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Differential
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abducens nerve paralysis, bilateral
acanthocytosis
advances in neurology
adverse drug reaction
amniocentesis
ANA
arrhythmia, cardiac
ataxia
ataxia, cerebellar
atrial fibrillation
autoimmune disease
baldness
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blindness
brainstem, lesion of
brainstem, tuberculoma of
calf hypertrophy
cancer of colon
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiomyopathy
CAT scan, abnormal
cataracts
central nervous system, infection of
cerebral cortical atrophy
cerebral palsy
cerebrovascular accident
cerebrovascular accident, young adult
chemosis
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
collagen vascular disease
complications
congenital birth defects
congenital heart disease
congestive heart failure
conjunctival injection
consanguinity
contractures, joint
cornea, abnormal
creatine phosphokinase(CPK)elevated
deafmute
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dermatomyositis
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
difficulty climbing stairs
digitalis intoxication
disability, neurological
distal muscle weakness
dropped head syndrome
dwarfism
dysphagia
dysthyroid ocularmyopathy
dystonia
dystroglycanopathies
dystrophin
edema, periorbital
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
extraocular muscle enlargement
eye, pain in
Fabry's disease
face, numbness of
facial appearance, abnormal
facial weakness
falling
familial
fetal movements, reduced
fetus
fine motor function, impaired
Fisher C.M.
floppy infant
fragile-X syndrome
Friedreich's ataxia
frontal balding
gait disorder
gargoylism
gaze palsy, horizontal
gene
gene mutation
gene therapy
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
glioma
Gowers maneuver
Graves ophthalmopathy
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
hemianopia, homonymous
high arched palate
hippus
histochemistry
histochemistry of muscle
Huntington's chorea
Hurler's syndrome
hyperthyroidism
hypoglycorrhachia
hypotonia
hypotonia, infants
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
intestinal pseudoobstruction
joint hypermobility
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
Leigh's disease
leukodystrophy
life expectancy
lipid storage disorder of CNS
liver function enzymes
malformation, CNS, congenital
malignancy screen
medulla oblongata, lesion of
MELAS syndrome
meningitis
meningitis, TB
mental retardation
merosin
MERRF syndrome
metachromatic leukodystrophy
methotrexate
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, serial
mucopolysaccharidoses
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myelopathy
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, inflammatory
myopathy, mitochondrial
myopathy, steroid induced
myopia
myositis
myotonia
myotonia dystrophica
myotonia dystrophica, classification
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neuritis
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuronal migration disorder
neuropathy
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
optic disc edema
optic neuritis
optic neuropathy
orbit, lesions of
ovarian tumor
pancytopenia
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poliomyelitis
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
pons, lesion of
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proptosis
proptosis, bilateral
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quality of life
ragged-red fibers
rash
Raynaud's phenomenon
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
risk factors
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate
seizure
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skin, tight
speech disorder, childhood
speech, delayed development of
Spielmeyer Vogt syndrome
spinal cord, neoplasm
spinocerebellar degeneration
steroid
steroid therapy, CNS treatment and complications with
suck, poor
sudden death
syringomyelia
systemic illness
Tay-Sachs disease
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tripping
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
Usher's syndrome
viral infection, CNS
visual field defect
visual fields, constricted
visual loss
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weight loss
white matter disease
xanthopsia
X-linked bulbospinal neuronopathy
Showing articles 50 to 100 of 15462 << Previous Next >>

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

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

Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
Neurol 70:1128-1133, Keegan,B.M.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
Neurol 70:1614-1619, McNeill,A.,et al, 2008

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Orthopedic Outcomes of Long-Term Daily Corticosteroid Treatment in Duchenne Muscular Dystrophy
Neurol 68:1607-1613, King,W.M.,et al, 2007

What Do We Really See When We Look at Magnetic Resonance Images?
Ann Neurol 62:207-208, Filippi,M. &Hartung,H.-P., 2007

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
AJNR 27:1037-1039, Mascalchi,M.,et al, 2006

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Practice Parameter: Corticosteroid Treatment of Duchenne Dystrophy
Neurol 64:13-20, Moxley,R.T. III.,et al, 2005

Intermittent Prednisone Therapy in Duchenne Muscular Dystrophy
Arch Neurol 62:128-132, Beenakker,E.A.C.,et al, 2005

West Nile Virus: A Case Report with Flaccid Paralysis and Cervical Spinal Cord MR Imaging Findings
AJNR 26:26-29, Kraushaar, G., et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Diffusion-Weighted and Conventional MR Imaging Findings of Neuroaxonal Dystrophy
AJNR 25:1269-1273, Sener,R.N., 2004

Severe Cardiac Arrhythmias in Young Patients with Myotonic Dystrophy Type 1
Neurol 63:1939-1941, Bassez,G.,et al, 2004

Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
Stroke 34:901-908, Boriani,G.,et al, 2003

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

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 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

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
Neurol 51:1454-1456, Laforet,P.,et al, 1998

Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
Arch Neurol 55:305-311, 2911998., Chang,L.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
JAMA 275:1335-1338, Politano,L.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
Lancet 345:1260-1264, Tracey,I.,et al, 1995

Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
JAMA 274:813-819, Tokgozoglu,L.S.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
Ann Int Med 119:900-905, Fishbein,M.C.,et al, 1993

Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993

Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993

Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992



Showing articles 50 to 100 of 15462 << Previous Next >>