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Differential
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abdominal reflex, absent
abducens nerve paralysis
abscess, intracerebral
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
amenorrhea
ammonia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
ankle clonous
anomic aphasia
anterior spinal artery
antiviral agents
aphasia
areflexia
Arnold Chiari malformation
arteritis, temporal
arthralgia
asterixis
asterixis, causes of
asterixis, unilateral
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
atlanto-axial subluxation
atypical
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, infarction
behavioral disorder
bladder dysfunction
brain atrophy
brain biopsy
brain biopsy, false negative
brainstem, dysfunction
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
burning feet
burning paresthesia
camptocormia
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
central nervous system, infection of
cerebral edema
cerebritis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, amonia
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glutamine
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
complications
confusion
consanguinity
cornea, opacity of
coronavirus
corpus callosum, lesion of
cough
COVID-19
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
decerebrate posture
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
depression
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
diaphragmatic paralysis, causes of
differential diagnosis
digiti quinti sign
diplopia
disability, neurological
distal muscle weakness
drowsiness
dysarthria
dysmorphic
dysphagia
dyspnea
electrical sensation
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
emotional lability
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
ependymal
epidemiology of neurology
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
falling
fasciculation
fatigue
fever
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
genu valgum
girdle sensation
glutamine
gram negative rod
granulomatosis with polyangiitis
granulomatous disease
hand weakness
headache
headache, recurrent
headache, severe
hearing loss
hearing problems in children
hemianopia
hemiparesis
hepatic encephalopathy
hepatolenticular degeneration, non-Wilsonian
Hispanics
Horner's syndrome
horse bite
hypercapnia
hyperreflexia
hypersegmented polys
hypertension
hypothalamus
hypothalamus, disturbance of
hypothermia
hypothermia, causes of
imbalance
incontinence, fecal
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
kyphoscoliosis, neurologic causes of
leg weakness, bilateral
lethargy
leukodystrophy
leukopenia
Lhermitte's sign
lymphadenopathy
lymphadenopathy, hilar
lymphoma involving CNS
lymphomatoid granulomatosis
lysosomal storage disease
mediastinum, lymph-node biopsy
mediastinum, mass of
medulla oblongata, lesion of
memory, impairment of
meningeal enhancement
meningitis
meningitis, bacterial
meningitis, brucellosis
meningitis, pneumococcal
mental retardation
mental status, abnormal
midbrain, lesion of
middle cerebellar peduncle, lesion
Mills syndrome
molecular genetics
mononeuropathy multiplex
Morquio syndrome
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, linear enhancement
MRI, nodular enhancement
MRI, ring sign
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
mucopolysaccharidoses
multiple sclerosis
muscle biopsy
muscle cramp
muscle weakness
myelitis, longitudinal
myelomalacia
myelopathy
myelopathy hand
nausea and vomiting
neck stiffness
neck weakness
nerve root enhancement
neuroendocrinology
neurogenic bladder
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neuropsychiatry
nystagmus
nystagmus, dissociated
nystagmus, vertical
ophthalmoplegia
optic nerve
optic nerve, lesion of
optic neuropathy
orthostatic hypotension
osteoporosis
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, hemiparesis in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
pernicious anemia
pes cavus
pituitary stalk
pituitary stalk, lesion of
pleocytosis of cerebrospinal fluid
posterior column disease
posterior leukoencephalopathy syndrome
postural abnormality
prognosis
progressive neurologic disorder
proprioception, abnormal
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyramidal tract dysfunction, unilateral
quadriparesis
rash
recurrent
remdesivir
renal failure
respiratory failure
retinal degeneration
retinal exudates
retinopathy
retropulsion
reversible neurologic disorder
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
risk factors
sarcoidosis
sarcoidosis, CNS
Saudi Arabia
scoliosis
scotoma
seizure
seizure, children
sensorineural hearing loss
sensory loss
sensory loss, cutaneous
short neck
short stature
skin, lesions in neurologic disorders
slow virus infection of CNS
spasticity
spinal cord
spinal cord, compression of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, pathologic exam of
splenomegaly
spongy degeneration of brain
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
syringomyelia
temporal lobe, lesion
temporal lobe, lesion, bilateral
thrombocytopenia
tinnitus
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
unconsciousness
urinary frequency
urinary incontinence
urinary urgency
vaccination, neurologic complications with
ventricular enlargement
vertigo
vertigo, episodic
vibratory sensation, abnormal
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
vitamin deficiency
weakness
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
wide based gait
zoonoses
Showing articles 0 to 50 of 5803 Next >>

Fewer COVID-19 Neurological Complications with Dexamethasone and Remdesivir
Ann Neurol 93:88-102, Grundmann,A.,et al, 2023

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020

A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
Neurol 86:e28, Lincoln, M.R.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

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

Depression-Induced Neurologic Dysfunction
NEJM 305:642, Brumback,R.A.,et al, 1981

The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

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

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,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

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

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

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

An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018



Showing articles 0 to 50 of 5803 Next >>