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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 1200 to 1250 of 1945 << Previous Next >>

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

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Familial Meningioma
Neurol 40:312-314, McDowell,J.R., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

Abnormal Respiration and Sudden Death During Sleep in Multiple System Atrophy with Autonomic Failure
Neurol 40:677-679, Munschauer,F.E.,et al, 1990

Diabetic Autonomic Neuropathy
NEJM 322:1078-1079, Watkins,P.J., 1990

Loss of Facial Sweating and Flushing in Holmes-Adie Syndrome
Neurol 40:847-849, Drummond,P.D.&Edis,R.H., 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
Ann Neurol 28:387-390, Gospe,S.M.&Gabor,A.J., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

MRI in Familial Multiple Sclerosis
Neurol 40:900-903, Lynch,S.G.,et al, 1990

A Comparison of Sporadic and Familial Multiple Sclerosis
Neurol 40:1354-1358, Weinshenker,B.G.,et al, 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Combined Resting-Postural Tremor of Lower Limbs:Another Essential Trem, or Variant
Neurol 40:1006, Rapoport,A.,et al, 1990

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990



Showing articles 1200 to 1250 of 1945 << Previous Next >>