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abdominal protrusion

acid maltase deficiency

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome, medical precautions with

acquired immunodeficiency syndrome-related complex

acyl CoA dehydrogenase deficiency

advances in neurology

adverse drug reaction

agenesis of corpus callosum

airway obstruction

alpha-fetoprotein

alveolar hypoventilation

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anesthesia, general

aneurysm, intracranial

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, absorption

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

arrhythmia, cardiac

arthrogryposis multiplex

ataxia, cerebellar

ataxia, paroxysmal

autoimmune disease

automatic implantable cardioverter-defibrillator

azidodeoxythymidine

bacterial infection

basal ganglia, calcification of

basal ganglia, infarction

Bassen-Kornzweig syndrome

benign congenital hypotonia

blindness, sudden

brainstem, lesion of

bulbar palsy, progressive

calcification, intracranial

calcium antagonist

calcium channel dysfunction

CAT scan, abnormal

CAT scan, muscle

cataracts, congenital

Central America

central core disease

central nervous system, infection of

central nuclei, muscle

cerebral cortical atrophy

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

chloride channel dysfunction

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

conduction block

congenital birth defects

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contractures, joint

cornea, abnormal

corpus callosum

corpus callosum, thinning

cortical blindness

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delivery, complicated

developmental abnormality of brain

developmental disability

developmental milestones

developmental retardation

differential diagnosis

difficulty climbing stairs

digits, abnormal

disability, neurological

dislocated hip, congenital

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

dystroglycanopathies

dystrophin associated proteins

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, induction

epidemiology of neurology

episodic disorders

episodic neurologic deficits

exome sequencing

face, elongated

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

familial hemiplegic migraine

Fazio-Londe's disease

feeding disorder

fetal movements, reduced

Friedreich's ataxia

frontal balding

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glycosyltransferase

gonadal dysgenesis

Gowers maneuver

Guillain Barre syndrome

Hallgren's syndrome

head circumference

heavy metal intoxication

hemorrhagic diathesis

hepatosplenomegaly

high arched feet

high arched palate

highly active antiretroviral therapy

histochemistry of muscle

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperkalemic periodic paralysis

hypertrophic cardiomyopathy

hypokalemic periodic paralysis

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

immunohistochemistry

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

intellectual deficit

intrauterine infection

intrauterine infection, viral

joint hypermobility

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

lid closure, weakness of

life expectancy

liver function enzymes

malformation, CNS, congenital

malignant hyperpyrexia

Melkersson's syndrome

mental retardation

metabolic acidosis

migraine, hemiplegic

Miller-Dieker syndrome

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

MRI, intrauterine

mucopolysaccharidoses

multicore myopathy

multiminicore disease

muscle atrophy, progressive

muscle atrophy, static

muscle hypertrophy

muscle hypertrophy, congenital

muscle stiffness

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, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myasthenic syndrome

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, focal

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myositis ossificans, progressive

myositis, bacterial

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonia, treatment of

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, primary of CNS

nerve conduction studies

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal migration disorder

neuropathy, ataxic

neuropathy, painful

neuropathy, peripheral

newborn, evaluation of

Noonan Syndrome

obstetric neurologic injuries

occipital lobe, infarction

occipital lobe, lesion of

ocular myopathy

oculopharyngeal muscular dystrophy

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

opportunistic infection

oral contraceptives

orbicularis oculi muscle

pacemaker, cardiac-transvenous

paramyotonia congenita

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paroxysmal neurologic deficits

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

poison, mercury

poison, neurologic problems with

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyositis, infantile

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

potassium channel antibodies

potassium channel dysfunction

practice guidelines

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive muscular dystrophy

progressive neurologic disorder

pseudohypertrophy

pseudoretinitis pigmentosa

psychiatric disorder

ptosis, bilateral

pulmonary stenosis

pyloric stenosis

quadriparesis, progressive

quadriplegia, transient

quality of life

ragged-red fibers

repetitive nerve stimulation

respiratory failure

retinitis pigmentosa

rigid spine syndrome

scoliosis, neurologic association with

seizure, children

seizure, injury following

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

serum alanine aminotransferase

skin, lesions in neurologic disorders

sloped shoulders

sodium channel dysfunction

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 6

standing difficulty

stem cell transplantation

stooped posture

systemic illness

temporalis muscle wasting

tongue, fasciculations of

transverse smile

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tubular aggregates, muscle

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

Usher's syndrome

viral infection

viral infection, CNS

visual field defect

visual fields, constricted

visual impairment

vitamin supplementation

vomiting, recurrent

Walker-Warburg syndrome

walking, difficulty with

weakness, congenital

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

whistle, inability to

white matter disease

wide based gait

winging of scapula

x-linked hydrocephalus

X-linked myopathy

Zika virus infection

Showing articles 750 to 800 of 1980 << Previous Next >>

Unruptured Intracranial Aneurysms - Risk of Rupture and Risks of Surgical Intervention
NEJM 339:1725-1733,1774, The Internat'l Study of Unruptured Intracranial An, 1998

Risk of Recurrent Subarachnoid Hemorrhage After Complete Obliteration of Cerebral Aneurysms
Stroke 29:2511-2513, Tsutsumi,K.,et al, 1998

Terson Syndrome:CT Evaluation in 12 Patients
AJNR 19:743-747, Swallow,C.E.,et al, 1998

Small Retinal Hemorrhages as the Only Sign of an Intracranial Aneurysm
Am J Ophthalmol 125:401-403, Kiriakopoulos,E.T.,et al, 1998

Double-Blind Randomized Trial of Tramadol for the Treatment of the Pain of Diabetic Neuropathy
Neurol 50:1842-1846, Harati,Y.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Subarachnoid Hemorrhage:Aneurysm Detection ahnd Preoperative Evaluation with CT Angiography
Radiology 208:423-430, Velthuis,B.K.,et al, 1998

Imaging of the Peripheral Nervous System:Evaluation of Peripheral Neuropathy and Plexopathy
AJNR 19:1011-1023, Maravilla,K.R.&Bowen,B.C., 1998

Dilemma of Discontin of Anticoag Therapy for Pts with Intracran Hem & Mech Heart Valves
Neurosurg 42:769-773, Eelco,F.M.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Mild Traumatic Brain Injury,Toward Understanding Manifestations and Treatment
Arch Int Med 158:90-97, Kushner,D., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Risk of Harboring an Unruptured Intracranial Aneurysm
Stroke 29:359-362, Ronkainen,A.,et al, 1998

Neurologic Outcomes in Children with Post-Pump Choreoathetosis
J Pediatr 132:162-164, Holden,K.R.,et al, 1998

Metabolic Abnormalities in Development Dyslexia Detected by 1H Magnetic Resonance Spectroscopy
Lancet 351:1849-1852, Rae,C.,et al, 1998

Calcium Antagonists in Patients with Aneurysmal Subarachnoid Hemorrhage
Neurol 50:876-883, Feigin,V.L.,et al, 1998

Quality of Life in Patients and Partners After Aneurysmal Subarachnoid Hemorrhage
Stroke 29:798-804, Hopp,J.W.,et al, 1998

Prevent of a 1st Stroke by Transfusions in Children/Sickle Cell Anemia & Abnorm Results on Transcr Doppler Ultrasonog
NEJM 339:5-11, Adams,R.J.,et al, 1998

Stroke in Children and Sickle-Cell Disease, Baltimore-Washington Cooperative Young Stroke Study
Neurol 51:169-176, Earley,C.J.,et al, 1998

Clinical Features of Moyamoya Disease in the United States
Stroke 29:1347-1351, Chiu,D.,et al, 1998

Mortality and Morbidity of Surgery for Unruptured Inracranial Aneurysms
Stroke 29:1531-1538, Raaymakers,T.W.M.,et al, 1998

Intracerebral Haemorrhage Caused by Drug Abuse
Lancet 351:1029, McEvoy,A.W.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Extramedullary Hematopoiesis Causing Paraparesis in Congenital Cyanotic Heart Disease
Neurol 51:636-637, Taylor,C.L.,et al, 1998

Cerebral Aneurysmal Arteriopathy in Childhood AIDS
Neurol 51:560-565, Dubrovsky,T.,et al, 1998

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 1998

Pupil Involvement in Patients with Diabetes-Associated Oculomotor Nerve Palsy
Arch Ophthalmol 116:723-727, 7981998., Jacobson,D.M., 1998

Managing Oculomotor Nerve Palsy
Arch Ophthalmol 116:798, Trobe,J.D., 1998

Diabetes Mellitus and the Nervous System
JNNP 65:620-632, Watkins,P.J.&Thomas,P.K., 1998

Management Issues for Women with Epilepsy,A Review of the Literature
Neurol 51:949-956, Zahn,C.A.,et al, 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Intracranial Aneurysm Rupture Presenting as Delayed Stroke Secondary to Cerebral Vasospasm
Stroke 28:2078-2080, Nussbaum,E.S.,et al, 1997

Long-Term Stroke Risk in Children with Sickle Cell Disease Screened with Transcranial Doppler
Ann Neurol 42:699-704, Adams,R.J.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Showing articles 750 to 800 of 1980 << Previous Next >>