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Differential
(Click to cross reference)
abdominal muscle paralysis
acetylcholine
acetylcholine in CNS
acetylcholine receptor
acetylcholine receptor antibody
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
agalsidase alfa
albinism
algorithm
alopecia
alpha galactosidase A deficiency
alpha glucosidase
Alzheimer's disease
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amnesia
amniocentesis
amphetamines
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
ANA
anemia
anemia, hemolytic
aneurysm
angiokeratoma
angiotensin-converting enzyme
anorexia nervosa
anterior horn cell disease
anti IgLON5
anticonvulsants
anticonvulsants, hypersensitivity syndrome
anticonvulsants, untoward effects of
antidepressant
antiendomysial antibodies
apraxia
apraxia of eye movements
areflexia
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
arrhythmia, CNS causes of
arteritides
arthralgia
arthritis
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
athetosis
autism
autoantibodies
autoimmune disease
automatic behavior
automobile accidents
autonomic dysfunction
azathioprine
B 12 deficiency
Babinski sign
bacterial infection
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Behcet's syndrome
biologic markers
biotin deficiency
biotinidase deficiency
blindness
blood dyscrasias, neurologic findings with
bone marrow transplantation
bradykinesia
brain atrophy
brain biopsy
brain purpura
brainstem
brainstem, dysfunction
brainstem, infarction of
brainstem, lesion of
bruit
bulbar dysfunction
bulbar palsy
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
campylobacter infection
Canavan's disease
carbamazepine
carbamazepine, toxicity
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
cardiomegaly
cardiomyopathy
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carotid siphon
carotid-siphon occlusion
CAT scan
CAT scan, abnormal
CAT scan, false negative
catalepsy
cataplexy
cataracts
caudate nucleus, lesion of
celiac disease, adult
celiac disease, childhood
central hypoventilation
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, glycine
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, pathophysiology
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
Chediak-Higashi syndrome
cherry red spot
cherry red spot-myoclonus syndrome
children
cholesterol
choline acetyltransferase
choline chloride
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
codfish vertebrae
coenzyme Q10 deficiency
Cogan's syndrome
cognition
coma
comorbidities
complications
compression fracture
confusion
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
coprolalia
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
cranial nerve enlargement
cranial nerve palsies
craniopharyngioma
creatine phosphokinase(CPK)elevated
creatinine, elevated
critical care unit
cry, abnormal
crying
cultured skin fibroblasts
cyclosporine
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
dermatitis herpetiformis
dermatomyositis
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
diarrhea
diet
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
dopamine
drooling
dropped head syndrome
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
dysmetria
dysmorphic
dysnomia
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
echolalia
efficacy
electrocardiogram, abnormal
electrocardiogram, loop
electromyogram
electron microscopy
emergencies, neurologic
encephalitis, autoimmune
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enteritis
enzyme treatment
enzyme, defect
enzyme, muscle disease
eosinophilia-myalgia syndrome
epidemiology of neurology
erythema nodosum
Europe
evoked potentials
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial weakness
failure to thrive
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
Fisher C.M.
Fisher's syndrome
floppy infant
flow study, carotid artery
fornix, lesion of
fracture, pathologic
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gait disorder
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gamma amino butyric acid
gammaglobulin therapy, intravenous
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis GM2-AB variant
gastrointestinal disease, neurologic complications
Gaucher's disease
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
Gilles de la Tourette syndrome
gliadin antibodies
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
gluten ataxia
gluten sensitivity
gluten-free diet
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hallucination, hypnagogic
hallucination, visual
hallucinosis
hand pain
hands, fisted
head lag
headache
headache, progressive
headache, thunderclap
headbanging
hearing loss
heart murmur
hematopoietic tissue, extramedullary
hemianopia, homonymous
hemifacial spasm
hemiparesis
hepatic failure
hepatitis
hepatitis B vaccine
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
hexosaminidase-A
hexosaminidase-A and B
histochemistry
histochemistry of muscle
HLA
hoarseness
homocystinuria
Hurler's syndrome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperbilirubinemia
hyperglycinemia
hyperhomocysteinemia
hyperlipoproteinemia
hyperreflexia
hypersensitivity reaction
hypersomnia
hypersomnia, idiopathic
hypertension
hypertonia
hypocretin
hypogammaglobulinemia
hypoglycemia
hypogonadism
hypomyelination
hyponatremia
hypopyon
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunologic disease
immunology and the nervous system
immunosuppression
immunosuppressive agents
immunotherapy
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
infection
infection, recurrent
insomnia
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
interferon
interferon beta 1-a
interferon beta 1-b
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal biopsy
intrauterine
iris, abnormal
iron, brain
irritability
ischemic exercise test
jaundice
jaw jerk, abnormal
Jewish
juvenile myoclonus epilepsy
Kearns-Sayre syndrome
keratitis
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lacunar infarction
L-dopa
Leber's hereditary optic neuropathy
left-right orientation
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukocyte alkaline phosphotase
leukocyte enzyme abnormality
leukocyte peroxidase
leukocytes
leukocytosis
leukodystrophy
life expectancy
lipid storage disorder of CNS
lipoprotein receptor-related protein 4
livedo reticularis
liver disease
Lyme disease
lymphadenopathy, hilar
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malabsorption
marihuana
McArdle's disease
meconium staining
mediastinum, mass of
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
memory, impairment of
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
methotrexate
microspherophakia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
modafinil
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, hypointense signal foci on
MRI, muscle
MRI, negative
MRI, paramagnetic effect
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, pathogenesis
multiple sclerosis, risk factors for
multiple sclerosis, treatment of
multiple sclerosis, with CSF bands
multiple sclerosis, without CSF bands
multiple sleep latency test
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle spasm, face
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
MuSK antibodies
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, diagnosis
myasthenia gravis, familial incidence of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, ocular
myasthenia gravis, receptor site in
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenia gravis, variants
myasthenic crisis
myelitis
myelitis, transverse
myelitis, transverse, recurrent
myelopathy
myocarditis
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, proximal
myopathy, vacuolar
myopia
myorhythmia
narcolepsy
narcolepsy, children
nausea and vomiting
neck weakness
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuromuscular junction
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuronal ceroid-lipofuscinosis
neuronal loss
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, painful
neuropathy, peripheral
neurotransmitter
nystagmus
obesity
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
optic neuritis
optic neuritis, recurrent
optic neuropathy
optic neuropathy, bilateral
oral ulcerations
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
pain, abdominal
palilalia
palmomental response
PANK2 mutation
paranoia
paraparesis, spastic
parasomnia
paraspinal muscle
paraspinal muscle weakness
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
Parkinsonism-dementia complex
PAS positive
PAS positive material in the brain
pathergy test
pathognomonic
pectus excavatum
pediatric neurology
peduncular hallucinosis
periarteritis nodosa
peroxisomal disease
peroxisomes
phenylketonuria
phosphorylase b kinase deficiency
photophobia
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polycythemia, primary
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic relapsing
polysomnogram
Pompe's disease of glycogen storage
porphyria
postpartum
postpartum coma
postural abnormality
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
proteinuria
pseudomyotonia
psoriasis
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
puberty
puberty, delayed
putamen, lesion of
pyramidal tract
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
quality of life
rash
recurrent
REM sleep
renal failure
renal tubular acidosis
respirations in CNS disease
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
RFLPs
rigidity
risk factors
ritalin
rituximab
salivation, excessive
Sandhoff's disease
Sanfilippo syndrome
sarcoidosis
sarcoidosis, CNS
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
seizure
seizure, cardiac arrhythmia resulting from
seizure, children
seizure, complications following
seizure, familial
seizure, focal
seizure, intractable
seizure, neonatal
seizure, psychomotor-temporal lobe
self-mutilation
semialdehyde dehydrogenase deficiency
serologic testing
serologic testing of cerebrospinal fluid
short stature
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep offset paralysis
sleep onset paralysis
sleep paralysis
sleep pathology and physiology
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
southeast asia
spasticity
speech disorder
speech disorder, childhood
sphingolipodoses
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
Stevens-Johnson syndrome
stimulant drugs
strabismus
striatum, lesion of
stuporous
stuttering
stuttering following CVA
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
suck reflex
suck, poor
sudden death
symmetric brain lesions
systemic illness
systemic lupus erythematosus
tachycardia
Taiwan
tauopathy
Tay-Sachs disease
temporal lobe, lesion
term infant
tetrahydrobiopterin
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
third ventricle, mass of
thrombocytosis
thrombosis, cerebral
thymectomy
thymic hyperplasia
thymoma
thyroiditis
thyrotoxicosis
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, ulcer
tongue, weakness
toxic epidermal necrolysis
transketolase
treatment of neurologic disorder
treatment, empirical
tremor
tremor, jaw
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
umbilical-cord blood transplantation
undiagnosed
upgaze
urea
urea-cycle enzymopathies
uremia
urinary incontinence
urine test for metabolic disorders
urine, dark
uveitis
vaccination, neurologic complications with
vasculitides
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
visual loss
vital capacity
vitamin deficiency
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight gain
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
winging of scapula
Showing articles 100 to 150 of 159 << Previous Next >>

Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

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

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Enzyme Replacement in Nervous Tissue After Allogeneic Bone-Marrow Transplantation for Fucosidoisis in Dogs
Lancet 2:772-774, Taylor,R.M.,et al, 1986

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
Arch Neurol 41:1293-1296, Dave,P.,et al, 1984

Multiple Sclerosis, (First of Two Parts)
NEJM 307:1183-1188, 1982, McFarlin,D.E.,et al, 1982

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,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

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

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

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

HLA & Neurologic Fisease
Neurol 28:413, Compston,A., 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

HLA & Cogan's Syndrome
NEJM 298:1094, Kaiser-Kuper,M.I.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Diagnostic Significance of Myeloperoxidase Assay in Neuronal Ceroidlipofuscinoses (Batten-Vogt Syndrome)
Neurol 28:924-927, Pilz,H.,et al, 1978

HLA Antigens in the Landry-Guillain-Barre Syndrome & Chronic Relapsing Polyneuritis
Ann Neurol 4:285-289, Stewart,G.J.,et al, 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
NEJM 296:210, VanWoert,M.H.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977



Showing articles 100 to 150 of 159 << Previous Next >>