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abdominal distention
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
ataxia
atrioventricular block
automatic implantable cardioverter-defibrillator
blepharophimosis
blepharospasm
bradycardia
bulging of biceps
cachexia
calcification, intracranial
calf atrophy
calf hypertrophy
calpain III deficiency
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
coma
complications
conduction block
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
creatine kinase
creatine phosphokinase(CPK)elevated
deafness
dementia
dermatomyositis
descending paralysis
developmental retardation
diarrhea
differential diagnosis
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspraxia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
exercise
exercise intolerance
extraocular muscle lesion
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fatigue
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
hammertoes
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
high arched feet
hip dysplasia
hip flexor weakness
hip pain
histochemistry of muscle
hyperthyroidism
hypoglycemia
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunohistochemistry
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
insulin
intestinal pseudoobstruction
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lactic dehydrogenase(LDH)
laminopathies
leg weakness, bilateral
leukodystrophy
lid closure, weakness of
life expectancy
LMNA gene
lordosis
lymphocyte capping, diminished
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
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, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hypokalemic
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia
myotonia dystrophica
myotonic discharges
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuroophthalmology
neuropathy
neuropathy, diabetic
next-generation sequencing
normal
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
pacemaker, cardiac-transvenous
pain, abdominal
pain, leg
pinched face
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
positive sharp waves
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
ragged-red fibers
recurrent
respirator
respiratory failure
retina, abnormal
retinal lesion
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
Schwartz-Jampel syndrome
scoliosis
seizure
sensorineural hearing loss
short stature
shoulder, pain in
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
syncope
systemic illness
toe walking
torticollis
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
Showing articles 700 to 750 of 2161 << Previous Next >>

Clinicopathologic Conference, Pulmonary Adenocarcinoma, Complicated by a Hypercoagulable State with a Nonbacterial Thrombotic Endocarditis
NEJM, Case 33-2018, 2018

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

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

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

Clinicopathologic Conference, Human Herpesvirus 6-Related Meningoencephalitis
NEJM 378:659-669, Case 5-2018, 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

Clinicopathologic Conference, Digitalis Toxicity
NEJM 378:1931-1938, Case 15-2018, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Prodromal Symptoms of Multiple Sclerosis in Primary Care
Ann Neurol 83:1162-1173, Disanto,G.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

A Patient With Multiple Cranial Nerve Palsies and Areflexic Paraparesis
Neurol 91:e392-e395, Garg,R.K.,et al, 2018

Varicella-Zoster Virus-Related Hemorrhagic Encephalomyelitis
Neurol 90:e1360-e1361, Ganesh, A.,et al, 2018

A 30-year-old man with acute paraplegia and left foot gangrene
Neurol 90:e1355-e1359, Paliwal, V.K.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

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

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

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

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Infratentorial Dural Arteriovenous Fistula Resulting in Brainstem Edema and Enhancement
Neurol 88:503-504, Emmer, B.J.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

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

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

A Young Woman with Respiratory Failure, Hearing Loss, and Paraplegia
Neurol 88:e78-e84, Ntranos, A.,et al, 2017

Management of Sciatica
NEJM 376:1175-1177, Ramaswami, Ramya, 2017

Trial of Pregabalin for Acute and Chronic Sciatica
NEJM 376:1111-1120, Mathieson, S.,et al, 2017

A 45-year-old Woman with Right Limb Weakness
Neurol 88:e103-e107, Li, S.,et al, 2017

Acute Spinal Cord Compression
NEJM 376:1358-1369, Ropper, A.E. & Ropper, A.H., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

A 45-year-old woman with Immobility and Incontinence
Neurol 88:e212-e218, Zhang, B.,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

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

A 61-year-old woman with Lower Extremity Paralysis and Sensory Loss
Neurol 89:e257-e263, Manners, J.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Clinical Phenotype and Outcome of Hepatitis E virus-asssociated Neuralgic Amyotrophy
Neurol 89:909-917, van Eijk, J.J.J.,et al, 2017

Overview of Acute Arterial Occlusion of the Extremities (Acute Limb Ischemia)
UptoDate Aug, Mitchell, M.E. & Carpenter, J.P., 2017

Neurocutaneous Melanosis with Diffuse Leptomeningeal Malignant Melanoma in an Adult
Neurol 86:e75-e79, Bhatia, R.,et al, 2016

Leptomeningeal Enhancement in a Patient with Progressive Cranial Neuropathies and Lumbosacral Radiculopathies
JAMA Neurol 73:345-346, Vargas, T.C.,et al, 2016



Showing articles 700 to 750 of 2161 << Previous Next >>