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

algorithm

amyloid

amyloidosis

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

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, 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

diphtheria

diplegia, atonic

diplegia, brachial

distal muscle atrophy

distal muscle weakness

electrophoretic pattern, serum

emotional lability

encephalitis

encephalitis, autoimmune

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

gynecomastia

hallucination

hand weakness

heavy metal intoxication

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

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

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

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

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

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

trauma

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 350 to 400 of 4151 << Previous Next >>

Neuropathy in Thyrotoxicosis-Correspondence-NEJM 289:219
1973., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Occult Normal Pressure Hydrocephalus Manifested by Parkinsonism-dementia Complex
Neurol 23:234-238, Sypert,G.W.,et al, 1973

Muscular Quivering
BMJ 3, 1972 Jan., , 1972

Amyotrophic Lateral Sclerosis
Richard Kisonak, Associated Press, Boston Globe Apr 30972., , 1972

Reversible Forms of Motor Neuron-Disease:Lead"Neuropathy"
Neurol 22:446, Boothby,J., 1972

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

Neurological Disorders in Patients Following Surgery for Peptic Ulcer
Neurol 22:450, Hoffman,P., 1972

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

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

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

Diagnostic Value of the Kappa Free light Chain Index to Distinguish MOGAD, NMOSD, and MS
Neurol 106:e214946, Tournier,A.,et al, 2026

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Radiologically Isolated Syndrome: A Review for Neuroradiologists
AJNR 41:1542-1549, Hosseiny, M.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

A Patient with a History of Weight Loss Presenting with Seizures
Neurol 95:e2038-e2042, Tang, G. & Benavides, D.R., 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Evaluation of the Central Vein Sign as a Diagnostic Imaging Biomarker in Multiple Sclerosis
JAMA Neurol 76:1446-1456, Sinnecker, T.,et al, 2019

"Better Explanations" in Multiple Sclerosis Diagnostic Workup
Neurol 92:e2527-e2537, Calabrese, M.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Misdiagnosis of Multiple Sclerosis
Neurol 92:15-16, Brownlee, W.J., 2018

A 56-year-old woman with acute vertigo and diplopia
Neurol 90:748-752, Sharma, R.,et al, 2018

IgG4-Related Disease and Intracranial Hypertension: Case Report of a Novel Mechanistic Association
J Neurol Sci 385:75-77, Healy, J.,et al, 2018

Showing articles 350 to 400 of 4151 << Previous Next >>