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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
afebrile
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anti MAG antibodies
anticonvulsants
areflexia
arrhythmia, cardiac
asymptomatic
autism
autoimmune disease
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebral cortical encephaliis
chewing, impaired
children
chromosome 17
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cotton-wool spots
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
delay in diagnosis
denervation of muscle
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
entrapment neuropathy
enzyme, defect
epidermal nevus syndrome
Epstein-Barr virus
exercise
exophthalmus
eye, pain in
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
falling
false positive
familial
fatigue
fever
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globe, flattened posteriorly
Gowers maneuver
headache
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
heterotopia
hirsutism
histochemistry
hoarseness
hypercalcemia
hypertension
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hypothyroidism
inability to sit up
infantile spasm
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
leg swelling
leukocytosis
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lymphadenopathy
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
malignant optic glioma of adulthood
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, orbit
MRI, venography
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelitis
myelitis, transverse
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
nerve conduction studies
nerve injury
neurocutaneous disease
neuroendocrinology
neuroinfectious diseases
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night sweats
obesity
optic chiasm, lesion of
optic disc
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, neoplasm of
optic nerve, tortuosity
optic neuritis
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optical coherence tomography
orthopnea
pain
pain, leg
palpitations
percussion induced muscle contraction
perineuritis
phakomatoses
plasma cell dyscrasia
polyneuropathy
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
radiculopathy
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
scoliosis
scotoma, central
seizure
shoulder, elevation
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
splenomegaly
steppage gait
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
subarachnoid hemorrhage
subcutaneous nodules
survival motor neuron gene
syringomyelia
systemic illness
telangiectases, retinal
third nerve palsy
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urinary frequency
urine, dark
visual acuity, decreased, monocular
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual symptoms
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
workup
Showing articles 150 to 200 of 1609 << Previous Next >>

Personalized iPSC-Derived Dopamine Progenitor Cells for Parkinsons Disease
NEJM 382:1926-1932, Schweitzer, J.S.,et al, 2020

Delayed Nonischemic Cerebral Enhancing Lesions Post Endovascular Coil Embolization
Neurol 94:e2402-e2403, Bettin, M.V. & Southerland, A.M., 2020

MR Target Sign in Cerebral Aspergillosis
Neurohospitalist doi:10.1177/1941874420929191, Finelli, P.F., 2020

Application of Deep Learning to Predict Standardized Uptake Value Ratio and Amyloid Status on 18F-Florbetapir PET Using ADNI Data
AJNR 41:980-986, Reith, F.,et al, 2020

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Ischemic Stroke
Stroke 51:e124-e127, Valdes Valderrama, E.,et al, 2020

Spinal Metastases
JAMA 323:2438, Chiu, R.G.,et al, 2020

Degenerative Cervical Spondylosis
NEJM 383:159-168, Theodore, N., 2020

Distal Symmetric Polyneuropathy in 2020
JAMA 324:90-92, Callaghan, B.C.,et al, 2020

CT Scanning in Suspected Stroke or Head Trauma: Is It Worth Going the Extra Mile and Including the Chest to Screen for COVID-19 Infection?
AJNR 41:1165-1169, Kwee, R.M.,et al, 2020

Childhood Multisystem Inflammatory Syndrome
NEJM 383:393-395, Levin, M., 2020

Arthralgia as an Initial Presentation of COVID-19
Rheumatol Int doi:10.1007/s00296-020-04561-0, Joob, B. & Wiwanitkit, V., 2020

Native-Valve Infective Endocarditis
NEJM 383:567-576, Chambers, H.F. & Bayer, A.S., 2020

Clinicopathologic Conference, Cerebrovascular Accident Probably Related to SARS-CoV2 Infection
NEJM 383:764-773, Case 26-2020, 2020

A Woman with Monocular Vision Loss
Neurol 95:e1105-e1109, Danish, H.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

A case of COVID-19-associated pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
Neurol 95:978-983, Liberatore, G.,et al, 2020

Migraine, hearing loss, and blurred vision in a young woman
Neurol 95:e2945-e2950, Sasikumar, S.,et al, 2020

A 62-year-old man with history of catheter ablation presenting with recurrent strokes
Neurol 95:e3065-e3069, Jeanneret, V.,et al, 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

Clinical and Radiologic Findings of Acute Necrotizing Encephalopathy in Young Adults
AJNR 41:2250-2254, Vanjare, H.A.,et al, 2020

A Rare Complication of Cardiac Ablation:Atrial-esophageal Fistula Presenting as Odynophagia
Cureus doi:10.7759/CUREUS.6871, Khan,M.,et al, 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

Immunoglobulin G4-related Hypertrophic Pachymeningitis Mimicking Temporal Arteritis
Neurol 94:(15 suppl), Han, J.Y.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

Clinical Manifestations and Diagnosis of Nocardiosis
UptoDate May, Spelman, D., 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Lyme Myelopathy:Case Report and Literature Review of a Rare But Treatable Disorder
Mult Scler Relat Disord 29:1-6, Kaiser,E.A.,et, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

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

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Clinicopathologic Conference, Lymphocytic Choriomeningitis Virus Infection
NEJM 381:2553-2560, Case Record 40-2019, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Artificially Sweetened Beverages and Stroke, Coronary Heart Disease, and All-Cause Mortality in the Womens Health Initiative
Stroke 50:555-562,549, Mossavar-Rahmani, Y.,et al, 2019

A Man with Headache, Fever, and Neck Stiffness
JAMA 321:1624-1625, Cooper, R.,et al, 2019

A 71-year-old Man Receiving Treatment for Cryptococcal Meningitis, Developing New-Onset Lethargy
Neurol 92:815-820, Peng, T.J.,et al, 2019

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,et al, 2019

Links in the Chain of Chronic Traumatic Encephalopathy
NEJM 380:1771-1772, Ropper, A.H., 2019

Pterygoid Myositis Mimicking Giant Cell Arteritis
Neurol 92:e2297, Na, S.,et al, 2019

Dog Licks Baby. Baby gets Pasteurella Multocida Meningitis
Lancet 393:e41, Ryan, J.M. & Feder Jr., H.M., 2019

Aspergillosis-Induced Vasculitis Presenting as Ischemic Stroke in an Immunocompetent Patient
Neurol 92:e2618-e2619, Lebeaux, D.,et al, 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019



Showing articles 150 to 200 of 1609 << Previous Next >>