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acid maltase deficiency
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
anterior tibial muscle weakness
apraxia of eye movements
areflexia
arthrogryposis multiplex
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atlanto axial dislocation, congenital
benign congenital hypotonia
Brugada syndrome
bulbar palsy, progressive
calf hypertrophy
carcinoembryonic antigen
carcinoma
cavernous sinus, syndrome
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
coma
complications
congenital heart disease
congenital myopathy
congestive heart failure
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
denervation of muscle
denervation potentials
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
Friedreich's ataxia
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
Guillain Barre syndrome
gynecomastia
heavy metal intoxication
hemangioma
history of neurology
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
infantile tremor syndrome
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mental retardation
misdiagnosis
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mononeuropathy
mortality
motor neuron disease
motor neuron disease, juvenile form
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
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, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, mitochondrial
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral, treatment
newborn, evaluation of
nusinersen
ocular motility, disorders of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
Oppenheim muscular dystrophy
paraparesis, familial spastic
Parkinson disease
pathology
patient information and support
periodic paralysis
periodic paralysis, thyrotoxic
phrenic nerve
placebo
poison, mercury
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
radiation hypersensitivity
radiculopathy
respiratory failure
review article
RFLPs
risk-benefit assessment
safety
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
skin, lesions in neurologic disorders
SMN1 gene
spina bifida
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stiff man syndrome
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
sudden death
survival motor neuron gene
telangiectases
term infant
Tolosa Hunt syndrome
tongue, fasciculations of
torticollis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 750 to 800 of 8383 << Previous Next >>

Idiopathic Hypertrophic Pachymeningitis
Neurol 62:686-694, Kupersmith,M.J.,et al, 2004

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Diagnosing Suprascapular Neuropathy in Patients with Shoulder Dysfunction: A Report of 5 Cases
Physther 84:359-372, Walsworth, M.K.,et al, 2004

Imaging Manifestations of Neurosarcoidosis
AJR 182:289-295, Smith, J.K.,et al, 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

Isolated Shoulder Paresis Caused by a Small Cortical Infarction
Neurol 61:1457, Komatsu,K.,et al, 2003

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

The Medial Brachial Fascial Compartment Syndrome Following Axillary Arteriography
Neurol 61:1037-1041, Tsao,B.E. &Wilbourn,A.J., 2003

Benign Calf Amyotrophy
Arch Neurol 60:1415-1420, Felice,K.J.,et al, 2003

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

MR Imaging in the Differential Diagnosis of Neurogenic Foot Drop
AJNR 24:1283-1289,1273, Bendszus,M.,et al, 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

West Nile Virus Infection
Neurol 61:55-59, Jeha,L.E.,et al, 2003

Neurologic Manifestations and Outcome of West Nile Virus Infection
JAMA 290:511-515,524,558, Sejvar,J.J.,et al, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Delayed Neuropathy and Myelopathy After Organophosphate Intoxication
NEJM 347:1119-1121, Chuang,C.,et al, 2002

Paresis Acquired in the Intensive Care Unit
JAMA 288:2859-2867, De Jonghe,B.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Carpal Tunnel Syndrome
NEJM 346:1807-1812, Katz,J.N &Simmons,B.P., 2002

Isolated Hand Palsy Due to Cortical Infarction: Localization of the Motor Hand Area
Neurol 58:1412-1414, Takahashi,N.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Posterior Circulation Stroke in Childhood
Neurol 59:1552-1556, Ganesan,V.,et al, 2002

Poliomyelitis Due to West Nile Virus
NEJM 347:1280-1281, Glass,J.D.,et al, 2002

West Nile Virus Encephalitis
NEJM 347:1225-1226, Peterson,L.R.,et al, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

Radiotherapy-induced Cerebral Abnormalities in Patients with Low-grade Glioma
Neurol 59:121-123,8, Postma,T.J.,et al, 2002

West Nile Virus: A Primer for the Clinician
Ann Int Med 137:173-179, Petersen,L.R. &Marfin,A.A., 2002

A Pain in the Neck
Lancet 359:1206, Latronico,N.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

Botulinum Toxin Type A in Primary Palmar Hyperhidrosis
Neurol 57:2095-2099, Saadia,D.,et al, 2001

Predominant Involvement of a Particular Group of Fingers Due to Small, Cortical Infarction
Neurol 56:1677-1682, Kim,J.S., 2001

Optic Neuropathy in Children With Lyme Disease
Pediatrics 108:477-481, Rothermel,H.,et al, 2001

A Diffusion-Weighted MRI Study of Acute Ischemic Distal Arm Paresis
Neurol 57:1589-1594, Gass,A.,et al, 2001

Multiple Sclerosis and Magnetic Resonance Imaging
Arch Neurol 58:35-36, Racke,M.K.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

Upper Cervical Spinal Cord Injury in Neonates: The Use of Magnetic Resonance Imaging
J Pediatr 138:105-108, Mills,J.F.,et al, 2001

A Controlled Study of Intravenous Immunoglobulin Combined with Prednisone in the Treatment of IBM
Neurol 56:323-327, Dalakas,M.C.,et al, 2001

Clinical Study of 222 Patients with Pure Motor Stroke
JNNP 71:239-242, Arboix,A.,et al, 2001

Sterile Cerebrospinal Fluid Ascites and Chronic Peritonitis
NEJM 345:297-298, Longstreth,G.F. &Buckwalter,N.R., 2001

Brain Magnetic Resonance Imaging in 23 Patients with Mucopolysaccharidoses and the Effect of Bone Marrow Transplantation
Ann Neurol 50:79-92, Seto,T.,et al, 2001

Clinical and Neuroradiologic Features of Acute Disseminated Encephalomyelitis in Children
Neurol 56:1308-1312,1257, Hynson,J.L.,et al, 2001

Acute Obstructive Hydrocephalus Heralding Neurocysticercosis
Conn Med 65:451-454, Finelli,P.F., 2001



Showing articles 750 to 800 of 8383 << Previous Next >>