Neudle.com: motor neuron disease 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

anterior horn cell disease

anti citrullinated antibody

aphasia, progressive, primary

apraxia of eye movements

ataxia telangiectasia

autonomic dysfunction

Babinski sign

basophilic stippling of red blood cells

brachial amyotrophic diplegia

bulbar palsy, progressive

cachexia

CAG repeats

cane

carcinoembryonic antigen

carcinoma

CAT scan, emission, abnormal

catalepsy

CD4 counts

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

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

chills

Chinese paralytic syndrome

chondroitin sulfate C

chorea

choreoathetosis

chromosomal abnormality

chromosome 11

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cortical-basal ganglionic degeneration

cranial neuropathy

crying, pathologic

cyclophosphamide

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

denervation of muscle

denervation potentials

differential diagnosis

distal muscle atrophy

distal muscle weakness

electroencephalogram, abnormalities of

electromyogram

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evoked potentials

executive dysfunction

exercise

eye movement, disorders of

facial weakness

facial weakness, bilateral

fine motor function, impaired

frontal behavioral spatial syndrome

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, apraxic

gamma amino butyric acid

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

GM1 ganglioside antibodies

grasp reflex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

heavy metal intoxication

heralding manifestation

highly active antiretroviral therapy

human immunodeficiency virus type 1

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

immunosuppressive agents

immunotherapy

impulsivity

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

India

inflexibility, mental

intellectual deficit

intrinsic hand muscles, wasting of

laminectomy, cervical

laughing, pathologic

L-dopa

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

lymphoma involving CNS

Man-In-The-Barrel syndrome

masked facies

masseter muscle wasting

meningitis

mental retardation

mental status, abnormal

monoclonal gammopathy

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelomalacia

myelopathy

myelopathy, ischemic

myelopathy, chronic progressive

myopathy, steroid responsive

nerve conduction studies

nerve conduction studies, motor

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuropathology, brain

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

night sweats

obsessive-compulsive disorder

ocular motility, disorders of

osteomalacia

pain

pain, abdominal

pain, increased response

pain, leg

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraspinal muscle

parathyroid adenoma

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism syndrome

pathology

patient information and support

penguin silhouette sign

personality change

Pick bodies

Pick's disease

pleocytosis of cerebrospinal fluid

poliomyelitis

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

porphyria

positive sharp waves

primary lateral sclerosis

progeria

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

rabies, nervous system involvement with

radial nerve, palsy of

radiation hypersensitivity

release phenomena

REM sleep

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

screening

sensory symptoms

sequencing difficulty

shell fish poisoning

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep offset paralysis

sleep onset paralysis

sleep paralysis

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

temporal lobe, atrophy

tick paralysis

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

trauma

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, acute

weakness, generalized

weakness, progressive

word-finding difficulty

wrist drop

X-linked bulbospinal neuronopathy

Showing articles 300 to 350 of 4074 << Previous Next >>

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

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

Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
JNNP 63:321-326, McGrath,N.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

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

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
JNNP 62:88-91, Waragai,M.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Motor Involvement in Acute Herpes Zoster
Muscle & Nerve 20:1433-1438997., Haanpaa,M.,et al, 1997

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Riluzole
Lancet 348:795-799, Wokke,J., 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,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

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid
Lancet 348:846-849, Zerr,I.,et al, 1996

Thalamic Haemorrhage
Brain 119:1873-1886, Chung,C-S.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

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

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

Clinicopath Conf
Intravascular Lymphomatosis Involving Brain & Other Organs, Case 30-1996, NEJM 335:952-9596., , 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Lid Nystagmus as a Sign of Intrinsic Midbrain Disease
J Neuro-Ophthalmol 15:236-240, Brodsky,M.C.&Boop,F.A., 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Prediction of Long-Term Outcome in the Early Hours Following Acute Ischemic Stroke
Arch Neurol 52:250-255, Fiorelli,M.,et al, 1995

Psychogenic Parkinsonism
Arch Neurol 52:802-810, Lang,A.E.,et al, 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Intramuscular Inject W/in 30 D of Immun with Oral Poliovirus Vaccine-Risk Factor for Vaccine-Assoc Paral Polio
NEJM 332:500-506, 5291995., Strebel,P.M.,et al, 1995

Showing articles 300 to 350 of 4074 << Previous Next >>