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abducens nerve paralysis
acoustic nerve
acral sensory symptoms
Adies pupil
advances in neurology
alcohol intolerance
alkylating agents
altered states of consciousness
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ankle reflex, absent
anterior tibial muscle weakness
antimetabolite
areflexia
arthrogryposis multiplex
asparginase
ataxia
ataxia, cerebellar
atonic bladder
autonomic dysfunction
Babinski sign
benign essential tremor
blood dyscrasias, neurologic findings with
burning paresthesia
caloric testing
carcinoma
carcinoma of thyroid
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central core disease
cerebrospinal fluid, pressure low
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosomal abnormality
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
constipation
corpus callosum, lesion of
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
dermatomyositis
differential diagnosis
diplopia
diplopia, transient
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dysarthria
dysphagia
electroencephalogram, inflammatory disease
electromyogram
encephalopathy
epidemiology of neurology
episodic neurologic deficits
evoked potentials
facial nerve palsy, bilateral
facial pain
falling
familial
fasciculation
Fazio-Londe's disease
fever
fine motor function, impaired
fluorouracil
flush syndrome
foot deformity
foot drop
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
Guillain Barre syndrome
hallucination
hammertoes
hand deformity
hand weakness
headache
hearing loss
heavy metal intoxication
hemiparesis
hemiparesis, transient
high arched feet
human genome
hyperreflexia
hyponatremia
hyporeflexia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intrinsic hand muscles, wasting of
isoniazid
jaw pain
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
laminectomy, cervical
laminectomy, lumbar
leg weakness, bilateral
leukemia, neurologic findings assoc.with
leukoencephalopathy
lumbosacral plexopathy
meningismus
meningoencephalopathy
methotrexate
methylhydrazine derivatives
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
monoparesis
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
multiple endocrine neoplasia
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelin protein zero gene
myelogram
myelopathy
myeloradiculopathy
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve growth factor
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuritis, causes of
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuroma
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, work up for
neurotoxin
neurotrophin-3
night blindness
nitrogen mustard
numbness, extremity
optic atrophy
optic atrophy, hereditary
orthostatic hypotension
pain
pain, foot
paralysis
paralysis, recurrent
paraparesis
paresthesias
paresthesias, feet
paresthesias, lower extremity
patient information and support
peroneal muscle atrophy, causes of
pes cavus
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, familial
porphyria
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
proptosis
ptosis
ptosis, bilateral
pulmonary function tests
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
quadriparesis
quadriplegia, transient
quality of life
radiculopathy
recombinant DNA
recurrent
Refsum's disease
respiratory failure
reversible neurologic disorder
review article
RFLPs
Romberg's sign
Roussy Levy syndrome
sarcoidosis
seizure
sensorineural hearing loss
sensory loss
spinal cord, compression of
spinal stenosis
spinal stenosis, familial
splenium of corpus callosum
spontaneous remission
steppage gait
stiff man syndrome
strokelike episodes
subdural hematoma
symmetric brain lesions
syncope
tinnitus
toe walking
tomaculous neuropathy
torticollis
transient neurologic deficit
treatment of neurologic disorder
tremor
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
ultrasonography, nerve
vestibular function, tests of
vinblastine
vincristine neurotoxicity
visual evoked response
visual impairment
vocal cord paralysis
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
white matter disease
wrist drop
X-linked neuropathy
x-ray, spine
Showing articles 400 to 450 of 4330 << Previous Next >>

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Riluzole
Lancet 348:795-799, Wokke,J., 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

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

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,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

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

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

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

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Recent Developments in the Drug Treatment of Motor Neurone Disease
BMJ 309:140-141, , 1994

Sequences Specific for Enterovirus Detected in Spinal Cord from Patients with Motor Neurone Disease
BMJ 308:1541-1543, Woodall,C.J.,et al, 1994

Clinical Significance of Hypointensity in the Motor Cortex on T2-Weighted Images
Neurol 44:1181, Iwasaki,Y.,et al, 1994

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



Showing articles 400 to 450 of 4330 << Previous Next >>