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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 850 to 900 of 2161 << Previous Next >>

Dyspnea as a Presenting Manifestation of Amyloid Myopathy
Neurol 81:e184, Ghosh, P.S.,et al, 2013

The Spectrum of Statin Myopathy
Curr Opin Rheumatol 25:747-752, Mohassel, P. & Mammen, A.L., 2013

Clinicopathologic Conference, Rabies Encephalitis
NEJM 368:172-180, Case 1-2013, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Magnetic Resonance Imaging in Follow-Up Assessment of Sciatica
NEJM 368:999-1007, Barzouhi, A.,et al, 2013

Clinical Reasoning: A 12-year-old Boy with Ascending Weakness
Neurol 80:e110-ee114, French, K.F.,et al, 2013

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

Clinicopatholic Conference, Acute Infection with Hepatitis B Virus
NEJM 368:1239-1245, Case 10-2013, 2013

Clinicopathologic Conference, Neurocysticercosis Involving the Cerebral Ventricles and Spinal Meninges
NEJM 366:1924-1934, Case 15-2012, 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

Bilateral Foot Drop in Polyarteritis Nodosa
NEJM 367:e9, Souza Neves, F. & Lin, K., 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Clinicopathologic Conference, Brucellosis Bacteremia and Discitis
NEJM 367:754-762, Case 26-2012, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Adult Primary Central Nervous System Vasculitis
Lancet 380:767-777, Salvarani, C.,et al, 2012

Clinicopathologic Conference, Paraneoplastic Stiff Person Syndrome with Limbic Encephalitis with Anti-Amphiphysin Antibodies with Metastatic Carcinoma of Breast
NEJM 367:851-861, Case 27-2012, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Surfers myelopathy
Neurol 79:2171-2176, Chang, C.J.,et al, 2012

Case Report: A Man Who Vomited until he couldnt Walk
Lancet 380:1966, Williams, D.,et al, 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Exercise-Associated Numbness and Tingling in the Legs
Arch Neurol 68:1599-1602, Sharp, L.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Functional Weakness: Clues to Mechanism from the Nature of Onset
JNNP 83:67-69, Stone, J.,et al, 2011

Epidemiology, Pathogenesis, Clinical Manifestations and Diagnosis of Waldenstrom Macroglobulinemia
UptoDate, May, Rajkumar, S.V., 2011

Metastatic spinal cord compression
BMJ 342:d2402, Quraishi, N. & Esler, C., 2011

Random skin biopsy and bone marrow biopsy for diagnosis of intravascular large B cell lymphoma
Ann Hematol 90:417-421, Matsue, K.,et al, 2011

Pediatric Sciatic Neuropathies: A 30-year Prospective Study
Neurol 76:976-979, Srinivasan,J.,et al, 2011

Recognizing Guillain-Barr� Syndrome in Preschool Children
Neurol 76:807-810, Roodbol,J.,et al, 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Pure Motor Monoparesis Due to Ischemic Stroke
The Neurologist 17:301-308, Hiraga, A., 2011

Diagnosis of intravascular lymphoma: usefulness of random skin biopsies
Brain Neurol 63:451-458, Nakano, N.M., 2011

Neurological disturbances caused by intravascular lymphomatosis
Brain Nerve 63:443-449, Mizutani, T., 2011

Effect of Caudal Epidural Steroid or Saline Injection in Chronic Lumbar Radiculopathy: Multicentre, Blinded, Randomised Controlled Trial
BMJ 343:d5278,d5310, Iversen, T.,et al, 2011

Clinical Reasoning: A young adult presents with focal weakness and hemorrhagic brain lesions
Neurol 76:e106-e109, Virmani, T.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Chronic Inflammatory Demyelinating Polyneuropathy: Etiology, Clinical Features, and Diagnosis
UpToDate, Sept, Lewis, R., 2010

Pain in Guillain-Barre Syndrome: A Long-Term Follow-Up Study
Neurol 75:1439-1447, Ruts,L.,et al, 2010

Hypertrophic Nerves Producing Myelopathy in Fulminant CIDP
Neurol 75:750, Staff,N.P.,et al, 2010

The Patient Has the Diagnosis
Lancet 378:1436, Jubany,L.I.,et al, 2010



Showing articles 850 to 900 of 2161 << Previous Next >>