Neudle.com: "bulbar palsy progressive"

Differential
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abdominal protrusion

abdominal x-ray

abducens nerve paralysis

abiotrophy

advance directives

advances in neurology

adverse drug reaction

agnosia

agnosia, visual

akinesia of eyelid function

algorithm

alpha coma

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

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, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anisocoria

anomic aphasia

anti GQ1b IgG antibody

aphasia, progressive, primary

apnea

applause sign

apraxia

apraxia of eyelid opening

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

Babinski sign

basal ganglia, lesion of

behavioral disorder

Bickerstaff's brainstem encephalitis

botulism immune globulin

botulism, infant

brain atrophy

brainstem

brainstem, dysfunction

bulbar palsy, childhood

bulbar palsy, juvenile

bulbar palsy, progressive

CAG repeats

calcification, intracranial

CAT scan, emission, abnormal

central hypoventilation

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction, subcortical

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

Clinical Pathologic Conference(C.P.C.)

corpus callosum, lesion of

corpus callosum, thinning

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

depression

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

diplopia

disorientation

distal muscle weakness

ears of the Lynx MR sign

electromyogram

electromyogram, decremental response

emergencies, neurologic

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalomyelitis

encephalopathy

enterovirus

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

executive dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

Fabry's disease

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fine motor function, impaired

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

genetic neurologic disorders

genetic testing

glabellar sign

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

heralding manifestation

histochemistry of muscle

inclusion bodies, intracytopasmic

infant, evaluation of

insomnia

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

intrinsic hand muscles, wasting of

Kugelberg-Welander syndrome

lacunar infarction

language disorder in adults

laughing, pathologic

L-dopa

leg weakness, bilateral

leg weakness, unilateral

lymphoma involving CNS

lymphomatoid granulomatosis

malignancy screen

masked facies

memory, impairment of

meningitis, aseptic

mental status, abnormal

microhemorrhage, intracerebral

monoclonal gammopathy

mood change

mortality

motor neuron disease

motor neuron disease, misdiagnosis

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis

myasthenia gravis, presenting manifestations

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

nerve injury

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuroprotective agents

neurotoxic

neurotoxin

next-generation sequencing

nystagmus

nystagmus, dissociated

nystagmus, vertical

obsessive-compulsive disorder

ocular myopathy

ocular myopathy, differential diagnosis

oculocephalic reflex

opened mouth

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, total

optic atrophy

pain

pain, abdominal

pain, management of chronic

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraparesis

paraparesis, familial spastic

paraparesis, spastic

parasomnia

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

Pick bodies

Pick's disease

pleocytosis of cerebrospinal fluid

poliomyelitis

poliomyelitis vaccine

polymerase chain reaction

polymyositis

post infectious polyneuropathy

post polio syndrome

postural abnormality

practice guidelines

prevention of neurologic disorders

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, oval

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

radiation therapy, CNS treatment and complications with

rash

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

saccadic eye movements, abnormal

salivation, excessive

saxitoxin

seizure

semantic dementia

sequencing difficulty

shell fish poisoning

sinemet

skin, lesions in neurologic disorders

sleep

sleep apnea, obstructive

sleep pathology and physiology

small vessel disease

spastic paraplegia, type 11

spasticity

speech disorder

speech, loss of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

splenomegaly

standing difficulty

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

subarachnoid hemorrhage

temporal lobe, atrophy

temporalis muscle wasting

thrombocytopenia

tinnitus

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

trauma

treatment of neurologic disorder

tremor

tremor, jaw

tremor, postural

trinucleotide repeats

tripping

unconsciousness

unconsciousness, episodic

unconsciousness, transient

urinary retention

vertigo

vestibular function, tests of

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

white matter disease, subcortical

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 0 to 50 of 3870 Next >>

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

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

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

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

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Anterior Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 763, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,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, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Difference in Distribution of Muscle Weakness Between Myasthenia Gravis and the Lambert-Eaton Myasthenic Syndrome
JNNP 73:766-768, Wirtz,P.W.,et al, 2002

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Delayed Radiation-Induced Bulbar Palsy
Neurol 46:1604-1606, Shapiro,B.E.,et al, 1996

Progressive Supranuclear Palsy:Neuropathologic and Clinical Heterogeneity
Neurol 44:1015-1024, Gearing,M.,et al, 1994

Dysphagia in Patients with the Post-Polio Syndrome
NEJM 324:1162-1167, 1206-12071991., Sonies,B.C.&Dalakas,M.C., 1991

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

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986

Botulism in an Adult Associated with Food-Borne Intestinal Infection with Clostridium Botulinum
NEJM 315:239-241, 254-2551986., Chia,J.K.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

'Locked-in Coma'in Postinfective Polyneuropathy
Arch Neurol 36:46-47, Carroll,W.M.,et al, 1979

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Showing articles 0 to 50 of 3870 Next >>