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abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
amyloidosis
anemia
angiography, cerebral
angiography, posterior fossa
anhidrosis
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arteriopathy
arthrogryposis multiplex
arylsulfatase B
atlanto-axial subluxation
band keratopathy
basal ganglia, calcification of
birth injury
blindness
bone marrow transplantation
calcification, intracranial
carcinoma
carotid artery occlusion, neck
CAT scan
CAT scan, abdomen
CAT scan, abnormal
cataracts
cataracts, congenital
cavernous sinus, syndrome
central nervous system, infection of
cerebellar hypoplasia
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cervical spine
children
chorioretinitis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital heart disease
congenital infection, CNS
conjunctival injection
contractures, joint
cornea
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corneal edema
corpus callosum
corpus callosum, hypoplastic
cranial neuropathy, multiple
cultured skin fibroblasts
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
dementia
dementia, presenile
developmental retardation
diarrhea
diplopia
diplopia, monocular
dissociated sensory loss
donut sign
dural sinus thrombosis
dwarfism
dysmorphic
dysostosis multiplex
dyspraxia
ear, abnormal
echocardiogram
ectatic basilar artery
eculizumab
edema, pedal
electroretinograph
empyema, epidural
empyema, subdural
encephalocele
enzyme treatment
enzyme, defect
epidermal nevus syndrome
eye movement, painful
Fabry's disease
facial appearance, abnormal
facial weakness, bilateral
fatty acid, elevated plasma content
fever
fungal infection, CNS
gangliosidosis GM1
gangliosidosis GM2
gene
genetic counselling
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genetic diagnosis, prenatal
genetic neurologic disorders
genu valgum
glaucoma
headache
headache, severe
hearing loss
hemianopia
hemiparesis
hemoglobinuria
hemolysis
hemorrhoids
hepatomegaly
hepatosplenomegaly
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydronephrosis
hypertension
hypopyon
hypotonia
hypotonia, infants
inclusion bodies
inclusion bodies, intracytopasmic
intelligence quotient
intracerebral hemorrhage
intraocular pressure, increase
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iritis
jugular foramen syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
life expectancy
lipid storage disorder of CNS
lissencephaly
lymphadenopathy
lymphoma
lymphoma, ocular
lymphoma, systemic
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mastoiditis
memory, impairment of
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micropolygyria
micropthalmia
mitral valve prolapse
monoclonal antibodies
Morquio syndrome
mortality
MRI
MRI, abnormal
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
myelopathy
myotonia dystrophica
nasal stuffiness
neck pain
neoplasm, metastatic to eye
nerve conduction studies
neurocutaneous disease
neurofibromatosis 2
neurolipidosis IV
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurosis
nevus
Niemann-Pick disease
nystagmus
ophthalmoplegia
optic atrophy
optic nerve
optic nerve, hypoplasia of
optic nerve, neoplasm of
optic neuritis
oral contraceptives
orbit, lesions of
osteomyelitis
osteomyelitis, skull
osteoporosis
otitis, neurologic complications with
pachygyria
pain
pain, abdominal
pain, head
papilledema
paraparesis, spastic
paroxysmal nocturnal hemoglobinuria
patent ductus arteriosus
pectus carinatum
periventricular leukomalacia
photosensitivity, skin
polycystic kidneys
polyneuropathy
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prognosis
proteinuria
pseudohypopyon
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
pupil, abnormality in neurologic disorders
quadriparesis
rash
red eye
renal failure
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rubella syndrome
sarcoidosis
seizure
seizure, neonatal
sensorineural hearing loss
short neck
short stature
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, bony defect on
slit lamp examination
spinal cord, compression of
splenic-vein thrombosis
splenomegaly
stem cell transplantation
stillbirth
sweating, abnormality of
Tangier's disease
third nerve palsy
thrombocytopenia
tinnitus
tongue, enlarged
torticollis
treatment of neurologic disorder
uremia
urinary incontinence
uveitis
varicose veins
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection, CNS
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual impairment
visual loss
Walker-Warburg syndrome
white matter disease
Showing articles 400 to 450 of 522 << Previous Next >>

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,J.,et al, 1982

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Prognosis in Nontraumatic Coma
Ann Int Med 94:293-301, Levy,D.E.,et al, 1981

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Neurologic Prognosis After Cardiopulmonary Arrest:IV. Brainstem Reflexes
Neurol 31:1092-1097, Snyder,B.D.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Human-To-Human Transmission of Rabies Virus by Corneal Transplant
NEJM 300:603-604, Houff,S.A.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Allopurinol Not Effective In Muscular Dystrophy
NEJM 301:785, Bakouche,P.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979



Showing articles 400 to 450 of 522 << Previous Next >>