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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
axonal degeneration
Babinski sign
bacterial infection
baroreceptors
bladder dysfunction
blood dyscrasias, neurologic findings with
botulism
bradycardia
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
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
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
dementia
dementia, familial
dementia, rapidly progressive
developmental retardation
diabetes mellitus
diarrhea
diplopia
dopamine
drug induced neurologic disorders
dysarthria
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
hypertension
hyperthermia
hyponatremia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypotonia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
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
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
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
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
psychosis
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
radiculopathy
review article
Riley-Day syndrome
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, 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
syncope
tachycardia
tardive dyskinesia
taste
thalamus, atrophy of
thalamus, lesion of
tinnitus
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
urinary incontinence
valsalva maneuver
vasospasm, cerebral
vinblastine
vincristine neurotoxicity
viral infection
visual loss, transient
vocal cord paralysis
weakness
weakness, progressive
weight loss
white matter disease
wrist drop
Showing articles 1150 to 1200 of 1916 << Previous Next >>

Detection of Tuberous Sclerosis in Parents by Magnetic Resonance Imaging
Neurol 41:262-265, Roach,E.S.,et al, 1991

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

A Genetic Study of Idiopathic Focal Dystonias
Ann Neurol 29:320-324, Waddy,H.M.,et al, 1991

Long-Term Suppression of Tremor by Chronic Stimulation of the Ventral Intermediate Thalamic Nucleus
Lancet 337:403-406, Benabid,A.L.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

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

Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
Neurol 41:1923-1927, Pulst,S.M.,et al, 1991

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Monozygotic Twins with Seizures, Shared Characteristics
Arch Neurol 48:1041-1045, Segal,R.A.,et al, 1991

Neurological Paraneoplastic Syndromes in Patients with Small Cell Lung Cancer, A Prospective Survey of 150 Pts
JNNP 54:764-767, Elrington,G.M.,et al, 1991

Prenatal Origin of Hemiparetic Cerebral Palsy:How Often and Why?
Pediatrics 88:1059-1062, Nelson,K.B., 1991

Autonomic Nervous Function in Progressive Supranuclear Palsy
Arch Neurol 48:1083-1084, vanDijk,J.G.,et al, 1991

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

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Recurrent Meningitis in a Patient with Congenital Deficiency of the C9 Component of Complement
Arch Int Med 150:2395-2399, Zoppi,M.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Multiple Sclerosis Sibling Pairs:Clustered Onset and Familial Predisposition
Neurol 40:1546-1552, Doolittle,T.H.,et al, 1990

Conjugal Temporal Arteritis
Neurol 40:1839-1842, Galetta,S.L.,et al, 1990

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

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

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

Cranial MR in Phenylketonuria
J Comput Assist Tomogr 14:458-460, Shaw,D.W.W.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

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

Effects of Pancreatic Transplantation on Diabetic Neuropathy
NEJM 322:1031-1037, Kennedy,W.R.,et al, 1990

Tangier Disease in a Black Patient:An Unusual Clinical Presentation
Am J Med 89:105-108, Lo,W.D.,et al, 1990

Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study
Ann Neurol 28:43-49, Claus,D.,et al, 1990

Familial Multiple Symmetric Lipomatosis with Peripheral Neuropathy
Neurol 40:1246-1250, Chalk,C.H.,et al, 1990

Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
Lancet 336:93-96, Shorvon,S.D., 1990

Acute Autonomic Neuropathy, Two Cases and a Clinical Review
Arch Int Med 150:2373-2376, Hart,R.G.&Kanter,M.C., 1990

Diabetic Autonomic Neuropathy
BMJ 301:565-566, Bilous,R.W., 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

The Triumph of Linkage Analysis, Editorial
Ann Neurol 27:111-113, Rosenberg,R.N., 1990

Screening for Prolonged Incubation of HTLV-1 in Relatives of British Patients with Tropical Spastic Paraparesis
BMJ 300:300-304, Cruickshank,J.K.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

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

Autonomic Neuropathy After Treatmant with Cisplatin, Vinblastine, and Bleomycin for Germ Cell Cancer
BMJ 300:511-512, Hansen,S.W., 1990

Adrenomyeloneuropathy Presenting as Addison's Disease in Childhood
NEJM 322:13-16, 54-551990., Sadeghi-Nejad,A.&Senior,B., 1990



Showing articles 1150 to 1200 of 1916 << Previous Next >>