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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 200 to 250 of 2440 << Previous Next >>

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

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

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

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

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

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

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

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

Anti-Ma and Anti-Ta Associated Paraneoplastic Neurological Syndromes: 22 Newly Diagnosed Patients and Review of Previous Cases
JNNP 79:767-773,742, Hoffmann,L.A.,et al, 2008

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

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

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

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

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

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

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

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

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 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

Spontaneous Spinal Cerebrospinal Fluid Leaks and Intracranial Hypotension
JAMA 295:2286-2296, Schievink,W.I., 2006

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
Neurol 64:1461-1464, Wolf,N.I.,et al, 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Cerebellar Ataxia and Central Nervous System Whipple Disease
Arch Neurol 62:618-620, Matthews,B.R.,et al, 2005

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
Arch Neurol 61:953-956, Umashankar,G.,et al, 2004

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Symmetric Deep Cerebellar Lesions After Smoking Heroin
Arch Neurol 60:1605-1606, Ropper,A.H. &Blair,R., 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002



Showing articles 200 to 250 of 2440 << Previous Next >>