Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acid maltase deficiency
acid maltase deficiency, adult
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
Alzheimer's disease
Alzheimer's disease, treatment of
anesthesia, general
anterior horn cell disease
arthritis
aspartate aminotransferase
asymptomatic
atidarsagene autotemcel
biologic markers
bone marrow transplantation
bradykinesia
calf hypertrophy
cardiomyopathy
carotid artery disease
cataracts
central nervous system, infection of
cerebrovascular accident
cerebrovascular disease
ceruloplasmin, serum
chelation therapy
children
choreoathetosis
chromosomal abnormality
cirrhosis
clinical trials
coenzyme Q10 deficiency
complications
congestive heart failure
copper
copper metabolism, abnormal
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
dementia, childhood
demyelinating disease
developmental retardation
diet
differential diagnosis
dysarthria
dyskinesia
dysphagia
dystonia
dystroglycanopathies
dystrophin
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
ethambutol
ethics in neurology
fatty acid, elevated plasma content
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glutamic acid decarboxylase
glycogen storage disease
Gowers maneuver
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
history of neurology
Hurler's syndrome
hypogonadism
hypotonia
in situ hybridization
inborn errors of metabolism, screening
Kayser-Fleischer ring
Kearns-Sayre syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Lesch-Nyhan syndrome
leukemia
leukocyte enzyme abnormality
leukodystrophy
Lewy body
life expectancy
lipid storage disorder of CNS
liver disease
liver transplantation
Lorenzo's oil
lysosomal storage disease
lysosomes, abnoral
MELAS syndrome
MERRF syndrome
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
motor system
MRI
MRI, abnormal
mucopolysaccharidoses
muscle biopsy
muscle wasting, diffuse
muscle weakness
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, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myelodysplasia
myoblast transfer
myopathy, mitochondrial
myopathy, quadriceps
neonatal screening, genetic neurologic disorders
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-recurrent
neoplasm, primary of CNS-treatment of
neuroleptic, atypical
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy, ataxia, retinitis pigmentosa
ophthalmoplegia, progressive external
pancreatitis
paraparesis, spastic
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, nonmotor problems of
Parkinson disease, on-off phenomena in
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
peroxisomal disease
polymerase chain reaction
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
ProSavin
psychiatric problems in neurologic disorders
quality of life
respirator
respiratory failure
review article
rigidity
rippling muscle disease
safety
scoliosis
screening
seizure
sham surgery
sinemet
skin, darkening of
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
subarachnoid hemorrhage
subthalamic nucleus
survival motor neuron gene
synucleinopathy
systemic illness
testicular atrophy
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
viral infection
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
white matter disease
Showing articles 950 to 1000 of 1660 << Previous Next >>

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Autosomal Dominant Parkinsoniam with Benign Course and Typical Lewy-Body Pathology
Neurol 43:2222-2227, Golbe,L.I.,et al, 1993

DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
JAMA 270:2316-2320, MacCollin,M.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993

Copper-Histidine Therapy for Menkes Disease
J Pediatr 123:828-830, Sarkar,B.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

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

A Neurological Gene Map
Arch Neurol 50:1269-1271, Rosenberg,R.N., 1993

Validity of Family History Data on Severe Headache and Migraine
Neurol 43:1954-1960, Ottman,R.,et al, 1993

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Familial Aggregation of Stroke
Stroke 24:1366-1371, Kiely,D.K.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
Lancet 341:1179-1181, Rose,J.,et al, 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

Conjugal Alzheimer's Disease:Is There an Increased Risk in Offspring?
Ann Neurol 34:396-399, Bird,T.D.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Migraine Madness:Recurrent Psychosis after Migraine
JNNP 56:416-418, Fuller,G.N.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Sleep Paralysis
Lancet 341:406-407, Dahlitz,M.&Parkes,J.D., 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
Lancet 341:595-596, Spitzer,E.D.,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

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,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

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992

Multiple Sclerosis in 54 Twinships:Concordance Rate is Independent of Zygosity
French Res. Gr. of MS, Ann Neurol 32:724-727, 7222., , 1992

Familial Multiple Sclerosis:MRI Findings in Clinically Affected and Unaffected Siblings
JNNP 55:883-886, Teinari,P.J.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

The Chiari Type I Malformation in Two Monozygotic Twins and First-Degree Relatives
Ann Neurol 31:220-222, Stovner,L.J.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992



Showing articles 950 to 1000 of 1660 << Previous Next >>