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Differential
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abdominal distention
abdominal muscle paralysis
abdominal protrusion
acid maltase deficiency
acid maltase deficiency, adult
acquired immunodeficiency syndrome
adverse drug reaction
alcohol
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alpha glucosidase
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
anterior horn cell disease
anti signal recognition particle antibody
aphonia
areflexia
arm weakness
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
aspartate aminotransferase
asymptomatic
ataxia
ataxia, sensory
ataxic gait
atrioventricular block
autoantibodies
autoimmune disease
azidodeoxythymidine
bone biopsy
bone pain
bone scanning
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, children
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
bradycardia
bulbar palsy
burning feet
burning paresthesia
cachexia
CAG repeats
calcification, intracranial
calf atrophy
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carpal tunnel syndrome
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar edema
cerebellar lesion
cerebral cortical atrophy
cerebral edema
cerebral embolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chromosomal abnormality
chromosome 5
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cold temperature
coma
conduction block
congenital heart disease
congestive heart failure
consanguinity
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deafness
delay in diagnosis
dementia
dementia, frontotemporal
dermatomyositis
developmental milestones
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic amyotrophy
diarrhea
differential diagnosis
difficulty climbing stairs
diplopia
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
drug induced neurologic disorders
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysmorphic
dysphagia
dysphonia
dyspnea
dyspraxia
dystrophic calcification
dystrophin
echocardiogram
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalomyelitis
encephalomyelitis, parainfectious
encephalopathy
encephalopathy, progressive
entrapment neuropathy
enzyme treatment
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
exercise
extraocular muscle lesion
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigable chewing
fatigue
fever
fibrillations
finger flexor weakness
finger weakness
flu-like illness
foot drop
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
gray matter
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
gynecomastia
hallucination
hand weakness
headache
headache, severe
headache, worst of life
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hoarseness
Hoesch test
human immunodeficiency virus type 1
hypercalcemia
hyperparathyroidism
hyperreflexia
hypertension
hyperthyroidism
hypoglycemia
hyponatremia
hypophonia
hyporeflexia
hypotelorism
hypotonia
hypotonia, infants
immediate recall
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
klippel feil syndrome
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lactic acidemia
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
level of consciousness, decreased
lid closure, weakness of
life expectancy
lumbosacral plexopathy
lumbosacral plexus
lumbosacral plexus, neuritis
lymphadenopathy
lymphadenopathy, cervical
lysosomal storage disease
lysosomes, abnoral
malignant hyperpyrexia
McArdle's disease
medulla oblongata, lesion of
MELAS syndrome
meningeal enhancement
meningismus
meningoencephalomyelitis
mental retardation
mental status, abnormal
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
MNGIE syndrome
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
monoparesis
mortality
motor neuron disease
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, muscle
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
mycoplasma
mycoplasma pneumoniae
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, amyloid
myopathy, autoimmune
myopathy, carcinomatous
myopathy, drug-induced
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
myopathy, mitochondrial
myopathy, necrotizing
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myositis, focal
myotonia dystrophica
myotonic discharges
nausea and vomiting
neck stiffness
neck weakness
negative
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuroophthalmology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neurotoxin
next-generation sequencing
night sweats
normal
nusinersen
nystagmus
nystagmus, rotary
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
osteomalacia
pacemaker, cardiac-transvenous
Paget's disease
pain
pain, abdominal
pain, leg
pain, severe
pain, thigh
paranoia
paraparesis
paraplegia
paraproteinemia
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias
photophobia
plasma cell dyscrasia
plasmapheresis
pleocytosis of cerebrospinal fluid
poliomyelitis
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
polyradiculoneuropathy
Pompe's disease of glycogen storage
porphyria
positive sharp waves
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
puerperium
quadriceps atrophy
quadriceps weakness
radionuclide imaging, heart
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
renal stones
repetitive nerve stimulation
respiratory failure
respiratory tract infection
retina, abnormal
retinal lesion
review article
rhabdomyolysis
rheumatoid arthritis
sarcoidosis
sclerosis, bone
scoliosis
scoliosis, neurologic association with
screening
seizure
sensorineural hearing loss
sensory symptoms
serologic testing
short stature
shoulder, subluxation
SMN1 gene
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
survival motor neuron gene
systemic illness
tandem gait, ataxic
temporalis muscle wasting
toe walking
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
toxins, nervous system
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
upward deviation of eyes
urine, dark
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
winging of scapula
X-linked bulbospinal neuronopathy
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 200 to 250 of 4234 << Previous Next >>

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Muscle Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

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

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

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

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

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

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

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Inflammatory Myopathies with Anti-Ku Antibodies
Medicine 91:95-102, Rigolet,A.,et al, 2012

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

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

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

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Ischemic Stroke of the Cortical "Hand Knob" Area: Stroke Mechanisms and Prognosis
J Neurol 256:1146-1151, Peters, N.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
Lancet 371:2201-2212, Feldman,B.M.,et al., 2008

Polymyalgia Rheumatica and Giant-Cell Arteritis
Lancet 372:234-245, Salvarani,C.,et al., 2008

What Are the Prospects of Stem Cell Therapy for Neurology?
BMJ 337:1325-1327, Chandran,S., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008



Showing articles 200 to 250 of 4234 << Previous Next >>