Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
adverse drug reaction
aneurysm, intracranial
areflexia
basal ganglia, calcification of
behavioral disorder
cachexia
calcification, intracranial
cardiomyopathy
caries
cataracts
children
chorionic gonadotropin
chromosomal abnormality
Cockayne's syndrome
complications
congenital heart disease
congenital heart disease, CNS complications with
contractures, joint
cry, weak
cryptorchidism
developmental retardation
differential diagnosis
drug induced neurologic disorders
dysmorphic
ear, abnormal
echocardiogram
eyes, sunken
facial anomalies
facial appearance, abnormal
familial
feeding disorder
genetic counselling
genetic neurologic disorders
growth retardation
gynecomastia
head circumference
hearing loss
hemorrhagic diathesis
hepatosplenomegaly
high arched palate
hypertelorism
hypertrophic cardiomyopathy
hypogonadism
hypotonia
hypotonia, infants
infertility
intellectual deficit
intracranial hypertension, benign
joint hypermobility
Klinefelter's syndrome
learning disability
mental retardation
micrognathia
misdiagnosis
mortality
MRI, abnormal
neck, webbed
neurologic disease, diagnoses of
Noonan Syndrome
obesity
optic neuropathy
osteoporosis
pectus excavatum
penis, small
photosensitivity, skin
pigmentary retinopathy
polyhydramnios
Prader-Labhart-Willi syndrome
precocious puberty
psychomotor retardation
puberty, delayed
pulmonary stenosis
rash
retinopathy
review article
seizure
seizure, children
seizure, injury following
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
stooped posture
testosterone
tremor
valvulopathy
visual impairment
vomiting, recurrent
white matter disease
Showing articles 0 to 5 of 5

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Pseudotumor Cerebri Following Beta-Human Chorionic Gonadotropin Hormone Treat for Undesc Testicles
Neurol 43:448-449, Haller,J.S.,et al, 1993

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

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

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



Showing articles 0 to 5 of 5