Neudle.com: dyspraxia

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Differential
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abscess, vertebral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

adverse drug reaction

agenesis of corpus callosum

agnosia, tactile

agranulocytosis

alexia without agraphia

alien hand syndrome

alternating rapid movement

aminoacidopathies

amyloid plaques

amyotrophic lateral sclerosis

anemia, megaloblastic

anesthesia, general

ankle reflex, absent

anticonvulsants

anticonvulsants, untoward effects of

antithyroid antibodies

apraxia of eye movements

apraxia, constructional

arrhythmia, cardiac

arylsulfatase B

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial fibrillation

atrioventricular block

auditory evoked brainstem potentials

autoimmune cerebellar ataxia

autoimmune disease

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

azidodeoxythymidine

B 12 deficiency

bacterial infection

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Bell's phenomenon

biologic markers

bladder dysfunction

blinking, reduced

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

burning paresthesia

carbamazepine, toxicity

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, myelogram with

CAT scan, ring sign

central cord syndrome

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, cardiac origin

cerebral hemisphere left-right asymmetry

cerebral palsy, associated problems with

cerebral peduncle

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cervical myelopathy

cervical spondylosis

Charcot-Marie-Tooth

Chediak-Higashi syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coin rotation test

concentration, impaired

congenital ocular motor apraxia

congestive heart failure

contractures, joint

convergence, impaired

cornea, opacity of

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, parenchymal

cyst, subcortical

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

differential diagnosis

disc space infection

disc space narrowing

disconnection syndrome

dissociated sensory loss

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drawing test in children

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dystonia musculorum deformens

dystonia, cervical

electrophoretic pattern, CSF

Emery-Dreifuss muscular dystrophy

empyema, epidural-spinal

episodic disorders

episodic neurologic deficits

evoked potentials

exome sequencing

eye movement, disorders of

failure to thrive

familial periodic ataxia

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

head circumference

heart block, complete

heel-knee-shin test

hemianopia, homonymous

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herniated disc, central

herniated disc, cervical

homocysteine, serum

Horner's syndrome

human immunodeficiency virus type 1

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hypogonadism, hypogonadotropic

iatrogenic neurologic disorders

immunohistochemistry

immunosuppressive agents

inborn errors of metabolism

inclusion bodies, intracytopasmic

industrial neurologic disorders

intellectual deficit

intellectual deterioration

intelligence quotient

intrathecal medication

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Kayser-Fleischer ring

lactic dehydrogenase(LDH)

lacunar infarction, differential diagnosis of

laminectomy, cervical

language disorder in adults

learning disability, in children

leg weakness, bilateral

leukocyte peroxidase

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

Lhermitte's sign

lipid storage disorder of CNS

liver function enzymes

lysosomal storage disease

medulla oblongata, neoplasm of

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

mental retardation

mental status, abnormal

metabolic disorder, primary-screening tests

methanol intoxication

methylmalonic acid, serum

methylmalonic acidemia

midbrain, atrophy

midbrain, infarction of

mitochondrial disease

molecular genetics

monoparesis, focal

motor dysfunction

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, spinal cord

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle spasm, paraspinal

muscle weakness

muscle weakness, proximal

muscular dystrophy

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, chronic progressive

myelopathy, vacuolar

myoclonic jerks

nausea and vomiting

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

nerve conduction studies, sensory

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neurologic testing

neuronopathy, sensory

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, sensory

neuropathy, toxic

next-generation sequencing

Niemann-Pick disease

numb clumsy hands syndrome

numbness, extremity

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection, CNS

optokinetic nystagmus, abnormal

ornithine transcarbamylase deficiency

osteomyelitis, spinal

ovarian dysgenesis

overuse syndrome

pacemaker, cardiac-transvenous

pain, abdominal

paraparesis, spastic

paresthesias, feet

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinsonism syndrome

pathologic reflex

peripheral blood smear, abnormal

pernicious anemia

Perrault syndrome

personality change

phenylketonuria

pons, lesion of

Poretti-Boltshauser syndrome

position sensation

positional head-hanging test

positive sharp waves

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

posterior fossa

posterior fossa, lesion of

postural abnormality

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

prion protein gene

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

pseudoathetosis

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pupil, light reflex, abnormal

pure sensory stroke

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

reflex sympathetic dystrophy

reflex, cutaneous

release phenomena

remote effect of cancer on the nervous system

retinal degeneration

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis

rubella encephalitis, progressive

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, drug-induced

seizure, laughing as manifestation

sensorineural hearing loss

sensory loss, asymmetric

sensory loss, cortical

serologic testing

serologic testing of cerebrospinal fluid

shoulder, pain in

Sjogren's syndrome

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

slit lamp examination

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar degeneration

square wave jerks

startle myoclonus

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

systemic illness

tandem gait, ataxic

thalamus, infarction of

thalamus, lesion of-bilateral

tongue, enlarged

tongue, swelling

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

vertebral erosion

vertigo, episodic

vibratory sensation

vibratory sensation, abnormal

viral infection, CNS

vision, blurred

visual field defect

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, difficulty with

weakness, progressive

Wernekinck commissure syndrome

white matter disease

wide based gait

winging of scapula

word-finding difficulty

Showing articles 50 to 71 of 71 << Previous

Parkinsonism and Defects of Praxis Following Methanol Poisoning
JNNP 54:843-844, Mozaz,M.J.,et al, 1991

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 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

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Neurologic Signs in Senescence
Arch Neurol 42:1154-1157, Jenkyn,L.R.,et al, 1985

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Asperger's Syndrome:A Clinical Account
Psychological Medicine 11:115-129, Wing,L., 1981

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Giant Axonal Neuropathy
Arch Neurol 36:107-108, Mizuno,Y.,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

Speech Defects in Children Aged 7 yrs, A National Study
BMJ 253, 1973 Feb., Butler,N.,et al, 1973

Specific Learning Disorders in Childhood
Psych Annals 2:, 1972 May., Gomez,M.R., 1972

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

Showing articles 50 to 71 of 71 << Previous