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Differential
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advances in neurology
alveolar hypoventilation
anesthesia, general
anxiety
arrhythmia, cardiac
arteriopathy
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
baldness
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
brain atrophy
cachexia
CAT scan
CAT scan, abnormal
cataracts
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
choreoathetosis
chromosomal abnormality
chromosome 19
chromosome 3
cognition
complications
confidentiality
creatine phosphokinase(CPK)elevated
dementia
dementia, cerebrovascular disease causing
dementia, subcortical
depression
diplopia
distal muscle weakness
dystonia
electrocardiogram, abnormal
electromyogram
emotional lability
eye movement, disorders of
facial appearance, abnormal
facial weakness
facial weakness, bilateral
failure to thrive
familial
familial hemiplegic migraine
familial periodic ataxia
fever
gene
gene mutation
genetic counselling
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genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
granular osmiphilic material
headache
heart block
hemiplegia
high arched palate
hypercapnia
hyperthermia
infantile bilateral striatal necrosis
intellectual deficit
lactic acidemia
lacunar infarction
leukoencephalopathy
malignant hyperpyrexia
mania
manic-depressive
metabolic acidosis
microangiopathy, brain
migraine
migraine with aura
migraine, hemiplegic
misdiagnosis
molecular genetics
MRI
MRI, abnormal
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
myoglobinuria
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neurologic disease, diagnoses of
neurologic evaluation
neuroophthalmology
Notch3 gene
nystagmus
nystagmus, gaze-paretic
optic atrophy
oscillopsia
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, dystonia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, rapid onset
Parkinsonism syndrome
paroxysmal neurologic deficits
percussion induced muscle contraction
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
proximal myotonic myopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
review article
rhabdomyolysis
rigidity
risk factors
seizure
skin, biopsy
slit lamp examination
striatum, lesion of
striatum, lesion of, bilateral
tachycardia
tachypnea
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trinucleotide repeats
vasculopathy
wheelchair
white matter disease
white matter disease, subcortical
Showing articles 800 to 850 of 1399 << Previous Next >>

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

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

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

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

Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Parkinson's Disease in Twins
Neurol 42:1453-1461, Vieregge,P.,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

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

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 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

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

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

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

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,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

Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
Ann Neurol 31:555-561, Gutmann,D.H.&Collins,F.S., 1992

Familial Intracranial Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Presymptomatic Testing for Huntington's Disease in the United Kingdom
BMJ 304:1593-1596, Tyler,A.,et al, 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992

Detecting Susceptibility to Malignant Hyperthermia
BMJ 304:791-792, Ellis,F.R., 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992



Showing articles 800 to 850 of 1399 << Previous Next >>