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Differential
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abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
amyloidosis
anemia
angiography, cerebral
angiography, posterior fossa
anhidrosis
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arteriopathy
arthrogryposis multiplex
arylsulfatase B
atlanto-axial subluxation
band keratopathy
basal ganglia, calcification of
birth injury
blindness
bone marrow transplantation
calcification, intracranial
carcinoma
carotid artery occlusion, neck
CAT scan
CAT scan, abdomen
CAT scan, abnormal
cataracts
cataracts, congenital
cavernous sinus, syndrome
central nervous system, infection of
cerebellar hypoplasia
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cervical spine
children
chorioretinitis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital heart disease
congenital infection, CNS
conjunctival injection
contractures, joint
cornea
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corneal edema
corpus callosum
corpus callosum, hypoplastic
cranial neuropathy, multiple
cultured skin fibroblasts
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
dementia
dementia, presenile
developmental retardation
diarrhea
diplopia
diplopia, monocular
dissociated sensory loss
donut sign
dural sinus thrombosis
dwarfism
dysmorphic
dysostosis multiplex
dyspraxia
ear, abnormal
echocardiogram
ectatic basilar artery
eculizumab
edema, pedal
electroretinograph
empyema, epidural
empyema, subdural
encephalocele
enzyme treatment
enzyme, defect
epidermal nevus syndrome
eye movement, painful
Fabry's disease
facial appearance, abnormal
facial weakness, bilateral
fatty acid, elevated plasma content
fever
fungal infection, CNS
gangliosidosis GM1
gangliosidosis GM2
gene
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genu valgum
glaucoma
headache
headache, severe
hearing loss
hemianopia
hemiparesis
hemoglobinuria
hemolysis
hemorrhoids
hepatomegaly
hepatosplenomegaly
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydronephrosis
hypertension
hypopyon
hypotonia
hypotonia, infants
inclusion bodies
inclusion bodies, intracytopasmic
intelligence quotient
intracerebral hemorrhage
intraocular pressure, increase
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iritis
jugular foramen syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
life expectancy
lipid storage disorder of CNS
lissencephaly
lymphadenopathy
lymphoma
lymphoma, ocular
lymphoma, systemic
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mastoiditis
memory, impairment of
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micropolygyria
micropthalmia
mitral valve prolapse
monoclonal antibodies
Morquio syndrome
mortality
MRI
MRI, abnormal
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
myelopathy
myotonia dystrophica
nasal stuffiness
neck pain
neoplasm, metastatic to eye
nerve conduction studies
neurocutaneous disease
neurofibromatosis 2
neurolipidosis IV
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurosis
nevus
Niemann-Pick disease
nystagmus
ophthalmoplegia
optic atrophy
optic nerve
optic nerve, hypoplasia of
optic nerve, neoplasm of
optic neuritis
oral contraceptives
orbit, lesions of
osteomyelitis
osteomyelitis, skull
osteoporosis
otitis, neurologic complications with
pachygyria
pain
pain, abdominal
pain, head
papilledema
paraparesis, spastic
paroxysmal nocturnal hemoglobinuria
patent ductus arteriosus
pectus carinatum
periventricular leukomalacia
photosensitivity, skin
polycystic kidneys
polyneuropathy
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prognosis
proteinuria
pseudohypopyon
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
pupil, abnormality in neurologic disorders
quadriparesis
rash
red eye
renal failure
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rubella syndrome
sarcoidosis
seizure
seizure, neonatal
sensorineural hearing loss
short neck
short stature
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, bony defect on
slit lamp examination
spinal cord, compression of
splenic-vein thrombosis
splenomegaly
stem cell transplantation
stillbirth
sweating, abnormality of
Tangier's disease
third nerve palsy
thrombocytopenia
tinnitus
tongue, enlarged
torticollis
treatment of neurologic disorder
uremia
urinary incontinence
uveitis
varicose veins
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection, CNS
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual impairment
visual loss
Walker-Warburg syndrome
white matter disease
Showing articles 200 to 250 of 522 << Previous Next >>

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

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 Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
NEJM 333:832-838, 8711995., Mendell,J.R.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Myotonic Dystrophy with No Trinucleotide Repeat Expansion
Neurol 35:269-272, 2551994., Thornton,C.A.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

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

Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
Lancet 344:302-303, Fassati,A.,et al, 1994

The Shoulder-Hand Syndrome after Stroke:A Prospective Clinical Trial
Ann Neurol 36:728-733, Braus,D.F.,et al, 1994

Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
Neurol 44:2006-2014, Jankovic,J., 1994

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

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,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

Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
NEJM 329:915-920, Sancho,S.,et al, 1993

Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma
Neurol 43:795-800, Ohlendieck,K.,et al, 1993

Gene Therapy for Duchenne Dystrophy
Ann Neurol 34:3-4, Engel,A.G., 1993

Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993

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

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

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

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,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

Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993

Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

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

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992



Showing articles 200 to 250 of 522 << Previous Next >>