Neudle.com: myoclonus familial

Differential
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absence

acrocyanosis

agitation

Aicardi-Goutieres syndrome

akathisia

alcohol

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amyloid angiopathy, cerebral

animal exposure

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, selection of

autonomic dysfunction

axonal spheroid

Babinski sign

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

beta adrenergic blocker

biologic markers

blindness

bone pain

bovine spongiform encephalopathy

calcification, intracranial

CAT scan

CAT scan, abnormal

CAT scan, false negative

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral vasculature

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

ceruloplasmin, serum

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

chilbran skin lesions

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

color vision, impaired

coma

confabulation

consanguinity

copper metabolism, abnormal

Creutzfeldt-Jakob disease, genetic

crying, pathologic

deafness

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, thalamic

dementia, transmissible

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

dizziness

Dravet syndrome

drooling

dropped head syndrome

dyssynergia cerebellaris myoclonica

dystonia

dystonia, children

dystonia, face

dystonia, treatment of

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

epsilon sarcoglycan gene

exome sequencing

eye movement, disorders of

failure to thrive

falling

familial

familial adult myoclonic epilepsy

fasciculation

fatal familial insomnia

fatigue

feeding disorder

fever

finger nose finger test

fingerprint bodies

fundus, abnormality of

gait disorder

gangliosidosis GM2

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

globus pallidus, lesion of

granular osmiphilic material

growth hormone

growth retardation

Hallervorden Spatz disease

hallucination

hallucination, visual

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hyperpyrexia, CNS disorder causing

hypertonia, congential

hypomyelination

hypothermia

hypotonia

iatrogenic neurologic disorders

imbalance

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

insight, loss

insomnia

intellectual deficit

intellectual deterioration

interferon alpha

intrauterine

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jewish

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Leigh's disease, adult variety

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

life expectancy

linear lesion

lipid storage disorder of CNS

liver biopsy

liver disease

lysosomal storage disease

macular degeneration

MELAS syndrome

memory, defect of recent

memory, impairment of

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, paroxysmal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, FLAIR

MRI, hypointense signal foci on

MRI, negative

MRI, punctate pattern

MRI, susceptibility weighted

multiple sclerosis, misdiagnosis

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myoclonus, stimulus sensitive

myopathy, mitochondrial

mysoline

negative

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic disease, diagnoses of

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuropsychiatry

next-generation sequencing

optic atrophy, hereditary

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pediatric neurology

penicillamine

pituitary, hormones of

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

pontocerebellar atrophy

prenatal

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

propranolol

protein 14-3-3, cerebrospinal fluid

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

ptosis

Purkinje cell

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

seizure, diagnosis of

seizure, drug resistance

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

short stature

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

speech disorder, childhood

speech, loss of

sphingolipodoses

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

spinopontine atrophy, dominant

spongy degeneration of brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

thalamus, lesion of-bilateral

titubation

tone, muscle, increased

topiramate

treatment of neurologic disorder

trinucleotide repeats

Unverricht-Lundborg disease

upgaze, paralysis of

visual acuity, decreased

visual loss

visuospatial disturbance

walking frame

walking, difficulty with

whole genome sequencing

wide based gait

Wolfram syndrome

workup

Showing articles 950 to 1000 of 2026 << Previous Next >>

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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
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Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
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Tourette's Syndrome:A Model Neuropsychiatric Disorder
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Clinicopath Conf
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A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
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Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Parkinsonism-Recognition and Differential Diagnosis
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Serotonin Syndrome
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
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Familial Occurrence of Cluster Headache
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Outcome in Familial Subarachnoid Hemorrhage
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
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Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Botulinum Toxin Treatment of Essential Head Tremor
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The Effect of Nimodipine on Essential Tremor
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
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Anticonvulsant Hypersensitivity Syndrome
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Non-Progressive Familial Idiopathic Intracranial Calcification:A Family Report
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Acute Anterior Interosseous Neuropathy in Pt with Hereditary Neuropathy with Liability to Press Palsies:Clin & EMG Study
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Familial Atrioventricular Septal Defect:Possible Genetic Mechanisms
Br Heart J 71:79-81, Kumar,A.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

The Nondystrophic Myotonias
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Superoxide Dismutase and ALS
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Monomelic Amyotrophy
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Trinucleotide Repeat Expansion in Neurological Disease
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Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
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On the Inheritance of Intracranial Aneurysms
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Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Periventricular Heterotopia and Epilepsy
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Showing articles 950 to 1000 of 2026 << Previous Next >>