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Differential
(Click to cross reference)
alcohol intolerance
alternating rapid movement
ataxia
ataxia, cerebellar
ataxia, progressive
Babinski sign
bladder dysfunction
blindness
CAG repeats
cerebellar atrophy, primary
choking
Clinical Pathologic Conference(C.P.C.)
clonus
cone-rod dystrophy
dementia
diplopia
dysarthria
dysmetria
dysphagia
electroretinograph
exome sequencing
eye movement, disorders of
familial
fatigue
finger nose finger test
fundus, abnormality of
gait disorder
gene mutation
genetic neurologic disorders
genetic testing
handwriting
heel-knee-shin test
hyperreflexia
imbalance
memory, impairment of
mortality
MRI, abnormal
myoclonus
neuropathology
neuropathy
next-generation sequencing
optic atrophy
optical coherence tomography
paraparesis, familial spastic
paraparesis, spastic
prognosis
progressive neurologic disorder
pyramidal tract
pyramidal tract dysfunction
retina, abnormal
retinal degeneration
Romberg's sign
spastic ataxia
spastic paraplegia, type 7
spasticity
spinocerebellar ataxia
spinocerebellar ataxia type 7
trinucleotide repeats
upgaze, paralysis of
urinary urgency
visual acuity, decreased
visual loss
visual loss, progressive
visual loss, slow
walking, difficulty with
wheelchair
Showing articles 1500 to 1550 of 23947 << Previous Next >>

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
NEJM 320:1592-1597, 1621-16231989., Mendell,J.R.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Increased Replication of HTLV-I in HTLV-I-Associated Myelopathy
Ann Neurol 26:331-335, Yoshida,M.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Laxative Abuse Causing Hypermagnesemia, Quadriparesis, & Neuromuscular Junction Defect
Neurol 39:746-747, Castelbaum,A.R.,et al, 1989

Hyponatremia and Inappropriate Secretion of Vasopressin (Antidiuretic Hormone) in Patients with Hypopituitarism
NEJM 321:492-496, 5381989., Oelkers,W., 1989

Intrathecal Baclofen for Severe Spinal Spasticity
NEJM 320:1517-1521, 1553-15551989., Penn,R.D.,et al, 1989

Chronic Progressive Multiple Sclerosis:Serial Magnetic Resonance Brain Imaging Over Six Months
Ann Neurol 26:248-256, Koopmans,R.A.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Plasmapheresis in Treatment of Human T-Lymphotropic Virus Type-I Associated Myelopathy
Lancet 2:1109-1113, Matsuo,H.,et al, 1988

Elevated Serum Antibody Titers to Epstein-Barr Virus in HTLV-I Associated Myelopathy (HAM)
Neurol 38:1650-1653, Itoyama,Y.,et al, 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Correlation of Neuropsychological and MRI Findings in Chronic/Progressive Multiple Sclerosis
Neurol 38:1826-1829, Franklin,G.M.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Involvement of JC Virus-Infected Mononuclear Cells From the Bone Marrow & Spleen in the Pathogen of PML
NEJM 318:301-305, 315-3171988., Houff,S.A.,et al, 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

CT & MRI in Maple Syrup Urine Disease
Neurol 38:486-488, Uziel,G.,et al, 1988

Role of Contrast Enhancement in Cerebral CT of Carbon Monoxide Poisoning
J Comput Assist Tomogr 12:341-343, Zeiss,J.&Brinker,R., 1988

Malignant Monophasic Multiple Sclerosis or"Marburg's Disease"
Neurol 38:1153-1155, Mendez,M.F.&Pogacar,S., 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Stiff-Man Syndrome, An Autoimmune Disease
NEJM 318:1060-1062, Layzer,R.B., 1988

Prolonged Survival & Partial Recovery in AIDS-Associated Progressive Multifocal Leukoencephalopathy
Neurol 38:1060-1065, Berger,J.R.&Mucke,L., 1988

Progressive Multifocal Leukoencephalopathy after Cardiac Transplantation
Neurol 38:995-996, Hall,W.A.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988



Showing articles 1500 to 1550 of 23947 << Previous Next >>