PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Korean Journal of Pediatrics10.3345/kjp.2016.59.11.45620165911456Edentulous child with Allgrove syndrome: a rare case reportMohammad Vahedi, Shima Fathi, Hanif Allahbakhshihttp://synapse.koreamed.org/pdf/10.3345/kjp.2016.59.11.456, http://synapse.koreamed.org/DOIx.php?id=10.3345/kjp.2016.59.11.456, http://kjp.or.kr/upload/pdf/kjped-59-456.pdf
Worldwide Medicine10.5455/ww.302644179201901A rare child red ear syndrome: Case reportHuseyin Keskin, Oguz guvenmezhttps://www.ejmanager.com/fulltextpdf.php?mno=302644179
Developmental Medicine & Child Neurology10.1111/j.1469-8749.2012.04433.x2012554385-389Reversible cerebral vasoconstriction syndrome: rare or underrecognized in children?REBECCA PROBERT, DAWN E SAUNDERS, VIJEYA GANESANhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.2012.04433.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2012.04433.x/fullpdf
Annals of Medicine and Surgery10.1016/j.amsu.2021.103009202172103009Allgrove syndrome: Case report of 18 years old male:the first case report from SyriaNagham Hanino, Sarya Swed, Mohammed Deeb Zakkor, Abdullah Hindawy, Hidar Alibrahim, Hachem Alhusseinhttps://api.elsevier.com/content/article/PII:S2049080121009596?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S2049080121009596?httpAccept=text/plain
Journal of Maxillofacial and Oral Surgery10.1007/s12663-009-0046-3200982188-191Ramsay-Hunt syndrome complicating osteonecrosis of edentulous maxilla and mandible: report of a rare caseSamprati J. Badjate, K. M. Cariappa, S. R. Shenoi, Shweta Nakhatehttp://link.springer.com/content/pdf/10.1007/s12663-009-0046-3.pdf, http://link.springer.com/article/10.1007/s12663-009-0046-3/fulltext.html, http://link.springer.com/content/pdf/10.1007/s12663-009-0046-3
10.21203/rs.3.rs-90287/v12020Thrombotic antiphospholipid syndrome in a child with Human Immunodeficiency Virus: A rare Case ReportRong-Jing Dong, Su-Yun Lei, Jun Li, Xin-Ping Yang, yuye li, Yun-Gui Zhanghttps://www.researchsquare.com/article/rs-90287/v1, https://www.researchsquare.com/article/rs-90287/v1.html
Sudanese Journal of Paediatrics10.24911/sjp.106-1583095341202189-94A rare haematological disorder in a Sudanese child: Evans syndrome, case report and literature reviewBashir Bashir, Suhair Othman, Amel Malikhttps://www.ejmanager.com/fulltextpdf.php?mno=90008
Surgical Case Reports10.1186/s40792-020-01051-0202061Ehlers–Danlos syndrome type IV: a case report of a rare cause of spontaneous sigmoid perforation and enteroatmospheric fistulae in a childHemal Kodikara, Sebastian K. King, Elizabeth McLeodhttp://link.springer.com/content/pdf/10.1186/s40792-020-01051-0.pdf, http://link.springer.com/article/10.1186/s40792-020-01051-0/fulltext.html, http://link.springer.com/content/pdf/10.1186/s40792-020-01051-0.pdf
VideoGIE10.1016/j.vgie.2020.02.007202056235-237Peroral endoscopic myotomy in a child with Triple A syndrome (Allgrove syndrome)Riccardo Rizzo, Valerio Balassone, Filippo Torroni, Paola De Angelis, Luigi Dall’Ogliohttps://api.elsevier.com/content/article/PII:S2468448120300503?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S2468448120300503?httpAccept=text/plain
Respirology10.1111/resp.13420_285201823192-193KARTAGENER'S SYNDROME: A RARE CASE REPORT IN MALEhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fresp.13420_285, http://onlinelibrary.wiley.com/wol1/doi/10.1111/resp.13420_285/fullpdf