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abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
agammaglobulinemia
alcoholism
aminoacidopathies
anterior tibial muscle weakness
anticonvulsants
anticonvulsants, selection of
antiviral agents
aphasia
areflexia
arrhythmia, cardiac
aspirin
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoimmune disease
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion, bilateral
basilar artery stenosis
Bassen-Kornzweig syndrome
black toenail sign
blindness
blindness, sudden
botulism
brain biopsy
brainstem, lesion of
bulbar palsy
cachexia
calcification, intracranial
carcinoma
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, gyral swelling
CAT scan, muscle
CAT scan, xenon-enhanced
cataracts
cataracts, congenital
cause of death
central core disease
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral blood flow
cerebral cortex
cerebral cortical atrophy
cerebral edema, cytotoxic
cerebral embolism
cerebral embolism, cardiac origin
cerebral glucose metabolism
cerebral infarction
cerebral ischemia
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
coma
congenital birth defects
congenital myopathy
consanguinity
cornea, abnormal
corpus callosum, lesion of
cortical blindness
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cultured skin fibroblasts
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
depression
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
diplopia
distal muscle weakness
dizziness
DNA probes
drug induced neurologic disorders
dwarfism
dyschromatopsia
dysphagia
dyspnea
dyspraxia
dystonia
Ekbom's Syndrome
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
emtricitabine
encephalomalacia
encephalomyopathy
encephalopathy
encephalopathy, progressive
enzyme, defect
epilepsia partialis continua
evoked potentials
exercise
exercise intolerance
extraocular muscle atrophy
extraocular muscle lesion
eye closure
eye movement, disorders of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
fatigue
fever
fibrillations
foot drop
foot ulcer, neuropathic
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
gonadal dysgenesis
growth retardation
gyrus, abnormal
Hallervorden Spatz disease
Hallgren's syndrome
headache
headache, sudden onset of
hearing loss
heart block
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
hirsutism
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hypocalcemia
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hypothyroidism
hypotonia
iatrogenic neurologic disorders
ileus, paralytic
imbalance
impulsivity
inclusion bodies
inclusion bodies, intranuclear
inclusion body myositis
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal pseudoobstruction
ischemic exercise test
Kearns-Sayre syndrome
keratoconus
lactate
lactic acidemia
Lafora's disease
laminar necrosis, cortical
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lid closure, weakness of
life expectancy
lipoma of skin
lipomatosis
lipomatosis, multiple symmetrical
lordosis
macular degeneration
malaise
malformation, CNS, congenital
MELAS syndrome
Melkersson's syndrome
memory, impairment of
meningeal enhancement
mental retardation
MERRF syndrome
mesial temporal lobe
microangiopathy, brain
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migratory lesion pattern
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
MRI
MRI lesion location
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, gyral enhancement
MRI, gyral swelling
MRI, linear enhancement
MRI, muscle
MRI, serial
MRI, T1 weighted high signal foci
MRS
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, drug-induced
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myopia
myotonia
myotonia dystrophica
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neoplasm, primary of CNS
nephrotic syndrome
neuritis
neuroendocrinology
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neurons
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, hereditary peripheral
neuropathy, peripheral
next-generation sequencing
night blindness
normal
nystagmus
obesity
occipital lobe, infarction
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic disc edema
optic nerve
optic nerve, compression of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
orbicularis oculi muscle
orbit, lesions of
pain
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
periodic paralysis
peroxisomal disease
personality change
pes cavus
pigmentary retinopathy
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
POLG1 gene
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyalgia rheumatica
polymyositis
polyneuropathy
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
prostigmine
proteinuria
proximal muscle atrophy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
ptosis
ptosis, bilateral
ragged-red fibers
rapidly progressing neurologic illness
recurrent
refractive errors
Refsum's disease
renal failure
research
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
Reye's syndrome
Reye's syndrome, adult
RFLPs
rhabdomyolysis
Romberg's sign
schizophrenia
screening
seizure
seizure, focal
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
seronegative
short stature
single photon emission computed tomography
sore throat
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar degeneration
spongy degeneration of brain
spontaneous remission
standing difficulty
Stephens syndrome
strokelike episodes
succinate dehydrogenase deficiency
symmetric brain lesions
systemic illness
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
transient neurologic deficit
transverse smile
treatment of neurologic disorder
trinucleotide repeats
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
Usher's syndrome
viral infection, CNS
visceral neuropathy
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
whistle, inability to
white matter disease
white matter disease, pattern
whole genome sequencing
wide based gait
winging of scapula
workup
Showing articles 350 to 400 of 1133 << Previous Next >>

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Isolated Dropped Head Due to Adult-Onset Nemaline Myopathy Treated by Posterior Fusion
Neurol 65:1504-1505, Katirji,B.,et al, 2005

Rhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Medicine 84:377-385, Melli,G.,et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Clinicopath Conf, Human Granulocytic Ehrlichiosis
NEJM 352:1358-1364, Case 10-2005, 2005

Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
AJNR 26:695-701,687, Tardieu,M.,et al, 2005

Axial Myopathy in Myasthenia: A Misleading Cause of Dropped Head
Muscle Nerve 29:329-330, Rodolico,C.,et al, 2004

The Dropped Head Sign: An Unusual Presenting Feature of Myasthenia Gravis
Neuromuscul Disord 14:378-379, Puruckherr,M.,et al, 2004

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

Intravenous Immunoglobulin in Autoimmune Neuromuscular Diseases
JAMA 291:2367-2375, Dalakas,M.C., 2004

Recurrent Meningitis of Unknown Aetiology
Lancet 363:1772, Ellerin,T.B.,et al, 2004

Fatal Myositis Due to the Microsporidian Brachiola algerae, a Mosquito Pathogen
NEJM 351:42-47, Coyle,C.M.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

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

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Neuromuscular Disorders in Severe Acute Respiratory Syndrome
Arch Neurol 61:1669-1673,1647, Tsai,L.-K.,et al, 2004

Incidence of Hospitalized Rhabdomyloysis in Patients Treated With Lipid-Lowering Drugs
JAMA 292:2585-2590, Graham,D.J.,et al, 2004

Primary Respiratory Failure in Inclusion Body Myositis
Neurol 63:2191-2192, Voermans,N.C.,et al, 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
Arch Neurol 61:106-113, Guis,S.,et al, 2004

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Asking the Right Question
Lancet 361:1786, Schattner,A.,et al, 2003

Neurologic Manifestations and Outcome of West Nile Virus Infection
JAMA 290:511-515,524,558, Sejvar,J.J.,et al, 2003

Polymyositis
Neurol 61:316-321, van der Meulen,M.F.G.,et al, 2003

Response to Sumatriptan in Headache of MELAS Syndrome
Neurol 61:577-578, Iizuka,T.,et al, 2003

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

Acute Effects and Recovery Time Following Concussion in Collegiate Football Players
JAMA 290:2556-2563,2604, McCrea,M.,et al, 2003

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Cumulative Effects Associated with Recurrent Concussion in Collegiate Football Players
JAMA 290:2549-2555,2604, Guskiewicz,K.M.,et al, 2003

Clinicopath Conf., Colchicine Myoneuropathy
NEJM 349:1656-1663, Case 33-2003, 2003

Proton MR Spectroscopy in the Diagnostic Evaluation of Suspected Mitochondrial Disease
AJNR 24:33-41, Lin,D.D.M.,et al, 2003

Clinicopath Conf., Penumococcal penumonia with Endocarditis and Endophtlhalmitis
NEJM 348:834-842, Case 7-2003, 2003

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003

Statin-Associated Myopathy
JAMA 289:1681-1690, Thompson,P.D.,et al, 2003

Alternate-Sided Homonymous Hemianopia as the Solitary Presentation of Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes Syndrome
Chang Gung Med J 26:199-203, Su,WY.,et al, 2003

Paresis Acquired in the Intensive Care Unit
JAMA 288:2859-2867, De Jonghe,B.,et al, 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Spontaneous "Second Wind" and Glucose-Induced Second "Second Wind" in McArdle Disease
Arch Neurol 59:1395-1402, Haller,R.G.&Vissing,J., 2002

AAC/AHA/NHLBI Clinical Advisory on the Use and Safety of Statins
Stroke 33:2337-2341, Pasternak,R.C.,et al, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

Mitochondrial Therapy for Parkinson Disease
Arch Neurol 59:1523, Rosenberg,R.N., 2002

A Tourist With Dengue Fever and Visual Loss
Lancet 360:1070, Haritoglou,C.,et al, 2002

Statin-Associated Myopathy With Normal Creatine Kinase Levels
Ann Int Med 137:581-585,617, Phillips,P.S.,et al, 2002

Is Coagulopathic Liver Disease a Factor in Spontaneous Cerebral Hemorrhage?
J Comput Assist Tomogr 26:69-72, Lee,H. &Hinrichs,C.R., 2002

Women With Pregnancy-related Polymyotis and High Serum CK Levels in the Newborn
Neurol 58:482-484, Messina,S.,et al, 2002



Showing articles 350 to 400 of 1133 << Previous Next >>