Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
about
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases.Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.AAA Syndrome, Case Report of a Rare Disease.Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.
P2860
Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
@en
Triple A
@nl
type
label
Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
@en
Triple A
@nl
prefLabel
Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
@en
Triple A
@nl
P2093
P2860
P356
P1476
Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
@en
P2093
Angela Huebner
Cesare Terzi
Danila Benevento
P2860
P2888
P356
10.1186/1824-7288-39-39
P577
2013-06-24T00:00:00Z
P5875
P6179
1027023400