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Differential
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aciduria
acquired immunodeficiency syndrome
acrocyanosis
acute ataxia of childhood
acute cerebellar ataxia
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
advances in neurology
affect, inappropriate
Africa
aggression
agitation
Aicardi-Goutieres syndrome
akinetic mute
alcohol
alcohol intolerance
alcohol, neurologic complications with
alcoholism
alopecia
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alveolar hypoventilation
amimia
aminoacidurias
anemia
anemia, hemolytic
Angelman syndrome
angiitis
angiitis, granulomatous of CNS
ankle, swelling of
anomic aphasia
anorexia
antibiotics, neurologic complications with
anxiety
aphasia
aphasia, children
aphasia, classification of
aphasia, recovery from
aphonia
apraxia, speech
areflexia
arylsulfatase A
ascending paralysis
ascites
aspiration
asterixis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ATP1A3 gene
attention deficit disorder with hyperactivity
attention span
atypical
audiologic test to localize site of pathology
audiology
auditory dominance
auditory processing, impaired
autism
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
behavior, combative
behavioral disorder
Benedict's solution test
benign essential tremor
bifid uvula
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
blindness
blood brain barrier
body image
bone marrow transplantation
botulinum toxin
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
bruxism
burning feet
burning feet, differential diagnosis of
CAG repeats
calcification, intracranial
calf hypertrophy
carcinoma
cardiomyopathy
carpo-pedal spasm
cassava
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, dense artery sign
catatonia
celiac disease, adult
Central America
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar lesion
cerebellar mutism
cerebellar vermis
cerebellitis
cerebellum, disease of
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral dominance
cerebral embolism
cerebral embolism, mechanical extraction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, young adult
Chagas'disease
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chilbran skin lesions
children
choking
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 7
cirrhosis
cirrhosis, causes of childhood
cleft palate
Clinical Pathologic Conference(C.P.C.)
clonus
clot retrieval
cochlear implant
cognition
cognitive delay
coma
comorbidities
complications
confusion
congenital bilateral perisylvian syndrome
congenital myasthenic syndromes
conjunctival biopsy
consanguinity
contractures, joint
conversion reaction
coronavirus
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cough
COVID-19
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying
crying, pathologic
cultured skin fibroblasts
cyanide poison
cytomegalic inclusion disease
cytomegalovirus infection
deafness
deafness, congenital
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, childhood
demyelinating disease
dense basilar artery sign
dense middle cerebral artery sign
dentate nuclei
dentate nuclei, lesion of
depression
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
dialysis
dialysis dementia
diarrhea
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disconnection syndrome
doll's head maneuver
dopa responsive dystonia
drooling
drought
dysarthria
dysdiadochokinesia
dysequilibrium syndrome
dyskinesia
dyskinesia, buccal lingual facial
dyslexia
dysmorphic
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, laryngeal
dystonia, painful
dystonia, treatment of
dystrophin
DYT1 mutation
echolalia
EDTA(ehtylenediamine tetraacetic acid)
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, sleep
electromyogram
electron microscopy
ELISA
embolism, paradoxical
embolism, vertebral-basilar artery
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
encephalopathy, parainfectious
encephalopathy, progressive
endovascular therapy
enuresis
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
epileptic encephalopathy
epsilon sarcoglycan gene
equinovarus
exome sequencing
eye movement, disorders of
eyedness
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
fish
fluctuate
fluorescene in situ hybridization
folic acid
footedness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal lobe, pathologic signs of
fucosidosis
fungal infection, CNS
gait disorder
gait, apraxic
galactorrhea
gastroenteritis
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycosuria
Gowers maneuver
grasp reflex
gray hair
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Hallervorden Spatz disease
hallucination
hallucination, visual
hand deformity
handedness
hands, fisted
handwriting
head circumference
head injury
head injury, pediatric
head lag
headache
headache, vascular
hearing loss
hearing problems in children
heavy metal intoxication
heel-knee-shin test
hemiballismus
hemichorea
hemiparesis
hemiparesis, transient
hemiplegia
hemisensory loss
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
herpes virus
hippocampus
hoarseness
human immunodeficiency virus type 1
hydrocephalus
hydroxyglutaric aciduria
hyperactivity
hyperintense vessel sign
hyperkalemia
hyperosmolality
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypokinetic left ventricle
hyponatremia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
illusions
imbalance
immunodeficiency
immunosuppression
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
incoordination
industrial neurologic disorders
infection
infection, recurrent
infertility
insomnia
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intestinal biopsy
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
intracranial pressure, increased
intrauterine
iron, brain
irritability
jaundice
joint hypermobility
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
konzo
lactic acidemia
Landau-Kleffner syndrome
language
language delay
language development, neurologic basis of
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
liver disease
liver function enzymes
locked-in syndrome
Lyme disease
Lyme disease, children
lymphoma involving CNS
lysosomal storage disease
macrocephaly
macrognathia
magnetic source image
magnetoencephalography
malabsorption syndrome
manganese intoxication
maple syrup urine disease
marche a petits pas
masked facies
medulla oblongata, neoplasm of
medulloblastoma
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, CSF cell count-normal
meningitis, recurrent
meningoencephalitis
mental retardation
mental status, abnormal
MERCI trial
MERS
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methotrexate
microcephaly
micrographia
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
midline defect in children
migraine
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal antibodies
monoparesis
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, cardiac
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR, hyperintense vessels
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRI, serial
MRI, T1 weighted high signal foci
MRS
muscle cramp
muscle stiffness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myelinolysis, extrapontine
myelodysplasia
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoglobinuria
nasal speech
negative
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve biopsy
nerve conduction studies
neurofibromatosis 1
neurologic complications
neurologic complications of, burns
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic examination, focal
neurologic testing
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, sensory
neurotoxic
neurotoxicity, acute
neurotoxin
NMDA antagonists
non-dominant hemisphere
nonverbal
nystagmus
nystagmus, rotary
nystagmus, spontaneous
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
opisthotonus
optic atrophy
optic neuritis
osmotic demyelination syndrome
ovarian insufficiency
palatal myoclonus
palatopharyngeal incompetence
palilalia
pancytopenia
PANK2 mutation
papilledema
paralysis, acute
paralysis, acute areflexic
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
parietal lobe, syndromes of
Parkinson disease
Parkinson disease, freezing phenomena in
Parkinsonism syndrome
paroxysmal neurologic deficits
patent foramen ovale
penicillamine
penicillin
Penumbra System
peroxisomal disease
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
poison, mercury
poliosis
polyneuropathy
polyneuropathy, uremic
pons, infarction of
pons, lesion of
positional head-hanging test
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
prosopagnosia
protozoan infection
pruritus
pseudobulbar palsy
pseudocoma
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
psychosomatic disease
ptosis
ptosis, bilateral
pulmonary infection
pure word deafness
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
reading disorder, acquired
recurrent
release phenomena
remote effect of cancer on the nervous system
renal transplantation
renal tubular acidosis
respirations in CNS disease
respirator
restless leg syndrome
reticulum cell sarcoma
retina, abnormal
retinal detachment
retinitis pigmentosa
Rett's syndrome
reversible neurologic disorder
reversible splenial lesion syndrome
review article
rhabdomyolysis
rheumatic brain disease
rheumatic fever
rheumatic heart disease
riboflavin transporter deficiency
rigidity
risk factors
rituximab
rocking
rooting reflex
rotavirus
rubella encephalitis, progressive
saccadic eye movements, abnormal
salivation, excessive
Saudi Arabia
schizophrenia
scoliosis
sea-blue histiocytes
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, focus
seizure, psychosocial aspects of
seizure, recurrent
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
sexual behavior, disorder of
sign language
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
slurred speech
smiling
snout reflex
South America
spastic diplegia
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, loss of
speech, pressured
speech, slowed
spina bifida
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenium of corpus callosum
splenomegaly
spongy degeneration of brain
stammering
startle reaction
stereotaxic surgery
stereotyped behavior
stimulation, deep brain
stimulation, deep brain, bilateral
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuttering
stuttering following CVA
subdural hematoma
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
tandem gait, ataxic
tantrum
tauopathy
teeth, wide-spaced
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
testicular enlargement
tetany
thrombectomy
thrombus, mural
tick bite
tick paralysis
tinnitus
titubation
toe walking
tongue, impaired movements of
tongue, protrusion of
tonic foot response
tonic spasms
torticollis
toxoplasmosis, acquired
toxoplasmosis, CNS
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
tripping
Trousseau's sign
trypanosoma cruzi
tuberculosis
tuberculosis, miliary
tyrosine hydroxylase deficiency
upgaze, paralysis of
uremia
uremic encephalopathy
uremic twitching
uric acid, low
urine test for metabolic disorders
urine, dark
uveitis
vasculopathy
vertigo
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
violent behavior
viral infection
viral infection, CNS
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin supplementation
vitiligo
Vogt-Koyanagi-Harada syndrome
voice, abnormality of
Wada test
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weight loss
welder
Wernicke's aphasia
Wernicke's encephalopathy
wheelchair
white hair
white matter disease
wide based gait
word-finding difficulty
workup
wrist drop
writing
x-linked intellectual deficit
x-linked mental retardation
Showing articles 150 to 200 of 17990 << Previous Next >>

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

Infectious Mononucleosis: Rapid Evidence Review
Am Fam Physician 107:71-78, Sylventer,J.E.,et al, 2023

Cerebral and Retinal Infarction in Bicuspid Aortic Valve
J Am Heart Assoc 12:e028789, Huntley,G.D.,et al, 2023

A Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023

Clinicopath Conf, Chronic Salicylate Toxicity
NEJM 388:264-272, Case Record 2, 2023

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

COVID-19-Booster Vaccine-Induced Encephalitis
Acta Neurol Belg 122:579-581, Sluyts,Y.,et al, 2022

Imaging Findings in Children Presenting with CNS Nelarabine Toxicity
AJNR 43:1802-1809, Serrallach,B.L.,et al, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Atypical Presentation of Primary Angiitis of Central Nervous System Responsive to Rituximab
Stroke 53:e490-e494, Kesav, P.,et al, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

Recent Advances in the Diagnosis and Management of Cluster Headache
BMJ 376:e059577, Schindler, E. & Burish, M.J., 2022

Brain Tumors in Children
NEJM 386:1922-1931, Cohen, A.R., 2022

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

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,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

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,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

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

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

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

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

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Efficacy and Safety of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1
Neurol 98:e938-e946, Hwang, J.,et al, 2022

Contemporary Trends in the Nationwide Incidence of Primary Intracerebral Hemorrhage
Stroke 53:e70-e74, Bako, A.T.,et al, 2022

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

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
J Med Case Reports doi:10.1186/s13256-022-03299-6, Talukder,N.T.,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

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
Clin Exp Immunol 206:266-281, Bartels,F.,et al, 2021

Anti-NMDAR Encephalitis Presenting as Stroke-Like Episodes in Children: A Case Series from a Tertiary Care Referral Centre from Southern India
J Pediatr Neurosci 16:194-198, Gowda,V.K.,et al, 2021

Focal Cerebral Arteriopathy of Childhood, Clinical and Imaging Correlates
Stroke 52:2258-2265, Oesch,G.,et al, 2021

Determination of Brain Death
NEJM 385:2554-2561, Greer, D.M., 2021

Clinicopathologic Conference, Moyamoya Disease
NEJM 385:2563-2572, Case 40-2021, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,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

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021



Showing articles 150 to 200 of 17990 << Previous Next >>