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cardiomyopathy
cerebellar atrophy, secondary
children
chorea
chromosomal abnormality
chronic progressive external ophthalmoplegia
cricopharyngeal bar
diplopia
dysarthria
dysdiadochokinesia
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fibrillations
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gaze palsy, horizontal
gene
gene mutation
genetic neurologic disorders
genetic testing
hammertoes
hearing loss
hepatic failure
imbalance
Leigh's disease
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
molecular genetics
movement disorder
movement disorder, extrapyramidal
MRI, abnormal
muscle biopsy
muscle pain
myopathy
myopathy, mitochondrial
neurologic disease, diagnoses of
neuronopathy
neuronopathy, sensory
neuropathy
next-generation sequencing
nystagmus
nystagmus, gaze-evoked
ophthalmoplegia
ophthalmoplegia, progressive external
Parkinson disease
Parkinsonism syndrome
POLG1 gene
polymerase chain reaction
progressive infantile poliodystrophy
progressive neurologic disorder
psychosis
ptosis
ptosis, bilateral
restless leg syndrome
screening
seizure
standing difficulty
strokelike episodes
tandem gait, ataxic
thalamus, lesion of
thalamus, lesion of-bilateral
upgaze, paralysis of
walking, difficulty with
weakness
weakness, progressive
web sites
wheelchair
Showing articles 1200 to 1250 of 2103 << Previous Next >>

Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Cerebrospinal Fluid
JNNP 59:349-357, Thompson,E.J., 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

The Interferons:Biological Effects, Mechanisms of Action, and Use in Multiple Sclerosis
Ann Neurol 37:7-15, Weinstock-Guttman,B.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

JC Virus DNA in CSF of HIV-Infected Pts:Predictive Value for Progressive Multifocal Leukoencephalopathy
Ann Neurol 37:395-399, McGuire,D.,et al, 1995

Expanded Spectrum of Herpes Simplex Encephalitis in Childhood
J Pediatr 126:234-241, Schlesinger,Y.,et al, 1995

Diagnosis of Whipple's Disease
NEJM 332:390-392, Dobbins,W.O., 1995

Chronic Encephalitis and Epilepsy (Rasmussen's Encephalitis)
Neurol 45:108-117, Jay,V.,et al, 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Non-Progressive Familial Idiopathic Intracranial Calcification:A Family Report
JNNP 59:432-434, Callender,J.S., 1995

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Eval of CSF EBV-DNA and IL-10 as Markers for In Vivo Dx of AIDS-Related Primary CNS Lymphoma
British J Haematology 90:844-849, DeLuca,A.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

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

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Diagnostic Value of Detecting JC Virus DNA in Cerebropsinal Fluid of Patients with Progressive Multifocal Leukoencephalopathy
J Clin Microbiol 33:484-486, Fong,I.W.,et al, 1995

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Familial Atrioventricular Septal Defect:Possible Genetic Mechanisms
Br Heart J 71:79-81, Kumar,A.,et al, 1994

Increased Risk of Parkinson's Disease in Parents and Siblings of Patients
Ann Neurol 36:659-661, Payami,H.,et al, 1994

DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
JNNP 57:1260-1262, Silander,K.,et al, 1994

Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
Neurol 44:2250-2252, Gouider,R.,et al, 1994

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
NEJM 331:1343-1346, Lowsky,R.,et al, 1994

Varicella-Zoster Virus Myelitis:An Expanding Spectrum
Neurol 44:1818-1823, Gilden,D.H.,et al, 1994

Cerebral Syphilitic Gumma Confirmed by the Polymerase Chain Reaction in a Man with HIV Infection
NEJM 331:1488-1491, 15161994., Horowitz,H.W.,et al, 1994

Herpes Simplex Virus Genomes in Human Nervous System Tissue Analyzed by Polymerase Chain Reaction
Ann Neurol 36:823-829, 8091994., Baringer,J.R.&Pisani,P., 1994

In Situ Polymerase Chain Reaction Demo of JC Virus in Progressive Multifocal Leukoencephalopathy, Incl Index Case
Ann Neurol 36:670-673, Ueki,K.,et al, 1994

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

Cytomegalovirus Multifocal Neuropathy in AIDS:Analysis of 15 Consecutive Cases
Neurol 44:2174-2182, Roullet,E.,et al, 1994

Polymerase Chain Reaction and the Diagnosis of Viral Central Nervous System Diseases
Ann Neurol 36:809-811, Tyler,K.L., 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994

Familial Occurrence of Neurocardiogenic Syncope
NEJM 331:205, Cooper,C.J.,et al, 1994



Showing articles 1200 to 1250 of 2103 << Previous Next >>