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

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 900 to 950 of 1088 << Previous Next >>

Clinical Valproate Toxicity Induced by Acetylsalicylic Acid
Neurol 37:1392-1394, Goulden,K.J.,et al, 1987

The Metabolic Pathology of the AIDS Dementia Complex
Ann Neurol 22:700-706, Rottenberg,D.A.,et al, 1987

The Importance of the Virology Laboratory in the Diagnosis & Management of Viral Meningitis
Am J Dis Child 141:454-457, Wildin,S.&Chonmaitree,T., 1987

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Movement Disorders & AIDS
Neurol 37:37-41, Nath,A.,et al, 1987

The Acquired Immunodeficiency Syndrome Dementia Complex as the Presenting or Sole Manifest of HIV Infection
Arch Neurol 44:65-69, Navia,B.A.&Price,R.W., 1987

Subacute Encephalomyelitis of AIDS & Its Relation to HTLV-III Infection
Neurol 37:562-569, delaMonte,S.M.,et al, 1987

Update on Parkinson Disease
NY State J Med, 87:147-1531987., Lieberman,A.N., 1987

About the Cheiro-Oral Syndrome
Neurol 37:1564-1565, Valzelli,L., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

ABC of AIDS, Neurological Manifestations
BMJ 294:1399-1401, Carne,C.A., 1987

Neurologic Manifestations of Infection with Human Immunodeficiency Virus, Clinical Features & Pathogenesis
Ann Int Med 107:383-391, Gabuzda,D.H.,et al, 1987

Virus Isolation From & Identification of HTLV-III/LAV-Producing Cells in Brain Tissue From a Pt. with AIDS
JAMA 256:2365-2371, 2390-23911986., Gartner,S.,et al, 1986

Orthostatic Tremor in Familial-Essential Tremor
Neurol 36:1241-1245, Wee,A.S.,et al, 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

The AIDS Dementia Complex:I. Clinical Features
Ann Neurol 19:517-524, Navia,B.A.,et al, 1986

HTLV/LAV Infection of the Central Nervous System in a 57-Year-Old Man with Progressive Dementia of Unknown Cause
NEJM 314:1191-1192, Mirra,S.S.,et al, 1986

The AIDS Dementia Comples:II. Neuropathology
Ann Neurol 19:525-535, Navia,B.A.,et al, 1986

Clinicopath. Conference
Amyloid Polyneuropathy, Case Record 26-1986, NEJM 315:45-55986., , 1986

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

Giant Axonal Neuropathy:Central Abnormalities Demonstrated by Evoked Potentials
Ann Neurol 19:394-396, Majnemer,A.,et al, 1986

The Neuroleptic Malignant Syndrome:Agent and Host Interaction
Acta Psychiatr Scand 73:337-347, Shaley,A.&Munitz,H., 1986

Parkinsonism Following Dystonia in Three Patients
Movement Disorders 1:151-157, Katchen,M.&Duvoisin,R.C., 1986

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985

Limb Shaking-A Carotid TIA
Stroke 16:444-448, Baquis,G.D.,et al, 1985

Repetitive Involuntary Movement Associated with Episodic Cerebral Ischemia
Ann Neurol 18:244-250, Yanagihara,T.,et al, 1985

Primary Writing Tremor & Myoclonic Writer's Cramp
Neurol 35:1387-1391, Ravits,J.,et al, 1985

Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging
Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985

The Heterogeneity of Parkinson's Disease:Clinical & Prognostic Implications
Neurol 35:522-526, Zetusky,W.J.,et al, 1985

Aphasia & Agraphia in Lesions of the Posterior Internal Capsule & Putamen
Neurol 35:1797-1801, Tanridag,O.&Kirshner,H.S., 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Frequent Neurologic Toxicity Associated with Amiodarone Therapy
Neurol 34:669-671, Charness,M.E.,et al, 1984

Orthostatic Tremor
Arch Neurol 41:880-881, Heilman,K.M., 1984

Vidarabine Encephalopathy
JNNP 47:1351-1354, Cullis,P.A.,et al, 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Acquired Immune Deficiency Syndrome & Multiple Tract Degeneration in a Homosexual Man
Ann Neurol 15:502-505, Horoupian,D.S.,et al, 1984

Cyclosporine-Associated Central-Nervous-System Toxicity after Allogeneic Bone-Marrow Transplantation
NEJM 310:527, Atkinson,K.,et al, 1984

Complex Visual Hallucinations & Cyclosponine
Arch Neurol 41:329-330, Noll,R.B.,et al, 1984

Action Tremor as a Manifestation of Chylomicron Retention Disease
Ann Neurol 14:591, Gauther,S.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Hand Difficulties Among Musicians
JAMA 249:1869-1872, Hochberg,F.H.,et al, 1983

Ischemic Monomelic Neuropathy
Neurol 33:447-451, Wilbourn,A.J.,et al, 1983

Aphemia Clinical-Anatomic Correlations
Arch Neurol 40:720-727, Schiff,H.B.,et al, 1983

Showing articles 900 to 950 of 1088 << Previous Next >>