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Differential
(Click to cross reference)
agenesis of corpus callosum
anticonvulsants
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
areflexia
arm weakness
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brain weight
cardiomyopathy
CAT scan
children
chromosomal abnormality
chromosome 17
cleft lip
cleft palate
cold temperature
congenital birth defects
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital malformation, dilantin therapy causing
congenital malformation, non CNS
cranial volume
Craniosynostosis
cryptorchidism
developmental abnormality of brain
developmental retardation
differential diagnosis
digits, abnormal
dilantin
dysmorphic
ear, abnormal
echocardiogram
electromyogram
facial anomalies
facial appearance, abnormal
familial
feeding disorder
fetal alcohol syndrome
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
head circumference
hearing loss
hemorrhagic diathesis
hepatosplenomegaly
heterotopia
high arched palate
holoprosencephaly
hypertelorism
hypertrophic cardiomyopathy
hypoplastic left heart syndrome
hypotelorism
hypotonia
hypotonia, infants
intellectual deficit
interpupillary distance
joint hypermobility
malformation, CNS, congenital
malformation, vascular
mental retardation
micrencephaly
microcephaly
micrognathia
midline defect in children
molecular genetics
MRI
muscle atrophy, focal
neck, webbed
neurologic disease, diagnoses of
neuropathy, hereditary peripheral
Noonan Syndrome
nose, abnormal
obesity
pain
pain, severe
pectus excavatum
polyhydramnios
Prader-Labhart-Willi syndrome
precipitating factors
precocious puberty
pregnancy, neurologic complications in
proximal muscle atrophy
puerperium
pulmonary stenosis
pyramidal tract dysfunction
recurrent
review article
seizure
seizure, children
seizure, injury following
short neck
short stature
simian crease
skin, lesions in neurologic disorders
valvulopathy
visual impairment
vomiting, recurrent
weakness
weakness, progressive
weakness, proximal
Showing articles 0 to 13 of 13

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy
Neurol 57:1963-1968, Jeannet,P.,et al, 2001

Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Minor Anomalies in Offspring of Epileptic Mothers
J Pediatr 112:521-529, 579-5811988., Gaily,E.,et al, 1988

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Tables of Cranial & Orbital Measurements, Cranial Volume, & Derived Indexes in Males & Females From 7 Days to 20 Years of Age
Ann Neurol 2:485, Dekaban,A., 1977

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Hypertelorism (Greigs Synd)
Year Book of Pediatric Opthal p. 181-Circa 1972-3., , 1972

Normal Inner Canthal & Outer Orbital Dimensions
J Pediatr 74:465, Laestadius,N.,et al, 1969

Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly
Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964

Patient Travel Distance to Neurologist Visits
Neurol 101:e1807-e1820, Lin,C.C.,et al, 2023



Showing articles 0 to 13 of 13