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Differential
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abulia
adrenoleukodystrophy
adult-onset leukodystrophy, with neuroaxonal spheroids
alopecia
apraxia
areflexia
ataxia
ataxia, cerebellar
axonal degeneration
axonal spheroid
axonal transection
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
blindness
bradykinesia
bradyphrenia
brain biopsy
calcification, intracranial
calcifications, intracranial, punctate
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral cortical atrophy
cerebral vasculature, calcification
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
Clinical Pathologic Conference(C.P.C.)
cognition
conjunctival biopsy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerves, toxins effecting
cranial neuropathy, multiple
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, frontal lobe type
dementia, presenile
dental pulp biopsy
dentate nuclei
dentate nuclei, lesion of
depression
developmental milestones, loss of
developmental retardation
differential diagnosis
disability, neurological
dysarthria
dyscalculia
dysdiadochokinesia
dysphagia
electromyogram
electron microscopy
encephalopathy
exome sequencing
falling
familial
fatigue
frontal lobe, anatomy and physiology
frontal lobe, lesion of
gait disorder
gait, spastic
gangliosidosis GM1
gangliosidosis, generalized
gaze palsy
gene mutation
genetic neurologic disorders
genetic testing
genu of corpus callosum
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
Hallervorden Spatz disease
handwriting
heavy metal intoxication
histochemistry
hyperreflexia
hypotonia
imbalance
incoordination
intellectual deficit
intellectual deterioration
intrathecal chemotherapy
iron, brain
jaundice
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
liver disease
lysosomal storage disease
memory, impairment of
metachromatic leukodystrophy
methotrexate
microangiopathy, brain
mimics
misdiagnosis
mortality
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, black holes on
MRI, demyelinating disease
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, high signal foci on
MRI, magnetization transfer sequence
MRI, paramagnetic effect
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, disability status scale
multiple sclerosis, misdiagnosis
muscle biopsy
muscle weakness
myoclonus
myoclonus, epilepsy
N-acetyl-L-aspartic acid
nerve biopsy
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuronal cell death
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neurotoxin
next-generation sequencing
Niemann-Pick disease
ophthalmoplegia, plus syndrome
optic atrophy
PANK2 mutation
personality change
posterior column disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract
quadriplegia
remote effect of cancer on the nervous system
review article
seizure
skin, biopsy
spinal cord
spinal cord, lesion of
thallium poisoning
tremor
tremor, intention
urinary incontinence
vibratory sensation, abnormal
vision, failure of in childhood
visual evoked response
visual impairment
vitamin deficiency
vitamin E deficiency
Wallerian degeneration
weakness, proximal
white matter disease
writing
Showing articles 300 to 350 of 539 << Previous Next >>

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

The Movement Disorder of Reflex Sympathetic Dystrophy
Neurol 40:57-61, Schwartzman,R.J.&Kerrigan,J., 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
Lancet 336:651-653, Wijmenga,C.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

Duchenne Muscular Dystrophy Carrieris
Neuroradiology 31:373-376, Matsumura,K., 1989

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
NEJM 320:1592-1597, 1621-16231989., Mendell,J.R.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Peripheral Neuropathy in Essential Mixed Cryoglobulinemia
Arch Neurol 45:1210-1214, Carcia-Bragado,F.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,et al, 1988

Reflex Sympathetic Dystrophy Syndrome in Children and Adolescents, Reports of 18 Cases and Review
Am J Dis Child 142:1325-1330, Silber,T.J.&Majd,M., 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Hearing Loss in Myotonic Dystrophy
Ann Neurol 23:202-203, Wright,R.B.,et al, 1988

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988



Showing articles 300 to 350 of 539 << Previous Next >>