Neudle.com: dysarthria clumsy hand syndrome

Differential
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acetazolamide

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

akinetic mute

alternating rapid movement

alternating rapid movement, impaired

amyotrophic lateral sclerosis

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

Babinski sign

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biologic markers

bone marrow transplantation

bradykinesia

brain atrophy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy

cerebral palsy, associated problems with

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

Charcot-Marie-Tooth

children

chorea

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cognition

congestive heart failure

consanguinity

corona radiata

cortical-basal ganglionic degeneration

cough

cranial neuropathy

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, rapidly progressive

depression

developmental milestones, loss of

down-beat nystagmus, primary position of gaze

drooling

dying

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

embolism

encephalitis

encephalopathy

epileptic encephalopathy

exome sequencing

eye movement, disorders of

failure to thrive

falling

familial

familial periodic ataxia

FARS2 deficiency

fatigue

fine motor function, impaired

finger nose finger test

Friedreich's ataxia, late onset

gait disorder

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glabellar sign

granular osmiphilic material

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hypogonadism, hypogonadotropic

hypometric saccades

hypotonia

iatrogenic neurologic disorders

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

Kayser-Fleischer ring

lacunar infarction

lacunar infarction, differential diagnosis of

lateropulsion

leg weakness, bilateral

leukodystrophy

leukoencephalopathy

lipid storage disorder of CNS

liver disease

Lorenzo's oil

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningitis, CSF cell count-normal

microcephaly

midbrain, atrophy

misdiagnosis

mitochondrial disease

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

myelomalacia

myelopathy

myelopathy, chronic progressive

myoclonic jerks

myoclonus

nausea and vomiting

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

neurofibrillary degeneration

neurofibromatosis 1

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuropathology

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, sensory

next-generation sequencing

Niemann-Pick disease

numb clumsy hands syndrome

nystagmus

ocular motility, disorders of

olivary degeneration, hypertrophic

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinsonism syndrome

positional head-hanging test

prevention of neurologic disorders

prion disease

prion protein gene

prognosis

progressive ataxia and palatal tremor

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychosis

pure dysarthria

pure motor hemiplegia

pursuit eye movements, abnormal

pyramidal tract dysfunction

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

sensorineural hearing loss

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

slit lamp examination

speech disorder, non aphasic

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

splenomegaly

spontaneous remission

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

tandem gait, ataxic

tau protein

tauopathy

thalamus, lesion of-bilateral

titubation

toe walking

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

upgaze, paralysis of

vertigo

vertigo, episodic

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

viral infection, CNS

vision, blurred

vitamin E deficiency

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, progressive

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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

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

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

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

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Clinical Study of 35 Patients with Dysarthria-Clumsy Hand Syndrome
JNNP 75:231-234, Arboix,A.,et al, 2004

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
Stroke 26:950-955, Kim,J.S.,et al, 1995

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

Clinical Anatomic Study of Pure Dysarthria
Stroke 22:809-812, Ichikawa,K.&Kageyama,Y., 1991

Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
Neurol 41:253-258, Amarenco,P.,et al, 1991

The Dysarthria-Clumsy Hand Syndrome:A Distinct Clinical Entity Related to Pontine Infarction
Ann Neurol 27:487-494, Glass,J.D.,et al, 1990

Dysarthria-Clumsy Hand Syndrome & Cerebellar Hemorrhage
Ann Neurol 21:415-416, Roy,E.P.,et al, 1987

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

Primary Pontine Hemorrhage & the Dysarthria-clumsy Hand Syndrome
Neurol 32:1027-1028, Tuhrim,S.,et al, 1982

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Current and Emerging Issues in Wilsons Disease
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

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

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
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Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Duchenne Muscular Dystrophy
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

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

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

A 60-year-old man with arm weakness and numbness
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Showing articles 0 to 50 of 1064 Next >>