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Differential
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abdominal reflex, absent
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome myelopathy
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
Africa
alcohol intolerance
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alopecia
alternating rapid movement
Alzheimer's disease
ammonia
amniocentesis
amphotericin B
amyloid plaques
amyloidoma
anemia
aneurysm, vertebral basilar system
angiitis, granulomatous of CNS
angiography, spinal
ankle reflex, absent
anterior horn cell disease
antioxidant
aphasia
areflexia
Arnold Chiari malformation
arthralgia
arthritis
astrocytoma
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atherosclerosis, generalized
atherosclerosis, premature
atypical
auditory evoked brainstem potentials
autism
autoantibodies
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal degeneration
axonal spheroid
B 12 deficiency
B12
Babinski sign
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
behavioral disorder
Behcet's syndrome
bladder dysfunction
blindness
bone marrow biopsy
brachial plexus neuropathy
brain biopsy
brain biopsy, negative
brain biopsy, stereotaxic
brainstem
brainstem, atrophy
brainstem, glioma
brainstem, glioma in children
brainstem, glioma, adult
brainstem, ischemia
brainstem, lesion of
brainstem, neoplasms of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
burning feet
burning paresthesia
CAG repeats
calcification, intracranial
cane
carcinoma of pancreas
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
caudate nucleus, atrophy
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemangioma
cerebellar lesion
cerebellar plaques, amyloid
cerebellar vermis
cerebral cortical atrophy
cerebral folate deficiency syndrome
cerebral palsy
cerebral palsy, associated problems with
cerebral venous thrombosis
cerebroretinal microangiopathy with calcifications and cysts
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
cervical myelopathy
cervical spondylosis
children
choking
cholestanol
chorea
chorea, causes of
chorea, familial
choreoathetosis
choroid plexus
choroid plexus, tumor of
chromosomal abnormality
chromosome 2
chromosome 6
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
cobalamin C deficiency
coccidioidomycosis
cognition
cold hands sign
color vision, impaired
coma
concentration, impaired
confusion
congenital infection, CNS
consanguinity
constipation
controversies in neurology
conversion reaction
corpus callosum, atrophy of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
crossed adductor reflex
crying, pathologic
cryptococcal meningitis
cyst, epidermoid of CNS
cysticercosis
deafness
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, childhood
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
demyelinating disease
depression
dermatitis
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
diplegia, spastic cerebral
diplopia
disability, neurological
disorientation
distal muscle atrophy
Dravet syndrome
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysphagia
dysphonia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystrophic calcification
ears of the Lynx MR sign
eczema
electrical sensation
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
emergency room
emotional lability
encephalitis
encephalitis, viral
encephalomyelitis
encephalopathy
endemic area
endovascular therapy
enzyme, muscle disease
ependymoma
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
equinovarus
evoked potentials
executive dysfunction
exome sequencing
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, recurrent
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatal familial insomnia
fatigue
fatty acid, elevated plasma content
fever
fine motor function, impaired
finger nose finger test
finger tapping
fistula, arterio-venous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
fluorescent treponema antibody absorption(FTA-ABS)
folic acid
folic acid deficiency
foot deformity
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
fundus, abnormality of
gadolinium
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gaze palsy
gender
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
geographic location
Gerstmann-Straussler-Scheinker disease
GFAP gene
girdle sensation
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucagonoma
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
glycogen storage disease
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
hallucination
hammertoes
hand weakness
handwriting
head tilt
headache
hearing loss
hearing problems in children
heel-knee-shin test
hemiparesis
hemosiderosis of CNS, superficial
hepatic failure
hepatitis
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
high arched feet
Hispanics
hoarseness
Hodgkin's disease
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
human T-lymphotropic virus type II(HTLV-II)
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperammonemic encephalopathy
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypersomnia
hypertension
hyperthermia
hyperthyroidism
hypertonia
hypodontia
hypoglycorrhachia
hypoglycorrhachia, causes of
hypomyelination
hypotension, systemic
hypothyroidism
hypotonia
imbalance
immunotherapy
impotence
impulsivity
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
iron, brain
irritability
Jakob-Creutzfeldt disease
Jewish
lactic acidemia
lathyrism
laughing
laughing, pathologic
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of, bilateral
leptospirosis
leukemia, neurologic findings assoc.with
leuko-araiosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
life expectancy
liver biopsy
liver disease
locked-in syndrome
low back pain
lymphoma
lymphoma involving CNS
macrocephaly
Madonna facies
Maghreb
mania
marche a petits pas
Marinesco-Sjogren syndrome
medulla oblongata, lesion of
megalencephaly
Melkersson's syndrome
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal gliomatosis
meningitis
meningitis, actinomycotic
meningitis, aseptic
meningitis, bacterial
meningitis, blastomyces
meningitis, brucellosis
meningitis, candida
meningitis, carcinomatous
meningitis, chronic
meningitis, chronic benign lymphocytic
meningitis, cladosporium
meningitis, coenurosis
meningitis, CSF cell count-normal
meningitis, cysticercosis
meningitis, echinococcal
meningitis, eosinophilic
meningitis, fungal
meningitis, helminthic
meningitis, histoplasma
meningitis, leptospira
meningitis, lymphomatous
meningitis, Mollaret's
meningitis, nocardia
meningitis, paracoccidioides
meningitis, post myelography
meningitis, recurrent
meningitis, syphilitic
meningitis, TB
meningitis, toxoplasma
meningoencephalitis
meningoencephalitis, toxoplasma
meningomyelitis
mental retardation
mental status, abnormal
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
methyl benzene
methylglutaconic aciduria
methylmalonic acidemia
microangiopathy, brain
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
mononeuritis multiplex
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, diffusion weighted
MRI, emergent
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, paramagnetic effect
MRI, spinal cord
MRI, spine
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myelopathy, hepatic
myelopathy, vacuolar
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, vacuolar
myositis
myositis, ocular
myxedema, neurologic manifestations of
Native Americans
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-metastasizing to subarachnoid space
neoplasm, primary of CNS-treatment of
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
neuropathy, sensory
neurosyphilis
neurotoxin
next-generation sequencing
night blindness
nitrous oxide
numb clumsy hands syndrome
nystagmus
nystagmus, rotary
obesity
ochronosis
octreotide
ocular motility, disorders of
oculodentodigital dysplasia
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
optic ataxia
optic atrophy
optic atrophy, hereditary
optic neuritis
optic neuropathy
optical coherence tomography
orthostatic hypotension
osteoarthrosis
osteoporosis
pain
pain, abdominal
pain, back
pain, foot
pain, leg
palatal myoclonus
palmomental response
pancytopenia
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paraplegin
paraspinal muscle
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
past pointing
Pelizaeus Merzbacher
penicillin
pernicious anemia
personality change
pes cavus
photosensitivity, skin
pinealoma
pleocytosis of cerebrospinal fluid
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
pons, lesion of
pontine glioma
portal caval shunt
posterior column disease
postural abnormality
precipitating factors
primary lateral sclerosis
prion disease
prisoners of war, neurologic complications in
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
pursuit eye movements, abnormal
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriparesis, progressive
quadriplegia
radiation therapy, CNS treatment and complications with
radiculopathy
Rankin score
rapidly progressing neurologic illness
Raynaud's phenomenon
rectal biopsy
recurrent
regional enteritis
release phenomena
remote effect of cancer on the nervous system
renal stones
reticulum cell sarcoma
retinal detachment
retinitis pigmentosa
Rett's syndrome
reversible neurologic disorder
review article
rigidity
risk factors
Romberg's sign
Rosenthal fibers
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
scalp tenderness
schizophrenia
scissors gait
sclerae, hyperpigmented
scleroderma
scleroderma, neurologic involvement with
SCN1A gene
scoliosis
scoliosis, neurologic association with
scotoma
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, tonic-clonic
sensorineural hearing loss
sensory level
sensory loss
sensory loss, cutaneous
serologic testing
serologic testing of cerebrospinal fluid
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea
sleep pathology and physiology
slow virus infection of CNS
sodium channel dysfunction
solitary scerlosis
somatosensory evoked potentials
somnolence
spartin
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spastic paraplegia, type 7
spasticity
spastin
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal cord, vascular malformation of
spinal xanthomatosis
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 7
spinocerebellar degeneration
spondylolysis
spongy degeneration of brain
startle reaction
status epilepticus
stereotyped behavior
stiff legs
stiff man syndrome
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
subcortical U fibers
substantia nigra
superior cerebellar peduncle
symmetric brain lesions
syndactyly
syphilis, diagnosis and treatment
syphilis, meningomyelitis
syphilis, neurologic complications with
syringomyelia
tachycardia
tectal glioma
teeth, abnormal
teeth, number of in infants
tendon, enlarged
thalamus, lesion of
thrombocytopenia
thyroiditis
thyrotoxicosis
titubation
toe walking
tone, muscle
tone, muscle, increased
tongue, enlarged
tongue, impaired movements of
tonsillar herniation of cerebellum
toxins, nervous system
toxoplasmosis, acquired
toxoplasmosis, CNS
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
ulcerative colitis
ulcers, fingertip
upgaze, paralysis of
urea-cycle enzymopathies
urinary frequency
urinary incontinence
urinary urgency
urine, dark
uveitis
valium
vegetarianism
vertigo
vibratory sensation, abnormal
viral infection
viral infection, CNS
viral isolation
virus, slow
visual acuity, decreased
visual evoked response
visual loss
vitamin deficiency
vitiligo
Vogt-Koyanagi-Harada syndrome
walking frame
walking, difficulty with
war
weakness
weakness, progressive
weakness, proximal
weight loss
Western immunoblot test
wheelchair
white matter disease
wide based gait
workup
xanthoma, tendon
xeroderma pigmentosa
 		Showing articles 100 to 150 of 1510 << Previous Next >>

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
JAMA Neurol 8:418-419, Liu,M.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Clinical Features and Diagnosis of Intramedullary Spinal Cord Abscess in Adults, A Systematic Review
Neurol 101:e836-e844, Harrold,G.K.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Longitudinally Extensive Spinal Cord Lesions in a Middle-Aged Man
Neurol 98:419-424, Xi, N. & Zhou, Y., 2022

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

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022



Showing articles 100 to 150 of 1510 << Previous Next >>