Add to ORKGLate-onset triple A syndrome caused by a novel homozygous missense mutation in the AAAS gene (A167V in exon 6) was diagnosed at least 17 years after symptom onse
Abstract Background Allgrove syndrome is a rare autosomal recessive disorder characterized by the tr...
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder character...
Triple A (Allgrove) syndrome is characterized by achalasia, alacrima, adrenal abnormalities and a pr...
Late-onset triple A syndrome caused by a novel homozygous missense mutation in the AAAS gene (A167V ...
Allgrove syndrome, also known as triple A syndrome (OMIM #231550), is a rare autosomal recessive dis...
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder character...
Allgrove syndrome (or triple A syndrome) is a rare autosomal recessive disorder characterized by ala...
Triple-A syndrome, also known as Allgrove syndrome, is a rare autosomal recessive disorder. The 3 fe...
Familial glucocorticoid deficiency due to corticotropin (ACTH) resistance consists of two distinct g...
Allgrove’s or "4 A" syndrome is a rare autosomal recessive condition with alacrima, achalasia, auton...
Triple A or Allgrove syndrome (AS) (MIM 231550) is a rare autosomal recessive disorder of adreno cor...
Background/Aims: A 33-year-old man was referred for the first time to the Division of Neurology beca...
Triple A syndrome (TAS) or Allgrove syndrome (OMIM #231550) is a rare autosomal recessive disorder c...
Abstract Background Triple A syndrome (or Allgrove syndrome) is a rare autosomal recessive disorder ...
Allgrove (Triple A) syndrome is a rare autosomal recessive disorder characterized by cardinal featur...
Abstract Background Allgrove syndrome is a rare autosomal recessive disorder characterized by the tr...
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder character...
Triple A (Allgrove) syndrome is characterized by achalasia, alacrima, adrenal abnormalities and a pr...
Late-onset triple A syndrome caused by a novel homozygous missense mutation in the AAAS gene (A167V ...
Allgrove syndrome, also known as triple A syndrome (OMIM #231550), is a rare autosomal recessive dis...
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder character...
Allgrove syndrome (or triple A syndrome) is a rare autosomal recessive disorder characterized by ala...
Triple-A syndrome, also known as Allgrove syndrome, is a rare autosomal recessive disorder. The 3 fe...
Familial glucocorticoid deficiency due to corticotropin (ACTH) resistance consists of two distinct g...
Allgrove’s or "4 A" syndrome is a rare autosomal recessive condition with alacrima, achalasia, auton...
Triple A or Allgrove syndrome (AS) (MIM 231550) is a rare autosomal recessive disorder of adreno cor...
Background/Aims: A 33-year-old man was referred for the first time to the Division of Neurology beca...
Triple A syndrome (TAS) or Allgrove syndrome (OMIM #231550) is a rare autosomal recessive disorder c...
Abstract Background Triple A syndrome (or Allgrove syndrome) is a rare autosomal recessive disorder ...
Allgrove (Triple A) syndrome is a rare autosomal recessive disorder characterized by cardinal featur...
Abstract Background Allgrove syndrome is a rare autosomal recessive disorder characterized by the tr...
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder character...
Triple A (Allgrove) syndrome is characterized by achalasia, alacrima, adrenal abnormalities and a pr...