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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
alopecia
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, familial
amniocentesis
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anasarca
anesthesia, general
anterior interosseous neuropathy
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticoagulant, treatment
anticoagulant, treatment in CVD
anticonvulsants
anticonvulsants, untoward effects of
antihistamines
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
aspirin
asymptomatic
ataxia
ataxia, paroxysmal
atelectasis
atrioventricular block
audiogram
auditory evoked brainstem potentials
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
baldness
basal ganglia, calcification of
botulism
brachial neuritis
bradycardia
brainstem, lesion of
cachexia
CAG repeats
calcification, intracranial
calcium antagonist
calcium channel dysfunction
cancer of colon
carbamazepine
carbamazepine, toxicity
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
cerebral blood flow
cerebral embolism
cerebral embolism, cardiac origin
cerebral ischemia
cerebrovascular accident
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
cholestasis
chromosomal abnormality
chromosome 19
chromosome 3
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
complications
compression neuropathy
conduction block
confidentiality
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
corneal dystrophy
corpus callosum
corpus callosum, thinning
coumarin
creatine phosphokinase(CPK)elevated
defibrillator, implanted
degenerative diseases of CNS
dementia, thalamic
dentatorubral-pallidoluysian atrophy
dermatomyositis
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
dilantin
dilantin, toxicity
diplopia
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dysphagia
echocardiogram
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
electronystagmography
electronystagmography, abnormal
electrophoretic pattern, serum
electroretinograph
embolism
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
epidemiology of neurology
erythrocyte
evoked potentials
exercise
exercise electrocardiography
eye closure
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
falling
false negative
familial
familial hemiplegic migraine
Fazio-Londe's disease
floppy infant
fluorescein angiography
fragile-X syndrome
Friedreich's ataxia
frontal balding
F-wave response
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glucose tolerance test, abnormal
gray matter
Guillain Barre syndrome
Guyon's canal
hand weakness
hearing loss
heart block
heart block, complete
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
H-reflex testing
huntingtin
Huntington's chorea
hydrocephalus
hydrops fetalis
hypercapnia
hyperinsulinism
hyperkalemic periodic paralysis
hyperostosis
hyperparathyroidism
hypersomnia
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
intellectual deficit
intelligence quotient
iris, abnormal
kaliuresis
Kearns-Sayre syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
lid abnormalities
lid closure, weakness of
lid retraction, lower
life expectancy
lordosis
malignancy screen
malignant hyperpyrexia
manic-depressive
median neuropathy
Melkersson's syndrome
mental retardation
metabolic acidosis
mexiletine
microcephaly
micrognathia
migraine
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
modafinil
molecular genetics
mononeuropathy
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, functional
MRI, muscle
MRS
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myasthenic syndrome
myocarditis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, proximal
myopathy, thyroid disease causing
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonia, causes of
myotonia, treatment of
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuritis, causes of
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic vs.myopathic atrophy
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuronal migration disorder
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
nifedipine
ocular myopathy
oculovestibular reflex
ophthalmoplegia
optic atrophy
orbicularis oculi muscle
orbit, lesions of
ovarian tumor
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
physical activity
platelet inhibiting drugs
pleural effusion
pneumonia
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
polyneuropathy
porphyria
posterior interosseous neuropathy
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prevention of neurologic disorders
procainamide
prognosis
proptosis
proximal myotonic myopathy
psychological testing
ptosis
ptosis, bilateral
pulmonary function tests
radionuclide angiocardiography
recombinant DNA
respiratory failure
review article
RFLPs
rhabdomyolysis
risk factors
saccadic eye movements
saccadic eye movements, abnormal
safety
sarcoidosis
screening
seizure
sensorineural hearing loss
single photon emission computed tomography
sleep apnea
slit lamp examination
sodium channel dysfunction
somnolence
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 6
spinocerebellar degeneration
stiff man syndrome
sudden death
taurine
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thoracic outlet syndromes
thyrotoxicosis
tocainide
torticollis
transient ischemic attack
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
twins
ulnar neuropathy
ultrasonography
ventricular tachycardia
viral infection, CNS
visual evoked response
weakness
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
white matter disease
white matter disease, periventricular
workup
X-linked bulbospinal neuronopathy
Showing articles 350 to 400 of 797 << Previous Next >>

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

Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

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

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

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

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 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 Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,J.,et al, 2023

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 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

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

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

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

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

Bilateral Pseudohypopyon Causing White Eyes in a Patient with Lymphoma
Lancet 395:e74, Radhakrishnan Iyer, S.S.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017



Showing articles 350 to 400 of 797 << Previous Next >>