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Differential
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abdominal cramps
abducens nerve paralysis
acoustic nerve
adult polyglucosan body disease
ageusia
akathisia
alcohol intolerance
alkylating agents
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
amyloidosis
anatomy of
angina pectoris
anhidrosis
anosmia
antimetabolite
areflexia
asparginase
asystole
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atonic bladder
attention deficit disorder with hyperactivity
autonomic dysfunction
autonomic dysfunction, acute
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal dominant leukodystrophy
axonal degeneration
Babinski sign
bacterial infection
baroreceptors
bladder dysfunction
blood dyscrasias, neurologic findings with
botulism
bradycardia
brain atrophy
brainstem, infarction of
bulbar palsy
burning paresthesia
carbamazepine
carcinoma
carcinoma of thyroid
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cataracts, congenital
catecholamine
cerebellar atrophy, secondary
cerebellar vermis
cerebral cortical atrophy
cerebral ischemia
cerebral vasculature
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chewing movements
children
chorea
choreoathetosis
cingulate island sign
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
coat-hanger pain
coma
confabulation
congestive heart failure
constipation
cranial neuropathy, multiple
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dementia, subcortical
developmental retardation
diabetes mellitus
diarrhea
differential diagnosis
diplopia
dopamine
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dystonia
dystonia musculorum deformens
encephalopathy
erectile dysfunction
exome sequencing
eye, pain in
Fabry's disease
facial nerve palsy
facial nerve palsy, bilateral
facial pain
failure to thrive
falling
familial
familial rectal pain
fatal familial insomnia
fever
flunarizine
fluorouracil
flush syndrome
flushing
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
gait disorder
gait, spastic
gamma amino butyric acid
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
glycogen storage disease
hallucination
head injury
headache
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
homovanillic acid
Horner's syndrome
human immunodeficiency virus type 1
hydrocephalus
hyperhidrosis
hyperreflexia
hypertension
hyperthermia
hyponatremia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypotonia
imbalance
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
isoniazid
jaw pain
Jewish
karyotyping
Korsakoff's psychosis
laughing
laughing, pathologic
L-dopa
leprosy
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
monoamine oxidase inhibitors
monoamines
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle pain
muscle weakness
myelomalacia
myeloneuropathy
myocardial infarction
myoclonic jerks
myoclonus
nausea and vomiting
neck pain
nerve biopsy
nerve growth factor
neuroendocrinology
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuroma
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, work up for
neurotoxin
neurotransmitter
next-generation sequencing
nitrogen mustard
norepinephrine
NOTCH2NLC
nystagmus
ocular dysmetria
orthostatic hypotension
orthostatic hypotension, idiopathic
pain
pain, anal
paraparesis
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, atypical
Parkinson disease, familial
Parkinsonism syndrome
paroxysmal extreme pain disorder
paroxysmal neurologic deficits
peroneal muscle atrophy, causes of
phenylketonuria
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polyneuropathy, familial
precipitating factors
prion disease
procarbazine
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
radiculopathy
review article
Riley-Day syndrome
Romberg's sign
screening
seizure
seizure, children
seizure, differential diagnosis of
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
shoulder, pain in
Shy-Drager syndrome
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
smell
SNCA duplication
sodium channel dysfunction
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
stuporous
subcortical U fibers
syncope
tachycardia
tardive dyskinesia
taste
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
urinary frequency
urinary incontinence
valsalva maneuver
vasospasm, cerebral
vinblastine
vincristine neurotoxicity
viral infection
visual loss, transient
vocal cord paralysis
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
wrist drop
Showing articles 750 to 800 of 1945 << Previous Next >>

Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997

Offspring Recurrence Rates and Clinical Characteristics of Conjugal Multiple Sclerosis
Lancet 349:1587-1590, Robertson,N.P.,et al, 1997

High-Frequency Unilateral Thalamic Stimulation in the Treatment of Essential and Parkinsonian Tremor
Ann Neurol 42:292-299, Koller,W.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

Apolipoprotein E e4 Associated with Chronic Traumatic Brain Injury in Boxing
JAMA 278:136-140, Jordan,B.D.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Comparison of First Degree Relatives and Spouses of Poeple with Chronic Tension Headache
BMJ 314:1092-1093, Ostergaard,S.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
Neurol 48:752-757, Polymeropoulos,M.H.,et al, 1997

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

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 Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Anhidrosis:An Unusual Presentation of Diabetes Insipidus
Neurol 49:1708-1710, Shimizu,H.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Olfactory Dysfunction in Familial Parkinsonism
Neurol 49:1262-1267, Markopoulou,K.,et al, 1997

Long-Term Effects of Pancreatic Transplantation on Diabetic Neuropathy
Ann Neurol 42:727-736, Navarro,X.,et al, 1997

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

Treatment of Gustatory Sweating with Botulinum Toxin
Ann Neurol 42:973-975, Naumann,M.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
Neurol 49:1231-1238, 11931997., Gardner,K.,et al, 1997

Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
JAMA 278:1237-1241, 12821997., Pericak-Vance,M.A.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

The Treatment of Postprandial Hypotension in Autonomic Failure with 3, 4-DL-Threo-Dihydroxyphenylserine
Neurol 47:1414-1420, 13701996., Freeman,R.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996

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

Abnormal Heart Rate Variability as a Manifestation of Autonomic Dysfunction in Hemispheric Brain Infarction
Stroke 27:2058-2063, Korpelainen,J.T.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

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

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996



Showing articles 750 to 800 of 1945 << Previous Next >>