|1.||Huebner, Angela: 21 articles (09/2015 - 02/2003)|
|2.||Koehler, Katrin: 14 articles (09/2015 - 03/2006)|
|3.||Huebner, A: 10 articles (08/2010 - 10/2000)|
|4.||Kind, Barbara: 5 articles (12/2010 - 12/2008)|
|5.||Krumbholz, Manuela: 4 articles (12/2010 - 09/2008)|
|6.||Clark, Adrian J L: 4 articles (12/2009 - 12/2002)|
|7.||Houlden, Henry: 4 articles (04/2009 - 12/2002)|
|8.||Lyonnet, S: 4 articles (05/2005 - 08/2000)|
|9.||Handschug, K: 4 articles (05/2003 - 11/2000)|
|10.||Ueno, Satoshi: 3 articles (09/2013 - 02/2006)|
|1.||Esophageal Achalasia (Megaesophagus)
05/01/2003 - "Achalasia of the cardia in Allgrove's (triple A) syndrome: histopathologic study of 10 cases."
05/01/1999 - "We describe a previously unreported finding of periventricular heterotopias in a brain magnetic resonance imaging (MRI) study, in a girl with adrenocortical insufficiency, alacrima, achalasia, and neurologic deterioration (Allgrove syndrome). "
09/01/2015 - "Organ-specific Neurodegeneration in Triple A syndrome-related Achalasia."
01/01/2012 - "Subsequent peripheral motor neuropathy, achalasia and alacrima raised the suspicion of triple A syndrome, which was confirmed by the presence of a homozygous R194X mutation in the AAAS gene. "
11/01/2011 - ""Triple A" syndrome is a rare, autosomal recessive condition whose main clinical features are alacrima, achalasia, and adrenal failure. "
|2.||Adrenal Insufficiency (Adrenal Gland Hypofunction)
02/01/2015 - "The combination of alacrima and adrenal insufficiency prompted screening for Allgrove syndrome, which was confirmed by genetic analysis showing homozygous c.1331+1G>A mutation within intron 14 of the gene encoding for ALADIN protein. "
10/15/2010 - "He lacked adrenal insufficiency that is frequently observed in patients with the classic phenotype of triple A syndrome. "
03/15/2010 - "Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency."
09/01/2007 - "In our patient, the absence of tears since birth followed by adrenal insufficiency were early signs of the triple A syndrome. "
08/01/2007 - "The human homolog of the Acd gene, mutated in a mouse model of adrenal insufficiency, was sequenced in 25 patients with a clinical diagnosis of familial glucocorticoid deficiency or triple A syndrome. "
|3.||Addison Disease (Addison's Disease)
10/01/2008 - "Larger studies about Addison's disease are needed to confirm the preponderance of the Allgrove syndrome."
07/01/2003 - "Allgrove syndrome--a syndrome of primary adrenocortical insufficiency with achalasia of the cardia and deficient tear production."
12/01/2015 - "Triple A or Allgrove Syndrome (OMIM#231550) is a rare, autosomal recessive genetic disorder in which patients typically suffer from chronic adrenal insufficiency due to resistance to ACTH (Addison's disease), esophageal achalasia, and defective tear formation (alacrima). "
|4.||Deglutition Disorders (Dysphagia)
09/01/2007 - "Triple A syndrome has to be considered in patients with dysphagia. "
09/01/2007 - "Dysphagia due to triple A syndrome: successful treatment of achalasia by balloon dilatation."
12/01/2007 - "The presence of achalasia with dysphagia, adrenal insufficiency, reduced tear production, optic atrophy and peripheral motor-sensory neuropathy with axonal loss led us to clinically diagnose Allgrove syndrome even though a genetic study showed no mutations in the ALADIN gene exons. "
|1.||Achalasia Addisonianism Alacrimia syndrome
|2.||Adrenocorticotropic Hormone (ACTH)
|4.||Steroidogenic Factor 1
|5.||Corticotropin Receptors (ACTH Receptor)
|8.||Nuclear Proteins (Protein, Nuclear)