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Differential
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abdominal muscle paralysis
acetylcholine receptor antibody
acid maltase deficiency
acid maltase deficiency, adult
ACTH, ectopic syndrome of
Addison's disease
advances in neurology
algorithm
alveolar hypoventilation
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
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, treatment of
amyotrophic lateral sclerosis-like syndrome
anemia
anesthesia, general
ankle edema
anosmia
anterior horn cell disease
anterior interosseous neuropathy
anterior tibial muscle weakness
aphonia
apnea
areflexia
arrhythmia, cardiac
arsenic
arthrogryposis multiplex
ascending paralysis
aspiration
asthma
asthma, poliomyelitis-like syndrome with
asymptomatic
ataxia, cerebellar
ataxia, sensory
ataxic gait
atrioventricular block
autoantibodies
autoimmune disease
azathioprine
BAL
baldness
basal ganglia, infarction
basophilic stippling of red blood cells
benign congenital hypotonia
bitemporal visual field defect
bone marrow suppression
brachial neuritis
brainstem, lesion of
bulbar palsy
bulbar palsy, acute
bulging of biceps
burning feet
burning paresthesia
cachexia
CAG repeats
calcification, intracranial
calf atrophy
calf hypertrophy
carcinoma
carcinoma of lung
cardiomegaly
cardiomyopathy
cardiovascular disease
carpo-pedal spasm
cataracts
central core disease
cerebellar degeneration
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
Charcot-Marie-Tooth
chewing, impaired
children
chromosomal abnormality
chromosome 17
chromosome 19
chromosome 5
chromosome 9
chronic polyneuritis, children
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
collagen vascular disease
coma
complications
compression neuropathy
concussion
conduction block
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
coronavirus
cortical hand knob
cost
cost effectiveness
COVID-19
coxsackievirus
coxsackievirus, myopathy with
CPAP
craniopharyngioma
creatine phosphokinase(CPK)elevated
critical illness
Cushing's syndrome
cystinosis
degenerative diseases of CNS
delay in diagnosis
dementia
dermatitis
dermatomyositis
desmin
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diaphragmatic paralysis
diarrhea
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dropped head syndrome
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dysphonia
dyspnea
dystrophic calcification
dystrophin
edema, pedal
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
encephalitis, brainstem
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
eosinophilia
epidemiology of neurology
erythrocyte
evidence-based research
evoked potentials
exercise
exophthalmus
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
familial
fasciculation
fatigable chewing
fatigue
Fazio-Londe's disease
fibrillations
fine motor function, impaired
finger drop
finger flexor weakness
finger weakness
fingernails, abnormal
flaccid paralysis
floppy infant
foot deformity
foot drop
foot drop, bilateral
fracture, long bone
fragile-X syndrome
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gastrocnemius muscle weakness
gastroenteritis
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guyon's canal
gynecomastia
hallucination
hallucination, auditory
hammertoes
hand deformity
hand weakness
Hand-Schuller-Christian disease
head injury
headache
heart block
heart block, complete
heavy metal intoxication
hemidiaphragm, paralysis of
hemoglobinuria
hepatitis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
high arched feet
high arched palate
histochemistry
histochemistry of muscle
hoarseness
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
hyperadrenalism
hyperamylasemia
hypercalcemia
hypercapnia
hyperinsulinism
hyperkalemia
hyperkeratosis
hyperparathyroidism
hyperreflexia
hypertension
hyperthyroidism
hypoglycemia
hypokalemia
hypokalemic alkalosis
hypokalemic periodic paralysis
hyponatremia
hypoparathyroidism
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
hypoxic encephalopathy
imbalance
immunohistochemistry
immunologic disease
immunosuppressive agents
inability to sit up
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intermittent positive pressure breathing
intrinsic hand muscles, wasting of
islet cell tumor
klippel feil syndrome
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
leg weakness, bilateral
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukopenia
level of consciousness, decreased
lid closure, weakness of
life expectancy
liver disease
liver function enzymes
lordosis
median neuropathy
Mees lines
MELAS syndrome
mental retardation
methotrexate
middle cerebral artery, occlusion of
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
monoparesis
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, muscle
multiple myeloma
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle strength, testing
muscle swelling
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, treatment of
myasthenic crisis
myelopathy
myelopathy, carcinomatous
myelopathy, chronic progressive
myocarditis
myoedema
myopathy
myopathy, amyloid
myopathy, autoimmune
myopathy, carcinomatous
myopathy, centronuclear
myopathy, desmin
myopathy, distal
myopathy, distal Laing
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, inflammatory
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, neurogenic hypothesis of
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nasal speech
nausea and vomiting
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, hormone producing
neoplasm, hormone producing, ectopic
neoplasm, pituitary
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
nerve hypertrophy
neuritis, causes of
neuritis, heavy metals causing
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal migration disorder
neuronopathy
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, toxic
newborn, evaluation of
next-generation sequencing
nusinersen
occipital lobe, infarction
occipital lobe, lesion of
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, total
Oppenheim muscular dystrophy
orthopnea
osteomalacia
overlap syndrome
pain
pancreatitis
pancytopenia
pandemic
papilledema
paranoia
paraparesis
paraplegia
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias, feet
paresthesias, hands
percussion induced muscle contraction
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
pes cavus
pheochromocytoma
phosphorylase b kinase deficiency
phrenic nerve pacemaker
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
poison, mercury
poison, neurologic problems with
poliomyelitis
poliomyelitis-like illness
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, variant form
polyneuropathy, chronic inflammatory demyelinating-pure motor syn
polyneuropathy, chronic inflammatory demyelinating-sens atax var
polyneuropathy, chronic inflammatory demyelinating-variant forms
polyneuropathy, familial
porphyria
position sensation, abnormal
positive sharp waves
post polio syndrome
posterior interosseous neuropathy
pregnancy, neurologic complications in
primary aldosteronism
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proprioception, abnormal
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
psychosis
ptosis
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
quality of life
rash
remote effect of cancer on the nervous system
renal stones
repetitive nerve stimulation
respirator
respiratory depression
respiratory failure
review article
RFLPs
rheumatoid arthritis
Romberg's sign
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
serologic testing
severe acute respiratory syndrome
short stature
skin, lesions in neurologic disorders
sleep apnea
slit lamp examination
SMN1 gene
spinal cord, injury of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar degeneration
standing difficulty
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
survival motor neuron gene
sweating, abnormality of
syringomyelia
tandem gait, ataxic
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
tetany
thoracic outlet syndromes
thrombocytopenia
thyrotoxicosis
titinopathy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trigger finger
trinucleotide repeats
Trousseau's sign
ulnar neuropathy
uremia
urine test in toxic screen
vasculitides
viral infection
viral infection, CNS
visual evoked response
vital capacity
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1200 to 1250 of 2033 << Previous Next >>

Distribution of Atherosclerosis and Risk Factors in Atherothrombotic Occlusion
Stroke 24:206-211, Yasaka,M.,et al, 1993

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
Lancet 341:265-268, Couratier,P.,et al, 1993

Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
Neurol 43:438-443, Moss,A.H.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Inclusion Body Myositis Presenting Solely as Dysphagia
Neurol 43:1241-1243, Riminton,D.S.,et al, 1993

Acute Myopathy Associated with Large Parenteral Dose of Corticosteroid in Myasthenia Gravis
JNNP 56:702-704, Panegyres,P.K.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Clinicopath Conf
Axonal Polyneuritis Assoc with IgA Lambda Multiple Myeloma, Case 21-1993, NEJM 328:1550-1558993., , 1993

Unilateral Amnesic Stroke:Six New Cases and a Review of the Literature
Stroke 24:1033-1042, Ott,B.R.&Saver,J.L., 1993

The Etiology of Posterior Circulation Infarcts:A Prospective Study Using MRI & MRA
Neurol 43:1528-1533, Bogousslavsky,J.,et al, 1993

Acute Neuromuscular Respiratory Paralysis
JNNP 56:334-343, Hughes,R.A.C.&Bihari,D., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Human Immunodeficiency Virus Type 1 Infection and Myopathy:Clinical Relevance of Zidovudine Therapy
Ann Neurol 34:206-211, Grau,J.M.,et al, 1993

Myopathies Assoc with HIV and Zidovudine:Can Their Effects be Distinguished?
Neurol 43:971-976, Simpson,D.M.,et al, 1993

Opportunistic Cerebral Vasculopathy & Stroke in Patients with Acquired Immunodeficiency Syndrome
Arch Neurol 50:430-432, Kieburtz,K.D.,et al, 1993

MRI Changes in Intracranial Hypotension
Neurol 43:919-926, Pannullo,S.C.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Fulminant Rhabdomyolysis in a Patient with Dermatomyositis
Neurol 43:844-845, Caccamo,D.V.,et al, 1993

Drug Therapy of Idiopathic Inflammatory Myopathies:Response to Prednisone Azathioprine, & Methotrexate
Am J Med 94:379-387, Joffe,M.M.,et al, 1993

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Thrombotic Occlusion of the Middle Cerebral Artery
Stroke 23:1761-1766, Ueda,S.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992

Cortical Blindness after Nifedipine Treatment
BMJ 305:693, Morton,C.&Hickey-Dwyer,M., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Centrum Ovale Infarcts:Subcortical Infarct in the Territory of Middle Cerebral Art
Neurol 42:1992-1998, Bogousslavsky,J.&Regli,F., 1992

Cerebral Infarction in a Heterozygote with Variant Antithrombin III
Stroke 23:1822-1825, Arima,T.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992



Showing articles 1200 to 1250 of 2033 << Previous Next >>