Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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
areflexia
arm weakness
aspiration
Babinski sign
basal ganglia, lesion of
BiPAP
botulinum toxin
Brugada syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
CAG repeats
camptocormia
cerebral cortex
cerebral cortical atrophy
chewing, impaired
Clinical Pathologic Conference(C.P.C.)
clonus
complications
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentatorubral-pallidoluysian atrophy
diabetes mellitus
differential diagnosis
distal muscle weakness
DNA probes
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
emotional lability
epidemiology of neurology
familial
fasciculation
fatigable chewing
fatigue
fibrillations
flail arm syndrome
foot drop
fragile-X syndrome
frontal lobe, atrophy
gag reflex, depressed
gastrostomy
gastrostomy, percutaneous endoscopic
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
hand weakness
hemiparesis
heralding manifestation
hoarseness
hospice
huntingtin
Huntington's chorea
hyperreflexia
hypertension
hyporeflexia
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
jaw clonus
jaw closure weakness
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg weakness, unilateral
life expectancy
liver disease
lobar atrophy
masseter muscle weakness
Mills syndrome
mimics
misdiagnosis
molecular genetics
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
myocardial injury
myocytolysis
myopathy
myotonia dystrophica
nasal speech
neck weakness
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuronal migration disorder
neuronopathy
neuropathology
neuropathology, brain
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
pain
pain, management of chronic
palliative care
paraparesis, spastic
polymerase chain reaction
polymyositis
practice guidelines
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pyramidal tract dysfunction
quality of life
repetitive nerve stimulation
respirator
respiratory failure
review article
riluzole
risk factors
salivation, excessive
sleep
sleep pathology and physiology
spasticity
speech disorder
spinal muscular atrophy
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
sudden death
temporal lobe, atrophy
temporalis muscle wasting
testicular atrophy
tongue, atrophy
tongue, fasciculations of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weight loss
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 350 to 400 of 2602 << Previous Next >>

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

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

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

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

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

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

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

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 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

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

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

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,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

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

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

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

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

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

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

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

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

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

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

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 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

Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
Neurol 103:e209883, Maya-Gonzalez,C.,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



Showing articles 350 to 400 of 2602 << Previous Next >>