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Differential
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adrenoleukodystrophy
adverse drug reaction
alternating rapid movement
amniocentesis
amyotrophic lateral sclerosis, guamian type of
anticonvulsants
anticonvulsants, selection of
arm swing, reduced
ataxia
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavioral disorder
blindness
bradykinesia
brain atrophy
brain biopsy
CAT scan, abnormal
cataracts
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebro hepato renal syndrome
cherry red spot
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cogwheel rigidty
conjunctival biopsy
deep gray nuclei
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
developmental milestones, loss of
developmental retardation
diagnostic criteria
DNA probes
drug induced neurologic disorders
dysarthria
dysmetria
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
eye movement, disorders of
falling
familial
fine motor function, impaired
fingerprint bodies
fundus, abnormality of
gait disorder
gangliosidosis GM1
gangliosidosis, generalized
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
granular osmiphilic material
Hallervorden Spatz disease
herpes virus infection
hyperreflexia
hypotonia
imbalance
immunofluorescence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intellectual deficit
intellectual deterioration
introverted
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
lead poisoning
leukocyte peroxidase
lymphocyte fingerprint profiles
lysosomal storage disease
macular degeneration
marche a petits pas
memory, impairment of
mental retardation
MERRF syndrome
metachromatic leukodystrophy
microcephaly
mimics
misdiagnosis
molecular genetics
mongolism
mortality
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
mucopolysaccharidoses
muscle biopsy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy, mitochondrial
myopia
negative
neuroaxonal dystrophy
neurofibrillary degeneration
neuroichthyosis
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
Niemann-Pick disease
night blindness
ophthalmoplegia, plus syndrome
optic atrophy
optic nerve
optic neuropathy
paraparesis, familial spastic
Parkinson disease, postencephalitic
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
peroxisomal disease
pigmentary retinopathy
prenatal diagnosis by amniocentesis
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
putamen, lesion of
putamen, lesion of, bilateral
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
schizophrenia
sea-blue histiocytes
seizure
seizure, children
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
skin, biopsy
skull x-ray, abnormal
slurred speech
spinocerebellar degeneration
storage disease of CNS
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
tapetoretinal degeneration
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
Unverricht-Lundborg disease
Usher's syndrome
ventricular enlargement
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
walking, difficulty with
Werdnig-Hoffman disease
West disease
wheelchair
wide based gait
Showing articles 450 to 500 of 756 << Previous Next >>

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Encephalitis Associated with Glutamic Acid Decarboxylase Autoantibodies
Neurol 56:814, Marchiori,G.C.,et al, 2001

Neurodegenerative Diseases and Prions
NEJM 344:1516-1526,1548, Prusiner,S.B., 2001

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Enzyme Replacement Therapy in Fabry Disease
JAMA 285:2743-2749, Schiffmann,R.,et al, 2001

CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
Neurol 56:1528-1533, Burkhard,P.R.,et al, 2001

Stem-Cell Research: Drawing the Line
Lancet 358:163,217, Greenberg,D.S., 2001

Positron Emission Tomography in Evaluation of Dementia
JAMA 286:2120-2127,2194, Silverman,D.H.S.,et al, 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

High-dose Intravenous Immune Globulin for Stiff-person Syndrome
NEJM 345:1870-1876, Dalakas,M.B.,et al, 2001

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Autoantibodies to Ganglionic Acetylcholine Receptors in Autoimmune Autonomic Neuropathies
NEJM 343:847-855, Verning,S. et al, 2000

Chorea Resulting From Paraneoplastic Striatal Encephalitis
JNNP 69:512-515, Tani,T.,et al, 2000

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Gray Matter Heterotopia
Neurol 55:1603-1608, Barkovich,A.J. & Kuzniecky,R.I., 2000

Antiphospholipid and Antinuclear Antibodies in Patients with Epilepsy or New-onset Seizure Disorders
Am J Med 109:712-717, Peltola,J.T.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Morvans Syndrome Associated With Voltage-Gated K+ Channel Antibodies
Neurol 54:771-772, Barber,P.A., et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Immune Cytopenias as the Presenting Finding in Primary Sjogrens Syndrome
QJM 93:825-829, Schattner,A.,et al, 2000

Epilepsia Partialis Continua:A New Manifestation of Anti-Hu-Associated Paraneoplastic Encephalomyelitis
Ann Neurol 45:255-258, Shavit,Y.B.,et al, 1999

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Antiamphiphysin Antibodies Are Associated with Various Paraneoplastic Neurological Syndromes and Tumors
Arch Neurol 56:172-177,151, Antoine,J.C.,et al, 1999

A New Metabolite Contributing to N-Acetyl Signal in 1H MRS of the Brain in Salla Disease
Neurol 52:1668-1672, Varho,T.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

A Serologic Marker of Paraneoplastic Limbic and Brain-Stem Encephalitis in Patients with Testicular Cancer
NEJM 340:1788-1795,1831, Voltz,R.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Carcinoma Associated Paraneoplastic Peripheral Neuropathies in Patients with and without Anti-Onconeural Antibodies
JNNP 67:7-14,4, Antoine,J.,et al, 1999

Paraneoplastic Painful Ulnar Neuropathy
Muscle & Nerve 22:952-955, Sharief,M.K.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Neuroimaging Findings in Late Infantile GM1 Gangliosidosis
AJNR 19:1628-1630, Chen,C-Y.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 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

Utility of Anti-Hu Antibodies in the Diagnosis of Paraneoplastic Sensory Neuropathy
Ann Neurol 44:976-980, Molinuevo,J.L.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Stiff-Leg Syndrome:A Focal Form of Stiff-Man Syndrome
Ann Neurol 43:400-403, Saiz,A.,et al, 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Multifocal Motor Neuropathy, Serum IgM Anti-GM1 Ganglioside Antibodies Detected Using Linkage of GM1 to ELISA Plates
Neurol 49:1289-1292, Pestronk,A.&Choksi,R., 1997



Showing articles 450 to 500 of 756 << Previous Next >>