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acanthocytosis
acetylcholine
advances in neurology
algorithm
Alzheimer's disease
amantadine
amyotrophic lateral sclerosis
anticholinesterase
antioxidant
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
Babinski sign
Bassen-Kornzweig syndrome
biologic markers
blindness
blood dyscrasias, neurologic findings with
brainstem, atrophy
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar vermis
cerebral glucose metabolism
cerebrovascular accident
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
congestive heart failure
consanguinity
controversies in neurology
cornea, abnormal
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diabetes mellitus
disability, neurological
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
endocardial fibrosis
ethics in neurology
eye movement, disorders of
falling
familial
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gargoylism
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
Hallgren's syndrome
hammertoes
head injury
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypotonia
imbalance
incoordination
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Laurence-Moon-Bardet-Biedl syndrome
lecithin
leg weakness, bilateral
Leigh's disease
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
malformation, CNS, congenital
malondialdehyde
Marinesco-Sjogren syndrome
mental retardation
metabolic disorder, primary
misdiagnosis
mitochondrial disease
molecular genetics
MRI
MRI, abnormal
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myelomalacia
myopathy
myopia
myotonia dystrophica
nerve conduction studies
neuritis
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, amyloid
nystagmus
obesity
ocular motility, disorders of
ocular myopathy
optic atrophy
paraparesis, familial spastic
Parkinson disease
pathologic reflex
pes cavus
physostigmine
polydactyly
polyneuropathy
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudoretinitis pigmentosa
psychiatric disorder
remote effect of cancer on the nervous system
retinitis pigmentosa
retinopathy
review article
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
sensory loss
spastic ataxia
spasticity
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
staggering
tandem gait, ataxic
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
Usher's syndrome
vibratory sensation
vibratory sensation, abnormal
visual evoked response
visual field defect
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
Showing articles 900 to 950 of 1254 << Previous Next >>

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Clinicopath Conf
Paraneoplastic Encephalitis (Limbic and Brain-Stem Encephalitis) , Case Record 39-1988, NEJM 319:849, 860,, 1988

Pontine Lesion in Opsoclonus-Myoclonus Syndrome Shown by MRI
JNNP 51:1572-1575, Hattori,T.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Opsoclunus, Myoclonus, Ataxia & Encephalopathy in Adults with Cancer:A Distinct Paraneoplastic Syndrome
Medicine 67:100-109, Anderson,N.E.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Thalamic Astasia:Inability to Stand After Unilateral Thalamic Lesions
Ann Neurol 23:596-603, Masdeu,J.C.&Gorelick,P.B., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Effect of Sulfamethoxazole & Trimethoprim on Neurologic Dysfunction in a Patient with Joseph's Disease
Arch Neurol 45:210-213, Mello,K.A.&Abbott,B.P., 1988

Clinicopath Conf
Infiltrating Carcinoma of Breast (Paraneoplastic Opsoclonus Syndrome & SIADH) Case 9-1988, NEJM 318:, 63-578., 1988

Alternating Skew on Lateral Gaze (Bilateral Abducting Hypertropia)
Ann Neurol 23:190-192, Moster,M.L.,et al, 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Ataxic Hemiparesis:Three Different Locations of Lesions Studied by MRI
Neurol 38:1322-1324, Helweg-Larsen,S.,et al, 1988

Cerebellar Stroke
Editorial, Lancet 1:1031-10321988., , 1988

The Clinical and Computed Tomographic Features of Cerebellar Peduncular Hemorrhage
Neurol 38:1485-1487, Wizer,B.,et al, 1988

Dissection of the Intracranial Vertebral Artery
Neurol 38:868-877, Caplan,L.R.,et al, 1988

Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Rett's Syndrome, Correlation of Electroencephalogram Characteristics with Clinical Staging
Arch Neurol 44:1053-1056, Glaze,D.G.,et al, 1987

Ataxia After Severe Head Injury:The Pathological Substrate
Ann Neurol 22:77-79, Chester,C.S.&Reznick,B.R., 1987

Somatosensory Evoked Potentials in Lacunar Syndromes of Pure Motor & Ataxic Hemiparesis
Stroke 18:1093-1097, Kelly,M.A.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Acute Trimethyltin Limbic-Cerebellar Syndrome
Neurol 37:945-950, Besser,R.,et al, 1987

Plasma R Binder Deficiency & Neurologic Disease
NEJM 317:1330-1332, Sigal,S.H.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Vitamin E Deficiency & Neurologic Disease in Adults with Cystic Fibrosis
Ann Int Med 107:51-54, Sitrin,M.D.,et al, 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Neurologic Manifestations of Heatstroke at the Mecca Pilgrimage
Neurol 37:1004-1006, Yaqub,B.A., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Clinicopath. Conf
Cryptococcal Meningitis & Septicemia, AIDS After Platelet Tranfusion, Case 41-1987, NEJM 317:946-953, , 1987

Delayed Cerebellar Ataxia:A New Complication of Falciparum Malaria
BMJ 294:1253-1254, Senanayake,N., 1987

Idiopathic Hypoparathyroidism with Extensive Brain Calcification & Persistent Neurologic Dysfunction
Neurol 37:307-309, Friedman,J.H.,et al, 1987

Long Term Exposure to Hydrogen Sulphide Producing Subacute Encephalopathy in a Child
BMJ 294:614, Gaitonde,U.B.&Sellar,R.J., 1987

Clinical & Magnetic Resonance Features of Primary Intracranial Arachnoid Cysts
Ann Neurol 21:342-348, Gandy,S.E.&Heier,L.A., 1987



Showing articles 900 to 950 of 1254 << Previous Next >>