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acanthocytosis
acetazolamide
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
Adies pupil
advances in neurology
adverse drug reaction
aggression
agitation
akathisia
alcohol
alcohol, neurologic complications with
algorithm
alien hand syndrome
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
amimia
aminoacidopathies
aminoacidurias
AMPA receptor antibodies
amphiphysin antibodies
amyotrophic chorea-acanthocytosis
anemia
anti basal ganglia antibodies
anti GQ1b IgG antibody
anti IgLON5
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, untoward effects of
antihistamines
anxiety
apraxia
apraxia of eye movements
apraxia, constructional
arthralgia
asterixis
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
athetosis
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune encephalopathy
autoimmune epilepsy
autonomic dysfunction
autonomic neuropathy
B 12 deficiency
Babinski sign
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery migraine
behavioral disorder
behavioral disorder, acute
benign essential tremor
beta adrenergic blocker
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
bladder dysfunction
blepharospasm
blinking, reduced
body odor
bone marrow biopsy
botulinum toxin
bradycardia
bradykinesia
brain biopsy
brainstem, atrophy
brainstem, lesion of
bruxism
burning skin
calcium antagonist
carbamazepine
carbamazepine, toxicity
carbon monoxide poisoning
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
catatonia
catecholamine
caudate nucleus, atrophy
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral ischemia
cerebral palsy
cerebral palsy, adults
cerebral palsy, associated problems with
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count, normal
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, young adult
ceruloplasmin, serum
channelopathy
children
chorea
chorea, familial
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 1
chromosome 7
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
cold intolerance
collapsin response mediator protein 5 IgG
coma
coma, causes of
coma, episodic
coma, unknown etiology
complications
computers, neurologic diagnosis and
confusion
conjugate gaze, forced
consanguinity
contactin associated protein like 2 antibodies
conversion reaction
copper metabolism, abnormal
cortical-basal ganglionic degeneration
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
diet
differential diagnosis
dilantin
dilantin, toxicity
diphenhydramine
diplopia
disability, neurological
dopamine
dopamine antagonist
down-beat nystagmus
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, drug induced
dyskinesia, facial
dysphagia
dyspnea
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, delayed onset
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, infancy
dystonia, painful
dystonia, paroxysmal
dystonia, psychogenic
dystonia, treatment of
dystonic reaction, acute
DYT1 mutation
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
ELISA
emergencies, neurologic
emotional lability
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, clinical picture and treatment of
encephalitis, etiology
encephalitis, focal
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, neonatal
encephalopathy, post anoxic
enuresis
enzyme, defect
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
epsilon sarcoglycan gene
exercise
exercise intolerance
exome sequencing
extralimbic encephalitis
eye color
eye movement, disorders of
face, contractions
facial nerve palsy
faciobrachial dystonic seizure
falling
familial
fatigue
felbamate
fever
fluctuate
flunarizine
gait disorder
gamma amino butyric acid
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze deviation
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of
GLUT1
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
glycine receptor antibodies
grimacing
Hallervorden Spatz disease
handedness
hands, fisted
head injury
head nodding
headache
hearing loss
heart block
hemiballismus
hemichorea
hemimyoclonic jerks
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
herpes simplex encephalitis
hippocampus
Hodgkin's disease
homovanillic acid
human immunodeficiency virus type 1
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperekplexia
hyperreflexia
hypertension
hypoglycorrhachia
hyponatremia
hyporeflexia
hyposmia
hypotension, systemic
hypotonia
hypotonia, infants
hypoxia, newborn
hypoxic encephalopathy
imbalance
immunologic disease
immunosuppression
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
incidence
incoordination
infantile hemiplegia
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
iron, brain
islet cell tumor
Jakob-Creutzfeldt disease
karyotyping
Kayser-Fleischer ring
Kearns-Sayre syndrome
ketogenic diet
lactic acidemia
lateropulsion
L-dopa
Leber's hereditary optic neuropathy
left handedness
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukodystrophy
level of consciousness, decreased
levitation
Lewy body disease, diffuse
limbic encephalitis
lipid storage disorder of CNS
liver disease
lobar atrophy
lumbar puncture
lysosomal storage disease
masked facies
mediastinum, mass of
medical-legal aspects of neurology
MELAS syndrome
memory
memory, defect of recent
memory, impairment of
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic disorder, primary
metabolic disorder, primary-screening tests
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoamines
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, paroxysmal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abdomen
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRS
multiple sclerosis
multiple sclerosis, paroxysmal symptoms in
muscle pain
muscle weakness
musicians
musician's dystonia
mutism
mycotoxin
myelitis, transverse, recurrent
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, segmental
myokymia
myopathy
myopathy, mitochondrial
myorhythmia
mysoline
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurexin-3 alpha antibodies
neuroleptic
neuroleptic malignant syndrome
neurologic complications
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, multifocal
neurologic signs
neurologic symptoms
neurologic testing
neuromyotonia
neuronal cell surface antigen
neuropathology
neuropathology, brain
neuropathy
neurotoxin
neurotransmitter
Niemann-Pick disease
nitroproprionic acid
NMDA antagonists
norepinephrine
nystagmus
nystagmus, periodic
nystagmus, vertical
occupational neurologic disorders
ocular motility, disorders of
oculogyric crisis
ophelia syndrome
ophthalmoplegia
opisthotonus
optic atrophy
optic neuropathy
optokinetic nystagmus, abnormal
pain
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, psychogenic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal exertion-induced dyskinesia
paroxysmal hypnogenic dyskinesia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
paroxysmal neurologic disorder
paroxysmal nonkinesigenic dyskinesia
pathognomonic
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
peroxisomal disease
personality change
phencyclidine poisoning
phenylketonuria
pigmentary retinopathy
pitfalls
PLEDs
pleocytosis of cerebrospinal fluid
polymyositis
pons, lesion of
potassium channel antibodies
practice guidelines
precipitating factors
primary episodic ataxia
prognosis
progressive neurologic disorder
propranolol
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
psychotic behavior
ptosis
pulmonary edema
pupil, abnormality in neurologic disorders
pupil, tonic
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
ragged-red fibers
rectal biopsy
recurrent
release phenomena
remote effect of cancer on the nervous system
respirator
respiratory failure
respiratory tract infection
retinitis pigmentosa
retinopathy
Rett's syndrome
reversible neurologic disorder
review article
rhabdomyolysis
rigidity
Riley-Day syndrome
rituximab
safety
salivation, excessive
Saudi Arabia
schizophrenia
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, adult onset
seizure, children
seizure, differential diagnosis of
seizure, dystonic
seizure, focal
seizure, neonatal
seizure, psychomotor-temporal lobe
seizure, stimulus sensitive
seizure, unknown origin
self harm
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
sensory loss
sensory loss, cortical
serologic testing
serologic testing, false negative
seronegative
sexual behavior, disorder of
short stature
sicca syndrome
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
somnolence
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
spinocerebellar ataxia type 16
splenomegaly
startle reaction
status dystonicus
status epilepticus, intractable
stereotaxic surgery
stereotypy
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
stimulation, deep brain, bilateral
strabismus
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
subarachnoid hemorrhage
substantia nigra
sugarcane, mildewed
symmetric brain lesions
tardive dyskinesia
tardive dystonia
tauopathy
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
tetrahydrobiopterin
thalamic tumors
thalamotomy
thalamus, lesion of
thymoma
tic
tonic foot response
tonic spasms
torticollis
toxic encephalopathy
toxins, nervous system
toxoplasmosis, CNS
transient neurologic deficit
transient paroxysmal dystonia in infancy
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, postural
tremor, psychogenic
tremor, treatment of
trigeminal neuralgia
trinucleotide repeats
twitching, face
undiagnosed
urea-cycle enzymopathies
urine test for metabolic disorders
urine test in toxic screen
vasospasm, cerebral
vigabatrin
viral infection
viral infection, CNS
visual evoked response
visual impairment
visuospatial disturbance
walking, difficulty with
weight loss
wheelchair
Whipple's disease
white matter disease
white matter disease, subcortical
wide based gait
Wolfram syndrome
workup
xerophthalmia
xerostomia
Showing articles 0 to 50 of 4126 Next >>

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

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

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Anti-LGI1 Encephalitis
Neurol 87:1449-1456,1428, Van Sonderen, A.,et al, 2016

Faciobrachial Dystonic Seizures
Neurol 86:e60-e61, Schmerler, D.A.,et al, 2016

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Limbic Encephalitis Associated with Anti-Voltage-Gated Potassium Channel Complex Antibodies Mimicking Creutzfeldt-Jakob Disease
JAMA Neurol 71:79-82, Yoo,J.Y. & Hirsch, L.J., 2014

Pathognomonic Seizures in Limbic Encephalitis Associated with Anti-LGl1 antibodies
Lancet 383:2018, Sen, A.,et al, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
Ann Neurol 74:648-654,627, Horisawa, S.,et al, 2013

Basal Ganglia Involvement in Facio-Brachial Dystonic Seizures Associated with LGI1 Antibodies
Neurol 80:e183-184, Plantone, D.,et al, 2013

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Autoimmune encephalitis
BMJ 342:d1918, Irani, S.R.,et all, 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Vigabatrin Improves Paroxysmal Dystonia in Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 68:1320-1321, Leuzzi,V.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

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

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999



Showing articles 0 to 50 of 4126 Next >>