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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 200 to 250 of 539 << Previous Next >>

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
Neurol 46:1350-1353, Sekizawa,A.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
Lancet 345:1260-1264, Tracey,I.,et al, 1995

Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
JAMA 274:813-819, Tokgozoglu,L.S.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
NEJM 333:832-838, 8711995., Mendell,J.R.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Head Injury in Sport
BMJ 308:1620-1624, McLatchie,G.&Jennett,B., 1994

The Shoulder-Hand Syndrome after Stroke:A Prospective Clinical Trial
Ann Neurol 36:728-733, Braus,D.F.,et al, 1994

Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
Neurol 44:2006-2014, Jankovic,J., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

Myotonic Dystrophy with No Trinucleotide Repeat Expansion
Neurol 35:269-272, 2551994., Thornton,C.A.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Imaging of Closed Head Injury
Radiology 191:1-17, Gentry,L.R., 1994

Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

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

Axonal Guillain-Barre Syndrome
Muscle & Nerve 17:678-679994., Feasby,T.E., 1994

Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
Lancet 344:302-303, Fassati,A.,et al, 1994

Imaging of Closed Head Injury
Radiology 191:1-17, Gentry,L.R., 1994

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
Ann Int Med 119:900-905, Fishbein,M.C.,et al, 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993

Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993

Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993

Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993

Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
NEJM 329:915-920, Sancho,S.,et al, 1993

Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma
Neurol 43:795-800, Ohlendieck,K.,et al, 1993

Gene Therapy for Duchenne Dystrophy
Ann Neurol 34:3-4, Engel,A.G., 1993



Showing articles 200 to 250 of 539 << Previous Next >>