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Differential
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achilles tendon, enlarged
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adult polyglucosan body disease
advances in neurology
affect, inappropriate
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
Angelman syndrome
antidepressant
antitoxin
apnea
applause sign
arm weakness
aspiration
asymmetric crying facies
ataxia
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
BiPAP
bladder dysfunction
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, infarction of
brainstem, lesion of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
calcification, intracranial
caries
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebral dominance
cerebrovascular accident
cerebrovascular accident, bilateral
children
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital birth defects
congenital heart disease
congenital malformation
constipation
contractures, joint
conversion reaction
cortical blindness
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cystatin C mutation
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, frontotemporal
depression
developmental disability
developmental retardation
differential diagnosis
disability rating scale, neurological
disability, neurological
distal muscle weakness
drooling
dying
dysarthria
dysdiadochokinesia
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
eating disorder
echocardiogram
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
epidemiology of neurology
Erdheim-Chester disease
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial asymmetry
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fibrillations
flail arm syndrome
floppy infant
fluoxetine
foam cells
food poisoning
food-borne infection
foot drop
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
growth hormone deficiency
growth retardation
hand flapping
head bobbing
hearing loss
heel swelling
hemiparesis
heralding manifestation
histiocytosis
honey
hospice
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hypogonadism
hypometric saccades
hypopigmentation of skin
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
infant, evaluation of
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
intubation
irritability
irritable baby
jaw jerk, abnormal
Jewish
laughing
laughing, pathologic
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
life expectancy
locked-in syndrome
masked facies
memory, defect of recent
memory, impairment of
mental retardation
merosin
middle cerebellar peduncle, lesion
mimics
misdiagnosis
molecular genetics
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, mouse ears
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscular dystrophy
muscular dystrophy, congenital
mutism
myelomalacia
myeloneuropathy
neck weakness
neurogenic bladder
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathy
neuroprotective agents
neurotoxin
next-generation sequencing
obesity
ocular bobbing
opened mouth
ophthalmoplegia
optic neuropathy
palliative care
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
peroxisomal disease
personality change
photosensitivity, skin
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymicrogyria
pons, infarction of
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychomotor retardation
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
rash
release phenomena
respirator
respiratory arrest
respiratory failure
retinopathy
review article
riluzole
risk factors
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sertraline
short stature
skew deviation
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
stooped posture
strabismus
suck, poor
symmetric brain lesions
systemic illness
tachycardia
temper tantrums
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
toxins, nervous system
tracheostomy
trauma
treatment of neurologic disorder
tremulousness
tripping
ultrasonography
urinary incontinence
very long chain fatty acids
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
wheelchair
white matter disease
wide based gait
Showing articles 1200 to 1250 of 2560 << Previous Next >>

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Simultaneous, Multiple Cranial Neuropathies in Diabetes Mellitus
J Neuro-Ophthalmol 15:219-224, Eshbaugh,C.G.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Neurologic Manifestations in Children with Lyme Disease
Pediatrics 96:1053-1056, Bingham,P.M.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Central Nervous System Disease in a Child with Primary Sjogren Syndrome
J Pediatr 127:961-963, Ohtsuka,T.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Renal Cell Carcinomatous Meningitis:Pathologic and Immunohistochemical Features
Neurol 45:189-191, Crino,P.B.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Permanent Hemiparesis Due to Partial Status Epilepticus
Neurol 45:187-188, Borchert,L.D.&Labar,D.R., 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

Hemiplegia Vegetativa Alterna (Ipsilateral Horner's Synd & Contralat Hemihyperhidrosis) Post Cerebral Art Occl
Stroke 26:702-704, Bassetti,C.&Staikov,I.N., 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

AIDS-Associated Progressive Multifocal Leukoencephalopathy Revealed by New-Onset Seizures
Am J Med 99:64-68, Moulignier,A.,et al, 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Cranial Nerve Enhancement in the Guillain-Barre Syndrome
AJNR 16:923-925, Fulbright,R.K.,et al, 1995

Clinical Relevance and Frequency of Transient Stenoses of the Middle and Anterior Cerebral Arteries in Bacterial Meningitis
Stroke 26:1399-1403, Muller,M.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Neuro-Ophthalmologic Manifestations of Lyme Disease
Ophthalmology 97:699-706, Lesser,R.L.,et al, 1995

Myelitis Due to Coxsackievirus B Infection
Neurol 45:1626-1627, Jadoul,C.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Intramuscular Inject W/in 30 D of Immun with Oral Poliovirus Vaccine-Risk Factor for Vaccine-Assoc Paral Polio
NEJM 332:500-506, 5291995., Strebel,P.M.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Pamidronate Treatment of the Neurologic Sequelae of Pagetic Spinal Stenosis
Arch Int Med 155:1813-1815, Wallace,E.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Pain and Remote Weakness in Limbs Injected with Botulinum Toxin A for Writer's Cramp
Lancet 346:154-156, Sheean,G.L.,et al, 1995



Showing articles 1200 to 1250 of 2560 << Previous Next >>