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Differential
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airway obstruction
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
analgesic
anxiety
aqueduct of Sylvius, stenosis
aqueductal stenosis
asymptomatic
ataxia
atrioventricular block
basal ganglia, calcification of
behavioral disorder
benzodiazepine
blindness
bradycardia
bruit, supraclavicular
calcification, intracranial
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
cerebellar hypoplasia
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cervical spine injury
cervical spondylosis
chronic progressive external ophthalmoplegia
claudication, extremity
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
concussion
contractures, joint
controversies in neurology
cornea, opacity of
corpus callosum
corpus callosum, thinning
cortical muscular atrophy
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
dementia, frontotemporal
dementia, presenile
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diplopia
dying
dyspnea
dyspraxia
dystonia
electromyogram
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, progressive
ethics in neurology
euthanasia
evidence-based research
evoked potentials
exercise intolerance
exercise-induced vascular symptoms
facial weakness, bilateral
familial
fasciculation
fetal movements, reduced
fetus
fibrillations
floppy infant
foot drop
frontal lobe, atrophy
gene mutation
genetic counselling
genetic neurologic disorders
glioma
gray matter
head injury
headache
hearing loss
heart block
heart block, complete
heart murmur
hemiplegia
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
high arched feet
histochemistry
histochemistry of muscle
hospice
hunger
hydrocephalus
hydrocephalus, congenital
hypotonia
hypotonia, infants
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
Leigh's disease
leukodystrophy
life sustaining treatment
lissencephaly
lobar atrophy
locked-in syndrome
malformation, CNS, congenital
medical-legal aspects of neurology
MELAS syndrome
mental retardation
merosin
MERRF syndrome
micrognathia
micropthalmia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monomelic amyotrophy
morphine
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, susceptibility weighted
MRS
multiple sclerosis
multiple sclerosis, diagnosis of
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelopathy
myoclonus
myopathy
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
negative
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuroophthalmology
neuropathology, brain
neuropathy
normal
ophthalmoplegia
optic atrophy
optic neuropathy
oxygen therapy
pacemaker, cardiac-transvenous
palliative care
pancytopenia
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinsonism syndrome
personality change
physician assisted suicide
pigmentary retinopathy
polyneuropathy
positive sharp waves
practice guidelines
prognosis
progranulin
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pyramidal tract
quality of life
ragged-red fibers
release phenomena
respiratory failure
retinal detachment
retinal dysplasia
retinopathy
review article
right to die
sedation
seizure
sensorineural hearing loss
short stature
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spinal cord, compression of
spinal cord, injury of
sternocleidomastoid muscle
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subclavian artery stenosis
suck, poor
sudden death
symmetric brain lesions
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
temporalis muscle wasting
term infant
thoracic outlet syndromes
toe walking
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
ultrasonography
upgaze, paralysis of
valium
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, progressive
weight loss
white matter disease
white matter disease, periventricular
winging of scapula
Showing articles 0 to 50 of 9131 Next >>

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Pseudoneurogenic Thoracic Outlet Syndrome
Muscle & Nerve 17:242-244, Simpson,D.M., 1994

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

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

Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
NEJM 390:522-529, Strong, N.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
Neurol 103:e209586, Taborda,M.H.,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

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

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

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

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

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

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

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



Showing articles 0 to 50 of 9131 Next >>