1. Allgrove syndrome with amyotrophy
   Míriam Carvalho Soares et al, 2021, Practical Neurology CrossRef
2. A novelTRAPPC11mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima
   Katrin Koehler et al, 2017, Journal of Medical Genetics CrossRef
3. Genetics in Oculoplastics
   Karthikeyan Arcot Sadagopan, 2021, Smith and Nesi’s Ophthalmic Plastic and Reconstructive Surgery CrossRef
4. The first report of a known 4A syndrome patient with suspected manifestations of COVID-19, what was the final outcome?
   Elham Azmoodeh et al, 2022, Heliyon CrossRef
5. Congenital alacrima
   Zhenyang Zhao et al, 2022, Orbit CrossRef
6. An Unusual Cause of Recurrent Pneumonia in a Child
   Manoj Madhusudan et al, 2022, Indian Pediatrics Case Reports CrossRef
7. Orbit
   Myron Yanoff et al, 2020, Ocular Pathology CrossRef
8. Triple-A Syndrome (TAS): An In-Depth Overview on Genetic and Phenotype Heterogeneity
   Gabriele Pogliaghi et al, 2020, Protein & Peptide Letters CrossRef
9. Cortisol deficiency
   John William Honour, 2023, Steroids in the Laboratory and Clinical Practice CrossRef
10. Case report of a familial triple: a syndrome and review of the literature
    Federica Gaiani et al, 2020, Medicine CrossRef
11. Orbit
    Myron Yanoff et al, 2025, Ocular Pathology CrossRef
12. Eponymous Terms and Selected Historical Figures in Endocrinology
    Andrea Manni et al, 2020, Endocrine Pathophysiology CrossRef
13. Isolated Congenital Lacrimal Gland Agenesis
    Gokce Belge Bilgin et al, 2024, Cureus CrossRef
14. Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report
    H. Berrani et al, 2018, BMC Pediatrics CrossRef
15. Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy
    Satyam Singh Jayant et al, 2021, Hormones CrossRef