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acid maltase deficiency
acoustic neurinoma
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
adult polyglucosan body disease
advance directives
advances in neurology
adverse drug reaction
alcoholic polyneuropathy
algorithm
alpha-fetoprotein
alveolar hypoventilation
Alzheimer's disease
aminoacidurias
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, cluster
amyotrophic lateral sclerosis, complications with
amyotrophic lateral sclerosis, conjugal
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, hospitalization
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, myasthenic syndrome with
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, sensory symptoms in
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
analgesic
anatomy of
aneurysm, cavernous sinus
aneurysm, internal carotid artery
animal exposure
ankylosing spondylitis
anterior horn cell disease
anterior interosseous neuropathy
anterior tibial muscle weakness
anti Hu antibody
antibodies to voltage-gated calcium channels
antiviral agents
anxiety
aphonia
apnea
apraxia of eye movements
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
atlanto axial dislocation, congenital
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavioral disorder
Bence Jones protein
benign congenital hypotonia
benzodiazepine
biologic markers
BiPAP
bladder dysfunction
bone marrow biopsy
botulinum toxin
botulinum toxin, complications of
brachial neuritis
brain atrophy
brainstem, infarction of
brainstem, lesion of
bright tongue sign
Brown Sequard syndrome
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
C0ORF72
cachexia
CAG repeats
calcium channel dysfunction
calf hypertrophy
camptocormia
carbon monoxide poisoning
carcinoembryonic antigen
carcinoma
carcinoma of breast
cardiomyopathy
caregiver
case studies
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cavernous sinus, syndrome
CD4 counts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral death
cerebral embolism
cerebral peduncle
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, young adult
cervical collar
cervical osteoarthritis
cervical osteophyte
cervical spine
cervical spine injury
cervical spine injury, treatment of
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Charcot-Marie-Tooth
chest x-ray, abnormal
chewing, impaired
children
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonus
cluster, geographic
cognition
cold temperature
coma
complications
compression neuropathy
concussion
conduction block
congenital heart disease
congenital myopathy
congestive heart failure
constipation
controversies in neurology
cost
cost effectiveness
cough
coxsackievirus
coxsackievirus, myopathy with
CPAP
creatine phosphokinase(CPK)elevated
crying, pathologic
cycad seed flour
cyclosporine
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
denervation of muscle
denervation potentials
dentatorubral-pallidoluysian atrophy
depression
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic mononeuropathy
diagnostic criteria
diaphragmatic paralysis
diaphragmatic paralysis, causes of
diet
differential diagnosis
difficulty climbing stairs
diplegia, atonic
disability rating scale, neurological
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dopamine
drooling
dropped head syndrome
drowning
drug interactions
dying
dysarthria
dysphagia
dysphonia
dyspnea
dystonia
dystrophin
efficacy
electrical injury of nervous system
electrical sensation
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
electrophoretic pattern, serum
emotional lability
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
encephalopathy, post anoxic
endocarditis, subacute bacterial
enterovirus
enterovirus infection of CNS
entrapment neuropathy
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
euthanasia
evidence-based research
evoked potentials
excitotoxin
exercise
extremity, cold
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
fatigable chewing
fatigue
Fazio-Londe's disease
fibrillations
finger weakness
flail arm syndrome
floppy infant
foot drop
football neurologic injuries
fragile-X syndrome
free radical
Friedreich's ataxia
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gangliosides
gastrostomy
gastrostomy, percutaneous endoscopic
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glutamic acid
GM1 ganglioside antibodies
growth retardation
guanidine
Guillain Barre syndrome
Gulf War syndrome
Guyon's canal
gynecomastia
hallucination
hand weakness
handlebar palsy
hanging
head injury
headache
health insurance
hearing loss
heart block
heavy metal intoxication
hemangioma
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
herniated disc
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
herpes zoster
highly active antiretroviral therapy
history of neurology
HLA
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hospice
human immunodeficiency virus type 1
hunger
huntingtin
Huntington's chorea
hypercalcemia
hypercapnia
hyperparathyroidism
hyperreflexia
hypertension
hypoglycemia
hypoglycemic coma
hypopnea
hyporeflexia
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immune complexes
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, ubiquitin
inclusion body myositis
infant, evaluation of
infantile tremor syndrome
insomnia
intellectual deficit
intermittent positive pressure breathing
internal capsule
internet
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
iron, brain
Isaacs syndrome
Jackson's syndrome
Jakob-Creutzfeldt disease
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Jewish
juvenile distal and segmental muscular atrophy
Kearns-Sayre syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
laminectomy, cervical
laughing, pathologic
lead and the nervous system
Leber's hereditary optic neuropathy
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
Leigh's disease
leukemia
leukoencephalopathy
level of consciousness, decreased
Lewy body disease, diffuse
Lhermitte's sign
lid closure, weakness of
life expectancy
life support, withdrawal of
life support, withholding of
life sustaining treatment
liver disease
lobar atrophy
locked-in syndrome
lordosis
lumbar puncture
Lyme disease
lymphadenopathy
lymphoma
lymphoma involving CNS
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
masseter muscle weakness
median neuropathy
medical-legal aspects of neurology
MELAS syndrome
meningitis
mental retardation
MERRF syndrome
Millard Gubler syndrome
Mills syndrome
mimics
minimally conscious state
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mobility
mobility aids
molecular genetics
monoclonal antibodies
monoclonal gammopathy
monomelic amyotrophy
mononeuropathy
mononeuropathy, motor
morphine
mortality
Motor Band Sign
motor neuron disease
motor neuron disease, juvenile form
motor neuron disease, spontaneous recovery
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, muscle
MRI, paramagnetic effect
MRI, spinal cord
MRI, spine
MRI, susceptibility weighted
MRS
multiple myeloma
multiple sclerosis
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle relaxant
muscle stiffness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myasthenic syndrome
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myelopathy, ischemic
myocardial infarction
myocardial injury
myoclonus
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, quadriceps
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
N-acetyl-L-aspartic acid
narcotic analgesics
nasal speech
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve growth factor
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurogenic bladder
neurogenic vs.myopathic atrophy
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic disease, incurable
neurologic evaluation
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction
neuromuscular junction, abnormality of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal migration disorder
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, bicycle
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuroprotective agents
neurotoxic
neurotoxin
neurotransmitter
neutropenia
newborn, evaluation of
NMDA antagonists
NMDA receptors
nusinersen
nystagmus
nystagmus, primary position of gaze
nystagmus, rotary
occupational neurologic disorders
ocular motility, disorders of
old age, neurology of
olivary degeneration, hypertrophic
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, progressive external
opiate
Oppenheim muscular dystrophy
optic neuropathy
orthopnea
osteomalacia
owl's eye sign of spinal cord
oxygen therapy
pain
pain, elbow
pain, foot
pain, management of chronic
palatal myoclonus
palliative care
pancytopenia
paranoia
paraoxonase
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraproteinemia
paraspinal muscle
parathyroid adenoma
paresthesias
Parkinson disease
Parkinson disease, motor neuron disease with
Parkinson disease, treatment of
Parkinsonism syndrome
Parkinsonism-dementia complex
pathology
patient information and support
penicillamine
periodic paralysis
periodic paralysis, thyrotoxic
persistent vegetative state
personality change
phrenic nerve
phrenic nerve pacemaker
physical activity
physical therapy
physician assisted suicide
Pick's disease
pigmentary retinopathy
placebo
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, mercury
poison, neurologic problems with
poliomyelitis
polyclonal gammopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
positive sharp waves
post polio syndrome
posterior fossa, differential diagnosis of lesions of
posterior inferior cerebellar artery syndrome
posterior interosseous neuropathy
practice guidelines
preclinical
pregnancy, neurologic complications in
pressure sores
prevention of neurologic disorders
primary lateral sclerosis
progeria
prognosis
progranulin
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pulmonary embolism
pulmonary function tests
pyramidal tract
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriplegia
quality of life
radiation hypersensitivity
radiation therapy, salivary gland
radiculopathy
ragged-red fibers
release phenomena
remote effect of cancer on the nervous system
renal stones
repetitive nerve stimulation
respirator
respiratory depression
respiratory failure
retinopathy
retrovirus
reverse split hand sign
review article
RFLPs
right to die
riluzole
risk factors
risk-benefit assessment
safety
salivation, excessive
sarcoidosis
scoliosis
scoliosis, neurologic association with
scooters
screening
sedation
seizure
seizure, children
seizure, treatment of
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory symptoms
sensory testing
serologic testing
serum alanine aminotransferase
short stature
shoulder, subluxation
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep
sleep apnea
sleep pathology and physiology
smell
Smell Identification Test
SMN1 gene
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
somnolence
spasticity
speech disorder
spina bifida
spinal cord
spinal cord degeneration
spinal cord, cervical
spinal cord, compression of
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary
spinal cord, neoplasm, intramedullary
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
spirometry
spondylosis
sports medicine, neurology of
standing difficulty
stem cell tourism
stem cell transplantation
sternocleidomastoid muscle
stiff legs
stiff man syndrome
strangulation
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subdural hematoma
sudden death
suicide
superoxide dismutase
survival motor neuron gene
symptomatic
syringomyelia
tabes dorsalis
tandem gait, ataxic
tau protein
telangiectases
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
temporalis muscle wasting
tensilon test
tensilon test, false positive
term infant
testicular atrophy
thoracic outlet syndromes
thrombophlebitis
thyrotropin-releasing hormone
Tolosa Hunt syndrome
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
tracheostomy
trauma
treatment of neurologic disorder
tremor
tremor, postural
triangle of Guillain and Mollaret
tricresylphosphate
trinucleotide repeats
tripping
tuberous sclerosis
ubiquitin
ulnar nerve
ulnar nerve, deep palmar branch of
ulnar neuropathy
unconsciousness
upgaze, paralysis of
urinary incontinence
valium
vasculopathy
venous thrombosis, non-cerebral
viral infection
viral infection, CNS
vitamin E
vitamin E deficiency
Waldenstrom's macroglobulinemia
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
web sites
Weber's syndrome
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 7323 << Previous Next >>

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

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

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,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 Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

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

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

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

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Rapid Multifocal Neurologic Decline in an Immunocompromised Patient
JAMA Neurol 73:226-231, Kromm, J.A.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

A Case of Hirayama Disease Presenting with Polymyoclonus
Neurol 85:e156, Ong, J.J.Y.,et al, 2015

Transient Cervical Cord Swelling in Monomelic Amyotrophy
Neurol 83:e77-e79, DeGregoris, L.M. & Engel, M., 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
Adams & Victors Principles of Neurology, Chp 30, pg 624, Ropper, A.H.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

MR Imaging Findings in Hepatic Encephalopathy
AJNR 29:1612-1621, Rovira,A.,et al, 2008

Orthopedic Outcomes of Long-Term Daily Corticosteroid Treatment in Duchenne Muscular Dystrophy
Neurol 68:1607-1613, King,W.M.,et al, 2007



Showing articles 300 to 350 of 7323 << Previous Next >>