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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 400 to 450 of 2020 << Previous Next >>

A Matter of Taste
JNNP 80:139-140, Theys,T.,et al, 2009

Genetic Aspects of Alzheimer Disease
The Neurologist 15:80-86, Williamson,J.,et al, 2009

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Genomewide Association Studies of Stroke
NEJM 360:1718-1728, Ikram,M.A.,et al, 2009

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,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

Neurofibromatosis
JAMA 300:352, Torpy,J.M.,et al., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Update on Blepharospasm: Report from the BEBRF International Workshop
Neurol 71:1275-1282, Hallett,M.,et al, 2008

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Familiality in Brain Tumors
Neurol 71:1015-1020, Blumenthal,D.T.&Cannon-Albright,L.A., 2008

Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
Neurol 71:1035-1037, V�lker,W.,et al, 2008

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Decoding Cryptogenic Cardioembolism
Ann Neurol 64:364-365, Meschia,J.F., 2008

Psychogenic Tremor Occurring After Deep Brain Stimulation Surgery for Essential Tremor
Neurol 70:1498-1499, McKeon,A.,et al, 2008

Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008

Complete Ophthalmoplegia: An Unusual Sign of Bilateral Paramedian Midbrain-Thalamic Infarction
Stroke 39:1355-1357, Thurtell,M.J. &Halmagyi,M., 2008

Tuberous Sclerosis Complex: A Tale of Two Genes
Neurol 70:904-905, Nass,R. &Crino,P.B., 2008

Nearly Completely Reversible Brain Abnormalities in a Patient With Incontinentia Pigmenti
AJNR 29:431-433, Lou,H.,et al, 2008

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

Klein-Levin Syndrome: A Systematic Study of 108 Patients
Ann Neurol 63:482-492, Arnulf,I.,et al, 2008

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

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

a-Synuclein Gene Duplication Is Present in Sporadic Parkinson Disease
Neurol 70:43-49,7, Ahn,T.-B.,et al, 2008

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

Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3
Neurol 70:2357-2363, Mineharu,Y.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Biochemical Markers in Persons With Preclinical Familial Alzheimer Disease
Neurol 71:85-92,78, Ringman,J.M.,et al., 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007

Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007

A Genetic Risk Factor for Periodic Limb Movements in Sleep
NEJM 357:639-647, Stefansson,H.,et al, 2007

Parental Transmission of MS in a Population-Based Canadian Cohort
Neurol 69:1208-1212,1202, Herrera,B.M.,et al, 2007

Deep Brain Stimulation
Neurologist 13:237-252, Kem,DS. &Kumar,R., 2007

Angelman Syndrome Revisited
Neurologist 13:305-312, Paprocka,J.,et al, 2007

Mysterious Falls and a Nasal Voice
Lancet 370:712, Bhandari,A. &Adenwalla,F., 2007

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

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007

Clinicopath Conf,Lyme Disease of the Nervous System
NEJM 356:1561-1570, Case Record 11-2007, 2007

Clinical Update:Diagnosis and Treatment of Essential Tremor
Lancet 369:1152-1154, Benito-Leon,J&Louis,E.D., 2007

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Phenylketonuria
eMedicine (December), Arnold,G.L., 2007

Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder
Neurol 69:2093-2104, Klein,C. &Schlossmacher,M.G., 2007



Showing articles 400 to 450 of 2020 << Previous Next >>