Neudle.com: myopathy necrotizing autoimmune

Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acne fulminans

Addison's disease

Adies pupil

adrenal crisis, acute

adverse drug reaction

amaurosis fugax

amaurosis fugax, unilateral vs.bilateral

amphiphysin antibodies

amyloid

amyotrophic lateral sclerosis, misdiagnosis

ANA

anemia

aneurysm

angiotensin-converting enzyme

anti signal recognition particle antibody

anti Yo antibody

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants, untoward effects of

aspartate aminotransferase

atlanto-axial subluxation

autonomic dysfunction

autonomic neuropathy

Balint's syndrome

Barkhof MR criteria for MS

basal ganglia

basal ganglia, lesion of

brain natriuretic peptide

brainstem

brainstem, infarction of

brainstem, lesion of

brainstem, tuberculoma of

bruising

bruit

burning skin

calcium channel dysfunction

cancer associated myopathy

cardiovascular disease

carpal tunnel syndrome

CAT scan, chest

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral infarction

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, young adult

cerebrovascular disease

chemical weapons

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

children

chills

chloride channel dysfunction

chorea

chronic fatigue syndrome

Clinical Pathologic Conference(C.P.C.)

cognition

collagen vascular disease

collapsin response mediator protein 5 IgG

coma

complications

compression neuropathy

concentration, impaired

confusion

congenital birth defects

congenital myasthenic syndromes

congestive heart failure

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

cost effectiveness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

delirium

demyelinating disease

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

dural rheumatoid nodules

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

electroencephalogram, abnormalities of

electromyogram

electromyogram, incremental response

electron microscopy

ELISA

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, recurrent

encephalomyelitis

encephalopathy

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epistaxis

evidence-based research

familial hemiplegic migraine

fatigue

fever

fibrillations

finger flexor weakness

finger weakness

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption/false positive

fundus, abnormality of

gag reflex, depressed

gait disorder

gait, waddling

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy, horizontal

gender

gene

genetic counselling

genetic neurologic disorders

genetic testing

glutamic acid decarboxylase, antibody

granulomatosis, allergic

Guillain Barre syndrome

Gulf War syndrome

gynecomastia

hallucination

hallucination, visual

hemianopia, homonymous

hemiparesis

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes virus

herpes virus infection

hip pain

HLA

HMGcoA reductase inhibitors

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperkalemia

hyperpigmentation of skin

hypersomnia

hypertension

hypertensive encephalopathy

hypokalemic periodic paralysis

hyponatremia

hyporeflexia

hypotension, systemic

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

insect repellent

insecticides

intellectual deterioration

interstitial pulmonary fibrosis

intracerebral hemorrhage

intracranial hypertension, benign

ipilimumab

irritability

joint hypermobility

juvenile idiopathic inflammatory myopathy

leg numbness

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

liver function enzymes

lymphadenopathy

lymphoma involving CNS

lymphoma, primary of CNS

malabsorption

malignancy screen

malignancy, occult

malignant hyperpyrexia

mastoiditis

medulla oblongata, lesion of

melanoma, malignant

meningitis

meningitis, aseptic

meningitis, neutrophilic

meningitis, noninfectious

meningoencephalitis

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mixed connective tissue disease

molecular genetics

monomelic myositis

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

MRI, disappearing lesion on

MRI, muscle

MRI, spinal cord

MRI, sulcal hyperintensity

multiple myeloma

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle strength, testing

muscle tenderness

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, etiology of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, paraneoplastic

myasthenia gravis, receptor site in

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

myelitis

myelopathy

myelopathy, chronic progressive

myocarditis

myocytolysis

myopathy

myopathy inflammatory, classification

myopathy, autoimmune

myopathy, carcinomatous

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, inflammatory, classification

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, quadriceps

myopathy, steroid induced

myopathy, steroid responsive

myopathy, toxic

myopathy, vacuolar

myositis

myositis specific autoantibody

myositis, bacterial

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

nasal septum, perforation of

nausea and vomiting

neck weakness

neoplasm, primary of CNS

nerve agents

nerve conduction studies

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronopathy, sensory

neuropathology, brain

neuropathy

neuropathy, iatrogenic

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

neurotoxic

neurotoxin

next-generation sequencing

night sweats

nivolumab

NMDA antagonists

ocular motility, disorders of

ocular myopathy

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, plus syndrome

opsoclonus-myoclonus syndrome

optic neuritis

optic neuropathy

otitis, neurologic complications with

paralysis, acute areflexic

paramyotonia congenita

paraneoplastic cerebellar degeneration

paresthesias

paroxysmal neurologic deficits

periodic paralysis, thyrotoxic

peripheral nerve, lesion of

photosensitivity, skin

plasmapheresis

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

POEMS syndrome

poison, organophosphate

polycythemia, primary

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

polymyositis

polymyositis, eosinophilic

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

positive sharp waves

posterior inferior cerebellar artery syndrome

postviral fatigue syndrome

potassium

potassium channel antibodies

potassium channel dysfunction

practice guidelines

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proximal muscle atrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis

ptosis

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

quadriplegia, transient

quality of life

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal biopsy

renal failure

renal failure, acute

repetitive nerve stimulation

research

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal artery occlusion

retinopathy

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid pachymeningitis

scleroderma, neurologic involvement with

scotoma

screening

sedimentation rate

sedimentation rate, elevated

seizure

sensorineural hearing loss

serologic testing

seronegative

serum alanine aminotransferase

sex reassignment surgery

sicca syndrome

single-fiber electromyography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, tight

skin, translucent

sodium channel dysfunction

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 6

splenomegaly

splinter hemorrhages

statin therapy

statin therapy, discontinuation

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

Still's disease

strokelike episodes

subarachnoid hemorrhage

subcutaneous edema

subcutaneous nodules

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tachycardia

telangiectases

telangiectases, periungual

temporal lobe, lesion

temporal lobe, lesion, bilateral

tensilon test, false positive

testicular biopsy

thalamus, infarction, bilateral

tongue, fasciculations of

toxic encephalopathy

transgender

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

unconsciousness

uremia

urine, dark

vaccination, neurologic complications with

vasculitides

vasospasm, cerebral

Venereal Disease Research Laboratory test

walking, difficulty with

weakness, generalized

weakness, progressive

Showing articles 900 to 950 of 1713 << Previous Next >>

A 9-Year-Old With Fever and Severe Muscle Pains
Lancet 349:1666, Punda-Polic,V.,et al, 1997

Treatment of Inflammatory Myopathies
Muscle & Nerve 20:651-664997., Mastaglia,F.L.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

Steroid Myopathy in Cancer Patients
Neurol 48:1234-1238, Batchelor,T.T.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
Ann Neurol 41:762-770, Said,G.,et al, 1997

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Paraneoplastic Encephalomyelitis:An Update of the Effects of the Anti-Hu Immune Response on the Nervous System & Tumour
JNNP 63:133-136, Voltz,R.D.,et al, 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

Clinical Features of Perineuritis
Muscle & Nerve 20:1153-1157997., Sorenson,E.J.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Small-Vessel Vasculitis
NEJM 337:1512-1523, Jennette,J.C.&Falk,R.J., 1997

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

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,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

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

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

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

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

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

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
Neurol 46:108-111, 21996., New,P.Z.,et al, 1996

Is Marfan Syndrome Associated with Symptomatic Intracranial Aneurysms?
Stroke 27:10-12, van den Berg,J.S.P.,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

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

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

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

Showing articles 900 to 950 of 1713 << Previous Next >>