Neudle.com: "ataxia acute onset"

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal distention

abdominal protrusion

abducens nerve paralysis, bilateral

abscess, brainstem

abscess, intracerebral

acute ataxia of childhood

acute cerebellar ataxia

adult polyglucosan body disease

advances in neurology

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, abdominal aortic

aneurysm, aortic arch

angiography, cerebral

angiography, posterior fossa

animal exposure

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

aorta, abdominal

aorta, abnormal

arterial dissection

arterial dissection, carotid

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, ruptured

arterial dissection, vertebral

ascending paralysis

ataxia, acute onset

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

axonal degeneration

bacterial infection

bacterial infection, CNS

basal ganglia, lesion of

basilar artery migraine

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

bladder dysfunction

blindness, monocular

blindness, transient

bone marrow biopsy

brachial plexus neuropathy

brainstem, infarction of

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy, progressive

carcinoma of bladder

carotid artery disease

CAT scan, abdomen

CAT scan, abnormal

cat-scratch disease

cauda equina, enhancement

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebral cortex

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, genetic

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

chorioretinitis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

conduction block

contractures, joint

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

degenerative diseases of CNS

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

disability, neurological

distal muscle atrophy

doll's head maneuver

Dravet syndrome

drug induced neurologic disorders in children

dysdiadochokinesia

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

enterovirus infection of CNS

epileptic encephalopathy

Epstein-Barr virus

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, recurrent

failure to thrive

FARS2 deficiency

fine motor function, impaired

Fisher's syndrome

flaccid paralysis

food-borne infection

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic neurologic disorders

genetic testing

glutamic acid decarboxylase, antibody

glycogen storage disease

gram negative rod

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

hand-foot-mouth disease

Hartnup's disease

headache, occipital

headache, severe

headache, sudden onset of

headache, throbbing

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

herpes, genital

heterophile antibody test

histochemistry of muscle

Hodgkin's disease

hyperosmolality

hypertension, cerebrovascular disease with

hyperthyroidism

hypokalemic periodic paralysis

hypotension, systemic

iatrogenic neurologic disorders

immunization, neurologic complications with

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

lactic acidemia

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

limbic encephalitis

listeria monocytogenes

listeriosis, CNS

lymphadenopathy

lymphadenopathy, paraaortic

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

meningoencephalitis, mumps

mental status, abnormal

migraine, children

migraine, visual symptoms in

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, brachial plexus

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, spinal cord

MRI, susceptibility weighted

multiple sclerosis

muscle atrophy, progressive

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

mycobacterial infection

mycobacterium bovis

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myeloneuropathy

myelopathy, chronic progressive

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, vacuolar

myositis, ocular

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

nerve conduction studies, motor

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuromuscular disease, electrodiagnosis of

neuronal intranuclear inclusion disease

neuropathy, acute

neuropathy, motor

neuropathy, motor, multifocal

NMDA antagonists

nystagmus, monocular

nystagmus, rotary

old age, neurology of

ophelia syndrome

ophthalmoplegia

oral ulcerations

osmotic demyelination syndrome

otitis, neurologic complications with

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis

periodic paralysis, thyrotoxic

pleocytosis of cerebrospinal fluid

poison, mercury

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

post infectious cerebellar ataxia

potassium channel antibodies

practice guidelines

precipitating factors

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary nodules

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

quadriplegia, transient

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

Refsum's disease

regional enteritis

renal tubular acidosis

respiratory failure

respiratory tract infection

retina, abnormal

riboflavin transporter deficiency

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory loss, band distribution

serologic testing

serologic testing, false negative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

sodium channel dysfunction

solitary scerlosis

spastic diplegia

speech, loss of

spinal cord, cervical

standing difficulty

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

suspended sensory loss

systemic illness

tandem gait, ataxic

temporal lobe, atrophy

tongue, fasciculations of

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

ulcerative colitis

urinary incontinence

urinary retention

vertebral-basilar insufficiency

viral infection

viral infection, CNS

visual acuity, decreased

visual impairment

visual loss, sudden-unilateral

visual loss, transient

walking, difficulty with

weakness, acute

weakness, episodic

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease

wide based gait

Showing articles 0 to 50 of 8117 Next >>

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

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

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

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Cerebellitis (Acute Ataxia of Childhood)
Adams & Victors Principles of Neurology, Chp 33, pg 754, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Autoantibodies in Postinfectious Acute Cerebellar Ataxia
Neurol 65:1114-1116, Uchibori,A.,et al, 2005

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,et al, 2004

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
Neurol 44:1506-1507, Ito,H.,et al, 1994

Course and Outcome of Acute Cerebellar Ataxia
Ann Neurol 35:673-679, Connolly,A.M.,et al, 1994

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Mumps-Associated Acute Cerebellar Ataxia
Am J Dis Child 146:930-931, Cohen,H.A.,et al, 1992

Acute Cerebellar Ataxia in a Child with Transient Pontine Lesions Demonstrated by MRI
Neuropediatrics 22:225-227, Groen,R.J.M.,et al, 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Dissection of the Intracranial Vertebral Artery
Neurol 38:868-877, Caplan,L.R.,et al, 1988

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Basilar Artery Migraine
Lancet 1:15-17, Bickerstaff,E.R., 1961

Acute Cerebellar Syndrome Secondary to Infectious Mononucleosis in a Fifty-Two Yealr Old Man
Ann Int Med 55:147-149, Bennett,D.R.&Peters,H.A., 1961

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Endovascular Therapy for Patients with Low NIHSS Scores and Large Vessel Occlusion in the 6- to 24-Hour Window
Neurol 104:e213442, Marto,J.P.,et al, 2025

Alteplase for Posterior Circulation Ischemic Stropke at 4.5 to 24 Hours
NEJM 392:1288-1296, Yan,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Showing articles 0 to 50 of 8117 Next >>