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acetazolamide
aciduria
acute ataxia of childhood
acute cerebellar ataxia
advances in neurology
aggression
alcohol intolerance
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
Alzheimer's disease
AMPA receptor antibodies
amyotrophic lateral sclerosis
anemia
aneurysm
aneurysm, children
aneurysm, fusiform
aneurysm, vertebral basilar system
Angelman syndrome
angiography, cerebral
angiography, posterior fossa
angiotensin-converting enzyme
aniridia
ankle reflex, absent
anti GQ1b IgG antibody
anticonvulsants
anticonvulsants, effectiveness
anxiety
apraxia of eye movements
areflexia
Arnold Chiari malformation
arterial dissection
arterial dissection, intracranial
arterial dissection, ruptured
arterial dissection, vertebral
arthritis
aspiration
astrocytoma
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, congenital
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
attention span
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
bacterial infection
bacterial infection, CNS
ballismus, bilateral
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavior, combative
behavioral disorder
behavioral disorder, acute
blindness
blood dyscrasias, neurologic findings with
brachycephaly
brainstem, atrophy
brainstem, dysfunction
brainstem, glioma in children
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
CAG repeats
calcification, intracranial
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, pelvis
cataplexy
cataracts
cataracts, congenital
cauda equina, enhancement
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar pontine angle
cerebellar pontine angle tumor
cerebellar vermis
cerebellitis
cerebellitis, autoimmune
cerebellum, neoplasms of
cerebral cortical atrophy
cerebral edema
cerebral folate deficiency syndrome
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, prognosis in
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
cerebrovascular disease, surgical treatment of
chickenpox
children
choking
chorea
choreoathetosis
choroid plexus
chromosomal abnormality
chromosome 11
chromosome 15
chromosome 2
cisterna magna
Clinical Pathologic Conference(C.P.C.)
clonus
coenzyme Q10
coenzyme Q10 deficiency
cognition
cognitive delay
coma
confusion
conjunctival biopsy
consanguinity
corpus callosum, thinning
counterimmunoelectrophoresis
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanide poison
cyst
cyst, parenchymal
cyst, subcortical
deafness
deep gray nuclei
degenerative diseases of CNS
delayed dentition
dementia
dementia, childhood
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
dermatitis herpetiformis
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
Dravet syndrome
drooling
drug induced neurologic disorders in children
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysmorphic
dysphagia
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis, postinfectious
encephalomyopathy
encephalopathy
ependymoma
epicanthal folds
Epstein-Barr virus
evoked potentials
excitotoxin
exercise intolerance
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
falling
familial
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fish
Fisher's syndrome
fluorescene in situ hybridization
folic acid
folic acid deficiency
foot deformity
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gait disorder
gait, spastic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gillespie syndrome
glioblastoma multiforme(astrocytoma Gr.III)
glutamic acid
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
granulomatous disease
growth hormone
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, variant forms of
hammertoes
hand flapping
handwriting
Hartnup's disease
head injury
head tilt
headache
headache, severe
headache, sudden onset of
hearing loss
heel-knee-shin test
hemosiderosis of CNS, superficial
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
HLA
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
huntingtin
Huntington's chorea
hydroxyglutaric aciduria
hyperactivity
hyperosmolality
hyperreflexia
hypertension
hypertension, cerebrovascular disease with
hypodontia
hypoglycemia
hypogonadism
hypomyelination
hypopigmentation of skin
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
immunization, neurologic complications with
immunodeficiency
immunosuppression
immunotherapy
inborn errors of metabolism
inclusion bodies
incoordination
infection
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
intracranial pressure, increased
intrathecal medication
iris, abnormal
irritability
Jakob-Creutzfeldt disease
jaundice
lactic acidemia
laughing, pathologic
learning disability
learning disability, in children
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
limbic encephalitis
lipid storage disorder of CNS
lymphoma
lysosomal storage disease
macrocephaly
macrognathia
macular degeneration
malabsorption
marche a petits pas
Marinesco-Sjogren syndrome
masked facies
mediastinum, mass of
memory, impairment of
meningismus
meningitis
meningitis, carcinomatous
meningoencephalitis, mumps
meningovascular syphilis
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, children
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal foci on
MRI, negative
MRI, serial
multiple sclerosis
multiple system atrophy
mumps virus
muscle biopsy
muscle cramp
muscle pain
muscle weakness
mycoplasma
mycoplasma pneumoniae
myelinolysis, extrapontine
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopia
myotonia dystrophica
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-treatment of
nephrotic syndrome
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, acute
neurosyphilis
neurotoxin
neurotransmitter
Niemann-Pick disease
NMDA antagonists
nystagmus
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, rotary
ocular motility, disorders of
oculodentodigital dysplasia
ophelia syndrome
ophthalmoplegia
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
optical coherence tomography
oral ulcerations
oscillopsia
osmotic demyelination syndrome
osteoporosis
ovarian tumor
ovary, enlarged
panic attacks
papilledema
paraparesis
paraparesis, spastic
paresthesias
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
parotitis
paroxysmal hemiplegia
paroxysmal neurologic deficits
past pointing
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
personality change
piperazine
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
poison, mercury
POLR3B
polyneuropathy
pons, lesion of
pontine glioma
Poretti-Boltshauser syndrome
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
progeria
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
puberty
puberty, delayed
pulmonary infection
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Refsum's disease
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinitis pigmentosa
review article
rituximab
safety
sarcoidosis
sarcoidosis, CNS
SCN1A gene
screening
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, laughing as manifestation
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing, false negative
seronegative
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
smiling
sodium channel dysfunction
spastic ataxia
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle myoclonus
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
strabismus
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
subarachnoid hemorrhage
subarachnoid hemorrhage, recurrent
symmetric brain lesions
syndactyly
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
teeth, wide-spaced
telangiectases
teratoma
teratoma, ovarian
tick bite
tick paralysis
titubation
tongue, protrusion of
topiramate
torticollis
toxins, nervous system
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremulousness
trinucleotide repeats
upgaze, paralysis of
urinary incontinence
urinary retention
urticaria
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
visual loss, progressive
visual loss, slow
Von Hippel Lindau
walking, difficulty with
weakness
weight loss
wheelchair
white matter disease
wide based gait
Wolfram syndrome
workup
X-linked bulbospinal neuronopathy
Showing articles 200 to 250 of 4245 << Previous Next >>

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

A Case of Delayed Encephalopathy after Carbon Monoxide Poisoning Longitudinally Monitored by Diffusion Tensor Imaging
AJNR 33:e52-e54, Kuroda,H.,et al, 2012

Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
JNNP 83:638-645, Zuliani,L.,et al, 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Brain Abnormalities in Neuromyelitis Optica Spectrum Disorder
Multiple Sclerosis International ID 735486, Kim, W.,et al, 2012

Basal Ganglia Involvement in Wernicke Encephalopathy: Report of 2 Cases
AJNR 32:E129-E131, Zuccoli, G.,et al, 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010

Childhood Posterior Circulation Arterial Ischemic Stroke
Stroke 41:2201-2209, Mackay,M.T.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Herpes Simplex Type 1 Encephalitis Restricted to the Brainstem in a Pediatric Patient
Case Reports in Medicine doi:10.1155/2010/606584, Arita, J.H., et al, 2010

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
BMJ 338:653, Beau-Salinas,F.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Slurred Speech and Spirochaetes
Lancet 373:978, Thukral,A.,et al, 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
JNNP 79:672-677, Wagner,J.N.,et al, 2008

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
Brain 131:2553-2563, Saiz,A., et al, 2008

JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008

Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
Diabetes Metab 34:386-388, Bayreuther,C.,et al, 2008

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Superficial Siderosis
Arch Neurol 64:491-496, Kumar,J, 2007

Causative Factors and Epidemiology of Bilateral Vestibulopathy in 255 Patients
Ann Neurol 61:524-532, Zingler,V.C.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

Upside Down Reversal of Vision Due to an Isolated Acute Cerebellar Ischemic Infarction
J Neurol 253:953-954, Hern�ndez,A.H.,et al, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
Brain 129:3150-3164, Jellema, K., et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Cerebellar Infarction int he Territory of the Medial Branch of the Superior Cerebellar Artery
Neurol 66:115-117, Sohn,S.-I.,et al, 2006



Showing articles 200 to 250 of 4245 << Previous Next >>