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acrochordon
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
alcoholism
anemia
anemia, megaloblastic
ankle, swelling of
anorexia
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
B 12 deficiency
bladder dysfunction
blindness
bone marrow transplantation
brain natriuretic peptide
burning hands
burning paresthesia
calf hypertrophy
cardiomyopathy
cardiovascular disease
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellum, disease of
cerebrovascular accident
cervical spondylosis
children
cirrhosis
Clinical Pathologic Conference(C.P.C.)
complications
contractures, joint
cortical blindness
cough
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
dantrolene sodium
deafness
decerebrate posture
delay in diagnosis
dementia, childhood
demyelinating disease
depression
dermal sinus tract
dermoid
developmental retardation
dexterity, impaired
diagnostic criteria
diamond on quadriceps
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dysraphism, spinal
dystrophin
electroencephalogram, abnormalities of
electromyogram
epidemiology of neurology
exercise
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fine motor function, impaired
foot numbness
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glucose tolerance test, abnormal
Gowers maneuver
hand weakness
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
HMGcoA reductase inhibitors
hung reflex
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertrichosis
hypogonadism
hypopigmentation of skin
hypothyroidism
iatrogenic neurologic disorders
intellectual deterioration
jaundice
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leukodystrophy
level of consciousness, decreased
limb-girdle weakness
lipoma of CNS
lipoma of skin
liver function enzymes
Lorenzo's oil
metabolic disorder, primary
methylmalonic acid, serum
misdiagnosis
mood change
mortality
movement disorder
MRI
MRI, abnormal
MRI, spine
multiple system atrophy
muscle biopsy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, necrotizing, autoimmune
myxedema, neurologic manifestations of
neurocutaneous disease
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathy
neuropathy, sensory
nutritional deficiency
nystagmus
ochronosis
osteoarthrosis
osteoporosis
pain, abdominal
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
personality change
phlebotomy
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pruritus
pseudobulbar palsy
ptosis
quadriparesis
renal failure
renal stones
respiratory failure
review article
RFC1 gene
rhabdomyolysis
rigidity
Romberg's sign
sarcoglycan
sarcoglycanopathy
sclerae, hyperpigmented
seizure
sensorineural hearing loss
sensory loss, leg
serum alanine aminotransferase
sex reassignment surgery
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
sleep apnea
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
spondylolysis
statin therapy
systemic illness
tandem gait, ataxic
testicular atrophy
tethered spinal cord
toe walking
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
tripping
urinary incontinence
urine, dark
very long chain fatty acids
vestibular areflexia
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
wide based gait
winging of scapula
workup
Showing articles 250 to 300 of 1579 << Previous Next >>

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A 30-year-old man with acute paraplegia and left foot gangrene
Neurol 90:e1355-e1359, Paliwal, V.K.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Dysphagia and a rash
BMJ 361:k1590, McFarlane, M. & Disney, B., 2018

Distinct Brain Microhemorrhage Pattern in Critical Illness Associated with Respiratory Failure
Neurol 90:e2011, Hall, J.P.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Respiratory Failure in Acute Infective Endocarditis, Trends and Outcomes: Data from the National Inpatient Sample from 1999-2014
Chest 152:A63, Khalif, A., et al, 2017

Cerebral Venus Sinus Thrombosis (CVST): A Review of the Deadly Threat
JOJ Case Stud 2:555588, Khan,A.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Infratentorial Dural Arteriovenous Fistula Resulting in Brainstem Edema and Enhancement
Neurol 88:503-504, Emmer, B.J.,et al, 2017

Rheumatoid Pannus of the Cervical Spine
Neurol 88:e51, Weerasinghe, D.,et al, 2017

MRI Findings in Collet-Sicard Syndrome
Neurol 88:811, , 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

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

Monitoring long-term Efficacy of Fampridine in Gait-Impaired Patients with Multiple Sclerosis
Neurol 88:832-841, Filli, L.,et al, 2017

A Young Woman with Respiratory Failure, Hearing Loss, and Paraplegia
Neurol 88:e78-e84, Ntranos, A.,et al, 2017

Clinicopathologic Conference, Primary Adrenal Insufficiency (Addisons Disease)
NEJM 376:1159-1167, Case 9-2017, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Acute Spinal Cord Compression
NEJM 376:1358-1369, Ropper, A.E. & Ropper, A.H., 2017

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

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

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

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A 45-year-old woman with Immobility and Incontinence
Neurol 88:e212-e218, Zhang, B.,et al, 2017



Showing articles 250 to 300 of 1579 << Previous Next >>