Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.
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Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases.Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide CohortAlacrima as a Harbinger of Adrenal Insufficiency in a Child with Allgrove (AAA) Syndrome.Familial glucocorticoid deficiency: a diagnostic challenge during acute illness.Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.Clinical and genetic characterisation of a series of patients with triple A syndrome.Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.
P2860
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P2860
Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.
description
2012 nî lūn-bûn
@nan
2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Long-term clinical follow-up a ...... tients with triple A syndrome.
@ast
Long-term clinical follow-up a ...... tients with triple A syndrome.
@en
type
label
Long-term clinical follow-up a ...... tients with triple A syndrome.
@ast
Long-term clinical follow-up a ...... tients with triple A syndrome.
@en
prefLabel
Long-term clinical follow-up a ...... tients with triple A syndrome.
@ast
Long-term clinical follow-up a ...... tients with triple A syndrome.
@en
P2093
P2860
P1476
Long-term clinical follow-up a ...... tients with triple A syndrome.
@en
P2093
Andrija Stanimirovic
Angela Huebner
Katrin Koehler
Mate Skegro
Miroslav Dumic
Nina Barišic
Vesna Kusec
P2860
P2888
P304
P356
10.1007/S00431-012-1745-1
P577
2012-04-28T00:00:00Z
P6179
1026367373