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Differential
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acid maltase deficiency
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
anterior horn cell disease
anterior tibial muscle weakness
areflexia
arthrogryposis multiplex
bulbar palsy
CAG repeats
calf atrophy
calf hypertrophy
cardiomyopathy
central core disease
Charcot-Marie-Tooth
children
chromosome 5
congenital heart disease
congenital myopathy
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
developmental retardation
diabetes mellitus
differential diagnosis
distal muscle atrophy
distal muscle weakness
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dystrophin
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
floppy infant
foot drop
fragile-X syndrome
gait disorder
gait, waddling
gastrocnemius muscle weakness
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
hand weakness
heavy metal intoxication
Huntington's chorea
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intrinsic hand muscles, wasting of
Kugelberg-Welander syndrome
leg weakness, bilateral
lid closure, weakness of
lordosis
misdiagnosis
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, mitochondrial
myopathy, quadriceps
myopathy, vacuolar
myotonia congenita
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurofibrillary degeneration
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuronal migration disorder
neuronopathy
neuropathy
newborn, evaluation of
nusinersen
old age, neurology of
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymyositis
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proximal muscle atrophy
quadriceps atrophy
quadriceps weakness
respiratory failure
review article
RFLPs
scoliosis
scoliosis, neurologic association with
screening
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar degeneration
steppage gait
survival motor neuron gene
tongue, fasciculations of
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trinucleotide repeats
walking frame
walking, difficulty with
weakness
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1500 to 1550 of 2055 << Previous Next >>

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,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

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Stroke in Patients with Fusiform Vertebrobasilar Aneurysms
Neurol 39:16-21, Pessin,M.S.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Occipital Infarction with Hemianopsia from Carotid Occlusive Disease
Stroke 20:409-411, Pessin,M.S.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Polymyositis and HTLV-I Antibodies
Ann Neurol 25:311, Francis,D.A.&Hughes,R.A.C., 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

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

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Trauma-Triggered Migraine:An Explanation for Common Neurological Attacks after Mild Head Injury
J Neurosurg 68:181-188, Haas,D.C.&Lourie,H., 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Neuro-Ophthalmologic Complications of Cardiac Catheterization
Neurol 38:483-485, Kosmorsky,G.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

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

Suxamethonium Myalgia
Editorial, Lancet 2:945-9461988., , 1988

Rhinocerebral Mucormycosis:MR Manifestations
J Comput Assist Tomogr 12:744-749, Press,G.A.,et al, 1988

Hypertensive Encephalopathy, Magnetic Resonance Imaging Demonstra of Reversible Cortical & White Matter Lesions
Arch Neurol 45:1078-1083, Hauser,R.A.,et al, 1988

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

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

The'Herald Hemiparesis'of Basilar Artery Occlusion
Arch Neurol 45:1301-1303, Fisher,C.M., 1988

Intra-arterial Thrombolytic Therapy Improves Outcome in Patients with Acute Vertebrobasilar Occlusive Disease
Stroke 19:1216-1222, Hacke,W.,et al, 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Successful Treatment of Ciguatera Fish Poisoning with Intravenous Mannitol
JAMA 259:2740-2742, Palafox,N.A.,et al, 1988

Overuse Syndrome:A Muscle Biopsy Study
Lancet 1:905-908, Dennett,X.&Fry,H.J.H., 1988

The Unilateral Hyperdense Middle Cerebral Artery:An Early CT-Sign of Embolism or Thrombosis
Neuroradiology 30:120-122, Schuierer,G.&Huk,W., 1988

Confusional States Following Posterior Cerebral Artery Infarction
Arch Neurol 45:160-163, Devinsky,O.,et al, 1988

Transcranial Doppler Sonographic Findings in Middle Cerebral Artery Disease
Arch Neurol 45:289-295, Mattle,H.,et al, 1988

Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
Ann Neurol 23:S38-S48, Dalakas,M.C.&Pezeshkpour,G.H., 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

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



Showing articles 1500 to 1550 of 2055 << Previous Next >>