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Differential
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acanthocytosis
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
amimia
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
anterior tibial muscle weakness
antiviral agents
aphasia
areflexia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic-dystonia syndromes
ATP1A3 gene
attention deficit disorder with hyperactivity
atypical
autonomic dysfunction
Babinski sign
basal ganglia, lesion, bilateral
behavioral disorder
beta-D-glucon
bladder dysfunction
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bronchoscopy
bulbar palsy
calcification, gyral
calcification, intracranial
candida albicans
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
ceruloplasmin, serum
Charcot-Marie-Tooth
chelation therapy
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 5
cingulate gyrus
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Coats plus
cobalamin C deficiency
cogwheel rigidty
coma
coma, sudden onset
complications
confusion
congenital myasthenic syndromes
consanguinity
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
corpus callosum, thinning
cortical ribbon sign
cranial nerve enhancement
cranial neuropathy
creatine phosphokinase(CPK)elevated
cyst
cyst, benign intracranial
cyst, cortical parenchyma
cyst, parenchymal
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dentate nuclei, lesion of
developmental disability
developmental retardation
diet
difficulty climbing stairs
difficulty going down stairs
disease modifying agents
distal muscle atrophy
distal muscle weakness
DNA sequencing
double-cortex syndrome
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
electromyogram
Embryonal tumors
encephalitis, brainstem
encephalopathy
encephalopathy, acute
enterovirus
enterovirus infection of CNS
eosinophilia
ependymoma
executive dysfunction
exome sequencing
Fabry's disease
facial appearance, abnormal
facial weakness
falling
false negative
familial
fatal familial insomnia
fatigue
feeding disorder
fever
fish
floppy infant
fourth ventricle, compression
fungal infection
fungal infection, CNS
gait disorder
gait speed
gait, spastic
GAMT gene
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis
genetic neurologic disorders
genetic screening
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
globus pallidus, lesion of, bilateral
gram positive cocci
gray hair
Guillain Barre syndrome
hammertoes
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
helminthic infection of CNS
hemianopia, homonymous
hemiparesis, transient
hemophagocytic lymphohistiocytosis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heterotopia
HHH syndrome
high arched feet
high arched palate
human genome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperammonemic encephalopathy
hyperbilirubinemia
hyperhomocysteinemia
hyperreflexia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
India
infection
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
interstitial pulmonary fibrosis
intracerebral hemorrhage
intrauterine infection, viral
intrauterine infection, viral of CNS
intravenous drug abuse
intrinsic hand muscles, wasting of
jaundice
Jewish
Krabbe's disease
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy with calcification and cysts
level of consciousness, decreased
lid
lid abnormalities
life expectancy
linear lesion
lipid storage disorder of CNS
liver biopsy
liver function enzymes
lung nodule
lung-brain syndromes
lysosomal storage disease
malformation, CNS, congenital
masked facies
McLeod syndrome
medulloblastoma
megalencephaly
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningitis
meningitis, basilar
meningitis, candida
meningitis, chronic
meningitis, fungal
meningitis, neutrophilic
mental retardation
mestinon
metabolic acidosis
methylmalonic acidemia
microcephaly
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
miglustat
mineralization
misdiagnosis
mitochondrial disease
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
moyamoya
moyamoya, adult
MRI, abnormal
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, muscle
MRI, negative
MRI, nodular enhancement
MRI, spinal cord
multiple sclerosis
muscle biopsy
muscle stiffness
muscle weakness, proximal
mutism
myelomalacia
myeloneuropathy
myelopathy
myoclonus
nasal speech
nausea and vomiting
needle tracks
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-treatment of
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic practice
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathy
neuropathy, demyelinating
newborn, evaluation of
next-generation sequencing
Niemann-Pick disease
night blindness
normal
NOTCH2NLC
nystagmus
occipital lobe
ocrelizumab
ocular motility, disorders of
opened mouth
ophthalmoplegia
organomegaly
ornithine transcarbamylase deficiency
ovarian dysgenesis
pachygyria
papilledema
paragonimiasis
paraparesis, familial spastic
paraparesis, spastic
parasitic infection, CNS
Parkinson disease
Parkinson disease, early symptoms
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal neurologic deficits
patient information and support
peripheral blood smear
Perrault syndrome
pes cavus
philtrum, tented
phonophobia
photophobia
PICU
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
polyglucosan body disease
polymicrogyria
pons, lesion of
precipitating factors
prion disease
PRKN gene
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
quality of life
recurrent
ReNU syndrome
respiratory tract infection
retinopathy
review article
risk factors
risus sardonicus
Romberg's sign
salivation, excessive
schizophrenia
scissors gait
scotoma
screening
sedimentation rate, elevated
seizure
seizure, drug-induced
seizure, focal
seizure, laughing as manifestation
sensorineural hearing loss
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sleep pathology and physiology
small vessel disease
spastic ataxia
spastic paraplegia, type 7
spasticity
speech disorder
speech, absence of
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
symmetric brain lesions
systemic illness
tandem gait, ataxic
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
tinnitus
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
tripping
tumefactive lesion
urea-cycle enzymopathies
urinary urgency
vasculitides
vasculopathy
vegetarianism
vestibular migraine
viral infection
viral infection, CNS
vision loss, sequential
vision, blurred
visual loss
visual loss, transient
visual obscurations, transient
visuospatial disturbance
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
white matter disease, unilateral
whole genome sequencing
wide based gait
workup
x-linked intellectual deficit
x-linked mental retardation
Zika virus infection
Showing articles 1000 to 1050 of 1063 << Previous Next >>

Retrovirus & Malignant Lymphoma in Homosexual Men
JAMA 254:1921-1925, Levine,A.M.,et al, 1985

Spinal Cord Degeneration in AIDS
Neurol 35:103-106, Goldstick,L.,et al, 1985

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

Intra-Blood-Brain-Barrier Synthesis of HTLV-III-Specific IgG in Patients with Neurologic Symp with AIDS or ARC
NEJM 313:1498-1504, 15381985., Resnick,L.,et al, 1985

Acquired Immune Defieiency Syndrome, Pathogenic Mechanisms of Ocular Disease
Ophthalmology 92:472-484, Pepose,J.S.,et al, 1985

A Prospective Study of the Ophthalmologic Findings in the Acquired Immune Deficiency Syndrome
Am J Ophthalmol 97:133-142, Freeman,W.R.,et al, 1984

Ophthalmologic Findings in Acquired Immune Deficiency Syndrome (AIDS)
Arch Ophthmol 102:201-206, Khadem,M.,et al, 1984

Progressive Multifocal Leukoencephalopathy in a Patient with Acquired Immune Deficiency Syndrome
Arch Neurol 41:780-782, Bernick,C.,et al, 1984

Acquired Immune Deficiency Syndrome & Multiple Tract Degeneration in a Homosexual Man
Ann Neurol 15:502-505, Horoupian,D.S.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Toxoplasmic Encephalitis in Patients with Acquired Immune Deficiency Syndrome
JAMA 252:913-917, Luft,B.J.,et al, 1984

Central-Nervous-System Toxoplasmosis in Homosexual Men & Parenteral Drug Abusers
Ann Int Med 100:36-42, Wong,B.,et al, 1984

Cerebral Toxoplasmosis in Acquired Immune Deficiency Syndrome
Arch Neurol 41:321-323, Alonso,R.,et al, 1984

Central Nervous System Toxoplasmosis in Homosexual Men
Am J Med 75:877-881, Anderson,K.P.,et al, 1983

Outbreak of Central-Nervous-System Toxoplasmosis in Western Europe & North America
Lancet 1:781-784, Luft,B.J.,et al, 1983

Fatal CNS Toxoplasmosis in a Homosexual Man
Neurol 33:926-927, Delaney,P.,et al, 1983

Precautions Recommended in Treating Patients with Aids
NEJM 308:156, Masci,J.R.,et al, 1983

Progressive Multifocal Leukoencephalopathy in Acquired Immunodeficiency Syndrome
NEJM 309:492-493, Bedri,J.,et al, 1983

Primary Lymphoma of the Nervous System Associated with Acquired Immune-Deficiency Syndrome
NEJM 308:45, Snider,W.D.,et al, 1983

Acquired Immunodeficiency
Malignant Lymphoma & Pneumocystis Carinii, Case Record NEJM 309:359-36983., , 1983

CNS Toxoplasmosis in Acquired Immunodeficiency Syndrome
Arch Neurol 40:649-652, Horowitz,S.L.,et al, 1983

Infection-Control Guidelines for Patients with Acquired Immunodeficiency Syndrome (AIDS)
Jr. , et al, NEJM 309:740-74483., Conte,J.E., 1983

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Intracerebral-Mass Lesions in the Acquired Immunodeficiency Syndrome (AIDS)
NEJM 309:1454-1455, Levy,R.M.,et al, 1983

Central-Nervous-System Toxoplasmosis In Homosexual & Heterosexual Adults
NEJM 307:498-499, Hauser,W.E.,et al, 1982

Multiple Sclerosis, (First of Two Parts)
NEJM 307:1183-1188, 1982, McFarlin,D.E.,et al, 1982

Progressive Multifocal Leukoencephalopathy In A Male Homosexual With T-Cell Immune Deficiency
NEJM 307:1436-1438, Miller,J.R.,et al, 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Herpes Simplex Virus & Recurrent Laryngeal Nerve Paralysis
Arch Int Med 139:1423-1424, Magnussen,C.R.,et al, 1979

Prevention Of Reactivated Herpes Simplex Infection By Human Leukocyte Interferon After Operation On The Trigeminal Root
NEJM 301:225-230, Paxin,G.J.,et al, 1979

HLA & Neurologic Fisease
Neurol 28:413, Compston,A., 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

HLA & Cogan's Syndrome
NEJM 298:1094, Kaiser-Kuper,M.I.,et al, 1978

HLA Antigens in the Landry-Guillain-Barre Syndrome & Chronic Relapsing Polyneuritis
Ann Neurol 4:285-289, Stewart,G.J.,et al, 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Case Records of the MGH
Metastatic Choreocarcinoma from Ovary, NEJM 296:9261977., , 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Urinary Retention Probably Secondary to Herpes Genitalis
NEJM 297:920, Caplan,L.R., 1977

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Cogan's Syndrome & HLA BW17
NEJM 295:1262, DelCarpio,J.,et al, 1976

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Virus Like Particles in Granulomatous Angiitis of the Central Nervous System
Neurol 26:797, Reyes,M.G.,et al, 1976

Herpes Simplex Neuropathy
Neurol 26:596, 1976, Krohel,G.B.,et al, 1976

Systemic Lupus Erythematosus
Arch Pathol 99:152, Jones,J.M.,et al, 1975

Herpes Simplex Virus in Idiopathic Facial Paralysis (Bell Palsy)
JAMA 233:527, Adour,K.K.,et al, 1975

The Bell Tolls for Decompression
NEJM 292:748, Adour,K.K., 1975



Showing articles 1000 to 1050 of 1063 << Previous Next >>