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Differential
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amyloidosis
amyotrophic lateral sclerosis
arrhythmia, cardiac
arthrogryposis multiplex
blepharophimosis
blepharospasm
cardiomyopathy
cataracts
Charcot-Marie-Tooth
chromosome 19
chromosome 3
confidentiality
creatine phosphokinase(CPK)elevated
delay in diagnosis
dermatomyositis
difficulty climbing stairs
dyspnea
ear, abnormal
electromyogram
electron microscopy
enzyme treatment
exercise intolerance
falling
familial
fibrillations
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Gowers maneuver
Guillain Barre syndrome
hammertoes
high arched feet
hip dysplasia
hip flexor weakness
hip pain
hypoxia
imbalance
klippel feil syndrome
leg weakness, bilateral
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
muscle biopsy
muscle diseases, characteristics of
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, hereditary
myopathy, metabolic
myopathy, myofibrillar
myopathy, proximal
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonic discharges
neck weakness
neuritis, causes of
neurologic disease, diagnoses of
neuropathy
neuropathy, diabetic
pinched face
poliomyelitis
polymyositis
polyneuropathy
Pompe's disease of glycogen storage
porphyria
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
pulmonary hypertension
respiratory failure
review article
sarcoidosis
Schwartz-Jampel syndrome
screening
short stature
shoulder, pain in
standing difficulty
stiff man syndrome
torticollis
treatment of neurologic disorder
trinucleotide repeats
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
white matter disease
winging of scapula
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 850 to 900 of 1115 << Previous Next >>

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

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

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

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

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

Hearing Loss in Myotonic Dystrophy
Ann Neurol 23:202-203, Wright,R.B.,et al, 1988

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,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

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

Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
Ann Neurol 23:470-476, Cros,D.,et al, 1988

Hydrops and Pleural Effusions in Congenital Myotonic Dystrophy
J Pediatr 113:555-557, Curry,C.J.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

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Association of Primary Hyperparathyroidism with Myotonic Dystrophy in Two Patients
Arch Int Med 147:777-778, Harada,S.,et al, 1987

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

Acute Lead Poisoning in Two Users of Illicit Methamphetamine
JAMA 258:510-511, Allcott,J.V.,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

The Spectrum of Neurol Dis Assoc with Antiphospholipid Antibd, Lupus Anticoag & Anticardiolipin Antibd
Arch Neurol 44:876-883, Levin,S.R.&Welch,K.M.A., 1987

Repetition Strain Injury
Editorial, Lancet 2:3161987., , 1987

Fibromyalgia Syndrome, An Emerging but Controversial Condition
JAMA 257:2782-2787, 2802-28031987., Goldenberg,D.L., 1987

Unusual Manifestations of Nervous System Borrelia Burgdorferi Infection
Arch Neurol 44:781-783, Midgard,R.&Hofstad,H., 1987

Computed Tomographic Findings of Brain & Skull in Myotonic Dystrophy
JNNP 50:435-438, Avrahami,E.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Cerebral Ischemia with Mitral Valve Prolapse
Am Heart J 113:1308-1315, Wolf,P.A.,et al, 1987

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

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986

Polymyositis Associated with AIDS Retrovirus
JAMA 256:2381-2383, Dalakas,M.C.,et al, 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Peripheral Neuropathy Associated with Mitochondrial Myopathy
Ann Neurol 20:249-257, Yiannikas,C.,et al, 1986



Showing articles 850 to 900 of 1115 << Previous Next >>