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acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
anterior horn cell disease
anterior tibial muscle weakness
antiviral agents
apraxia of eye movements
areflexia
arm atrophy
arm weakness
arthrogryposis multiplex
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
brachial amyotrophic diplegia
Brugada syndrome
bulbar palsy
bulbar palsy, progressive
CAG repeats
calf hypertrophy
carcinoembryonic antigen
carcinoma
CD4 counts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
Clinical Pathologic Conference(C.P.C.)
clinodactyly
coma
complications
congenital heart disease
congenital myopathy
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
denervation of muscle
denervation potentials
dentatorubral-pallidoluysian atrophy
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
diplegia, brachial
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dysphagia
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
fragile-X syndrome
Friedreich's ataxia
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
gynecomastia
heavy metal intoxication
heralding manifestation
highly active antiretroviral therapy
history of neurology
human immunodeficiency virus type 1
huntingtin
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
jaw closure weakness
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
Man-In-The-Barrel syndrome
masseter muscle weakness
mental retardation
misdiagnosis
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myeloradiculopathy
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myopathy, quadriceps
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal degeneration
neuronal migration disorder
neuronopathy
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
newborn, evaluation of
nusinersen
ocular motility, disorders of
Parkinson disease
pathology
patient information and support
peroneal muscle atrophy, causes of
placebo
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymyositis
polyneuropathy
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
radiation hypersensitivity
radiculopathy
Refsum's disease
respiratory failure
retrovirus
review article
RFLPs
risdiplam
risk-benefit assessment
Roussy Levy syndrome
safety
scoliosis
scoliosis, neurologic association with
screening
skin, lesions in neurologic disorders
SMN1 gene
spinal cord
spinal cord degeneration
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
sudden death
survival motor neuron gene
telangiectases
term infant
testicular atrophy
tongue, fasciculations of
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
viral infection
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 600 to 650 of 7326 << Previous Next >>

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

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

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Postradiation Motor Neuron Syndrome
Arch Neurol 33:786, Sadowsky,C.H.,et al, 1976

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Frequency of Nerve Fiber Degeneration of Peripheral Motor & Sensory Neurons in Amyotrophic Lateral Sclerosis
Neurol 25:781, Dyck,P.J.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Poliomyelitis-A Persistent Problem
NEJM 288:370, Weinstein,L., 1973

Neuropathy in Thyrotoxicosis-Correspondence-NEJM 289:219
1973., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Reversible Forms of Motor Neuron-Disease:Lead"Neuropathy"
Neurol 22:446, Boothby,J., 1972

Amyotrophic Lateral Sclerosis
Richard Kisonak, Associated Press, Boston Globe Apr 30972., , 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Neurological Disorders in Patients Following Surgery for Peptic Ulcer
Neurol 22:450, Hoffman,P., 1972

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Muscular Quivering
BMJ 3, 1972 Jan., , 1972

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

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

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

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,



Showing articles 600 to 650 of 7326 << Previous Next >>