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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
algorithm
alpha glucosidase
alpha-fetoprotein
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
aphasia
aphasia, progressive, primary
apraxia of eye movements
areflexia
arm weakness
aspartate aminotransferase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
Babinski sign
behavioral disorder
bulbar palsy
calf hypertrophy
camptocormia
cane
carcinoembryonic antigen
carcinoma
cardiomyopathy
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
cognition
congenital heart disease
congenital myopathy
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dystonia
efficacy
emotional lability
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
epidemiology of neurology
exercise
eye movement, disorders of
facial weakness, bilateral
familial
fasciculation
floppy infant
fluency
foot drop
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
growth retardation
hallucination
hand weakness
hemiparesis
hepatomegaly
heralding manifestation
history of neurology
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inflexibility, mental
intellectual deficit
intrinsic hand muscles, wasting of
jaw jerk, abnormal
Kugelberg-Welander syndrome
laughing, pathologic
leg atrophy
leg weakness, bilateral
leukemia
life expectancy
lobar atrophy
lymphoma
lysosomal storage disease
lysosomes, abnoral
mental retardation
Mills syndrome
mimics
misdiagnosis
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
motor system
movement disorder
movement disorder, extrapyramidal
MRI, abnormal
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myelomalacia
myopathy
myotonia congenita
neck weakness
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic evaluation
neuronal degeneration
neuropathology
neuropathy
newborn, evaluation of
next-generation sequencing
nusinersen
ocular motility, disorders of
pain, increased response
palliative care
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
Parkinsonism syndrome
Parkinsonism-dementia complex
pathology
patient information and support
personality change
Pompe's disease of glycogen storage
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
radiation hypersensitivity
release phenomena
respiratory failure
review article
risk factors
safety
scoliosis
scoliosis, neurologic association with
screening
single photon emission computed tomography
skin, lesions in neurologic disorders
SMN1 gene
spastic ataxia
spasticity
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
stereotyped behavior
superoxide dismutase
survival motor neuron gene
telangiectases
tongue, enlarged
tongue, fasciculations of
trauma
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
wheelchair
word-finding difficulty
workup
Showing articles 1050 to 1100 of 7771 << Previous Next >>

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Thalamic Hemorrhage with Intraventricular Hemorrhage in the Full-Term Newborn
Pediatrics 85:737-742, Rowland,E.H.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

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

Acute Relapsing Guillain-Barre Syndrome after Long Asymptomatic Intervals
Arch Neurol 47:82-84, Wijdicks,E.F.&Ropper,A.H., 1990

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Traumatic Basal Ganglia Hemorrhage:Clinicopathologic Features and Outcome
Neurol 39:897-904, Katz,D.I.,et al, 1989

Short-Term Outcomes of Skull Fracture:A Population-Based Study of Survival and Neurologic Complications
Neurol 39:96-102, Wiederholt,W.C.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Cardiorespiratory Responses to Aerobic Training by Patients with Postpoliomyelitis Sequelae
JAMA 261:3255-3258, 32941989., Jones,D.R.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

Traumatic Monocular Blindness and Associated Carotid Injuries
Pediatrics 84:128-134, King,M.A.,et al, 1989

Neck Sprains after Car Accidents, A Common Cause of Long Term Disability
BMJ 298:973-974, Porter,K.M., 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Brain Damage by Neonatal Hypoglycaemia
Editorial, Lancet 1:882-8831989., , 1989

Tuberculous Meningitis in Children:Treatment with Isoniazid and Rifampicin for Twelve Months
J Pediatr 114:875-879, Visudhiphan,P.&Chiemchanya,S., 1989

Neurological Outcome after Out-of-Hospital Cardiac Arrest, Prediction by Cerebrospinal Fluid Enzyme Analysis
Arch Neurol 46:753-756, Roine,R.O.,et al, 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
Neurol 39:282-283, Sadeh,M.,et al, 1989

Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
J Pediatr 114:194-203, Levin,M.,et al, 1989

Morbidity for Survivors of Extracorporeal Membrane Oxygenation:Neurodevelopmental Outcome at 1 Year of Age
Pediatrics 83:72-78, Glass,P.,et al, 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Primary Lateral Sclerosis in a Child
Neurol 39:1530-1532, Grunnet,M.L.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Neurologic Status and Intracranial Hemorrhage in Very-Low-Birth Weight Preterm Infants
Am J Dis Child 143:1186-1190, Ford,L.M.,et al, 1989

Perioperative Nerve Lesions
Arch Neurol 46:1355-1360, Dawson,D.M.&Krarup,C., 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Incidence of Guillain-Barre Syndrome During a Nationwide Oral Poliovirus Vaccine Campaign
Neurol 39:1034-1036, Kinnumen,E.,et al, 1989

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Prediction of Delayed Cerebral Ischemia, Rebleeding, and Outcome After Aneurysmal Subarachnoid Hemorrhage
Stroke 19:1250-1256, Hijdra,A.,et al, 1988

Quality of Life 4 Years After Stroke
Stroke 19:1101-1107, Niemi,M.L.,et al, 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Septic Thrombosis of the Cavernous Sinuses
Arch Neurol 45:567-572, DiNubile,M.J., 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

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

Medical Decisions and Prognostications of Pediatricians for Infants with Meningomyelocele
J Pediatr 113:835-840, Siperstein,G.N.,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

Pituitary Apoplexy
BMJ 297:1526-1527, Lewin,I.G.,et al, 1988

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



Showing articles 1050 to 1100 of 7771 << Previous Next >>