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Differential
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acanthocytosis
Aicardi-Goutieres syndrome
algorithm
amyotrophic chorea-acanthocytosis
areflexia
ataxic gait
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, hemorrhage
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bicaudate index
biotin
blepharospasm
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, lesion of
calcification, intracranial
calcification, intracranial, rim
cardiac arrest
cardiac arrest and resuscitation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, hemorrhage of
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid, oligoclonal IgG in
children
chorea
chorea, familial
chorein
choreoathetosis
chromosomal abnormality
chromosome 19
cognition
coma
cortical infarction
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanide poison
cyst
cyst, parenchymal
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei, lesion of
differential diagnosis
disability rating scale, neurological
disability, neurological
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonic reaction, acute
electroencephalogram, focal delta activity
electromyogram
encephalitis, focal
encephalitis, Rasmussen's
encephalopathy
encephalopathy, anoxic
encephalopathy, post anoxic
enzyme, defect
failure to thrive
familial
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutaric acidemia
glutaric aciduria
gray matter
Huntington's chorea
Huntington's chorea, presymptomatic detection of
Huntington's disease, children
hydrocephalus
hyperreflexia
hyporeflexia
hypotension, systemic
hypotonia
hypoxia
hypoxic encephalopathy
inborn errors of metabolism
infantile bilateral striatal necrosis
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
lacunar infarction
laminar necrosis, cortical
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
Lesch-Nyhan syndrome
leukoencephalopathy
level of consciousness, decreased
lip, biting
lobar atrophy
mammillary bodies
McLeod syndrome
memory, impairment of
methanol intoxication
midbrain, lesion of
movement disorder
MRI
MRI, abnormal
MRI, gradient-echo
MRI, serial
MRI, susceptibility weighted
MRI, volumetry
multiple sclerosis
multiple sclerosis, plaque
myoclonus
myopathy
neurologic disease, diagnoses of
neuropathology
neuropathy
neurotoxin
nutritional deficiency
nystagmus
optic atrophy
optic nerve, lesion of
optic neuropathy
optic neuropathy, toxic
Parkinson disease, arteriosclerotic
Parkinsonism syndrome
periaqueductal lesion
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
putamen, lesion of
putamen, lesion of, bilateral
rigidity
screening
seizure
seizure, focal
seizure, intractable
self-mutilation
sensory nerve action potentials
single photon emission computed tomography
spasticity
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
thalamus, lesion of
thalamus, lesion of-bilateral
third ventricle, wall
tic
tongue, biting
treatment of neurologic disorder
trinucleotide repeats
ventriculostomy
vocalizations
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
Showing articles 50 to 100 of 2327 << Previous Next >>

Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
Neurol 103:e209489, Hartnett,P.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Occipital Condyle Syndrome
Neurol 103:e210067, Mirian,A.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
NEJM 391:2036-2046, Case 37-2024, 2024

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

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Primary Diffuse Leptomeningeal Melanocytosis, A Diagnoatic Conundrum
Neurol 101:e576-3580, Selvarajan,J.M.P.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

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

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 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

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

Trial of Globus Pallidus Focused Ultrasound Ablation in Parkinsons Disease
NEJM 388:683-693, 759, Krishna,V.,et al, 2023

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

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

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 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, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

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

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Neuroimaging Findings in CHANTER Syndrome
AJNR 43:1136-1141, Mallikarjun, K.S.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022



Showing articles 50 to 100 of 2327 << Previous Next >>