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abiotrophy
adult polyglucosan body disease
advance directives
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anti IgLON5
apnea
areflexia
arm weakness
aspiration
autoantibodies
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, lesion of
behavioral disorder
BiPAP
bladder dysfunction
botulinum toxin
brain atrophy
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
C9orf72
CAG repeats
camptocormia
CAT scan, abnormal
CAT scan, emission, abnormal
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
coma, episodic
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
disability, neurological
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
encephalitis
encephalitis, autoimmune
encephalomyelitis
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
fibrillations
fine motor function, impaired
flaccid paralysis
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gag reflex, depressed
gait disorder
gait, spastic
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
gynecomastia
hand weakness
hearing loss
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
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hyperreflexia
hypersomnia
hypertension
hypophonia
hyporeflexia
hypotension, systemic
imbalance
immunotherapy
inclusion bodies
intellectual deficit
intellectual deterioration
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Jewish
Kugelberg-Welander syndrome
laughing
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukoencephalopathy
life expectancy
liver disease
lobar atrophy
locked-in syndrome
masseter muscle weakness
memory, defect of recent
memory, impairment of
Mills syndrome
mimics
misdiagnosis
molecular genetics
mortality
motor neuron disease
motor neuron disease, misdiagnosis
MRI
MRI, abnormal
multiple sclerosis, differential diagnosis of
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muscle wasting, diffuse
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muscle weakness, proximal
muscular dystrophy
mutism
myelomalacia
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myocardial injury
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myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
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neuroendocrinology
neurogenic bladder
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optic atrophy
pain
pain, management of chronic
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polyglucosan body
polyglucosan body disease
polymerase chain reaction
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practice guidelines
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progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
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pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiculopathy
REM sleep behavior disorder
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
review article
riluzole
risk factors
saccadic eye movements, abnormal
salivation, excessive
sensorineural hearing loss
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
tandem gait, ataxic
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
vestibular function, tests of
vocalizations
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
West Nile fever
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 450 to 500 of 2707 << Previous Next >>

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

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

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
Neurol 104:e213519, Ioannidis,S.,et al, 2025

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

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

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

Automated Detection of Normal Pressure Hydrocephalus Using CT Imaging for Calculating the Ventricle-to-Subarachnoid Volume Ratio
AJNR 46:141-146, Knittel,J.J.,et al, 2025

Automated Idiopathic Normal Pressure Hydrocephalus Diagnosis via Artificial Intelligence-Based 3D T1 MRI Volumetric Analysis
AJNR 46:33-40, Lee,J.,et al, 2025

Bilaterally Symmetrical Globus Pallidus Infarction
Ann Neurol 97:254-255, Chen,L.,et al, 2025

Black Turbinate Sign as an Early Clue of Rhino-Orbital-Cerebral Mucormycosis
Neurol 104:e210202, Xie,J.S.,et al, 2025

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

A 66-Year-Old Female Patient with Rapidly Progressive Memory Changes
Neurol 105:e214211, Fokas,J.A.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

Intercostal Muscle Wasting is the Clue to a Diagnosis of Diabetic Thoracic Radiculopathy
Neurol 105:e214290, Lau,T.M. & Coebergh,J.A., 2025

Clinicopathologic Conference, Diffuse Meningeal Melanomatosis
NEJM 393:2152-2162, Case 34-2025, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

Complex Regional Pain Syndrome
NEJM 393:2338-2348, Goebel,A., 2025

A 27-Year-Old Man with Progressive Bilateral Vision Loss Resistant to Steroid Therapy
Neurol 105: e213897, Zhang,W.,et al, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025



Showing articles 450 to 500 of 2707 << Previous Next >>