Neudle.com: amyotrophic lateral sclerosis misdiagnosis

Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute intermittant porphyria

advances in neurology

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

anemia

angiostrongylus cantonensis

anterior horn cell disease

anti citrullinated antibody

anti IgLON5

antiviral agents

aphasia

aphasia, progressive, primary

autonomic dysfunction

Babinski sign

basophilic stippling of red blood cells

brachial amyotrophic diplegia

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

CAT scan, emission, abnormal

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, proteincytologic dissociation

cervical osteophyte

cervical spine

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Chinese paralytic syndrome

chondroitin sulfate C

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

creatine phosphokinase(CPK)elevated

crying, pathologic

cyclophosphamide

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontotemporal

dementia, presenile

denervation of muscle

denervation potentials

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, autoimmune

encephalopathy

endemic area

eosinophilia

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evoked potentials

exercise

facial weakness

facial weakness, bilateral

fine motor function, impaired

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gene

gene mutation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

headache, progressive

heavy metal intoxication

helminthic infection of CNS

heralding manifestation

highly active antiretroviral therapy

hoarseness

hospice

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

immunosuppressive agents

immunotherapy

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

inflexibility, mental

intellectual deficit

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

laminectomy, cervical

laughing, pathologic

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

lymphoma involving CNS

Man-In-The-Barrel syndrome

masseter muscle wasting

meningismus

meningitis, eosinophilic

mimics

misdiagnosis

monoclonal gammopathy

monomelic amyotrophy

mortality

motor neuron disease

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

MRI

MRI, abnormal

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelopathy, chronic progressive

myopathy, steroid responsive

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronopathy

neuropathology

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, amyloid

neuropathy, diphtheritic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral, treatment

neuropathy, toxic

neuroprotective agents

neurotoxin

next-generation sequencing

osteomalacia

pain

pain, abdominal

pain, increased response

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

parasitic infection

parasitic infection, CNS

Parkinsonism syndrome

pathology

patient information and support

personality change

Pick's disease

pleocytosis of cerebrospinal fluid

poison, mercury

poliomyelitis

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

porphyria

positive sharp waves

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

radial nerve, palsy of

raw fish ingestion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retrovirus

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

single photon emission computed tomography

sleep

sleep pathology and physiology

snail

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spondylosis

stereotyped behavior

sternocleidomastoid muscle

steroid

steroid therapy, CNS treatment and complications with

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

trauma

travel history

travel, foreign

treatment of neurologic disorder

tremor

tremor, postural

trinucleotide repeats

tripping

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

wheelchair

word-finding difficulty

wrist drop

X-linked bulbospinal neuronopathy

Showing articles 200 to 250 of 4087 << Previous Next >>

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
Neurol 44:547-548, Camu,W.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
Lancet 341:265-268, Couratier,P.,et al, 1993

Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
Neurol 43:438-443, Moss,A.H.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Showing articles 200 to 250 of 4087 << Previous Next >>