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Differential
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abdominal distention
abducens nerve paralysis
abiotrophy
acoustic nerve
agammaglobulinemia
alcohol intolerance
alkylating agents
alopecia
altered states of consciousness
alveolar hypoventilation
anesthesia, general
antimetabolite
aphasia
areflexia
arrhythmia, cardiac
arthralgia
asparginase
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atonic bladder
autonomic dysfunction
baldness
basal ganglia, calcification of
blood dyscrasias, neurologic findings with
brainstem, dysfunction
cachexia
calcification, intracranial
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosome 19
chronic progressive external ophthalmoplegia
cleft palate
Clinical Pathologic Conference(C.P.C.)
coma
congenital heart disease
congenital malformation
congenital myasthenic syndromes
congenital myopathy
consanguinity
cough
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
dementia
developmental retardation
diabetes mellitus
diarrhea
diplopia
distal muscle weakness
Duane syndrome
dysphagia
dyspnea
dyspraxia
dystonia
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, progressive
exercise intolerance
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fatigue
fever
fluorescein angiography
fluorouracil
flush syndrome
foot drop
gait disorder
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
granulomatosis with polyangiitis
granulomatous disease
hallucination
headache
hearing loss
heart block
hemianopia
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
high arched palate
Hirschprung's disease
Holt-Oram syndrome
hypercapnia
hypogonadism
hyponatremia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
intestinal pseudoobstruction
iris, abnormal
isoniazid
jaw pain
Kearns-Sayre syndrome
klippel feil syndrome
Korsakoff's psychosis
lactic acidemia
Leber's hereditary optic neuropathy
Leigh's disease
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
lymphoma involving CNS
lymphomatoid granulomatosis
MELAS syndrome
meningismus
meningoencephalopathy
mental retardation
MERRF syndrome
methotrexate
methylhydrazine derivatives
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
movement disorder
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, familial incidence of
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myelopathy
myoclonus
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular blockade
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
neuropathy, peripheral
neurotoxin
nitrogen mustard
normal
nystagmus
nystagmus, dissociated
nystagmus, vertical
ocular motility, disorders of
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuropathy
orthostatic hypotension
pain
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
paresthesias
Parkinsonism syndrome
percussion induced muscle contraction
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polyneuropathy
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
prostigmine
pseudomyasthenia
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
ptosis, classification of
ptosis, familial
ptosis, unilateral
pulmonary infiltrates
ragged-red fibers
rash
retina, abnormal
retinal degeneration
retinal lesion
retinopathy
review article
seizure
sensorineural hearing loss
seronegative
short stature
skin, lesions in neurologic disorders
slit lamp examination
spasticity
spina bifida
splenomegaly
steroid therapy, CNS treatment and complications with
strokelike episodes
syringomyelia
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
testicular atrophy
thrombocytopenia
tinnitus
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
vertigo
vinblastine
vincristine neurotoxicity
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
white matter disease
wide based gait
Wildervanck's syndrome
wrist drop
Showing articles 650 to 700 of 2020 << Previous Next >>

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Topiramate and Essential Tremor
Ann Neurol 47:837-838, Galvez-Jimenez,N. &Hargreave,M., 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
Radiology 214:209-216, Brunereau,L.,et al, 2000

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

Pulmonary Arteriovenous Malformations
Neurol 55:959-964, Moussouttas,M.,et al, 2000

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
Neurol 55:1661-1667, Iglesias,S.,et al, 2000

Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000

MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

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

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

Headache: Cortical Vein Thrombosis and Response to Anticoagulation
J Emerg Med 17:449-453, Minadeo,J.P &Karaman,B.A., 1999

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,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

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Multicentre European Study of Thalamic Stimulation in Paarkinsonisn and Essential Tremor
JNNP 66:289-296, Limousin,P.,et al, 1999

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Treatment of Attention-Deficit-Hyperactivity Disorder
NEJM 340:780-788, Elia,J.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

What Level of Care for the Neurofibromatoses?
Lancet 353:1114-1116, Huson,S.M., 1999

Familial Subarachnoid Hemorrhage, Outcome Study
Stroke 30:1099-1102, Ronkainen,A.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

A Randomized Placebo-Controlled Comparative Trial of Gabapentin and Propranolol in Essential Tremor
Arch Neurol 56:475-480, Gironell,A.,et al, 1999

MR Imaging of Dejerine-Sottas Disease
AJNR 20:378-380, Make,D.D.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Stereotactic Radiosurgical Pallidotomy and Thalamotomy with the Gamma Knife:MR Imaging Findings with Clinical Correlation-Preliminary Experience
Radiology 212:143-150, Friedman,D.P.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Ptosis, Blepharospasm, and Apraxia of Eyelid Opening Secondary to Putaminal Hemorrhage
Neurol 53:652, Verghese,J.,et al, 1999

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
Neurol 53:982-988, Raaymakers,T.W.M.&the MARS Study Group, 1999



Showing articles 650 to 700 of 2020 << Previous Next >>