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Differential
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aminoacidurias
ammonia
anatomy of
anorexia
Arnold Chiari malformation
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
Behcet's syndrome
beriberi
beriberi, infantile
blood dyscrasias, neurologic findings with
brain atrophy
brainstem
brainstem, lesion of
bulimia
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, false negative
cataracts
caudate nucleus
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
children
chorea
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
dizziness
dysarthria
dystonia
electron microscopy
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enkephalins
enzyme, defect
eye movement, disorders of
Fabry's disease
Fahr disease
failure to thrive
familial
flavivirus
fontanel, bulging
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glioma
glutaric acidemia
gyrus, abnormal
head injury
head lag
headache
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
histochemistry
histochemistry of muscle
hyperglycemia
hyperphagia
hyperreflexia
hypoglycemia
hyponatremia
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
inborn errors of metabolism
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal pseudoobstruction
intraventricular hemorrhage
iron, brain
irritability
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
magnetic susceptibility
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metronidazole
microhemorrhage, intracerebral
midbrain, lesion of
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
myelitis, longitudinal
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
neoplasm, primary of CNS
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neurotoxin
nutritional deficiency
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
paraparesis, spastic
Parkinson disease
pes cavus
pigmentary retinopathy
POLG1 gene
polyneuropathy
pons, lesion of
progressive infantile poliodystrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinopathy
review article
Romberg's sign
seizure
seizure, children
sensorineural hearing loss
sensory loss
short stature
spasticity
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
substantia nigra
suck, poor
symmetric brain lesions
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
titubation
tonic spasms
treatment of neurologic disorder
tremor
tremor, intention
urine test for metabolic disorders
visual acuity, decreased
vitamin deficiency
Von Hippel Lindau
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 650 to 700 of 763 << Previous Next >>

Isolation of Herpes Simplex Virus Type 1 in Recurrent (Mollaret) Meningitis
Ann Neurol 11:17-21, Steel,J.G.,et al, 1982

Periodic Meningitis & Familial Mediterranean Fever
Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982

Chronic Blastomycotic Meningitis
Am J Med 71:501-505, Kravitz,G.R.,et al, 1981

Focal Intracranial Mucormycosis Presenting as Chronic Meningitis
JAMA, 246:2063-20641981., Jones,P.G.,et al, 1981

Neurologic Disease & Nutrition
Res & Staff Physician August 1981, pp. 77-81., Dreyfus,P.M., 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Biologic Distinction Between Sporadic & Familial Alzheimer Disease by an in vitro Cell Fusion Test
Neurol 31:323-325, Dubois-Moreau,M.C.,et al, 1981

Evoked Responses in Vitamin B12 Deficiency
Ann Neurol 9:407-409, Krumholz,A.,et al, 1981

Lhermitte's Sign in Cobalamin (Vitamin B12) Deficiency
JAMA 245:1059, Butler,W.M.,et al, 1981

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

Two Cases of Rapidly Progressive Subacute Sclerosing Panencephalitis
Arch Neurol 38:109-113, Silva,C.A.,et al, 1981

Meningitis, In Clinical Neurology
Harper & Row Publishers, 1981, p. 1-55., Sahs,A.L.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Mollaret Meningitis:Report of a Case with Recovery after Colchicine
Ann Neurol 8:631-633, Mora,J.S.,et al, 1980

CSF B-Glucoronidase Assay in the Diagnosis of Neoplastic Meningitis
Arch Neurol 37:684-687, Shuttleworth,E.,et al, 1980

Cerebral Embolism in Libman-Sacks Endocarditis
Neurol 30:487-491, Fox,I.S.,et al, 1980

Transissible Dementias:Current Problems in Tissue Handling
Neurol 30:302-303, Baringer,J.R.,et al, 1980

Serial EEG Findings in 27 Cases of Creutzfeldt-Jakob Disease
Arch Neurol 37:143-145, Chiofalo,N.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

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

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

The Neuropsychiatry of Megaloblastic Anaemia
BMJ 281:1036-1038, Shorvon,S.D.,et al, 1980

Unreliability of Radiodilution Assays as Screening Tests for Cobalamin (Vitamin B12) Deficiency
JAMA 244:1942-1945, Cohen,K.L.,et al, 1980

Studies Of A Patient With Megaloblastic Anemia & An Abnormal Transcobalamin II
NEJM 303:1209-1212, Seligman,P.A.,et al, 1980

Clin. Path. Conference. Lymphoblastic lymphoma
Nonbacterial Thrombotic Endocarditis, Cerebral Infarction, Case Record 27-1980, NEJM 303:92-10080., , 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Periodic Lateralized Epileptiform Complexes (PLEDs) in Creutzfeldt-Jakob Disease
Neurol 30:611-617, Au,W.J.,et al, 1980

Failure of Interferon to Modify Creutzfeldt-Jakob Disease
BMJ 280:902, Kovanen,J.,et al, 1980

Review of 38 Cases of S. S. P. E. :Effect of Amantadine on the Natural Course of the Disease
Jr. , et al, Ann Neurol 8:422-42580., Robertson,W.C., 1980

Histoplasma Meningitis:Diagnostic Value of Cerebrospinal Fluid Serology
Ann Int Med 92:189-191, Plouffe,J.F.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Visual Evoked Responses in Pernicious Anemia
Arch Neurol 36:168-169, Troncoso,J.,et al, 1979

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Subacute Sclerosing Panencephalitis During Pregnancy
Arch Neurol 36:314-316, Gaines,K.J.,et al, 1979

Radionuclide Imaging in Subacute Sclerosing Panencephalitis
Neurol 29:749-752, , 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

Clinical Similarity of Alzheimer & Creutzfeldt-Jakob Disease
Ann Neurol 6:368-369, Watson,C.P., 1979

Creutzfeldt-Jakob Disease Treated with Amantadine
JNNP 42:960-961, Sanders,W.L., 1979

The Variable Natural History of Subacute Sclerosing Panencephalitis
Arch Neurol 36:610-614, Risk,W.S.,et al, 1979

Myasthenia Gravis, Pernicious Anemia, & Hashimoto's Thyroiditis
Arch Neurol 36:594-595, Krol,T.C., 1979

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Cobalamin Analog Present In Human Plasma Mask Cobalamin Defic Current Radioistope Dil. Assays Not Spec for Cobalamin
NEJM 299:785, Kolhouse,J.F.,et al, 1978

Evidence That Some Patients With Pernicious Anemia Are Not Recogn By Radiodil Assay For Cobalamin In Serum
NEJM 299:816, Cooper,B.A.,et al, 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Recurrent Meningitis Due to an Intracranial Epidermoid
Neurol 28:124, Schwartz,J.F.,et al, 1978

Bacterial Endocarditis in 4 Young Infants
Clin Peds 16:607-609, Edwards,K.,et al, 1977



Showing articles 650 to 700 of 763 << Previous Next >>