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Current Therapeutic Options in Sturge-Weber SyndromeSturge-Weber syndrome and epilepsy: an argument for aggressive seizure management in these patients.Cell proliferation and oxidative stress pathways are modified in fibroblasts from Sturge-Weber syndrome patientsUpdates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvementFocal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge-Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American OphthalmologicEpilepsy Mechanisms in Neurocutaneous Disorders: Tuberous Sclerosis Complex, Neurofibromatosis Type 1, and Sturge-Weber Syndrome.Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome.Importance of utilizing a sensitive free thyroxine assay in Sturge-Weber syndrome.Sturge-weber syndrome.
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
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2006年论文
@zh-cn
name
Growth hormone deficiency in Sturge-Weber syndrome.
@ast
Growth hormone deficiency in Sturge-Weber syndrome.
@en
type
label
Growth hormone deficiency in Sturge-Weber syndrome.
@ast
Growth hormone deficiency in Sturge-Weber syndrome.
@en
prefLabel
Growth hormone deficiency in Sturge-Weber syndrome.
@ast
Growth hormone deficiency in Sturge-Weber syndrome.
@en
P2093
P2860
P356
P1476
Growth hormone deficiency in Sturge-Weber syndrome.
@en
P2093
E L Germain-Lee
R S Miller
P2860
P304
P356
10.1136/ADC.2005.082578
P407
P577
2006-04-01T00:00:00Z