Neudle.com: amyotrophic lateral sclerosis prognosis

Differential
(Click to cross reference)

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

advance directives

advances in neurology

algorithm

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

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, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

anterior horn cell disease

aphasia, progressive, primary

asthma, poliomyelitis-like syndrome with

bulbar palsy, progressive

cachexia

camptocormia

cane

carbon monoxide poisoning

carcinoma of lung

caregiver

CAT scan, abnormal

CAT scan, emission, abnormal

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebral death

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

children

chills

chromosomal abnormality

chromosome 5

climate change

Clinical Pathologic Conference(C.P.C.)

cognition

coma

confusion

congenital heart disease

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontotemporal

dementia, presenile

depression

developmental milestones

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

diplegia, brachial

disability rating scale, neurological

distal muscle atrophy

distal muscle weakness

encephalitis, central European

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, post anoxic

enterovirus

enterovirus infection of CNS

epidemiology of neurology

ethics in neurology

euthanasia

exercise

facial weakness, bilateral

football neurologic injuries

frontotemporal dementia, behavioral variant

gastrostomy, percutaneous endoscopic

genetic neurologic disorders

genetic screening

genetic testing

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

heralding manifestation

highly active antiretroviral therapy

hospice

human immunodeficiency virus type 1

hunger

hypercapnia

hyperreflexia

hypogammaglobulinemia

hypoxic encephalopathy

immunohistochemistry

immunosuppression

inclusion body myositis

infection

inflexibility, mental

insomnia

intellectual deficit

intermittent positive pressure breathing

internal capsule

intrinsic hand muscles, wasting of

jaw jerk, abnormal

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laminectomy, cervical

laughing, pathologic

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

leukemia

leukemia, neurologic findings assoc.with

leukoencephalopathy

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

limbic encephalitis

lobar atrophy

locked-in syndrome

medical-legal aspects of neurology

meningismus

mental status, abnormal

Mills syndrome

mimics

minimally conscious state

motor neuron disease, spontaneous recovery

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 pain

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy

myelitis

myelitis, longitudinal

myocardial infarction

nerve conduction studies

neurologic complications

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neuronal degeneration

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuroprotective agents

next-generation sequencing

nusinersen

old age, neurology of

opiate

owl's eye sign of spinal cord

oxygen therapy

pain

pain, back

pain, increased response

pain, management of chronic

palliative care

paralysis, acute

paralysis, acute areflexic

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

persistent vegetative state

personality change

phrenic nerve pacemaker

physician assisted suicide

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis

poliomyelitis-like illness

polymerase chain reaction

positive sharp waves

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

public health

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quality of life

radiculitis

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirator

respiratory arrest

respiratory failure

respiratory tract infection

salivation, excessive

scoliosis

scoliosis, neurologic association with

screening

sedation

sensory symptoms

serologic testing, false negative

single photon emission computed tomography

sleep

sleep pathology and physiology

spinal cord degeneration

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

survival motor neuron gene

syringomyelia

thalamus, lesion of

tick bite

tick-borne encephalitis

tongue, atrophy

tongue, fasciculations of

tracheostomy

trauma

treatment of neurologic disorder

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

word-finding difficulty

Showing articles 50 to 100 of 6941 << Previous Next >>

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

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

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

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

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 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

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

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

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Physician-Assisted Death
Neurol 87:1152-1160, Abrahao, A.,et al, 2016

Mills Syndrome
Neurol 87:e54, Porto, F.H.G.,et al, 2016

Responsibilities of Health Care PRofessionals in Counseling and Educating Patients with Incurable Neurological Diseases Regarding "Stem Cell Tourism"
JAMA Neurol 72:1342-1345, Bowman, M.,et al, 2015

Owls Eye Sign
Neurol 84:1500, Kumar, S.,et al, 2015

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Venous Thromboembolism in Amyotrophic Lateral Sclerosis
Neurol 82:1674-1677, Gladman, M.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Spectrum of Paraneoplastic Disease Associated With Lymphoma
Neurol 76:705-710, Briani,C.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

What Are the Prospects of Stem Cell Therapy for Neurology?
BMJ 337:1325-1327, Chandran,S., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Showing articles 50 to 100 of 6941 << Previous Next >>