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Differential
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abducens nerve paralysis
acoustic nerve
acral sensory symptoms
Adies pupil
advances in neurology
alcohol intolerance
alkylating agents
altered states of consciousness
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ankle reflex, absent
anterior tibial muscle weakness
antimetabolite
areflexia
arthrogryposis multiplex
asparginase
ataxia
ataxia, cerebellar
atonic bladder
autonomic dysfunction
Babinski sign
benign essential tremor
blood dyscrasias, neurologic findings with
burning paresthesia
caloric testing
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central core disease
cerebrospinal fluid, pressure low
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chromosomal abnormality
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
corpus callosum, lesion of
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
dermatomyositis
differential diagnosis
diplopia
diplopia, transient
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dysarthria
dysphagia
electroencephalogram, inflammatory disease
electromyogram
encephalopathy
epidemiology of neurology
episodic neurologic deficits
evoked potentials
facial nerve palsy, bilateral
facial pain
falling
familial
fasciculation
Fazio-Londe's disease
fever
fine motor function, impaired
fluorouracil
flush syndrome
foot deformity
foot drop
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
Guillain Barre syndrome
hallucination
hammertoes
hand deformity
hand weakness
headache
hearing loss
heavy metal intoxication
hemiparesis
hemiparesis, transient
high arched feet
human genome
hyperreflexia
hyponatremia
hyporeflexia
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intrinsic hand muscles, wasting of
Isaacs syndrome
isoniazid
jaw pain
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
laminectomy, cervical
laminectomy, lumbar
leg weakness, bilateral
leukemia, neurologic findings assoc.with
leukoencephalopathy
lumbosacral plexopathy
meningismus
meningoencephalopathy
methotrexate
methylhydrazine derivatives
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
monoparesis
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelin protein zero gene
myelogram
myelopathy
myeloradiculopathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve growth factor
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuritis, causes of
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuropathy
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, work up for
neurotoxin
neurotrophin-3
night blindness
nitrogen mustard
numbness, extremity
optic atrophy
optic atrophy, hereditary
orthostatic hypotension
pain
pain, foot
paralysis
paralysis, recurrent
paraparesis
paresthesias
paresthesias, feet
paresthesias, lower extremity
patient information and support
peroneal muscle atrophy, causes of
pes cavus
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, familial
porphyria
post polio syndrome
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
proptosis
ptosis
ptosis, bilateral
pulmonary function tests
pupil
pupil, dilated and fixed, bilateral
pyramidal tract dysfunction
quadriparesis
quadriplegia, transient
quality of life
radiculopathy
recombinant DNA
recurrent
Refsum's disease
respiratory failure
reversible neurologic disorder
review article
RFLPs
Romberg's sign
Roussy Levy syndrome
sarcoidosis
seizure
sensorineural hearing loss
sensory loss
spinal cord, compression of
spinal muscular atrophy
spinal stenosis
spinal stenosis, familial
splenium of corpus callosum
spontaneous remission
steppage gait
stiff man syndrome
strokelike episodes
subdural hematoma
symmetric brain lesions
syncope
tinnitus
toe walking
tomaculous neuropathy
torticollis
transient neurologic deficit
treatment of neurologic disorder
tremor
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
ultrasonography, nerve
vestibular function, tests of
vinblastine
vincristine neurotoxicity
visual evoked response
visual impairment
vocal cord paralysis
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
white matter disease
wrist drop
X-linked neuropathy
x-ray, spine
Showing articles 500 to 550 of 7753 << Previous Next >>

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

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Characteristics of Motor Vehicle Crashes Associated with Seizure
Neurol 91:e1102-e1111,543, Neal, A.,et al, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Inflammatory Demyelinating Polyneuropathy Versus Leptomeningeal Disease Following Ipilimumab
J Immunother Cancer 6:11, Cafuir, L.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Gasperini Syndrome
Neurol 90:e261, Lorio, R., 2018

Facial Ulceration in stroke
Neurol 90:e1448-e1449, May, L.M.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Acute demyelinating polyneuropathy induced by nivolumab
JNNP 89:435-437, Fukumoto, Y.,et al, 2018

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

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

Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
Neurol 88:e52-e54, da paz Oliveira, G.,et al, 2017

A 74-year-old Woman with Bilateral Foot Pain and a Palmar Rash
Neurol 88:e44-e50, Wynn, D.P.,et al, 2017

Guillain-Barre Syndrome following tuberculosis: A rare association
J Neurosci Rural Pract 8:296-299, Lakhotia, A.N.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

A Comparative Study of CIDP in a Cohort of HIV-Infected and HIV-Uninfected Patients
Neurol Neuroimmunol Neuroinflamm 4:e315, Moodley, K.,et al, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Long-Term Benefit of Enzyme Replacement Therapy in Pompe Disease
Neurol 89:2365-2373, Kuperus, E.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

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

Neurologic Complications Associated with the Zika Virus in Brazilian Adults
JAMA Neurol 74:1190-1198,1164, Ferreira da Silva, I.R.,et al, 2017

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

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Pure Sensory Ganglionopathy as the First Sign of Relapse in Non-Hodgkin Lymphoma
Neurol 88:1976-1977, Hossack, M. & McClean, J., 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

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

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

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

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

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

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

A Rare Case of Bilateral Optic Neuritis and Guillain-Barre Syndrome Post Mycoplasma Pneumoniae Infection
Neuro Opth 41:41-47, Baheerathan, A.,et al, 2017

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Zika Virus
NEJM 374:1552-1563, Petersen, L.R.,et al, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Stepwise Paralysis in a Patient with Adenocarcinoma of Lung
Neurol 86:e122-e127, Furlan, J.C.,et al, 2016

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Guillain-Barre Syndrome Outbreak Associated with Zika Virus Infection in French Polynesia: A Case-Control Study
Lancet 387:1531-1539,1486, Cao-Larmeau, V-M., et al, 2016

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Neurologic Signs and Symptoms Frequently Manifest in Acute HIV Infection
Neurol 87:148-154, Hellmuth, J.,et al, 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016



Showing articles 500 to 550 of 7753 << Previous Next >>