Neudle.com: "dystonia truncal"

Differential
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acetazolamide

adverse drug reaction

agnosia, color

akathisia

akinesia of eyelid function

alexia without agraphia

anticholinergic drugs

anticholinesterase

anxiety

aphasia

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia of eyelid opening

ataxia telangiectasia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

brainstem, dysfunction

calcification, intracranial

camptocormia

carbamazepine

carcinoembryonic antigen

carcinoma

CAT scan

CAT scan, abnormal

CAT scan, false negative

CAT scan, muscle

cataracts

caudate nucleus, atrophy

central hypoventilation

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar pontine angle

cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy

cerebral palsy, associated problems with

cerebral peduncle

cerebrovascular accident

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

conjugate gaze, forced

consanguinity

conversion reaction

cortical-basal ganglionic degeneration

cranial nerve palsies

creatine phosphokinase(CPK)elevated

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

differential diagnosis

diplopia

diurnal variation

donepezil

dopa responsive dystonia

down-beat nystagmus

downward gaze

drooling

drug induced neurologic disorders

dying

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

encephalitis, autoimmune

enzyme, defect

ependymoma

episodic disorders

episodic neurologic deficits

exercise-induced neurologic dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial expression abnormality

falling

familial

fever

fine motor function, impaired

fluctuate

foot deformity

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

grasp reflex

grimacing

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hemianopia, homonymous

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

heralding manifestation

HLA

hoarseness

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

iatrogenic neurologic disorders

intellectual deterioration

internet

intracranial pressure, increased

iron, brain

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Kayser-Fleischer ring

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

liver function enzymes

low back pain

lymphoma

lysosomal storage disease

manganese intoxication

masked facies

memory, defect of recent

memory, impairment of

meningismus

meningitis

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

midbrain

midbrain, atrophy

midbrain, infarction of

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, psychogenic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, negative

MRI, paramagnetic effect

MRI, spine

MRI, T1 weighted high signal foci

MRS

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

myelopathy, chronic progressive

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neurocutaneous disease

neuroendocrinology

neuroleptic

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic evaluation

neurologic examination

numb clumsy hands syndrome

nystagmus

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

paraspinal muscle weakness

parkin gene

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

pathology

penguin silhouette sign

penicillamine

personality change

pigmentary retinopathy

Pisa syndrome

pitfalls

pleocytosis of cerebrospinal fluid

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postural abnormality

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

procyclidine

progeria

prognosis

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Red flags

release phenomena

renal stones

respirations in CNS disease

reversible neurologic disorder

saccadic eye movements, abnormal

salivation, excessive

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory tricks

sequencing difficulty

short stature

shoulder, elevation

sinemet

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

somnolence

spasticity

speech disorder

speech disorder, childhood

spinal cord

spinal cord, lesion of

spinal muscular atrophy

splenomegaly

stare

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

symmetric brain lesions

thalamus, infarction of

treatment of neurologic disorder

tricyclic antidepressant

trientine dihydrochloride

trinucleotide repeats

urinary sulfatidase excretion

vision, blurred

visual evoked response

walking, difficulty with

weakness, progressive

Showing articles 0 to 50 of 1169 Next >>

A 6-Year-Old Girl with Progressive Toe Walking
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

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

Lithium-Induced Reversible Pisa Syndrome
Neurol 88:e184, Kumar, N.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

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

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

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

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Camptocormia
Neurol 65:355-359, Azher,S.N. &Jankovic,J., 2005

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Drug-Induced Pisa Syndrome (Pleurothotomus)
CNS Drugs 10:166-174, Suzuki, T. & Matsuzaka, H., 2002

Bilateral Pallidal Deep Brain Stimulation for Cervical and Truncal Dystonia
Neurol 57:557-558, Andaluz,N.,et al, 2001

Relation Between Cholinesterase Inhibitor and Pisa Syndrome
Lancet 355:2222, Kwak,Y.T. et al, 2000

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Post-Traumatic Shoulder 'Dystonia':Persistent Abnormal Postures of the Shoulder After Minor Trauma
Neurol 51:1205-1207, Thyagarajan,D.,et al, 1998

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

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

Showing articles 0 to 50 of 1169 Next >>