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acute cerebellar ataxia
acute disseminated encephalomyelitis
Adies pupil
advances in neurology
aggression
algorithm
alternating rapid movement
AMPA receptor antibodies
amphiphysin antibodies
anemia
anti GQ1b IgG antibody
anti Hu antibody
anti La antibody
anti Ma
anti MAG antibodies
anti mGluR1 encephalitis
anti Ri antibody
anti Ro antibody
anti Tr antibodies
anti Yo antibody
antiamphiphysin
antibiotics
antibodies to voltage-gated calcium channels
antithyroid antibodies
anxiety
aphasia
arthritis
ataxia
ataxia, cerebellar
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
autonomic neuropathy
bacterial infection
ballismus, bilateral
behavioral disorder
behavioral disorder, acute
Behcet's syndrome
Bickerstaff's brainstem encephalitis
biologic markers
blindness
brachial neuritis
brainstem, atrophy
brainstem, dysfunction
brainstem, lesion of
brucellosis, nervous system involvement with
Brudzinski's sign
bulbar dysfunction
CA-125
calcium channel dysfunction
CAR syndrome
carbon monoxide poisoning
carcinoma
carcinoma of bladder
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of testis
carcinoma of uterus
CAT scan, abdomen
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, pelvis
celiac disease, adult
celiac disease, childhood
central core disease
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebellitis
cerebellitis, autoimmune
cerebellum
cerebellum, disease of
cerebral cortex
cerebral folate deficiency syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
chairbound
children
chloride channel dysfunction
chorea
choreoathetosis
choroid plexus
Clinical Pathologic Conference(C.P.C.)
cognition
collapsin response mediator protein 5 IgG
confusion
contactin associated protein like 2 antibodies
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
deep gray nuclei
dementia
demyelinating disease
dermatitis herpetiformis
dermatomyositis
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
diplopia
disorientation
dizziness
down-beat nystagmus
DPPX
DPPX, antibodies, encephalitis
drowsiness
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysphagia
dystonia
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
Epstein-Barr virus
eye movement, disorders of
face, numbness of
falling
familial hemiplegic migraine
fasciculation
fever
fine motor function, impaired
Fisher's syndrome
folic acid
folic acid deficiency
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
genetic neurologic disorders
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
growth retardation
gynecomastia
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hemiparesis
hepatitis
heralding manifestation
HLA
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hot cross bun sign
hyperesthesia
hypogonadism
hypokalemic periodic paralysis
hypothyroidism
imbalance
immune-mediated pathogenesis
immunologic disease
immunology and the nervous system
immunomodulation
immunosuppressive agents
immunotherapy
incoordination
infection
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
irritability
kelch-like protein 11 antibodies
Kernig's sign
lateropulsion
leg spasms, painful
leucine rich glioma inactivated 1 antibodies
leukopenia
level of consciousness, decreased
limbic encephalitis
lip biopsy
listeriosis, CNS
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
malabsorption
malignancy screen
malignancy, occult
malignant hyperpyrexia
memory, impairment of
meningeal enhancement
meningismus
meningitis
mental status, abnormal
mesial temporal lobe
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
misdiagnosis
monoclonal antibodies
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, negative
MRI, serial
multiple sclerosis
muscle cramp
muscle spasm
myasthenia gravis, paraneoplastic
myasthenic syndrome
mycoplasma
mycoplasma pneumoniae
myelitis
myelopathy
myelopathy, chronic progressive
myoclonus
myopathy
myotonia congenita
nausea and vomiting
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular junction
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, paraneoplastic
neuropathy, sensory
NMDA antagonists
NMDA receptors
nystagmus
nystagmus, primary position of gaze
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular motility, disorders of
oculocephalic reflex
onconeural antibodies
ophelia syndrome
ophthalmoplegia
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
oral ulcerations
oscillopsia
osteoporosis
ovarian tumor
ovary, enlarged
palatal myoclonus
panic attacks
paramyotonia congenita
paraneoplastic brainstem encephalitis
paraneoplastic cerebellar degeneration
parietal lobe, lesion of
Parkinsonism syndrome
Parkinsonism, freezing phenomena in
parotid gland neoplasm
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
periodic paralysis
peripheral nerve, lesion of
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
POEMS syndrome
polyneuropathy
pons, lesion of
post infectious cerebellar ataxia
potassium channel antibodies
potassium channel dysfunction
practice guidelines
precipitating factors
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, bilateral
puberty
puberty, delayed
Purkinje cell
purkinje cell cytoplastic autoantibody
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
recurrent
Red flags
remote effect of cancer on the nervous system
respiratory tract infection
retinopathy
retropulsion
reversible neurologic disorder
review article
rheumatoid arthritis factor(R.A.factor)
rhomboencephalopathy
rigidity
rituximab
saccadic eye movements, abnormal
scannig speech
Schirmer test
screening
sedimentation rate, elevated
seizure
seizure, intractable
seminoma
serologic testing
serologic testing, false negative
seronegative
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
speech disorder
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
staphylococcal protein A column therapy
startle reaction
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
striatal encephalitis
superior cerebellar peduncle
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thymoma
thyroiditis
tinnitus
titubation
transglutaminase antibodies
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
tuberculosis
vertigo
viral infection
visual loss
vitiligo
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
Showing articles 250 to 300 of 2440 << Previous Next >>

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Vertigo and Gait Ataxia Without Usual Signs of Lateral Medullary Infarction: A Clinical Variant Related to Rostral-dorsolateral Lesions
Cerebrovasc Dis 10:471-474, Kim,J.S., 2000

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

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

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,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

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,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

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

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



Showing articles 250 to 300 of 2440 << Previous Next >>