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Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abducens nerve paralysis, bilateral

acetylcholine receptor

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome-related complex

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adverse drug reaction

alcohol, heart involvement with

alcohol, neurologic complications with

alpha glucosidase

amaurosis fugax

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

angiotensin-converting enzyme

ankle reflex, preserved

anterior horn cell disease

anterior tibial muscle weakness

anti HMGCR antibody

anti Jo1 antibody

anti Ku antibody

anti Mi2 antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antiviral agents

arrhythmia, cardiac

arthrogryposis multiplex

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial fibrillation

atrioventricular block

autoimmune disease

autonomic dysfunction

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

Balint's syndrome

beta adrenergic blocker

biologic markers

blepharophimosis

bone marrow transplantation

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain natriuretic peptide

bulbar palsy, acute

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calf hypertrophy

cancer associated myopathy

carcinoma of esophagus

carcinoma of lung

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, false negative

cauda equina, enhancement

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chewing, impaired

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cold temperature

collagen vascular disease

conduction block

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

contractures, joint

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine kinase

creatine phosphokinase(CPK)elevated

critical care unit

cultured skin fibroblasts

Cushing's syndrome

deep tendon reflexes

delay in diagnosis

dementia, frontotemporal

dementia, rapidly progressive

dementia, subcortical

dental procedure, neurologic complications with

dermatomyositis

descending paralysis

developmental milestones

developmental retardation

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, congenital and infectious disease with

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic cranialneuropathies

diabetic mononeuropathy

diabetic radiculopathy

diabetic spinal syndromes

diabetic visceral neuropathy

diamond on quadriceps

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

dilantin, hypersensitivity to

diplegia, brachial

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug abuse, inhalation

drug induced neurologic disorders

dysferlinopathy

dystrophic calcification

echocardiogram, LVH

electrocardiogram, abnormal

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, human immunodeficiency virus type 1

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

eosinophilia-myalgia syndrome

epidemiology of neurology

epsilon-aminocaproic acid(E.A.C.A.)

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, elongated

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fatigable chewing

finger flexor weakness

finger weakness

Fisher's syndrome

flu-like illness

foot ulcer, neuropathic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

gag reflex, depressed

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

hallucination, auditory

headache, severe

headache, worst of life

heart block, complete

heat intolerance

hepatosplenomegaly

heralding manifestation

high arched feet

high arched palate

highly active antiretroviral therapy

hip flexor weakness

histochemistry of muscle

HMGcoA reductase inhibitors

H-reflex testing

human immunodeficiency virus type 1

hyperadrenalism

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperparathyroidism

hyperparathyroidism, secondary

hyperphosphatasia

hypersensitivity reaction

hyperthyroidism

hypokalemic periodic paralysis

hypoosmolality of serum

hypoparathyroidism

hypopituitarism

hypotonia, infants

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

ileus, paralytic

immediate recall

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunomodulation

immunosuppressive agents

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

intellectual deficit

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

ischemic exercise test

jaw jerk, abnormal

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg weakness, bilateral

leg weakness, unilateral

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid storage myopathy

lipomatosis, multiple symmetrical

livedo reticularis

liver function enzymes

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lumbosacral radiculopathy

lung transplantation

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lysosomal storage disease

lysosomes, abnoral

malabsorption syndrome

malignancy screen

malignancy, occult

malignant hyperpyrexia

McArdle's disease

McArdle's disease, adult onset

McLeod syndrome

medulla oblongata, lesion of

Melkersson's syndrome

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningoencephalomyelitis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic alkalosis

middle cerebellar peduncle

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

motor neuron disease, spontaneous recovery

movement disorder

MRI, brachial plexus

MRI, disappearing lesion on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multicore myopathy

multiple myeloma

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, presenting manifestations

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma pneumoniae

myeloneuropathy

myelopathy, chronic progressive

myelopathy, tract-specific

myopathy, acquired

myopathy, acute

myopathy, alcoholic

myopathy, amyloid

myopathy, autoimmune

myopathy, carcinomatous

myopathy, critically ill

myopathy, drug-induced

myopathy, glycogen storage

myopathy, hereditary

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, painful

myopathy, proximal

myopathy, quadriceps

myopathy, scleromyxedema

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis, focal

myositis, granulomatous

myositis, ocular

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

nausea and vomiting

Nelson's syndrome

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

nerve conduction studies

nerve root enhancement

neuritis, causes of

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology, brain

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

oral contraceptives

overlap syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

palate, paralysis

paralysis, acute areflexic

paralysis, use-related

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinsonism syndrome

parotid gland swelling

perhexiline maleate

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

personality change

physical activity

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

poison, organophosphate

poliomyelitis, provocation

polymerase chain reaction

polymyositis, eosinophilic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyradiculoneuropathy

Pompe's disease of glycogen storage

position sensation, abnormal

positive sharp waves

posterior column disease

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

proximal myotonic myopathy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

pupil, abnormality in neurologic disorders

purkinje cell cytoplastic autoantibody

quadriceps atrophy

quadriceps weakness

quadriparesis, acute

rabies, nervous system involvement with

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

regional enteritis

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retrograde axonal flow

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rigid spine syndrome

salivation, excessive

sarcoglycanopathy

Schwartz-Jampel syndrome

sclerosis, bone

scoliosis, neurologic association with

sedimentation rate, elevated

sensorineural hearing loss

sensory symptoms

serologic testing

serum alanine aminotransferase

sex reassignment surgery

shoulder, pain in

shoulder, subluxation

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sloped shoulders

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

spirochete infection

splinter hemorrhages

standing difficulty

starvation, therapeutic

statin therapy, discontinuation

status asthmaticus

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

subcutaneous edema

survival motor neuron gene

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

telangiectases, periungual

temporal lobe, lesion

temporalis muscle wasting

tensilon test, false positive

thymus and neuromuscular function

thyroid function tests

tick-borne encephalitis

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

transient ischemic attack

transverse smile

treatment of neurologic disorder

tremor, intention

trinucleotide repeats

type 1 muscle fiber

type 2 muscle fiber

ulcerative colitis

upgaze, paralysis of

upward deviation of eyes

urinary frequency

urinary incontinence

urine osmolality, elevated

vestibular migraine

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

vitamin deficiency

vitamin E deficiency

vocal cord paralysis

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, episodic

weakness, fatiguable

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

white matter disease

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 1350 to 1400 of 3168 << Previous Next >>

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Fluoroquinolone Antibiotics Block Neuromuscular Transmission
Neurol 50:804-807, Sieb,J.P., 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

Secondary Hyperkalaemic Paralysis
JNNP 64:249-252, Evers,S.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

Amyloid Neuropathy Simulating Lower Motor Neuron Disease
Neurol 51:600-602, Quattrini,A.,et al, 1998

Prognosis of patients with Primary Systemic Amyloidosis Who Present with Dominant Neuropathy
Am J Med 104:232-237, Rajkumar,S.V.,et al, 1998

Prognosis of Patients with Symptomatic Vertebral or Basilar Artery Stenosis
WASID Study Group, Stroke 29:1389-13921998., , 1998

Hemopericardium and Cardiac Tamponade after Thrombolysis for Acute Ischemic Stroke
Neurol 50:1857-1859, Kasner,S.E.,et al, 1998

Baclofen Overdose:Drug Experimentation in a Group of Adolescents
Pediatrics 101:1045-1048, Perry,H.E.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Long Term Results of Botulinum Toxin Type A (Dysport) in the Treatment of Hemifacial Spasm:A Report of 175 Cases
JNNP 64:751-757, Jitpimolmard,S.,et al, 1998

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

Cortical Myoclonus
Neurol 50:933-942, Mima,T.T.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Guillain-Barre Syndrome
Lancet 352:635-641, Hahn,A.F., 1998

Guillain-Barre Syndrome:MR Imaging Findings of the Spine in Eight Patients
Radiology 208:137-141, Byun,W.M.,et al, 1998

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,et al, 1998

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998

Magnetic Resonance Imaging of Muscle in Amyotrophic Lateral Sclerosis
Neurol 51:110-113, Bryan,W.W.,et al, 1998

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Leukotriene C4-synthesis Deficiency:A New Inborn Error of Metabolism Linked to a Fatal Developmental Syndrome
Lancet 352:1514-1517,1487, Mayatepek,E.&Flock.B., 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Primary Aldosteronism
NEJM 339:1828-1834, Ganguly, A., 1998

AIDS Dementia Complex with Generalized Myoclonus
Mov Disord 12:593-597, Maher,J.,et al, 1997

Clinical Epidemiology of Nocturnal Leg Cramps in Male Veterans
Am J Med Sci 313:210-214, Haskell,S.G.&Fiebach,N.H., 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

An Infant with Encephalitis
Lancet 350:1594, Yeung,W.L.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Guillain-Barre Syndrome Following Allogeneic Bone Marrow Transplantation
Neurol 49:1711-1714, Wen,P.Y.,et al, 1997

Showing articles 1350 to 1400 of 3168 << Previous Next >>