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Differential
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aciduria
adolescent medicine
adverse drug reaction
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
anticholinergic drugs
aphonia
areflexia
ataxia
ataxia, cerebellar
ATP1A3 gene
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
Babinski sign
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
brain atrophy
camptocormia
carbamazepine
CAT scan, emission
CAT scan, emission, abnormal
central nervous system, infection of
cerebral palsy
children
chorea
chromosomal abnormality
chromosome 14
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
contractures, joint
delay in diagnosis
depression
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dysarthria
dyskinesia
dysphagia
dystonia
dystonia musculorum deformens
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
DYT1 mutation
encephalitis, autoimmune
encephalitis, brainstem
encephalopathy
encephalopathy, progressive
enzyme, defect
equinovarus
eye movement, disorders of
falling
familial
foot deformity
gait disorder
galactorrhea
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
GLUT1 deficiency syndrome
hand weakness
hands, fisted
head nodding
hearing loss
hemidystonia
hepatolenticular degeneration(Wilson's disease)
hyperreflexia
hypertonia
hyporeflexia
hypotonia
imbalance
imbalance, postural
inborn errors of metabolism
inclusion bodies, intranuclear
intellectual deficit
L-dopa
leg spasms
leg spasms, painful
masked facies
meningitis, carcinomatous
microcephaly
mimics
misdiagnosis
molecular genetics
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, treatment of
MRI
MRI, negative
neurochemistry
neurologic disease, diagnoses of
neurologic signs
neuronal intranuclear inclusion disease
neuropathology
neurotomy
next-generation sequencing
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
optic atrophy
pain
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
postural abnormality
precipitating factors
PRKN gene
prognosis
progressive neurologic disorder
prolactin, elevated
psychiatric problems in neurologic disorders
pull test
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
reversible neurologic disorder
review article
rigidity
scoliosis
seizure
sensorineural hearing loss
sensory tricks
short stature
sinemet
speech disorder
speech disorder, childhood
status epilepticus
stimulation, deep brain
striatal encephalitis
substantia nigra
swallow evaluation
tardive dystonia
tetrahydrobiopterin
toe walking
tonic foot response
torticollis
treatment of neurologic disorder
tremor
tremor, postural
tripping
tyrosine hydroxylase deficiency
walking
walking frame
walking, difficulty with
wheelchair
wide based gait
workup
Showing articles 0 to 22 of 22

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Familial Dopa-Responsive Cervical Dystonia
Neurol 66:599-601, Schneider,S.A.,et al, 2006

Dopa-responsive Dystonic Camptocormia
Neurol 66:1779, Van Gerpen,J.A., 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

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

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
Ann Neurol 35:396-402, 3811994., Rajput,A.H.,et al, 1994

Comparison of Striatal 18F-dopa Uptake in Adult-Onset Dystonia-Parkinsonism, Parkinson's & Dopa-Responsive Dystonia
Neurol 43:1563-1568, Turjanski,N.,et al, 1993

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Dopa-responsive Dystonia:[18F]Dopa Positron Emission Tomography
Ann Neurol 30:24-30, Sawle,G.V.,et al, 1991

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

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986



Showing articles 0 to 22 of 22