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Differential
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ACTH, ectopic syndrome of
addiction, heroin
Addison's disease
advances in neurology
alcohol
alcohol, neurologic complications with
amphotericin B
ankle edema
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
Asians
asymptomatic
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atrial fibrillation
autoimmune disease
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bitemporal visual field defect
brachial neuritis
brainstem, lesion of
cachexia
calcification, intracranial
calcium channel dysfunction
carbenoxolone
carcinoma of lung
carpo-pedal spasm
CAT scan
CAT scan, muscle
CD4 counts
central core disease
cerebellar degeneration
chloride channel dysfunction
chloroquine
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
clofibrate
coinfection
coma
congenital myopathy
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cystoisospora belli
deep tendon reflexes
Dengue fever
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diarrhea
diuretic
drug induced neurologic disorders
electrocardiogram, abnormal
electron microscopy
encephalitis
encephalopathy
enteritis
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
exercise
exophthalmus
familial hemiplegic migraine
fasciculation
flavivirus
gait disorder
genetic neurologic disorders
giardiasis
Guillain Barre syndrome
gynecomastia
hallucination, auditory
Hand-Schuller-Christian disease
homosexual
human immunodeficiency virus type 1
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperkalemic periodic paralysis
hyperparathyroidism
hyperthyroidism
hypocalcemia
hypokalemia
hypokalemic alkalosis
hypokalemic paralysis
hypokalemic periodic paralysis
hyponatremia
hypoparathyroidism
hyporeflexia
hypothalamus
hypothalamus, disturbance of
inclusion body myositis
India
infection
insomnia
insulin
intrinsic hand muscles, wasting of
ipecac
islet cell tumor
leg numbness
leg weakness, bilateral
leukocytosis
liquorice
liver function enzymes
malignant hyperpyrexia
migraine
migraine, hemiplegic
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle pain
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Duchenne
myasthenia gravis
myasthenic syndrome
myelopathy
myelopathy, carcinomatous
myoedema
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, mitochondrial
myopathy, proximal
myopathy, steroid induced
myositis
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nausea and vomiting
neoplasm, hormone producing
neoplasm, hormone producing, ectopic
neoplasm, pituitary
Nepal
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuropathy, peripheral
ophthalmoplegia
ophthalmoplegia, total
pain, abdominal
pain, leg
papilledema
paralysis, acute areflexic
paramyotonia congenita
paranoia
paraparesis
parasitic infection, CNS
parathyroid adenoma
paroxysmal neurologic deficits
perhexiline maleate
periodic paralysis
periodic paralysis, thyrotoxic
pheochromocytoma
pleocytosis of cerebrospinal fluid
polymyositis
potassium
potassium channel antibodies
potassium channel dysfunction
primary aldosteronism
prognosis
protozoan infection
psychosis
quadriparesis
quadriplegia, transient
rash
remote effect of cancer on the nervous system
review article
rhabdomyolysis
risk factors
seizure
snuff dipping
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
tetany
thyroid function tests
thyroid gland, enlarged
thyrotoxicosis
travel, foreign
treatment of neurologic disorder
tremor
Trousseau's sign
tubular aggregates, muscle
vincristine neurotoxicity
viral infection
viral infection, CNS
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
yersinia enterocolitica
Showing articles 450 to 500 of 1024 << Previous Next >>

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

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

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

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

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

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

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,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

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

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
Ann Neurol 37:806-810, Dalakas,M.C.&Illa,I., 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

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

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Distal Vacuolar Myopathy in Nephropathic Cystinosis
Ann Neurol 35:181-188, Charnas,L.R.,et al, 1994

Relation of Alcoholic Myopathy to Cardiomyopathy
Ann Int Med 120:529-536, Fernandez-Sola,J.,et al, 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994



Showing articles 450 to 500 of 1024 << Previous Next >>