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Differential
(Click to cross reference)
abdominal distention
abdominal muscle paralysis
abducens nerve paralysis
abscess, intracerebral
acetazolamide
acid maltase deficiency
acid maltase deficiency, adult
acoustic nerve
acquired immunodeficiency syndrome
activities of daily living scale
acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
alcohol
alcohol intolerance
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alkylating agents
alpha glucosidase
altered states of consciousness
aminoacidopathies
amiodarone
amitriptyline
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anemia
aneurysm
aneurysm, intracranial
ankle, swelling of
anterior horn cell disease
anterior tibial muscle weakness
antiarrhythmic drugs
anticholinesterase
antimetabolite
antiviral agents
aphasia
areflexia
arrhythmia, cardiac
arsenic
arthralgia
arthrogryposis multiplex
ascending paralysis
asparginase
aspartate aminotransferase
asthma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atonic bladder
atypical
auditory evoked brainstem potentials
autoimmune disease
autonomic dysfunction
azidodeoxythymidine
Babinski sign
BAL
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery stenosis
basophilic stippling of red blood cells
Bassen-Kornzweig syndrome
bent spine syndrome
biological warfare
black toenail sign
blacks
blindness, sudden
blood dyscrasias, neurologic findings with
bone marrow suppression
bone marrow transplantation
botulism
bradycardia
brain biopsy
brain purpura
brainstem, dysfunction
brainstem, lesion of
bright tongue sign
bulbar palsy
burning paresthesia
calcification, intracranial
calf hypertrophy
caloric testing
camptocormia
cancer, cerebrovascular accident complicating patients with
canned food
carbon monoxide poisoning
carbon monoxide poisoning, chronic
carboxyhemoglobin
carcinoid tumor
carcinoma
cardiomegaly
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebral ischemia
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemical weapons
chemotherapy, CNS treatment and complications with
cherry red spot-myoclonus syndrome
chest pain
children
chills
chloroquine
chromosomal abnormality
chromosome 11
chronic fatigue syndrome
chronic graft versus host disease
chronic progressive external ophthalmoplegia
Chvostek sign
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
cognition
coma
compartment syndrome
complications
confusion
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
conversion reaction
cortical blindness
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
critical care unit
cultured skin fibroblasts
Cushing's syndrome
cyclic vomiting
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytokines
deafness
DEET
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
depression
dermatitis
dermatomyositis
descending paralysis
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diarrhea
differential diagnosis
difficulty climbing stairs
diphtheria
diplopia
distal muscle atrophy
distal muscle weakness
dizziness
DNA probes
docetaxel
down-beat nystagmus
drooling
dropped head syndrome
drowsiness
drug induced neurologic disorders
duvalumab
dysarthria
dysgeusia
dyskinesia
dysmorphic
dysphagia
dyspnea
dystonia
echocardiogram
echocardiogram, LVH
edema, pedal
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
electronystagmography
electroretinograph
emergencies, medical
emergencies, neurologic
emtricitabine
encephalitis
encephalitis, autoimmune
encephalomalacia
encephalomyopathy
encephalopathy
encephalopathy, anoxic
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
epidemiology of neurology
epilepsia partialis continua
episodic disorders
episodic neurologic deficits
erythrocyte
evoked potentials
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exercise-related muscle strength increase
extraocular muscle atrophy
eye movement, disorders of
facial appearance, abnormal
facial hair, excessive
facial nerve palsy
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
fatigue
Fazio-Londe's disease
feeding disorder
fever
fibrillations
fingernails, abnormal
fish
fish poisoning
floppy infant
fluctuate
fluorouracil
flush syndrome
food poisoning
foot drop
fundus, abnormality of
gag reflex, depressed
gait disorder
gammaglobulin therapy, intravenous
gangliosidosis GM2
gastroenteritis
gastrointestinal motility
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen debranching enzyme deficiency
glycogen storage disease
gonadal dysgenesis
Gowers maneuver
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Gulf War syndrome
gyrus, abnormal
Hallervorden Spatz disease
hallucination
hand weakness
headache
headache, sudden onset of
hearing loss
heart block
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemoglobinuria
hepatitis
hepatomegaly
heralding manifestation
hexosaminidase-A
hip flexor weakness
hirsutism
histochemistry of muscle
human immunodeficiency virus type 1
hydroxychloroquine
hyperamylasemia
hyperbaric oxygen
hyperkalemia
hyperkeratosis
hypertension
hypocalcemia
hypoglycemia
hypoglycemic coma
hypokalemia
hypomagnesemia
hypomyelination
hyponatremia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hyporeflexia
hypotension, systemic
hypothyroidism
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immune checkpoint inhibitors
immune-related adverse events
immunologic disease
immunosuppression
immunosuppressive agents
immunotherapy
impotence
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
insect repellent
insecticides
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal pseudoobstruction
intracerebral hemorrhage
ipecac
ipilimumab
ischemic exercise test
isoniazid
jaundice
jaw pain
Jewish
kaliuresis
Kearns-Sayre syndrome
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphosis
lactic acidemia
lactic dehydrogenase(LDH)
Lafora's disease
laminar necrosis, cortical
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
leg swelling
leg weakness, bilateral
Leigh's disease
lens, dislocation of
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocytes
leukocytosis
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
lid closure, weakness of
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
lipid storage myopathy
liver disease
liver function enzymes
lordosis
low back pain
lymphopenia
lysosomal storage disease
lysosomes, abnoral
macular degeneration
mannitol
McArdle's disease
McArdle's disease, adult onset
Mees lines
MEK inhibitor
melanoma, malignant
MELAS syndrome
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, leukemic
meningoencephalopathy
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
mestinon
metabolic acidosis
metabolic alkalosis
metabolic disorder, primary
metallic taste
methotrexate
methylhydrazine derivatives
microcephaly
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
molybdenum cofactor deficiency
monoamine oxidase inhibitors
mononeuropathy
mortality
motor neuron disease
movement disorder
MRI
MRI lesion location
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, gyral enhancement
MRI, gyral swelling
MRI, hypointense signal foci on
MRI, muscle
MRI, serial
MRI, T1 weighted high signal foci
MRS
mucopolysaccharidoses
multiple organ failure
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenic crisis
myasthenic syndrome
myelopathy
myocarditis
myoclonus
myoclonus, epilepsy
myoglobinuria
myoneuropathy
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, carcinomatous
myopathy, centronuclear
myopathy, critically ill
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, immune-mediated
myopathy, proximal
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, toxic
myopathy, vacuolar
myopia
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia, treatment of
myotonic discharges
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
neoplasm, metastatic
neoplasm, metastatic to CNS
nephrotic syndrome
nerve agents
nerve biopsy
nerve conduction studies
nerve conduction studies, sensory
neuritis, causes of
neuritis, heavy metals causing
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neurons
neuroophthalmology
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, ataxia, retinitis pigmentosa
neuropathy, diabetic
neuropathy, diphtheritic
neuropathy, hereditary peripheral
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, motor
neuropathy, peripheral
neuropathy, sensory
neuropathy, toxic
neurotoxic
neurotoxin
neutropenia
newborn, evaluation of
next-generation sequencing
night blindness
night sweats
nitrogen mustard
nivolumab
normal
nose, abnormal
numbness, extremity
nystagmus
occipital lobe, lesion of
occupational neurologic disorders
ocular motility, disorders of
ocular myopathy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
orbit, lesions of
organ transplantation
orthopnea
orthostatic hypotension
oxygen therapy
pain
pain, arm
pain, back
pain, leg
palpitations
pancreatitis
pancuronium
pancytopenia
paramyotonia congenita
paraparesis
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
PAS positive
patient in waiting
patient information and support
pediatric neurology
pembrolizumab
pericardial effusion
periodic paralysis
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
peroxisomal disease
personality change
phosphorylase b kinase deficiency
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
poison, mercury
poison, neurologic problems with
poison, organophosphate
POLG1 gene
poliomyelitis
polymerase chain reaction
polymyalgia rheumatica
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, critically ill
Pompe's disease of glycogen storage
Pompe's disease, infantile
porphyria
position sensation, abnormal
postpartum
postural abnormality
precipitating factors
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
procarbazine
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
proximal muscle atrophy
pruritus
pseudomyotonia
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary embolism
pulmonary function tests
pulmonary hypertension
pulmonary infiltrates
quadriparesis
quadriparesis, acute
quadriparesis, progressive
quadriplegia
quadriplegia, transient
radionuclide imaging, heart
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
recurrent laryngeal nerve paralysis
refractive errors
Refsum's disease
renal failure
respirator
respiratory failure
respiratory tract infection
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
riboflavin
rigidity
risk factors
sarcoidosis
screaming
screening
second wind phenomena
seizure
seizure, intractable
seizure, neonatal
selumetinib
sensorineural hearing loss
sensory symptoms
sensory testing
sensory testing, quantitative
short stature
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sodium valproate
sodium valproate, toxicity
somatosensory evoked potentials
Southern immunoblot test
spasticity
spinal cord, compression of
spinal cord, metastasis to
spinal muscular atrophy
spinocerebellar degeneration
spongy degeneration of brain
spontaneous remission
standing difficulty
startle reaction
status asthmaticus
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stooped posture
storage disease of CNS
strokelike episodes
subarachnoid hemorrhage
suicide
sweating, abnormality of
symmetric brain lesions
systemic illness
tachycardia
tapetoretinal degeneration
taxol
Tay-Sachs disease
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thirst
thrombocytopenia
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, weakness
torticollis
toxic oil syndrome
toxins, nervous system
transient neurologic deficit
transverse smile
treatment of neurologic disorder
tremor
tremor, jaw
tricresylphosphate
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
uremia
uric acid, low
urinary frequency
urinary incontinence
urine test in toxic screen
urine, dark
Usher's syndrome
vaccination, neurologic complications with
vecuronium
vinblastine
vincristine neurotoxicity
visual field defect
visual loss
vital capacity
vocal cord paralysis
walking, difficulty with
war
weakness
weakness, acute
weakness, chronic
weakness, episodic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
whole genome sequencing
winging of scapula
workup
wrist drop
 		Showing articles 100 to 150 of 1936 << Previous Next >>

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
NEJM 316:761-763, 807-8081987., Senanayake,N.&Karalliedde,L., 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Neurologic Complications of Carcinoid
Neurol 36:745-749, Parchell,R.A.&Posner,J.B., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Peripheral Neuropathy Associated with Mitochondrial Myopathy
Ann Neurol 20:249-257, Yiannikas,C.,et al, 1986

Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Ciguatera Fish Poisoning in Miami
JAMA 244:254-258, Lawrence,D.N.,et al, 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

The Ultrastructure of the Sural Nerve in Pompe's Disease
Ann Neurol 2:111, Goebel,H.H.,et al, 1977

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

The Neuromyopathy of Vincristine in Man, Clinical, Electrophysiol & Pathological Studies
J Neurol Sci 10:107-131, Bradley,W.G.,et al, 1970

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

An 81-Year-Old Woman with Chronic Isolated Neck Extensor Weakness
Neurol 106:e218060, Chen,J.,et al, 2026

Inflammatory Myopathies
NEJM 394:1925-1938, AllenBach,Y. & Benveniste,O., 2026

Niemann-Pick Disease Type C
Gene Reviews www.genereview.org, Bremova-Ertl,T. & Patterson, M., 2025

From Stroke Workup to Mitochondrial Disease: A Case Report of MELAS
Radiol Case Reports 20:6248-6252, Sevencan,Y.,et al, 2025

A 69-Year-Old Woman with Ophthalmoplegia
Neurol 104:e213763, Yu, H & Frey, J, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

Chasing the New Dragon, Toxic Spongiform Leukoencephalopathy with Chronic Fentanyl Inhalation
Neurol 106:e214517, Maisenbacher,M. & Jayagopal, L.A., 2025

Clinicopathologic Conference, Lyme Carditis
NEJM 393:799-807, Case 24-2025, 2025

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

The Multifactorial Nature of Ischemic Stroke in Malignancy
Stroke 56:e303-e306, Doyle,C.L.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
Neurol 105:e214086, McGuire,J.L.,et al, 2025

Tiger Man Sign in Sarcoid Myopathy
Neurol 105:e214323, Sun,Q.,et al, 2025



Showing articles 100 to 150 of 1936 << Previous Next >>