weakness
antiarrhythmic drugs
anticholinesterase
antimetabolite
aphasia
areflexia
arrhythmia, cardiac
arsenic
arthralgia
arthrogryposis multiplex
ascending paralysis
asparginase
aspartate aminotransferase
asthma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atonic bladder
atypical
auditory evoked brainstem potentials
autoimmune disease
autonomic dysfunction
azidodeoxythymidine
Babinski sign
BAL
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
Bassen-Kornzweig syndrome
bent spine syndrome
biological warfare
blacks
blindness, sudden
blood dyscrasias, neurologic findings with
bone marrow suppression
bone marrow transplantation
botulism
bradycardia
brain biopsy
brain purpura
brainstem, dysfunction
brainstem, lesion of
bulbar palsy
burning paresthesia
calcification, intracranial
calf hypertrophy
caloric testing
camptocormia
cancer, cerebrovascular accident complicating patients with
canned food
carbon monoxide poisoning
carbon monoxide poisoning, chronic
carboxyhemoglobin
carcinoid tumor
carcinoma
cardiomegaly
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral glucose metabolism
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemical weapons
chemotherapy, CNS treatment and complications with
cherry red spot-myoclonus syndrome
chest pain
children
chills
chloroquine
chromosome 11
chronic fatigue syndrome
chronic graft versus host disease
chronic progressive external ophthalmoplegia
Chvostek sign
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
cognition
coma
compartment syndrome
complications
confusion
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
conversion reaction
cortical blindness
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
critical care unit
cultured skin fibroblasts
Cushing's syndrome
cyclic vomiting
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytokines
deafness
DEET
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
depression
dermatitis
dermatomyositis
descending paralysis
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
diarrhea
differential diagnosis
difficulty climbing stairs
diphtheria
diplopia
distal muscle atrophy
distal muscle weakness
dizziness
DNA probes
docetaxel
down-beat nystagmus
drooling
dropped head syndrome
drowsiness
drug induced neurologic disorders
duvalumab
dysgeusia
dyskinesia
dysmorphic
dysphagia
dyspnea
dystonia
echocardiogram
echocardiogram, LVH
edema, pedal
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
electronystagmography
electroretinograph
emergencies, medical
emergencies, neurologic
encephalitis
encephalitis, autoimmune
encephalomyopathy
encephalopathy
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
epidemiology of neurology
epilepsia partialis continua
episodic disorders
episodic neurologic deficits
erythrocyte
evoked potentials
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exercise-related muscle strength increase
extraocular muscle atrophy
eye movement, disorders of
facial appearance, abnormal
facial hair, excessive
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
fatigue
Fazio-Londe's disease
feeding disorder
fever
fibrillations
fingernails, abnormal
fish
fish poisoning
floppy infant
fluctuate
fluorouracil
flush syndrome
food poisoning
foot drop
fundus, abnormality of
gag reflex, depressed
gait disorder
gammaglobulin therapy, intravenous
gangliosidosis GM2
gastroenteritis
gastrointestinal motility
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glucocerebrosidase
glycogen debranching enzyme deficiency
glycogen storage disease
gonadal dysgenesis
Gowers maneuver
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Gulf War syndrome
Hallervorden Spatz disease
hallucination
hand weakness
headache
headache, sudden onset of
hearing loss
heart block
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemoglobinuria
hepatitis
hepatomegaly
hexosaminidase-A
hip flexor weakness
hirsutism
histochemistry of muscle
human immunodeficiency virus type 1
hydroxychloroquine
hyperamylasemia
hyperbaric oxygen
hyperkalemia
hyperkeratosis
hypertension
hypocalcemia
hypoglycemia
hypoglycemic coma
hypokalemia
hypomagnesemia
hypomyelination
hyponatremia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hyporeflexia
hypotension, systemic
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immune checkpoint inhibitors
immune-related adverse events
immunologic disease
immunosuppression
immunosuppressive agents
immunotherapy
impotence
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
insect repellent
insecticides
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal pseudoobstruction
intracerebral hemorrhage
ipecac
ipilimumab
ischemic exercise test
isoniazid
jaundice
jaw pain
Jewish
kaliuresis
Kearns-Sayre syndrome
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphosis
lactic acidemia
lactic dehydrogenase(LDH)
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
leg swelling
leg weakness, bilateral
Leigh's disease
lens, dislocation of
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocytes
leukocytosis
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
lid closure, weakness of
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
lipid storage myopathy
liver disease
liver function enzymes
lordosis
low back pain
lymphopenia
lysosomal storage disease
lysosomes, abnoral
macular degeneration
mannitol
McArdle's disease
McArdle's disease, adult onset
Mees lines
MEK inhibitor
melanoma, malignant
MELAS syndrome
memory, impairment of
meningismus
meningitis
meningitis, leukemic
meningoencephalopathy
mental retardation
mental status, abnormal
MERRF syndrome
mestinon
metabolic acidosis
metabolic alkalosis
metabolic disorder, primary
metallic taste
methotrexate
methylhydrazine derivatives
microcephaly
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
molybdenum cofactor deficiency
monoamine oxidase inhibitors
mononeuropathy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, hypointense signal foci on
MRI, muscle
MRI, serial
mucopolysaccharidoses
multiple organ failure
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenic crisis
myasthenic syndrome
myelopathy
myocarditis
myoclonus
myoclonus, epilepsy
myoglobinuria
myoneuropathy
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, carcinomatous
myopathy, centronuclear
myopathy, critically ill
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, immune-mediated
myopathy, proximal
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, toxic
myopathy, vacuolar
myopia
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia, treatment of
myotonic discharges
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
neoplasm, metastatic
neoplasm, metastatic to CNS
nephrotic syndrome
nerve agents
nerve biopsy
nerve conduction studies
nerve conduction studies, sensory
neuritis, causes of
neuritis, heavy metals causing
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neurons
neuroophthalmology
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, ataxia, retinitis pigmentosa
neuropathy, diabetic
neuropathy, diphtheritic
neuropathy, hereditary peripheral
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, motor
neuropathy, peripheral
neuropathy, sensory
neuropathy, toxic
neurotoxic
neurotoxin
neutropenia
newborn, evaluation of
night blindness
night sweats
nitrogen mustard
nivolumab
normal
nose, abnormal
numbness, extremity
nystagmus
occupational neurologic disorders
ocular motility, disorders of
ocular myopathy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
orbit, lesions of
organ transplantation
orthopnea
orthostatic hypotension
oxygen therapy
pain
pain, arm
pain, back
pain, leg
palpitations
pancreatitis
pancuronium
pancytopenia
paramyotonia congenita
paraparesis
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
PAS positive
patient information and support
pediatric neurology
pembrolizumab
pericardial effusion
periodic paralysis
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
peroxisomal disease
personality change
phosphorylase b kinase deficiency
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
poison, mercury
poison, neurologic problems with
poison, organophosphate
POLG1 gene
poliomyelitis
polymerase chain reaction
polymyalgia rheumatica
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, critically ill
Pompe's disease of glycogen storage
porphyria
position sensation, abnormal
postpartum
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
procarbazine
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
proximal muscle atrophy
pruritus
pseudomyotonia
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary embolism
pulmonary function tests
pulmonary hypertension
pulmonary infiltrates
quadriparesis
quadriparesis, acute
quadriparesis, progressive
quadriplegia
quadriplegia, transient
radionuclide imaging, heart
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
recurrent laryngeal nerve paralysis
refractive errors
Refsum's disease
renal failure
respirator
respiratory failure
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
riboflavin
rigidity
risk factors
sarcoidosis
screaming
screening
second wind phenomena
seizure
seizure, intractable
seizure, neonatal
selumetinib
sensorineural hearing loss
sensory symptoms
sensory testing
sensory testing, quantitative
short stature
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sodium valproate
sodium valproate, toxicity
somatosensory evoked potentials
Southern immunoblot test
spasticity
spinal cord, compression of
spinal cord, metastasis to
spinal muscular atrophy
spinocerebellar degeneration
spongy degeneration of brain
standing difficulty
startle reaction
status asthmaticus
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stooped posture
strokelike episodes
subarachnoid hemorrhage
suicide
sweating, abnormality of
systemic illness
tachycardia
tapetoretinal degeneration
taxol
Tay-Sachs disease
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thirst
thrombocytopenia
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, weakness
torticollis
toxic oil syndrome
toxins, nervous system
transverse smile
treatment of neurologic disorder
tremor
tremor, jaw
tricresylphosphate
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
uremia
uric acid, low
urinary frequency
urinary incontinence
urine test in toxic screen
urine, dark
Usher's syndrome
vaccination, neurologic complications with
vecuronium
vinblastine
vincristine neurotoxicity
visual field defect
visual loss
vital capacity
vocal cord paralysis
walking, difficulty with
war
weakness
weakness, acute
weakness, chronic
weakness, episodic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
workup
wrist drop
Showing articles 1600 to 1650 of 1908 << Previous Next >>

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Sources of Error in the Diagnosis of Guillain-Barre Syndrome
Muscle & Nerve 5:111-117, Feit,H.,et al, 1982

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

Acute Polymyopathy During Total Parenteral Nutrition
BMJ 283:1578, Stewart,P.M.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Methyl Bromide Poisoning Seen Initially as Psychosis
Arch Neurol 38:529-530, Zatuchni,J.,et al, 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Neurological Complications of Ethylene Glycol Intoxication
Arch Neurol 38:724-726, Berger,J.R.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Dural Sinus Thrombosis in Children With Acute Lympho-blastic Leukemia
JAMA 246:2837-2839, Steinherz,P.G.,et al, 1981

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Plasmapheresis in Idiopathic Inflammatory Myopathy Experience With 35 Patients
Arch Neurol 38:544-552, Dau,P.C., 1981

Effects of Prophyl. Treat. of CNS on Intellect. Funct. of Children with Acute lymph. Leuk
Am J Med 71:47-52, Moss,H.A., 1981

Disulfiram Neuropathy
Neurol 31:730-735, Mokri,B.,et al, 1981

Polyneuropathy After Massive Exposure to Parathion
Neurol 31:603-605, deJager,A.E.J.,et al, 1981

Brainstem Auditory Evoked Response in the Diagnosis of Pediatric Neurologic Diseases
Neurol 31:832-840, Hecox,K.E.,et al, 1981

Pharyngeal Dysphagia in Alcoholic Myopathy
Ann Int Med 95:189-191, Weber,L.D.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Fatal Vidarabine Toxicity in a Patient With Normal Renal Function
JAMA 246:1703-1705, VanEtta,L.,et al, 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Cimetidine Toxic Reactions Masquerading as Delirium Tremens
JAMA 245:1058-1059, Weddington,W.W.,et al, 1981

Successful Treat. of Echovirus Meningoenceph & Myo Fasciitis With Immune Glob Therapy In X-Linked Agammaglob
NEJM 304:1278-1281, Mease,P.J.,et al, 1981

Polymyositis & Diffuse Interstitial Lung Disease
Arch Int Med 141:1005-1010, Salmeron,G.,et al, 1981

Polymyositis Beginning as a Focal Process
Arch Neurol 38:439-442, Heffner,R.R.Jr.,et al, 1981

Eosinophilic Myositis, An Unusual Cause of Pseudotumor & Eosinophilia
JAMA 246:70-71, Agrawal,B.L.,et al, 1981

Labetalol-induced Toxic Myopathy
BMJ 282:1824-1825, Teicher,A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

Focal Encephalopathy Following Methotrexate Therapy
Arch Neurol 38:450-452, Packer,R.J.,et al, 1981

Rhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Arch Neurol 37:187-188, Britt,C.W.,et al, 1980

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

Neurological Dysfunction of the Bladder in Workers Exposed to Dimethylaminopropronitrile
JAMA 243:741-745, Kreiss,K.,et al, 1980

Immunosppressive Agents in Corticosteroid-Refractory Childhood Dermatomyositis
Neurol 30:286-291, Niakan,E.,et al, 1980

Acute Myopathy Associated with Influenza A/Texas/l/77 Infection
JAMA 243:461-462, Kessler,H.A.,et al, 1980

Detection of Phenylketonuria in Autistic & Psychotic Children
JAMA 243:126-128, Lowe,T.L.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Clinical Significance of Periodic EEG Patterns
Arch Neurol 37:15-20, Kuroiwa,Y.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

A Diagnostic Index of Active Demyelination:Myelin Basic Protein in Cerebrospinal Fluid
Ann Neurol 8:25-31, Cohen,S.R.,et al, 1980

Is Acanthamoeba Encephalitis an Opportunistic Infection
Neurol 30:567-574, Martinez,A.J., 1980

Influenzal Acute Myositis in the Elderly
Neurol 30:877-878, Congy,F.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Acute Hydrocortisone Myopathy
BMJ 281:271-272, Marle,W.V., 1980

Cramps, Muscle Pain, & Tubular Aggregates
Arch Neurol 37:715-717, Lazaro,R.P.,et al, 1980



Showing articles 1600 to 1650 of 1908 << Previous Next >>