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Differential
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airway obstruction
alopecia
alveolar hypoventilation
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
anesthesia, general
aneurysm, thoracic aortic
antibiotics
aortic wall, thickened
aortitis
arrhythmia, cardiac
arterial dissection, aorta
arterial dissection, wall thickness
arteritis, temporal
aspiration
atrophy, muscle
baldness
blink reflex
Borrelia miyamotoi infection
botulinum toxin
bruxism
bulbar palsy
cachexia
cardiac arrest
cardiac arrest and resuscitation
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission, abnormal
CAT scan, muscle
cataracts
central nervous system, infection of
cerebrospinal fluid, elevated protein of
chewing movements
chewing, impaired
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
confusion
corneal reflex, abnormal
corneal reflex, absent
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
diagnostic criteria
distal muscle atrophy
distal muscle weakness
dysarthria
dysphagia
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
encephalitis
eosinophilic fasciitis
eye movement, painful
eye, pain in
face, numbness of
facial appearance, abnormal
facial pain
facial weakness
facial weakness, bilateral
false negative
familial
fasciculation
fatigable chewing
fatigue
fever
floaters
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
giant cell arteritis
gynecomastia
halo sign
headache
headache, bilateral
headache, temporal
heart block
hemiparesis
high arched feet
high arched palate
hydrocephalus
hypercapnia
hypoglycorrhachia
hypotonia
hypotonia, infants
idiopathic
immunosuppression
infection
intrinsic hand muscles, wasting of
jaw claudication
leukocytosis
lid closure, weakness of
masseter muscle hypertrophy
masseter muscle wasting
masseter muscle weakness
memory, defect of recent
meningitis
meningitis, neutrophilic
meningitis, treatment of
meningoencephalitis
mental status, abnormal
micrognathia
misdiagnosis
molecular genetics
mononeuropathy
mononeuropathy, motor
motor neuron disease
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, orbit
MRI, sulcal hyperintensity
MRI, vessel wall
MRI, vessel wall enhancement
multimodal neuroimaging
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myoclonus
myopathy
myositis
myositis, pterygoid
myotonia
myotonia congenita
myotonia dystrophica
neck stiffness
neck weakness
nerve conduction studies
neurologic disease, diagnoses of
neurologic evaluation
neuronopathy
neuronopathy, sensory and motor
neutropenia
New England
ophthalmic artery
papilledema
percussion induced muscle contraction
phonophobia
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proximal muscle atrophy
ptosis
ptosis, bilateral
repetitive nerve stimulation
respiratory failure
retro-orbital pain
review article
scalp tenderness
sedimentation rate, elevated
seizure
slit lamp examination
somnolence
sonophobia
spirochete infection
standing difficulty
stare
staring spells
steppage gait
temporal artery
temporalis muscle enhancement
temporalis muscle hypertrophy
temporalis muscle swelling
temporalis muscle tenderness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
tongue, fasciculations of
tongue, weakness
transient neurologic deficit
treatment of neurologic disorder
trigeminal nerve, abnormality of
trigeminal neuropathy
trigeminal neuropathy, motor
trinucleotide repeats
vasculitis, large vessel
vertebral artery wall thickness
vision, blurred, monocular
visual loss
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
word-finding difficulty
Showing articles 250 to 300 of 2760 << Previous Next >>

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

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

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

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

A 35-year-old Woman with Hyperstartling Stiffness, and Accidental Falls
Neurol 88:e38-e41, Russo, S.P.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 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

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

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

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

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

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

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

Clinicopathologic Conference, Probable Acute Leptospirosis
NEJM 377:268-278, Case 22-2017, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

A Case of Altered Mental Status, Not Otherwise Specified
Neurol 89:e154-e158, Swor, D.E.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Rituximab as Treatment for anti-MuSK myasthenia gravis
Neurol 89:1069-1077, Hehir, M.K.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Clinicopathologic Conference, Eosinophilic Granulomatosis with Polyangiitis
NEJM 377:1569-1578, Case 32-2017, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

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

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

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

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016

Leptomeningeal Enhancement in a Patient with Progressive Cranial Neuropathies and Lumbosacral Radiculopathies
JAMA Neurol 73:345-346, Vargas, T.C.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016



Showing articles 250 to 300 of 2760 << Previous Next >>