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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 250 to 300 of 539 << Previous Next >>

Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993

Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
Neurol 42:1783-1790, Ioannou,P.,et al, 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992

Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
Arch Neurol 49:954-960, Verhagen,W.I.M.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
Neurol 42:1815-1817, Dubel,J.R.,et al, 1992

Fasioscapulohumeral and Scapuloperoneal Syndromes
In Handbook Clin Neurol 62:161-177, Munsat,T.L.&Serratrice,G., 1992

Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
Neuroradiol 34:396-398, Aihara,M.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Ventricular Late Potentials in Myotonic Dystrophy
Ann Int Med 115:607-613, Milner,M.R.,et al, 1991

Hearing Loss in Facioscapulohumeral Muscular Dystrophy
Neurol 41:1878-1881, Brouwer,O.F.,et al, 1991

The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
Neurol 41:38-40, Miller,R.G.,et al, 1991

Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Prednisone in Duchenne Dystrophy, A Randomized, Controlled Trial Defining the Time Course & Dose Response
Arch Neurol 48:383-388, Griggs,R.C.,et al, 1991

Mononuclear Cell Analysis of Muscle Biopsies in Prednisone-Treated & Untreated Duchenne Muscular Dystrophy
Neurol 41:667-672, Kissel,J.T.,et al, 1991

A Comparison of Daily and Alternate-Day Prednisone Therapy in the Treatment of Duchenne Muscular Dystrophy
Arch Neurol 48:575-579, Fenichel,G.M.,et al, 1991

Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Long-Term Benefit from Prednisone Therapy in Duchenne Muscular Dystrophy
Neurol 41:1874-1877, Fenichel,G.M.,et al, 1991

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990



Showing articles 250 to 300 of 539 << Previous Next >>