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acid maltase deficiency
acid maltase deficiency, adult
acyl CoA dehydrogenase deficiency
advances in neurology
adverse drug reaction
alcohol
alcohol, heart involvement with
alcohol, neurologic complications with
alcoholism
alpha glucosidase
amyloid
amyloidosis
ANA
ankle edema
anterior horn cell disease
antiphospholipid antibody syndrome
areflexia
arrhythmia, cardiac
aspartate aminotransferase
aspiration
asthma
asymptomatic
ataxia
atrioventricular block
autoimmune disease
bradycardia
brain biopsy
brainstem, lesion of
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
carpal tunnel syndrome
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, nonvascular territory
cerebrovascular accident, postpartum
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
chemosis
chest pain
chloroquine
chronic progressive external ophthalmoplegia
Churg-Strauss syndrome
Clinical Pathologic Conference(C.P.C.)
complications
congestive heart failure
conjunctivitis
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
dementia
dementia, cerebrovascular disease causing
depression
dermatomyositis
desmin
developmental retardation
diabetes mellitus
differential diagnosis
distal muscle weakness
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dystroglycanopathies
dystrophic calcification
dystrophin
echocardiogram
edema, leg
edema, periorbital
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
enzyme, muscle disease
eosinophilia
eosinophilic granulomatosis with polyangiitis
epidemiology of neurology
episcleritis
exercise intolerance
exercise-induced neurologic dysfunction
extraocular muscle enlargement
facial weakness
falling
familial
fatigue
fever
fibrillations
fluctuate
fluorescein angiography
fundus, abnormality of
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glycogen storage disease
granular atrophy, cerebral cortex
hammertoes
headache
heart block
hemianopia
hepatomegaly
high arched feet
hip pain
hirsutism
histochemistry
histochemistry of muscle
hypoglycemia
hypotonia
iatrogenic neurologic disorders
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
intellectual deficit
intellectual deterioration
ipecac
Kearns-Sayre syndrome
lactic acidemia
leg swelling
Leigh's disease
life expectancy
lipid storage myopathy
lordosis
lung biopsy
lysosomal storage disease
lysosomes, abnoral
MELAS syndrome
metabolic acidosis
microinfarcts
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
molecular genetics
mortality
motor neuron disease
MRI, abnormal
MRI, muscle
MRI, orbit
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenic syndrome
myocardial biopsy
myocardial infarction
myocarditis
myocytolysis
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, amyloid
myopathy, desmin
myopathy, drug-induced
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, painful
myopathy, proximal
myopathy, steroid induced
myopathy, toxic
myositis
myositis, bacterial
myotonic discharges
neck weakness
nerve biopsy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuropathology
neuropathy
neuropathy, toxic
neurotoxin
nystagmus
occipital lobe, infarction, bilateral
old age, neurology of
ophthalmoplegia
optic atrophy
orthopnea
pacemaker, cardiac-transvenous
pain
pain, calf
pain, leg
periarteritis nodosa
pericardial effusion
perineuritis
perineuritis, optic
peripheral vascular disease
poison, neurologic problems with
polymyositis
Pompe's disease of glycogen storage
postpartum
postpartum cardiomyopathy
postpartum cortical blindness
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
psychiatric problems in neurologic disorders
ptosis
ptosis, unilateral
pulmonary edema
quadriplegia
quality of life
radionuclide imaging, heart
renal biopsy
renal failure
renal failure, acute
repetitive nerve stimulation
respirator
respiratory failure
retinal vasculitis
retinopathy
review article
rhabdomyolysis
rigid spine syndrome
sedimentation rate, elevated
seizure
shoulder, pain in
sick sinus syndrome
skin, biopsy
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
systemic illness
tachycardia
thrombophlebitis
thrombotic microangiopathy
tongue, enlarged
toxins, nervous system
transient ischemic attack
treatment of neurologic disorder
type 1 muscle fiber
uveitis
viral myopathy
visual field defect
visual loss
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
winging of scapula
workup
Showing articles 1050 to 1100 of 1607 << Previous Next >>

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

Cerebral Vasculitis:MR Imaging and Angiographic Correlation
Radiology 182:65-72, Greenan,T.J.,et al, 1992

Radiation Necrosis vs High-Grade Recurrent Glioma:Differentiation by Using Dual-Isotope SPECT with 201TI and 99mTc-HMPAO
AJR 158:399-404, Schwartz,R.B.,et al, 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

CNS Sarcoidosis:Evaluation with Contrast-Enhanced MR Imaging
AJR 158:391-397, Seltzer,S.,et al, 1992

Physical Activity and Stroke in British Middle Aged Men
BMJ 304:597-601, Wannamethee,G.&Shaper,A.G., 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Multifocal Inflammatory Leukoencephalopathy with 5-Fluorouracil and Levamisole
Ann Neurol 31:262-267, Hook,C.C.,et al, 1992

Cholesterol Emboli Neuropathy
Neurol 42:428-430, Bendixen,B.H.,et al, 1992

Use of MR Angiography for Stereotactic Planning
J Comput Assist Tomogr 16:35-40, Ehricke,H.,et al, 1992

Subacute Necrotizing Myelopathy:MR Imaging in Four Pathologically Proved Cases
AJR 158:163-169, 1701992., Mirich,D.R.,et al, 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Adult-Onset Metachromatic Leukodystrophy Presenting as Isolated Peripheral Neuropathy
Neurol 42:1396-1398, Fressinaud,C.,et al, 1992

Clinicopath Conf
Multiple Myeloma, Presenting as Plasmacytoma of Bone Extending into Sphenoid Sinus, Case 21-1992, NE, M 31417-1424,1992., 1992

Clinicopath Conf
Systemic Amyloidosis with Involvement of Heart, Autonomic Nerves, Kidneys, and Lungs, Case 38-1992,, EJM 33-950,1992., 1992

Neurocysticercosis in an Orthodox Jewish Community in New York City
NEJM 327:692-695, 7271992., Schantz,P.M.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Relationship of Cardiac Disease to Stroke Occurrence, Recurrence, and Mortality
Stroke 23:1250-1256, Broderick,J.P.,et al, 1992

Presenting Features and Outcomes in Patients Undergoing Temporal Artery Biopsy, Review of 98 Pts
Arch Int Med 152:1690-1695, Chmelewski,W.L.,et al, 1992

Spontaneous Vertebal Artery Dissection Initially Mimicking Myocardial Infarction
Stroke 23:1021-1023, Linden,D.,et al, 1992

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

The Risk of Stroke in Patients with Acute Myocardial Infarction after Thrombolytic and Antithrombotic Treatment
NEJM 327:1-6, Maggioni,A.P.,et al, 1992

Intracranial Hemorrhage After Coronoary Thrombolysis with Tissue Plsminogen Activator
Am J Med 92:384-390, Kase,C.S.,et al, 1992

Transeophageal Echocardiographic Detection of Aortic Arch Disease in Patients with Cerebral Infarction
Stroke 23:1005-1009, Amarenco,P.,et al, 1992

Effect of Stereotactic Thalamic Lesion on Essential Tremor
Lancet 340:206-207, Lakie,M.,et al, 1992

Valve Disease Associated with Ergot Alkaloid Use:Echocardiographic and Pathologic Correlations
Ann Int Med 117:50-52, Redfield,M.M.,et al, 1992

Clinicopath Conf
Case 7-1992, Systemic Mastocytosis, NEJM 326:472-481992., , 1992

Cerebral Hemorrhage with Biopsy-Proved Amyloid Angiopathy
Arch Neurol 49:51-58, Yong,W.H.,et al, 1992

Cardiogenic Embolism to the Brain
Lancet 339:589-594, Hart,R.G., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

CT patterns of Intracranial Hemorrhage Complicating Thrombolytic Therapy for Acute Myocardial Infarction
Radiology 181:555-559, Uglietta,J.P.,et al, 1991

Stereotaxic Implantation of Autologous Adrenal Medulla Into Caudate Nucleus in Parkinsonism, One-Year Follow-up
Arch Neurol 48:813-820, Fazzini,E.,et al, 1991

Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
Ann Neurol 29:566-569, Berkovic,S.F.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

Multiple Sclerosis:Histopath and MR and/or CT Correlation in 37 Cases at Biopsy and Three Cases at Autopsy
Radiology 180:467-474, Nesbit,G.M.,et al, 1991

Brain Magnetic Resonance Imaging & Neuropsychologic Evaluation of Patients with Idiopathic Dilated Cardiomyopathy
Stroke 22:195-199, Schmidt,R.,et al, 1991

Eosinophilia-Myalgia Syndrome Associated with Ingestion of L-Tryptophan:Muscle Biopsy Findings in 4 Patients
Neurol 41:319-321, Hollander,D.&Adelman,L.S., 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

MR Imaging of Pineal Region Neoplasms
J Comput Assist Tomogr 15:56-63, Zee,C.,et al, 1991

Prognosis and Prognostic Factors of Retinal Infarction:A Prospective Cohort Study
BMJ 302:499-504, Hankey,G.J.,et al, 1991

Clinicopath Conf
Spinal Cord Infarction, Acute, Secondary to Fibrocartilaginous Emboli, Case 5-1991, NEJM 324:322-332, 1991, 1991

Cranial Neuropathy Associated with Primary Amyloidosis
Ann Neurol 29:451-454, Traynor,A.E.,et al, 1991

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Adult Polyglucosan Body Disease:The Diagnostic Value of Axilla Skin Biopsy
Ann Neurol 29:448-451, Busard,H.L.S.M.,et al, 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Clinicopath Conf
Hepatic Encephalopathy in a 40-Year-Old Woman, Am J Med 90:374-3801991., , 1991



Showing articles 1050 to 1100 of 1607 << Previous Next >>