Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal reflex, absent
abducens nerve paralysis
abscess, spinal cord
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome myelopathy
acrocyanosis
addiction, heroin-neurologic complications with
Addison's disease
adducted thumb
adrenal biopsy
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
Africa
Aicardi-Goutieres syndrome
alcohol
alcohol injection
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
Alzheimer's disease
aminoacidopathies
aminoacidurias
ammonia
amyloid plaques
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anemia
anemia, megaloblastic
anesthesia, general
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, neurologic complications with
ankle reflex, absent
anterior spinal artery
antispasticity drugs
aphasia
arteritis, temporal
arthralgia
arthritis
asterixis
asterixis, causes of
asterixis, unilateral
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atherosclerosis, premature
atlanto-axial subluxation
atrioventricular block
atypical
auditory evoked brainstem potentials
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
azospermia
B 12 deficiency
Babinski sign
baclofen
bacterial infection
bacterial infection, CNS
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Behcet's syndrome
blacks
bladder dysfunction
blink reflex
blood dyscrasias, neurologic findings with
blood transfusion
bone marrow transplantation
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, dysfunction
brainstem, lesion of
breast feeding
Brown Sequard syndrome
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
bulbar palsy, progressive
CAG repeats
calcification, intracranial
camptocormia
cane
carotid angiogram
cassava
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, myelogram with
CAT scan, serial
CAT scan, spinal cord
CAT scan, spine
cataracts
cavernous hemangioma
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral edema
cerebral palsy
cerebritis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, amonia
cerebrospinal fluid, culture of, viral
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, glutamine
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrotendinous xanthomatosis
cerebrovascular accident
cervical spine
cervical spine injury, compression
cervical spondylosis
Charcot-Marie-Tooth
chilbran skin lesions
children
cholestanol
chorea, causes of
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 2
chromosome 6
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
color vision, impaired
complications
compression fracture
confusion
conjunctivitis
consanguinity
constipation
cornea, opacity of
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cortical blindness
cough
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
crossed adductor reflex
crying, pathologic
cultured skin fibroblasts
cyanide poison
cystinuria
DARS
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, familial
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
diet
differential diagnosis
digits, abnormal
diplopia
distal muscle atrophy
distal muscle weakness
Dravet syndrome
drought
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
dysarthria
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
ears of the Lynx MR sign
electrical sensation
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
ELISA
emergencies, neurologic
emergency room
emotional lability
encephalitis
encephalopathy
encephalopathy, metabolic
endemic area
enzyme, defect
enzyme, muscle disease
epicanthal folds
epidemiology of neurology
epileptic encephalopathy
erythema migrans
evoked potentials
exome sequencing
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatal familial insomnia
fatigue
fatty acid, elevated plasma content
feeding disorder
fetus
fever
fibrillations
fine motor function, impaired
finger nose finger test
fistula, arterio-venous, dural
flexor spasm
fluorosis
foot deformity
foot drop
Friedreich's ataxia
gadolinium
gait disorder
gait, spastic
galactocerebrosidase
gamma amino butyric acid-mimetic drug
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu valgum
geographic location
Gerstmann-Straussler-Scheinker disease
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamine
gram negative rod
granulomatosis with polyangiitis
granulomatous disease
Hallervorden Spatz disease
hammertoes
hand weakness
head lag
headache
hearing loss
hearing problems in children
heart block
heart block, complete
hemangioma
hemangioma, vertebral
hematopoietic tissue, extramedullary
hematuria, microscopic
hemianopia
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
herpes virus
herpes virus infection
high arched feet
hoarseness
Horner's syndrome
human herpesvirus 6
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
human T-lymphotropic virus type II(HTLV-II)
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperammonemic encephalopathy
hypercalcemia
hyperhidrosis
hyperparathyroidism
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hyperthermia
hyperthyroidism
hypogonadism
hypomyelination
hypopigmentation of skin
hypothalamus, disturbance of
hypothermia
hypothermia, causes of
hypothyroidism
hypotonia
iatrogenic neurologic disorders
imbalance
immunosuppression
immunosuppressive agents
impotence
impulsivity
inborn errors of metabolism
inclusion bodies
incontinence, fecal
incoordination
infection
insomnia
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intracerebral hemorrhage
intrathecal antispasticity drugs
intrauterine
intrinsic hand muscles, wasting of
iron, brain
irritability
Jamaica ginger paralysis
jaw jerk, abnormal
Jewish
konzo
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic acidemia
lathyrism
laughing, pathologic
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukopenia
Lhermitte's sign
liver disease
Lorenzo's oil
low back pain
Lyme disease
lymphadenopathy
lymphocytic pneumonitis
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
Maghreb
magnetic stimulation
magnetic stimulation, brain
malformation, vascular
malformation, vascular, treatment of
medulla oblongata, lesion of
meningeal enhancement
meninges
meningitis
meningitis, brucellosis
meningitis, CSF cell count-normal
meningomyelitis
meningovascular syphilis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
methylmalonic aciduria
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion, bilateral
Mills syndrome
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mononeuropathy multiplex
Morquio syndrome
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, demyelinating disease
MRI, emergent
MRI, false negative
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, T1 weighted high signal foci
MRI, target sign
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, chronic progressive
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sclerosis, prognosis
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
muscle cramp
muscle culture
muscle twitching
muscle wasting, diffuse
muscle weakness
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelofibrosis
myelogram
myelogram, thoracic
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myelopathy, hepatic
myelopathy, vacuolar
myeloradiculopathy
myocarditis
myoclonic jerks
myoclonus
myoclonus, epilepsy
nasal speech
Native Americans
neck pain
neck weakness
nerve biopsy
nerve conduction studies
nerve culture
nerve root enhancement
neurocutaneous disease
neuroendocrinology
neurogenic bladder
neuroichthyosis
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
neuropathy, vasculitic, systemic
neurosyphilis
neurotoxin
next-generation sequencing
night blindness
nitrous oxide
nystagmus
nystagmus, dissociated
nystagmus, rotary
nystagmus, vertical
occupational neurologic disorders
ochronosis
ocular motility, disorders of
oculodentodigital dysplasia
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
optic ataxia
optic atrophy
optic atrophy, hereditary
optic nerve, lesion of
oral ulcerations
orchitis
osteoarthrosis
osteomyelitis
osteopetrosis
osteoporosis
pain
pain, abdominal
pain, arm
pain, back
pain, foot
pain, leg
palatal myoclonus
pancytopenia
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, painful
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paraplegin
parathormone
parathyroid adenoma
paresthesias
Parkinson disease
Parkinsonism syndrome
past pointing
Pelizaeus Merzbacher
pericarditis
pernicious anemia
peroneal nerve palsy
peroneal nerve, lesion of
peroxisomal disease
personality change
pes cavus
phenylketonuria
phenylketonuria, adult onset
phlebotomy
pleocytosis of cerebrospinal fluid
poison, organophosphate
polycythemia, primary
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy, familial
pons, lesion of
portal caval shunt
posterior longitudinal ligament, ossification of
precocious puberty
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prion disease
prisoners of war, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proteinuria
pseudobulbar palsy
pseudomonas aeruginosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pursuit eye movements, abnormal
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation encephalopathy, delayed
radiation therapy, CNS treatment and complications with
radiculopathy
rash
Raynaud's phenomenon
release phenomena
renal stones
respiratory failure
reticulum cell sarcoma
retinitis pigmentosa
retrovirus
reversible neurologic disorder
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
risk factors
Romberg's sign
Rosenthal fibers
sarcoidosis
sarcoidosis, CNS
Saudi Arabia
Schilder's disease
schizophrenia
scissors gait
sclerae, hyperpigmented
scleroderma
scleroderma, neurologic involvement with
SCN1A gene
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
serologic testing
serologic testing of cerebrospinal fluid
short neck
short stature
sicca syndrome
sickle cell disease
Sjogren-Larsson syndrome
Sjogren's syndrome
skin, darkening of
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
somatosensory evoked potentials
spartin
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spastic paraplegia, type 15
spastic paraplegia, type 7
spasticity
spasticity, treatment of
spastin
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, biopsy
spinal cord, cervical
spinal cord, compression of
spinal cord, enlargement
spinal cord, herniation
spinal cord, infarction of
spinal cord, injury of
spinal cord, injury, management of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary
spinal cord, neoplasm, meningioma
spinal cord, pathologic exam of
spinal cord, vascular disorders Affecting
spinal cord, vascular malformation of
spinal xanthomatosis
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spirochete infection
splenomegaly
spondylolysis
spongy degeneration of brain
startle reaction
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stiff legs
striatonigral degeneration
striatonigral degeneration, infantile
striopallidodentate calcifications, familial idiopathic
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subcortical U fibers
substantia nigra
symmetric brain lesions
syndactyly
syphilis, meningomyelitis
syphilis, neurologic complications with
systemic illness
tachycardia
teeth, abnormal
tendon, enlarged
testicular atrophy
tetanus
thalamus, lesion of
thalassemia
thrombocytopenia
tick bite
tinnitus
titubation
toe walking
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
toxins, nervous system
transposition of the great vessels
trauma
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, spinal
tuberous sclerosis
undiagnosed
urinary frequency
urinary incontinence
urinary urgency
urine, dark
vasculitides
vertigo
vibratory sensation, abnormal
viral infection
viral infection, CNS
viral isolation
visual acuity, decreased
visual evoked response
visual loss
walking frame
walking, difficulty with
war
weakness
weakness, progressive
weight loss
Werdnig-Hoffman disease
Werner's syndrome
West disease
Western immunoblot test
wheelchair
white matter disease
wide based gait
xanthoma, tendon
x-linked hydrocephalus
x-ray, spine
 		Showing articles 300 to 350 of 2156 << Previous Next >>

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Retroviruses in the Nervous System:Neurological Involv in AIDS
Neurological Disorders Assoc with HTLV-I, NIH Symposium (Suppl) , Ann Neurol 23:S1-S2178., , 1988

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Familial Cases of HTLV-I-Associated Myelopathy
Ann Neurol 22:601-605, Miyai,I.,et al, 1987

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Retrovirus-Associated Myelopathies
Arch Neurol 44:659-663, Roman,G.C., 1987

Tropical Spastic Paraparesis Associated with Human T Lymphotropic Virus Type I in an East African Naturalised in Sweden
BMJ 295:1380-1381, Ryberg,B.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Cranial Magnetic Resonance Imaging in the Evaluation of Myelopathy of Undetermined Etiology
Neurol 37:840-843, Miska,R.M.,et al, 1987

Radiculomeningeal Vascular Malformations of the Spine:MR Imaging
Radiology 164:845-849, Nasaryk,T.J.,et al, 1987

Clinicopathological Conference
Paget's Disease of Bone, Giant-Cell Reparative Granuloma, Case 1-1986, NEJM 314:105-11386., , 1986

Neurologic Sequelae of Chronic Solvent Vapor Abuse
Neurol 36:698-702, Hormes,J.T.,et al, 1986

Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Pyramidal Tract Deficits & Polyneuropathy in Hyperthyroidism
Am J Med 78:1041-1044, Fisher,M.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Dominant Chondrodysplasia Punctata with Neurologic Symptoms
Neurol 33:1095-1097, Curless,R.G., 1983

Multiple Sclerosis After Age 50
Neurol 33:1537-1544, Noseworthy,J.,et al, 1983

Multifocal Central Nervous System Damage Caused by Toluene Abuse
Neurol 33:1337-1340, Lazar,R.B.,et al, 1983

Coma & Thyrotoxicosis
Ann Neurol 14:689-690, Newcomer,J.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Paraparesis in Hereditary Multiple Exostoses:Case Report
Neurol 29:973-977, Ferrari,G.,et al, 1979

Hereditary-Multiple Exostoses With Myelopathy
Arch Neurol 36:714, Ho,S.U.,et al, 1979

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

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

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

Pediatric Neurology
Psych Annals 2:1, , 1972

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

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

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

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

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

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

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

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

Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
JAMA Neurol 81:939-946, Kaplitt,M.G.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024



Showing articles 300 to 350 of 2156 << Previous Next >>