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acromegaly
Addison's disease
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
ANA
anemia
anorexia
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
Asians
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
atrial fibrillation
autoimmune disease
bitemporal visual field defect
bulbar palsy
bulbar palsy, acute
bulbar palsy, acute-causes of
calcification, intracranial
carpo-pedal spasm
CAT scan
CAT scan, abnormal
cerebrospinal fluid, elevated protein of
Charcot-Marie-Tooth
chemosis
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10
collagen vascular disease
coma
complications
concentration, impaired
confusion
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
deafness
deep tendon reflexes
delusion
dementia
dermatomyositis
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diarrhea
digitalis intoxication
diplopia
disorientation
dropped head syndrome
dysarthria
dysphagia
dysphonia
dysthyroid ocularmyopathy
edema, periorbital
electrocardiogram, abnormal
electromyogram
epidemiology of neurology
exercise
exophthalmus
extraocular muscle enlargement
eye movement, disorders of
eye, pain in
facial nerve palsy
fasciculation
fatigue
fever
Fisher C.M.
gag reflex, depressed
gait disorder
gait, spastic
genetic neurologic disorders
Graves ophthalmopathy
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, auditory
Hand-Schuller-Christian disease
headache
hearing loss
hemianopia, homonymous
hippus
HLA
hoarseness
hung reflex
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperreflexia
hypersomnia
hyperthyroidism
hypocalcemia
hypokalemia
hypokalemic paralysis
hypokalemic periodic paralysis
hypoparathyroidism
hypoparathyroidism, idiopathic
hypopituitarism
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypothyroidism
immunology and the nervous system
impotence
insomnia
intellectual deterioration
intrinsic hand muscles, wasting of
islet cell tumor
Kearns-Sayre syndrome
klippel feil syndrome
leg numbness
leg weakness, bilateral
level of consciousness, decreased
lid abnormalities
lid retraction, lower
mania
marche a petits pas
memory, impairment of
meningitis, TB
mental retardation
mental status, abnormal
mononeuropathy
mortality
motor neuron disease
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscle weakness, sudden onset of
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, neuromuscular junction in
myasthenia gravis, receptor site in
myasthenia gravis, treatment of
myasthenic crisis
myoedema
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, drug-induced
myopathy, focal
myopathy, mitochondrial
myopathy, proximal
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, toxic
myositis
myotonia
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nasal speech
neck weakness
Nelson's syndrome
neoplasm, pituitary
neuritis, causes of
neuroendocrinology
neuromuscular disease, electrodiagnosis of
neuroophthalmology
neuropathy
neuropathy, diabetic
neuropathy, peripheral
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic disc edema
optic neuritis
optic neuropathy
orbit
orbit, lesions of
pain, leg
papilledema
paralysis, acute areflexic
paranoia
paraparesis
paraplegia, acute
parathyroid adenoma
paresthesias
periodic paralysis
periodic paralysis, thyrotoxic
personality change
pheochromocytoma
photophobia
photophobia, central
poliomyelitis
polymyositis
polyneuropathy
porphyria
potassium
primary aldosteronism
prognosis
proptosis
proptosis, bilateral
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quadriparesis
quadriplegia
quadriplegia, transient
ragged-red fibers
rash
review article
rhabdomyolysis
sarcoidosis
scintillations
seizure
sensorineural hearing loss
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea
somnolence
spasticity
statin therapy
steroid therapy, CNS treatment and complications with
stiff man syndrome
systemic lupus erythematosus
tachycardia
telangiectases
telangiectases, periungual
tetany
thymectomy
thymoma
thyroid function tests
thyroid gland, enlarged
thyroiditis
thyrotoxicosis
tongue, enlarged
torticollis
treatment of neurologic disorder
tremor
Trousseau's sign
tuberculosis
visual loss
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, proximal
weight loss
Werdnig-Hoffman disease
xanthopsia
Showing articles 500 to 550 of 1200 << Previous Next >>

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Pituitary Enlargement on Magnetic Resonance Imaging in Congenital Hypothyroidism
Arch Pediatr Adolesc Med 150:623-628, Desai,M.P.,et al, 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
Lancet 346:1387-1390, Henderson,A.S.,et al, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
Arch Neurol 52:1074-1079, Seshadri,S.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
Neurol 45:390-391, Sato,K.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Superior Saggital Sinus Thrombosis and Thyrotoxicosis:Possible Assoc in Two Cases
Stroke 26:496-497, Siegert,C.E.H.,et al, 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Medical Complications During Stroke Rehabilitation
Stroke 26:990-994, Kalra,L.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Electroencephalographic Findings in Hashimoto's Encephalopathy
Neurol 45:977-981, Henchey,R.,et al, 1995

Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
Neurol 45:1253-1260, 12511995., Alexander,M.P., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995



Showing articles 500 to 550 of 1200 << Previous Next >>