Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
bulbar palsy
chromosome 11
compartment syndrome
creatine phosphokinase(CPK)elevated
electrocardiogram, abnormal
electromyogram
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
familial
fatigue
floppy infant
gene
genetic neurologic disorders
glycogen storage disease
hypotonia, infants
iatrogenic neurologic disorders
ischemic exercise test
leukocytes
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
molecular genetics
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, metabolic
neurologic disease, diagnoses of
pain
pain, arm
PAS positive
phosphorylase b kinase deficiency
polymerase chain reaction
proximal muscle atrophy
renal failure
respiratory failure
review article
RFLPs
second wind phenomena
seizure
treatment of neurologic disorder
urine, dark
weakness
weakness, generalized
Showing articles 1350 to 1400 of 1454 << Previous Next >>

Outbreak of Central-Nervous-System Toxoplasmosis in Western Europe & North America
Lancet 1:781-784, Luft,B.J.,et al, 1983

Fatal CNS Toxoplasmosis in a Homosexual Man
Neurol 33:926-927, Delaney,P.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Joseph Disease in a Non-Portuguese Family
Neurol 33:74-80, Sakai,T.,et al, 1983

Transderm Pupil & Confusion in a 10-Year-Old
Ann Neurol 13:583, Johnson,S.F.,et al, 1983

Scopalamine Psychosis Revisited
Ann Neurol 13:582, Cairncross,J.G., 1983

Precautions Recommended in Treating Patients with Aids
NEJM 308:156, Masci,J.R.,et al, 1983

Progressive Multifocal Leukoencephalopathy in Acquired Immunodeficiency Syndrome
NEJM 309:492-493, Bedri,J.,et al, 1983

Central-Nervous-System Toxoplasmosis In Homosexual & Heterosexual Adults
NEJM 307:498-499, Hauser,W.E.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Electro-oculographic Findings in Machado-Joseph Disease
Neurol 32:1272-1276, Dawson,D.M.,et al, 1982

Anisocoria From Scopolamine Patches
JAMA 248:353-354, McCrary,J.A.,et al, 1982

Progressive Multifocal Leukoencephalopathy In A Male Homosexual With T-Cell Immune Deficiency
NEJM 307:1436-1438, Miller,J.R.,et al, 1982

Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy
Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
Neurol 32:1295-1299, Longstreth,W.T.Jr.,et al, 1982

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,J.,et al, 1982

Cycloplegia From Transdermal Scopolamine
NEJM 306:174, Chiaramonte,J.S., 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Needle Biopsy of Skeletal Muscle In The Diag of Myopathy & Clinical Study of Muscle Funct & Repair
NEJM 302:261-271, Edwards,R.,et al, 1980

Dejerine-Sottas Disease Revisited
Arch Neurol 37:67-68, Stran,R., 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

Cramps, Muscle Pain, & Tubular Aggregates
Arch Neurol 37:715-717, Lazaro,R.P.,et al, 1980

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978



Showing articles 1350 to 1400 of 1454 << Previous Next >>