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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 100 to 150 of 2440 << Previous Next >>

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Autoimmune Pancerebellitis Associated with Pembrolizumab Therapy
Neurol 91:91-93, Vitt, J.R.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

Metronidazole-Associated Encephalopathy
NEJM 374:1465, Baden, L.R., 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

A 52-year-old Man with Diplopia and Ataxia
Neurol 87:e140-e143, Bradshaw, M.J.,et al, 2016

Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
AJNR 37:1256-1261, Capizzano, A.A.,et al, 2016

A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
Neurol 87:e110-e113, Paliwal, V.K.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016



Showing articles 100 to 150 of 2440 << Previous Next >>