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Differential
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acetazolamide
alcohol
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidopathies
aminoacidurias
antibodies to voltage-gated calcium channels
areflexia
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
calcium channel dysfunction
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
channelopathy
Charcot-Marie-Tooth
children
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
coma
coma, episodic
conjunctivitis
cryopyrin-associated periodic syndrome
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei, lesion of
developmental retardation
diagnostic criteria
differential diagnosis
diplopia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
dysarthria
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
familial
familial hemiplegic migraine
familial periodic ataxia
fever
fever, recurrent
fingerprint bodies
Friedreich's ataxia
frontal bossing
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of, bilateral
granular osmiphilic material
head circumference
headache
hearing loss
hypertrophic intracranial pachymeningitis
hypokalemic periodic paralysis
hypotonia
imbalance
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intellectual deficit
lactic acidemia
leukodystrophy
leukoencephalopathy
lysosomal storage disease
malignant hyperpyrexia
maple syrup urine disease
memory, impairment of
meningitis, aseptic
meningitis, carcinomatous
metabolic acidosis
metabolic disorder, primary
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
molecular genetics
motor neuron disease
movement disorder
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
muscle weakness
myasthenic syndrome
myoclonus
myoclonus, epilepsy
myokymia
myotonia
myotonia congenita
nausea and vomiting
negative
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic testing
neuromyotonia
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathy
neuropathy, hereditary peripheral
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
optic atrophy
optic atrophy, bilateral
oscillopsia
paralysis
paramyotonia congenita
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
periodic paralysis
peroxisomal disease
pleocytosis of cerebrospinal fluid
pons, lesion of
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
respiratory tract infection
review article
seizure
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skull bone, thickening
slurred speech
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
status epilepticus
storage disease of CNS
stress, emotional
strokelike episodes
stuttering
symmetric brain lesions
tinnitus
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
urea-cycle enzymopathies
vertigo
vertigo, episodic
vertigo, treatment of
vitamin E deficiency
walking, difficulty with
weakness
wheelchair
white matter disease
Showing articles 0 to 50 of 3240 Next >>

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

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

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

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

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

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

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

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

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

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

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

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

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

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

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

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021



Showing articles 0 to 50 of 3240 Next >>