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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
carcinoma
carcinoma of thyroid
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
constipation
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
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
multiple endocrine neoplasia
muscle cramp
muscle diseases, characteristics of
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
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
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuroma
neuromuscular disease, electrodiagnosis of
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
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 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 1000 to 1050 of 4667 << Previous Next >>

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

A 73-Year-Old Woman with Episodic Dysarthria and Horizontal Binocular Diplopia
Neurol 98:767-772, Bower, A.S.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Babesiosis: Clinical Manifgestations and Diagnosis
www.UptoDate.com, Oct, Krause,P.J. & Vannier,E.G., 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

Saturday Night Myelopathy Flexion Myelopathy Related to Drug Intoxication
Neurologist 27:27-29, Martin, A.J.&Garcia,M.C., 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022

Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
Mol Genet Genomic Med 10:e1906, Vo,M.L.,et al, 2022

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

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

An Unusual Case of Acute Psychosis and Tetraparesis in a Young Zambian Man
Neurol 97:1002-1005, Zimba, S.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

A 79-Year-Old Woman with Subacute Bilateral Visual Loss
Neurol 97:e1159-e1165, Rossi, S.,et al, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021

Lumbar Sediment Sign Seen in an Unusual Presentation of Meningitis
Lancet 398:1436, Hegde, A.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Pain in Right Buttock after Carbon Monoxide Poisoning
BMJ 373:n1233, Hu, H. & Sun, Q., 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Silent Myocardial Infarction and Subsequent Ischemic Stroke in the Cardiovascular Health Study
Neurol 95:e436-e443, Merkler, A.E.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

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

Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Neurologic Involvement in Children and Adolescents Hospitalized in the United States for Covid-19 or Multisystem Inflammatory Syndrome
JAMA Neurol 78:536-547, LaRovere, K.L.,et al, 2021

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Recurrent Perimesencephalic Nonaneurysmal Subarachoid Hemmorrhage Within a Short Period of Time:A Case Report
World J Clin Cases 16:3356-3364, Li,J.,et al, 2021

Complication of Hepatitis A Infection: Case Report of Acute Inflammatory Demyelinating Polyneuropathy
Clin Prac Case Emerg Med 5:113-116, Laursen,D.,et al, 2021

CNS Demyelinating Attacks Requiring Ventilatory Support With Myelin Oligodendrocyte Glycoprotein or Aquaporin-4 Antibodies
Neurol 97:e1351-e1358, Zhao-Fleming,H.H.,et al, 2021

Transocular Sonography in Acute Arterial Occlusions of the Eye in Elderly Patients
PlusOne doi.org/10.1371/journal.pone.0247072, Czihal, M.,et al, 2021

A Case of Primary Leptomeningeal Lymphoma Presenting with Hydrocephalus Characterized by Disproportionately Large Fourth Vehicle
NMCCRJ 8:399-404, Nohira, S.,et al, 2021

Anti-cN1A Antibodies are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis
Cells 10:1146, Lucchini,M.,et al, 2021



Showing articles 1000 to 1050 of 4667 << Previous Next >>