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Differential
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abdominal distention
acetylcholine receptor antibody
acid maltase deficiency
aciduria
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acrocyanosis
acromicria
adverse drug reaction
agenesis of corpus callosum
Aicardi-Goutieres syndrome
airway obstruction
alternating hemiplegia
alternating hemiplegia of childhood
aminoacidurias
amitriptyline
amniocentesis
anemia
anemia, megaloblastic
Angelman syndrome
angiokeratoma
anorexia
anterior horn cell disease
antitoxin
antiviral agents
apnea
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
aspartocyclase
ataxia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
athetosis, infant
ATP1A3 gene
attention deficit disorder with hyperactivity
atypical
autism
autonomic dysfunction
B 12 deficiency
B 12 deficiency, infants
Babinski sign in new born
bacterial infection
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
biopterin deficiency
birth injury
blindness
bone biopsy
bone density
bone density, increased
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
bradycardia
brain atrophy
brain biopsy
brainstem, atrophy
breast feeding
breech delivery
Brown-Vialetto-Van Laere syndrome
bulbar palsy
bulbar palsy, childhood
calcification, intracranial
Canavan's disease
canned food
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiomyopathy
CAT scan
CAT scan, abnormal
celiac disease, childhood
central core disease
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral gigantism
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, neonatal
cerebrovascular accident, postpartum
cervical spine injury
cherry red spot
chilbran skin lesions
child abuse
children
chorea
choreoathetosis
chorioamnionitis
chorioretinitis
chromosomal abnormality
chromosome 1
chromosome 15
chromosome 5
chromosome 6
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cobalamin C deficiency
cognition
cognitive delay
coma
congenital heart disease
congenital heart disease, CNS complications with
congenital infection, CNS
congenital infection, viral
congenital myopathy
congenital myopathy, inflammatory
consanguinity
constipation
contractures, joint
cornea, opacity of
corpus callosum
corpus callosum, thinning
cortical blindness
cranial neuropathy
cranial neuropathy, multiple
Craniosynostosis
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cyanosis
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
deep gray nuclei
delay in diagnosis
delayed dentition
delivery, complicated
dementia
dementia, childhood
dentate nuclei
dentate nuclei, lesion of
descending paralysis
developmental abnormality of brain
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
diet
differential diagnosis
diphtheria-tetanus-pertussis immunization
dislocated hip, congenital
DNA sequencing
drooling
drug overdose
dural sinus thrombosis
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dystonia
dystonia, children
ear, abnormal
eating disorder
ecchymoses
echocardiogram
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism, paradoxical
encephalitis
encephalomyelitis
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
evoked potentials
exome sequencing
eye movement, disorders of
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
familial
FARS2 deficiency
fasciculation
fatigue
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
fine motor function, impaired
floppy infant
fontanel, bulging
food poisoning
food-borne infection
forceps delivery
fucosidosis
fundus, abnormality of
gag reflex, depressed
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genital hypoplasia
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GLUT1
GLUT1 deficiency syndrome
gluten-free diet
glycogen storage disease
glycoprotein
Gowers maneuver
growth hormone deficiency
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, infantile and childhood form
hallucination
hand clapping
hand deformity
hand flapping
hand wringing
head bobbing
head circumference
head lag
hearing loss
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
high arched feet
high arched palate
histochemistry
histochemistry of muscle
hoarseness
homocystinuria
honey
Horner's syndrome
Horner's syndrome, bilateral
Horner's syndrome, congenital
human genome
Hunter's syndrome
hydrocephalus
hydrocephalus, communicating
hydrocephalus, congenital
hydrocephalus, exvacuo
hydroxyglutaric aciduria
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperhomocysteinemia
hyperphagia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertelorism
hypertension
hypertonia
hypertrophic cardiomyopathy
hypodontia
hypogammaglobulinemia
hypoglycorrhachia
hypogonadism
hypokinesia
hypomyelination
hypopigmentation of skin
hyporeflexia
hypothermia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
imbalance
immunization, neurologic complications with
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
infant, evaluation of
infantile neuronal degeneration
infantile spasm
infection, recurrent
intellectual deficit
intellectual deterioration
interferon alpha
intestinal biopsy
intracranial hemorrhage
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intubation
irritability
irritable baby
islet cell tumor
jaundice
Jewish
joint hypermobility
karyotyping
ketogenic diet
kyphoscoliosis, neurologic causes of
lactic acidemia
leg weakness, bilateral
Leigh's disease
lethargy
leukodystrophy
leukoencephalopathy
leukotrienes
lid closure, weakness of
lissencephaly
listeria monocytogenes
liver disease
liver function enzymes
lumbar puncture
lysosomal storage disease
macrocephaly
malabsorption
malformation, CNS, congenital
malformation, vascular
malignant hyperpyrexia
McArdle's disease
meningitis, carcinomatous
meningitis, CSF cell count-normal
mental retardation
merosin
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
methylmalonic acidemia
microcephaly
micrognathia
micropthalmia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine, seizures in
misdiagnosis
mitochondrial disease
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, fetal
MRI, high signal foci on
MRI, muscle
MRI, spinal cord
MRI, spine
mucopolysaccharidoses
mucopolysacchariduria
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle diseases, characteristics of
muscle phosphorylase deficiency
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscle-eye-brain disease
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, LAMA2
myasthenia gravis, neonatal
myelomalacia
myoclonic jerks
myoclonus
myopathy
myopathy, centronuclear
myopia
myositis
myotonia congenita
myotonia dystrophica
nasal bridge, wide
nausea and vomiting
neck weakness
neck, webbed
nemaline rod myopathy
neonatal infection, viral
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
nerve conduction studies
nerve conduction studies, motor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurologic disease, diagnoses of
neurologic evaluation
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neurophysiology
neurotoxin
newborn, evaluation of
Noonan Syndrome
nusinersen
nystagmus
nystagmus, monocular
obesity
obstetric neurologic injuries
opened mouth
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, total
optic atrophy
optic atrophy, infants
optic nerve, hypoplasia of
osteopetrosis
pachygyria
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
patient information and support
pectus excavatum
pediatric neurology
periventricular leukomalacia
pertussis immunization
petechiae
phenylketonuria, variant form of
PICU
placenta
placenta, infection of
placenta, thrombosis of
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
poliomyelitis
poliomyelitis vaccine
POLR3B
polyhydramnios
polymerase chain reaction
polymicrogyria
polymyositis
polymyositis, infantile
pons, atrophy
pons, lesion of
postoperative neurologic complications
postpartum
Prader-Labhart-Willi syndrome
precipitating factors
precocious puberty
pregnancy, neurologic complications in
premature infant
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, childhood
ptosis
ptosis, bilateral
pulmonary stenosis
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriparesis, acute
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
reflex, stretch
reflex, tonic stretch
renal tubular acidosis
repetitive nerve stimulation
respirator
respiratory arrest
respiratory depression
respiratory distress syndrome, neurologic status with
respiratory failure
respiratory tract infection
Rett's syndrome
review article
RFLPs
riboflavin transporter deficiency
rigid spine syndrome
rubella vaccine
scoliosis
scoliosis, neurologic association with
screaming
screening
segmental demyelination
seizure
seizure, children
seizure, focal
seizure, injury following
seizure, neonatal
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
serum alanine aminotransferase
short stature
shunt procedure, ventricular
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
small for dates infant, problems in
SMN1 gene
spastic diplegia
spasticity
speech disorder, childhood
speech, delayed development of
spinal cord, enlargement
spinal cord, injury of
spinal cord, injury, New Born
spinal cord, intramedullary cyst of
spinal cord, transection
spinal muscular atrophy
spinal muscular atrophy, classification
splenomegaly
spongy degeneration of brain
standing difficulty
startle reaction
status epilepticus
stereotyped behavior
stereotypy
stillbirth
strabismus
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural effusion
subdural hematoma, neonates and infants
subgaleal hematoma
suck, poor
superior sagittal sinus thrombosis
symmetric brain lesions
systemic lupus erythematosus
systemic lupus erythematosus, neonatal
systemic lupus erythematosus, neurologic complications with
tachycardia
Tay-Sachs disease
teeth, abnormal
teeth, number of in infants
temper tantrums
temporalis muscle wasting
term infant
tetrahydrobiopterin
thiamine deficiency
thrombocytopenia
titinopathy
titubation
toe walking
tone, muscle
tongue, fasciculations of
tongue, protrusion of
tongue, weakness
tonic spasms
toxins, nervous system
toxoplasmosis, CNS
tracheostomy
transilumination of skull
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
trinucleotide repeats
type 1 muscle fiber
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
urine test for metabolic disorders
vaccination, neurologic complications with
vaccine
vacuum delivery
valvulopathy
vasculopathy
vegetarianism
vein of Galen
vision, failure of in childhood
visual evoked response
visual impairment
visual loss
visual tracking
vitamin deficiency
vomiting, recurrent
walking, difficulty with
weakness
weakness, acute
weakness, congenital
weakness, generalized
weakness, infant
weakness, progressive
Werdnig-Hoffman disease
white matter disease
wide based gait
workup
wrist drop
Showing articles 1500 to 1550 of 1556 << Previous Next >>

Perinatal intracranial hemorrhage
Arch Neurol 34:570, Schoenberg,B.S.,et al, 1977

Neonatal Meningitis, The Ventricle as a Bacterial Reservoir
Arch Neurol 34:560, Gilles,F.H.,et al, 1977

Strokes in Children & Adolescents
Current Concepts of Cerebrovascular Disease, Stroke 2:291977., , 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Apparent Emergence of Aminoglycoside-Resistant Escherichia Coli During Neonatal Meningitis
NEJM 293:913, Echeverria,P.,et al, 1975

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,et al, 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Neonatal Intracranial Hemorrhage Iatrogenic Etiology? NEJM 291:43
1974, 291:10881974., , 1974

Visual Symptoms in the Migraine Syndrome
Neurol 23:570, Hachinski,V.,et al, 1973

Huntington's Disease in Children
Neurol 23:561, Byers,R.,et al, 1973

Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis
Letter Lancet Feb 1973., Wadia,N.H.,et al, 1973

Neonatal Hypoglycemia
NEJM 289:790, Senior,B., 1973

Drug Use within an Adolescent Treatment Center
Psych Ann 2:26, 1972 May., Crabtree,L.,et al, 1972

Psychiatry in the Schools
Psych Ann 2, 1972 May., Balser,B.H., 1972

Lead & Hyperactivity
Lancet 900, 1972 Oct., David,O.,et al, 1972

Juvenile Cerebral Arteriosclerosis & other Cerebral Arteriopathies of Childhood (Six Autopsied cases)
Acta Neurol Scand 48:479, Harvey,F.H.,et al, 1972

Head Injuries in Children
BMJ 196, 1972 Jan., , 1972

Perinatal Risk Associated with Maternal Genital Herpes Simplex Virus Infection
Am J OB Gyn 110:825-837, Nahmias,A.J.,et al, 1971

Drug-Induced Neurologic Disorders in Childhood
Current Problems in Pediatrics 1:1, Schwartz,J., 1971

Polyarteritis Nodosa in Infancy
JAMA 217:1666, Tang,P.,et al, 1971

CNS Damage in the Human Fetus & Newborn Infant
Amer J Dis Child 119:529, Towbin,A., 1970

Natural History of Acute Hemiplegia of Childhood
Brain 93:107, Soloman,G.E.,et al, 1970

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Acquired Sixth-Nerve Paresis in Children
Arch Ophthal 83:574-579, Robertson,D.M.,et al, 1970

Abnormal Head Size, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970

Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970

Benign Intracranial Cyst, In Neurosurgery of Infancy & Childhood
(Ed) , 1969, Charles C. Thomas p. 179., Matson,D.D., 1969

How to Talk Sense to Adolescent Rebels
Hosp Physician, Sept 1969, p. 143., Bates,R., 1969

Acute Hemiplegia in Infancy & Childhood
Develop Med Child Neurol 2:162, Aicardi,J.,et al, 1969

Unusual Cause of Progressive Head Enlargement Following Proteus Mirabilis Meningitis
Develop Med Child Neurol 11:633, Mukhergee,S.K.,et al, 1969

CNS Abnormalities after Neonatal Hemolytic Disease of Hyperbilirubinemia
Am J Dis Child 117:395, Hyman,C.,et al, 1969

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Intracranial Ventricular Haemorrhage as a First Presentation of Haemophilia
JNNP 32:470-473, Adeloye,A.,et al, 1969

Cerebrospinal Fluid in the Healthy Newborn Infant
African Med J 42:933, Naidoo,B.S., 1968

The Hazard of Infection Following Splenectomy in Children
Amer J Dis Child 116:1-12, Erickson,W.D.,et al, 1968

Subdural Effusions in Infants
Pediatr Clin North Am 14:832, Rabe,E., 1967

Benign Intracranial Hypertension
Pediatr Clin North Am 14:819-830, Greer,M., 1967

Epilepsy in Children
Current Therapy, 1966, p. 574., Scholl,M.L., 1966

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
NEJM 274:384, Renuart,A., 1966

Neuro CPC of MGH
Acute Multiple Sclerosis, NEJM 273:760-7671965., , 1965

Orthopaedic Aspects of Intraspinal Tumors in Infants & Children
J Bone & Joint Surg 47A:223965., Tachdjian,M.&Matson,D., 1965

Optic Atrophy in Childhood
Pediatrics 34:670, 1964 (Nov) ., Schwartz,J.F.,et al, 1964

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

The Diagnosis & Treatment of Seizures
Pediatr Clin North Am 9:353, Scholl,M.L., 1962

Basilar Artery Migraine
Lancet 1:15-17, Bickerstaff,E.R., 1961

Subdural Hematoma:A Review of 389 Cases
Lancet 1:1365, , 1960

Infectious Neuronitis (Guillain-Barre Syndrome) in Children
Neurol 9:533-539, Peterman,A.F.,et al, 1959

Polyneuritis in Children
Pediatrics 22:972-990, Low,N.L.,et al, 1958



Showing articles 1500 to 1550 of 1556 << Previous Next >>