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Addison's disease
adrenoleukodystrophy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
aminoacidurias
amniocentesis
arylsulfatase A
arylsulfatase A pseudodeficiency
asymptomatic
ataxia
ataxia, cerebellar
atidarsagene autotemcel
auditory evoked brainstem potentials
behavioral disorder
bone marrow transplantation
burning feet
Canavan's disease
carcinoma of pancreas
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral edema, cytotoxic
cerebrospinal fluid, elevated protein of
children
cholelithiasis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
cognition
complications
conjunctival biopsy
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, lesion of
cortical blindness
cranial nerve enhancement
cultured skin fibroblasts
Cushing's syndrome
deafness
dementia
dementia, childhood
demyelinating disease
depression
developmental milestones, loss of
differential diagnosis
dysmorphic
dystonia
dystonia, focal
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalopathy
enzyme treatment
enzyme, defect
evoked potentials
Fabry's disease
facial appearance, abnormal
falling
familial
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gene mutation
gene therapy
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
Hallervorden Spatz disease
hallucination
hallucination, auditory
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
Hurler's syndrome
hyperadrenalism
hyperparathyroidism
hyperthyroidism
hypoglycemia
hypoparathyroidism
hypothyroidism
imbalance
inborn errors of metabolism
inborn errors of metabolism, screening
intellectual deterioration
internal capsule
Krabbe's disease
leg weakness, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
lysosomal storage disease
memory, impairment of
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
mitochondrial disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, gradient-echo
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
muscular dystrophy, Duchenne
neonatal screening, genetic neurologic disorders
neoplasm, intracranial
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropsychiatry
Niemann-Pick disease
ophthalmoplegia, plus syndrome
optic atrophy
pain, abdominal
paraparesis
paraparesis, spastic
Pelizaeus Merzbacher
penicillamine
pernicious anemia
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
porphyria
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, cause of
pyramidal tract dysfunction
quadriparesis
review article
safety
Sandhoff's disease
Schilder's disease
schizophrenia
screening
seizure
short stature
skin, biopsy
somatosensory evoked potentials
speech disorder
speech disorder, childhood
sphingolipodoses
spongy degeneration of brain
stem cell transplantation
sural nerve
symmetric brain lesions
syphilis, neurologic complications with
systemic lupus erythematosus
Tay-Sachs disease
titubation
treatment of neurologic disorder
tremor
urinary sulfatidase excretion
visual evoked response
white matter disease
white matter disease, periventricular
Showing articles 100 to 150 of 151 << Previous Next >>

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Leukodystrophy in Patients with Ovarian Dysgenesis
Ann Neurol 41:654-661, Schiffman,R.,et al, 1997

Progressive Familial Leukodystrophy of Late Onset
Neurol 46:429-434, Knopman,D.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Immunosuppression-Induced Leukoencephalopathy from Tacrolimus (FK506)
Ann Neurol 40:575-580, Small,S.L.,et al, 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

X-Linked Adrenoleukodystrophy:Adult Cerebral Variant
Neurol 43:1518-1522, Farrell,D.F.,et al, 1993

A Two-Year Trial of Oleic and Erucic Acids ("Lorenzo's Oil") as Treatment for Adrenomyeloneuropathy
NEJM 329:745-752, 8011993., Aubourg,P.,et al, 1993

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Adrenomyeloneuropathy Presenting as Addison's Disease in Childhood
NEJM 322:13-16, 54-551990., Sadeghi-Nejad,A.&Senior,B., 1990

The Leukodystrophies
NEJM 322:54-55, Menkes,J.H., 1990

MR Findings in Globoid Cell Leucodystrophy
Neuroradiology 32:520-522, Demaerel,Ph.,et al, 1990

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987

Krabbe Disease:Specific MRI & CT Findings
Neurol 36:111-115, Baram,T.Z.,et al, 1986

Infantile Sudanophilic Leukodystrophy:Computed Tomography Demonstration
Neuroradiology 28:170-172, Sano,N.,et al, 1986

Computed Tomography in White Matter Diseases
Ann Neurol 17:314-315, Ferriero,D.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

MR Imaging in Adrenoleukomyeloneuropathy
J Comput Assist Tomogr 9:793-796, Bewermeyer,H.,et al, 1985

Hereditary Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
NEJM 311:948-953, Eldridge,R.,et al, 1984

Computed Tomography in Krabbe's Disease:Comparison with Neuropathology
Neuroradiology 25:323-327, Ieshima,A.,et al, 1983

Usefulness of BAER Studies in the Early Diagnosis of Pelizaeus-Merzbacher Disease
Neurol 33:955-956, Garg,B.P.,et al, 1983

Noninvasive CT Diagnosis of Infantile Alexander Disease:Pathologic Correlation
J Comput Assist Tomogr 7:509-516, Trommer,B.L.,et al, 1983

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,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

Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease
Arch Neurol 37:446-447, Lieberman,J.S.,et al, 1980

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Leukoencephalopathy in Childhood Leukemia
et al. , Neurol 27:609977., Devivo,D.C., 1977

Computerized Tomography in Demyelinating Disease of the Young
Neurol 27:838, Robertson,W.C.,et al, 1977

Rapid Diagnosis of Meningoencephalitis, Encephalitis
Neurol 24:l43, Lindeman,J.,et al, 1974



Showing articles 100 to 150 of 151 << Previous Next >>