Neudle.com: genetic linkage

Differential
(Click to cross reference)

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

amniocentesis

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

apraxia of eye movements

arteriopathy

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

Bassen-Kornzweig syndrome

benign familial neonatal convulsions

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain biopsy

brainstem, lesion of

brainstem, neoplasms of

bulbar palsy, progressive

cafe au lait spots

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebro hepato renal syndrome

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chorea

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

clubfoot as related to neurologic disease

Cockayne's syndrome

coma

compression neuropathy

compression neuropathy, recurrent

cost effectiveness

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cyst, neoplastic cerebellum

cytomegalovirus infection

degenerative diseases of CNS

dementia

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dentate nuclei

dentate nuclei, lesion of

developmental retardation

diabetes mellitus

DNA probes

drooling

drug induced neurologic disorders

dysarthria

dysmorphic

dystonia

dystonia musculorum deformens

electronystagmography

electroretinograph

encephalitis

encephalitis, focal

encephalitis, Rasmussen's

encephalitis, viral

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

eye movement, disorders of

face, elongated

facial appearance, abnormal

familial

fasciculation

fatal familial insomnia

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gadolinium

gait disorder

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

GFAP gene

gonadotropin-releasing hormone

growth retardation

gynecomastia

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hyperactivity

hyperekplexia

hyperhidrosis

hyperkalemic periodic paralysis

immunoperoxidase staining

immunosuppression

in situ hybridization

inclusion bodies, intracytopasmic

insomnia

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

Jakob-Creutzfeldt disease

joint hypermobility

Kallmann's syndrome

Kearns-Sayre syndrome

KRIT1 gene

Kugelberg-Welander syndrome

Laurence-Moon-Bardet-Biedl syndrome

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malignant hyperpyrexia

manic-depressive

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

meningitis

meningitis, recurrent

meningitis, relapse

mental retardation

mental retardation, familial

mononeuropathy, recurrent

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscular dystrophy, Becker

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myelin basic protein gene

myoclonus

myopathy

myopathy, mitochondrial

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, posterior fossa

neoplasm, primary intracranial

neoplasm, primary of CNS

neurocutaneous disease

neurofibromatosis 2, presymptomatic

neurologic disease

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, peripheral

night blindness

Notch3 gene

ocular motility, disorders of

oculopharyngeal muscular dystrophy

paraparesis, familial spastic

paraparesis, spastic

paroxysmal dystonic choreoathetosis

paroxysmal neurologic deficits

pathology

patient information and support

periodic paralysis

peroxisomal disease

pheochromocytoma

pigmentary retinopathy

polycystic kidneys

polymerase chain reaction

polyneuropathy, familial

posterior fossa, lesion of

practice guidelines

prenatal diagnosis by amniocentesis

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive spinal muscular atrophy

proximal myotonic myopathy

radiation hypersensitivity

seizure, intractable, treatment of

seizure, neonatal

sensorineural hearing loss

simian crease

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small vessel disease

Southern immunoblot test

spasticity

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spondylosis

spongy degeneration of brain

startle reaction

stuporous

subarachnoid hemorrhage

synkinesis

tapetoretinal degeneration

telangiectases

testicular enlargement

thalamus, lesion of

tinnitus

tomaculous neuropathy

trauma

treatment of neurologic disorder

trinucleotide repeats

Usher's syndrome

ventricular garlands

vibratory sensation, abnormal

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, difficulty with

Werdnig-Hoffman disease

Western immunoblot test

wheelchair

white matter disease

X-linked bulbospinal neuronopathy

x-linked mental retardation

X-linked neuropathy

Showing articles 1650 to 1700 of 1744 << Previous Next >>

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Autosomal Dominant Neurological Disorders
Ann Neurol 4:548-552, Brady,R.O.,et al, 1978

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

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Supratentorial Leptomeningeal Hemangioblastoma
Neurol 28:727, Lee,K.R.,et al, 1978

Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 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

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

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
Neurol 27:1107-1113, Griffin,J.W.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Neuroectodermal Tumors in the Cerebellum in Two Sisters
JNNP 40:886, Thomas,M.,et al, 1977

An unusual Cause of Apparent Epilepsy:ECG & EEG Findings in a Case of Jervell Lange-Neilson Syndrome
JNNP 40:1102, Selby,P.J.,et al, 1977

Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
Ann Neurol 2:285, Lance,J.W., 1977

Hereditary Chorea Without Dementia
JNNP 40:687, Behan,P.O.,et al, 1977

Clinical Neurogenetics
Neurol 27:1057, Bird,T.D.,et al, 1977

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Intracranial Aneurysms:Characteristics of Aneurysms in Siblings
NEJM 297:115, 1977. (Letter), Andrews,R.J., 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Familial Spasmodic Torticollis
Neurol 27:11, Gilbert,G.J., 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Familial Nonprogressive Involuntary Movements of Childhood
Ann Neurol 1:602 1977., Damasio,H.,et al, 1977

Gilles de la Tourette's syndrome:Clinical, Genetic, Psychologic, & Biochemical Aspects in 21 Selected Families
Neurol 27:115, Eldridge,R.,et al, 1977

Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
NEJM 296:210, VanWoert,M.H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 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

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

Juvenile Parkinsonism Treated with Levodopa
Arch Neurol 34:244, Sachdev,K.K.,et al, 1977

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

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976

Myasthenic Abduction Nystagmus in a Patient with Hyperthyroidism
Neurol 26:589, Finelli,P.F.&Hoyt,W., 1976

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
NEJM 295:62, Blass,J.P.,et al, 1976

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Showing articles 1650 to 1700 of 1744 << Previous Next >>