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abdominal distention

acquired immunodeficiency syndrome

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

aminoacidopathies

anterior tibial muscle weakness

anticonvulsants

anticonvulsants, selection of

antiviral agents

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

autoimmune disease

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion, bilateral

basilar artery stenosis

Bassen-Kornzweig syndrome

black toenail sign

blindness, sudden

brainstem, lesion of

calcification, intracranial

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, gyral swelling

CAT scan, muscle

CAT scan, xenon-enhanced

cataracts, congenital

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral ischemia

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

congenital birth defects

congenital myopathy

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dentatorubral-pallidoluysian atrophy

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

distal muscle weakness

drug induced neurologic disorders

dyschromatopsia

Ekbom's Syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalomalacia

encephalomyopathy

encephalopathy, progressive

epilepsia partialis continua

evoked potentials

exercise intolerance

extraocular muscle atrophy

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

foot ulcer, neuropathic

Friedreich's ataxia

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

gonadal dysgenesis

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

headache, sudden onset of

hemianopia, homonymous

hemianopia, transient

hepatic failure

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

histochemistry of muscle

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hypoparathyroidism

hypoparathyroidism, idiopathic

iatrogenic neurologic disorders

ileus, paralytic

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

ischemic exercise test

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

life expectancy

lipomatosis, multiple symmetrical

macular degeneration

malformation, CNS, congenital

Melkersson's syndrome

memory, impairment of

meningeal enhancement

mental retardation

mesial temporal lobe

microangiopathy, brain

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migratory lesion pattern

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

motor neuron disease

movement disorder

MRI lesion location

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, linear enhancement

MRI, T1 weighted high signal foci

mucopolysaccharidoses

muscle atrophy, progressive

muscle biopsy, extraocular

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myoclonic jerks

myoclonus, epilepsy

myopathy, centronuclear

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, proximal

myopathy, toxic

myopathy, vacuolar

myotonia dystrophica

nausea and vomiting

nemaline rod myopathy

neoplasm, primary of CNS

nephrotic syndrome

neuroendocrinology

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

next-generation sequencing

night blindness

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic disc edema

optic nerve, compression of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

orbicularis oculi muscle

orbit, lesions of

pain, abdominal

paraparesis, spastic

Parkinsonism syndrome

periodic paralysis

peroxisomal disease

personality change

pigmentary retinopathy

PLEDs, bilateral independent

PLEDs, etiology of

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychosis, acute

ptosis, bilateral

ragged-red fibers

rapidly progressing neurologic illness

refractive errors

Refsum's disease

respiratory tract infection

retina, abnormal

retinal degeneration

retinitis pigmentosa

Reye's syndrome

Reye's syndrome, adult

seizure, paradoxical

seizure, treatment of

sensorineural hearing loss

single photon emission computed tomography

Southern immunoblot test

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

Stephens syndrome

strokelike episodes

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

tapetoretinal degeneration

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

transient neurologic deficit

transverse smile

treatment of neurologic disorder

trinucleotide repeats

Unverricht-Lundborg disease

upgaze, paralysis of

Usher's syndrome

viral infection, CNS

visceral neuropathy

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss, progressive

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

whistle, inability to

white matter disease

white matter disease, pattern

whole genome sequencing

wide based gait

winging of scapula

Showing articles 1050 to 1100 of 1133 << Previous Next >>

Cardiac Myxoma:A Diagnostic Challenge for the Neurologist
Neurol 26:1060, Yufe,R.,et al, 1976

The Extra-Intestinal Complications of Crohn's Disease & Ulcerative Colitis:A Study of 700 Patients
Medicine 55:401, Greenstein,A.J.,et al, 1976

Granulomatous Myositis & Myopathy Assoc. with Crohn's Colitis
NEJM 295:818, Menard,D.B.,et al, 1976

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Long-term Administration of Corticosteroids in Myasthenia Gravis
Neurol 26:729, Mann,J.D.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Pseudomalignant Myositis Ossificans, A Pathological Study of Eight Cases
Human path 6:653-665, Lagier,R.&Cox,J.N., 1975

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
JAMA 235:1142, Finelli,P.F.,et al, 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

Reye's Syndrome-Virus or Artifact in Muscle
NEJM 293:505, Hanson,P.A.,et al, 1975

Chronic Myopathy Associated with Coxsackievirus Type A9-A Combined Electron Microscopical & Viral Isolation Study
NEJM 292:608, 6411975., Tang,T.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Serum Creatine Phosphokinase in Leptospirosis
JAMA 233:981, Johnson,W.D.,et al, 1975

Posttraumatic Dysautonomic Cephalgia
Arch Neurol 32:649, Vijayan,N.,et al, 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Neurologic Complications of Rheumatoid Arthritis
Orth Clin North Am 6:861-881, Nakano,K.K., 1975

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Specificity of the Urine Inhibitor Test for Leigh's Disease
Neurol 24:885, Pincus,J.H.,et al, 1974

Polymyalgia Rheumatica & Giant Cell Arteritis
Disease-A-Month, 1974. , Jan., Anderson,L.,et al, 1974

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Acute Bulbar Dysfunction & Hyperthyroidism
Am J Med 56:464, Kammer,G.M.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Coccidioidomycosis in N. Calif
Calif Med 119:16, Werner,S.B.&Pappagianis,D., 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Neurologic Complications of Heroin Addiction
Bull NY Acad Sci 49:4, Ritcher,R.W.,et al, 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

Trichinosis with Central Nervous System Involvement
Neurol 22:485-491, Kramer,M.D.,et al, 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Acute & Chronic Alcoholic Myopathy
Neurol, April 1972. Vol. 22., Martinez,A.J.,et al, 1972

SLE in the Elderly
Arch Int Med 130:743, Foad,B.S.,et al, 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Case Record of MGH
NEJM Amyloidosis & Multiple Myeloma, 86:53472., , 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 1972

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Trigeminal Neuropathy in Connective Tissue Disease
Neurol 21:609, Ashworth,B.,et al, 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Electrodiagnosis Studies in Neuromuscular Disease
NEJM 285:1244, Samaha,F., 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Showing articles 1050 to 1100 of 1133 << Previous Next >>