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Differential
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advances in neurology
amyloid
amyotrophic lateral sclerosis, misdiagnosis
anesthesia, general
areflexia
arrhythmia, cardiac
autoantibodies
autoimmune disease
cachexia
calf hypertrophy
cardiomyopathy
cardiovascular disease
case studies
children
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
creatinuria
delay in diagnosis
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic amyotrophy
diamond on quadriceps
differential diagnosis
distal muscle weakness
dysphagia
dystrophin
electromyogram
epidemiology of neurology
exercise
falling
fibrillations
finger flexor weakness
finger weakness
gait disorder
gender
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
hand weakness
heralding manifestation
hip flexor weakness
histochemistry of muscle
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
Kugelberg-Welander syndrome
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
life expectancy
limb-girdle weakness
mercaptopropionyl glycine
misdiagnosis
multiple myeloma
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myoglobinuria
myopathy
myopathy, autoimmune
myopathy, drug-induced
myopathy, inclusion body
myopathy, quadriceps
myositis
myositis, focal
nerve conduction studies
neurologic disease, diagnoses of
neuropathy
neuropathy, diabetic
osteoarthritis, knee
pain
pain, leg
pain, thigh
paraproteinemia
polymyositis
polyradiculoneuropathy
prognosis
progressive neurologic disorder
proximal muscle atrophy
quadriceps atrophy
quadriceps weakness
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
scoliosis
steroid therapy, CNS treatment and complications with
toe walking
treatment of neurologic disorder
urine, dark
weakness, proximal
web sites
weight loss
wheelchair
winging of scapula
workup
Showing articles 700 to 750 of 1006 << Previous Next >>

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

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

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

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

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

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Pyogenic Myositis:CT Evaluation
J Comput Assist Tomogr 12:1002-1005, Tumeh,S.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 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

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

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

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 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

Lyme Myositis:Muscle Invasion by Borrelia Burgdorferi
Ann Int Med 109:245-246, Atlas,E.,et al, 1988

Subacute Structural Myopathy Associated with Human Immunodeficiency Virus Infection
Arch Neurol 45:585-587, Gonzales,M.F.,et al, 1988

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

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

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,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 Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 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

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

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Syndrome De Gougerot Sjogren Primitif Avec Polymyosite Necrosante:Effet Favorable de L'Hydroxychloroquine
Rev Neurol 143:147-148, Ponge,T.,et al, 1987

Whiplash and Its Relationship to Migraine
Headache 27:452-457, Winston,K.R., 1987

Cluster Headache after Head Injury
Headache 27:509-510, Reik,L., 1987

Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
NEJM 316:761-763, 807-8081987., Senanayake,N.&Karalliedde,L., 1987

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Acetazolamide-Responsive Myotonia Congenita
Neurol 37:488-491, Trudell,R.G.,et al, 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Tick-Bite Meningoradiculoneuritis:Clinical, Electrophysiologic, & Histolic Findings in 10 Cases
Neurol 37:749-753, Vallat,J.M.,et al, 1987

Neurologic Disease as the Presenting Manifestation of Acquired Immunodefieicney Syndrome
South Med J 80:683-686, Berger,J.R.,et al, 1987



Showing articles 700 to 750 of 1006 << Previous Next >>