Neudle.com: molecular genetics

Differential
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abscess, intracerebral

acanthocytosis

acetazolamide

aciduria

acoustic nerve, vestibular division of

acoustic neurinoma

acquired immunodeficiency syndrome

acromicria

Adies pupil

adrenal mass

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agitation

Alexanders disease

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, pathogenesis

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid beta protein

amyloid plaques

amyotrophic lateral sclerosis

anaplastic large cell lymphoma

aneurysm, intracranial, screening for

anterior horn cell disease

anterior tibial muscle weakness

antibiotic prophylaxis

antibiotics

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, selection of

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arteriovenous malformation, cerebral

arthralgia

arthritis

arthrogryposis multiplex

ataxia telangiectasia

ataxic-dystonia syndromes

ATP1A3 gene

atrioventricular block

attention deficit disorder with hyperactivity

atypical

autism

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic dysfunction

azidodeoxythymidine

Babinski sign

bacterial infection

bacterial infection, CNS

baldness

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biotinidase deficiency

bitemporal visual field defect

brachial plexus neuropathy

brachial plexus neuropathy, familial

bradycardia

brain atrophy

brain biopsy

brain biopsy, negative

calcification, intracranial

carcinoma of pancreas

CAT scan, emission, abnormal

CAT scan, false negative

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, origin and treatment

cerebral edema, vasogenic

cerebral embolism

cerebral palsy

cerebral palsy, etiology

cerebral palsy, work up

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, childhood

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, silent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

children

chloride channel dysfunction

cholecystitis

chorea

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate gyrus

cirrhosis

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

cognition

collagen vascular disease

coma

coma, sudden onset

complications

compression neuropathy

compression neuropathy, recurrent

conduction block

confidentiality

confusion

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

controversies in neurology

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical ribbon sign

cranial nerve enhancement

cranial nerve tumor

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cry, abnormal

cry, weak

cultured skin fibroblasts

cyst

cyst, benign intracranial

cyst, cortical parenchyma

degenerative diseases of CNS

dementia, rapidly progressive

dementia, transmissible

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental abnormality of brain

developmental disability

developmental evaluation

developmental retardation

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

diplopia

disease modifying agents

distal muscle atrophy

distal muscle weakness

diurnal variation

DNA probes

DNA sequencing

dopa responsive dystonia

dopaminergic dysfunction

double-cortex syndrome

drooling

drug induced neurologic disorders

dystonia musculorum deformens

dystonia, children

dystonia, etiology of

dystonia, painful

dystroglycanopathies

dystrophin

dystrophin associated proteins

eating disorder

edema, pedal

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electromyogram

electron microscopy

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, diagnosis of

encephalitis, viral

encephalitis, viral-causes of

encephalopathy

encephalopathy, acute

encephalopathy, progressive

endolymphatic sac tumors

epidemiology of neurology

executive dysfunction

exercise

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

fatal familial insomnia

fine motor function, impaired

fingerprint bodies

fish

fistula, arterio-venous, pulmonary

fourth ventricle, compression

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gastrointestinal bleeding

Gaucher's disease

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1 deficiency syndrome

glycogen storage disease

gram positive cocci

gray hair

grimacing

growth hormone deficiency

growth retardation

Guillain Barre syndrome

headache, awakening with

headache, positional

headache, progressive

hearing loss

heart block

heart block, complete

heart murmur

helminthic infection of CNS

hemangioblastoma

hemianopia, homonymous

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniation syndromes, intracranial

histochemistry of muscle

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hyperactivity

hyperammonemic encephalopathy

hypercapnia

hyperhomocysteinemia

hyperkalemic periodic paralysis

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

immunosuppressive agents

immunotherapy

in situ hybridization

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

insular cortex, lesion

intellectual deficit

intellectual deterioration

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intranasal medication

intrauterine infection

intrauterine infection, viral

intravenous drug abuse

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Kayser-Fleischer ring

Kearns-Sayre syndrome

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms

leg spasms, painful

leg weakness, bilateral

leukoencephalopathy with calcification and cysts

leukopenia

level of consciousness, decreased

lipid storage disorder of CNS

lissencephaly

liver disease

liver function enzymes

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malignant hyperpyrexia

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, leptospira

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylmalonic acidemia

mexiletine

microcephaly

micrognathia

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

miglustat

migraine

Miller-Dieker syndrome

mimics

mineralization

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

molecular markers

mononeuropathy

mononeuropathy, recurrent

MRI, contrast enhanced

MRI, diffusion weighted

MRI, nodular enhancement

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelin protein zero gene

myelitis, longitudinal

myopathy, centronuclear

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, mitochondrial

myotonia dystrophica, classification

myotonia dystrophica, type 2

nemaline rod myopathy

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nephritis

nerve biopsy

nerve biopsy, indication

nerve conduction studies

nerve hypertrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurofibromin

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic practice

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, work up for

neurotomy

newborn, evaluation of

next-generation sequencing

obsessive-compulsive disorder

occipital lobe

ocular motility, disorders of

oculogyric crisis

oculopharyngeal muscular dystrophy

ophthalmoplegia, progressive external

optic atrophy

optic atrophy, hereditary

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

organomegaly

ornithine transcarbamylase deficiency

orthostatic hypotension

ovarian dysgenesis

overlap syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paraparesis, spastic

paraplegin

parasitic infection, CNS

paresthesias

Parkinson disease

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, pathogenesis of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

patient information and support

penicillamine

percussion induced muscle contraction

periodic paralysis

peripheral blood smear

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

POLG1 gene

polyglucosan body disease

polymerase chain reaction

polymicrogyria

polyneuropathy, familial

pons, lesion of

positive sharp waves

posterior fossa, lesion of

postural abnormality

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, dilated and fixed, bilateral

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia

quality of life

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly fatal neurologic illness

respiratory tract infection

reversible neurologic disorder

rhabdomyosarcoma of heart

saccadic eye movements, abnormal

salivation, excessive

sedimentation rate, elevated

seizure

seizure, focal

seizure, laughing as manifestation

seizure, paradoxical

seizure, treatment of

senile plaques

sensorineural hearing loss

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

shagreen patch

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

sleep pathology and physiology

slit lamp examination

small vessel disease

SMN1 gene

sodium channel dysfunction

South America

spartin

spastic ataxia

spastic paraplegia, type 7

spinal cord degeneration

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar degeneration

spirochete infection

splenomegaly

spongy degeneration of brain

striatal encephalitis

strokelike episodes

subarachnoid hemorrhage

survival motor neuron gene

symmetric brain lesions

telangiectases, retinal

temozolomide

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

thalassemia

thalassemia/mental retardation syndrome

tomaculous neuropathy

tongue, protrusion of

trauma

travel, foreign

treatment of neurologic disorder

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis, screening for

tumefactive lesion

twins

ultrasonography, head

ultrasonography, head, fetus-neonate

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary catecholamines

urinary urgency

urine test for metabolic disorders

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, transient

visual obscurations, transient

visuospatial disturbance

vitamin E deficiency

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, delayed

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

Western immunoblot test

white matter disease, unilateral

whole genome sequencing

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Zika virus infection

zinc

Showing articles 1200 to 1250 of 1775 << Previous Next >>

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Brain Tumors
NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991

Detection of Tuberous Sclerosis in Parents by Magnetic Resonance Imaging
Neurol 41:262-265, Roach,E.S.,et al, 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

A Genetic Study of Idiopathic Focal Dystonias
Ann Neurol 29:320-324, Waddy,H.M.,et al, 1991

Mental Retardation in Turner Syndrome
J Pediatr 118:415-417, VanDyke,D.L.,et al, 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
Neurol 41:437-439, Bird,S.J.&Sladky,J.T., 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991

Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
Neurol 41:1313-1315, Visy,J.M.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers
Neurol 41:992-999, Farrer,L.A.,et al, 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Recurrent Meningitis in a Patient with Congenital Deficiency of the C9 Component of Complement
Arch Int Med 150:2395-2399, Zoppi,M.,et al, 1990

Cytomegalovirus and Rasmussen's Encephalitis
Lancet 336:1282-1284, Power,C.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Conjugal Temporal Arteritis
Neurol 40:1839-1842, Galetta,S.L.,et al, 1990

Multiple Sclerosis Sibling Pairs:Clustered Onset and Familial Predisposition
Neurol 40:1546-1552, Doolittle,T.H.,et al, 1990

Risk Factors for Multiple Sclerosis:Race or Place? Editorial
JNNP 53:821-823, 903, 906990., Compston,A., 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

AIDS-Assoc Progressive Multifocal Leukoencephalopathy (PML) :Comparison to Non-AIDS PML
Neurol 40:1073-1078, Aksamit,A.J.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Familial Meningioma
Neurol 40:312-314, McDowell,J.R., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy & Adrenomyeloneuropathy Present in the Same Family
Arch Neurol 47:665-669, Willems,P.J.,et al, 1990

Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
Ann Neurol 28:387-390, Gospe,S.M.&Gabor,A.J., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
NEJM 322:1293-1298, Albin,R.L.,et al, 1990

Progress in Tuberous Sclerosis
Editorial, Lancet 336:598-5991990., , 1990

Showing articles 1200 to 1250 of 1775 << Previous Next >>