Neudle.com: dysarthria clumsy hand syndrome

Differential
(Click to cross reference)

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

behavioral disorder

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

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, presenile

dementia, rapidly progressive

depression

developmental milestones, loss of

disease modifying agents

dizziness

down-beat nystagmus

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

lysosomal storage disease

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

salivation, excessive

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

Showing articles 1000 to 1050 of 1088 << Previous Next >>

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Peripheral Nerve Conduction in Patients with a Cervical Rib & Band
Ann Neurol 4:124-129, Gilliatt,R.W.,et al, 1978

Tricyclic Antidepressants
NEJM 299:1106-1109, 1168-11721978., Hollister,L., 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Propranolol for Severe Post-head Injury Action Tremor
Neurol 28:197, Ellison,P.H., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Chlordecone Intoxication in Man
Neurol 28:626, Taylor,J.R.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Case Record of the M. G. H.
Glioblastoma Multiforme of Pons, NEJM 296:8651977., , 1977

The Serological Diagnosis of St. Louis Encephalitis in Patient with Syndr. of Opsoclonia, Body Tremulousness, & Benign Encephalitis
Ann Neurol 1:596, Estrin,W., 1977

Hangman's Fracture Subsequent to Shaking in an Infant
Ann Neurol 2:82, McGrory,B.E., 1977

Lymphomatoid Granulomatosis Clinically Confined to the CNS
Arch Neurol 34:782, Kokmen,E., 1977

Clonazepam & Branchial Myoclonus
Ann Neurol 1:306, Gledhill,R.F., 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Radicular Compression in Multifocal Eosinophilic Granuloma
Arch Neurol 34:786, Eil,C.,et al, 1977

Familial Essential Myoclonus
Brain 93:131-138, Korten,J.J.,et al, 1977

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976

Dystonia & Choreoathetosis in Multiple Sclerosis
Arch Neurol 33:590, Bachman,D.S.,et al, 1976

Dapsone Motor Neuropathy--An Axonal Disease
Neurol 26:514, Gutmann,L.,et al, 1976

Anticonvulsant-induced Dyskinesias:A Comparison with Dyskinesias Induced by Neuroleptics
JNNP 39:1210, Chadwick,D.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Phenytoin-induced Ophthalmoplegia
Neurol 26:1031, Spector,R.H.,et al, 1976

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Case Record MGH
Necrotizing Myelopathy with Carcinoma, NEJM 294:14471976., , 1976

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

A Wasted Hand
JNNP 38:100, Bergquist,E.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Non-Beta Blocking Action of Propranolol
NEJM 293:988, Koch-Weser,J., 1975

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

Ulnar Neuropathy in Bicycle Riders
Arch Neurol 32:130-131, Eckman,P.B.,et al, 1975

Neuropathy Due To Physical Agents, In Peripheral Neuropathy
Phila. 1975, Ch. 36, p. 741., Dyck,T.&Lambert.,W.B.Saunders Co., 1975

Case Records of MGH-Polycythemia
Carotid Occlusion & Cerebral Infarcts, NEJM 291:96674., , 1974

Efficacy of Chronic Propranolol Therapy in Action Tremors of the Familial, Senile or Essential Varieties
NEJM 290:984, Winkler,G.,et al, 1974

Anterior Interosseous Nerve Palsy:Spontaneous Recovery in Two Patients
JNNP 37:1146, Gardner-Thorpe,C., 1974

Case Records of MGH-NEJM 287:1291
1972, 289:1039, 1973 Arterio-Venous Malformation of Cerebellum., , 1973

Showing articles 1000 to 1050 of 1088 << Previous Next >>