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Gernay Caroline

Département des sciences cliniques > Médecine générale

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Main Referenced Co-authors
Boros, Emese (1)
Bours, Vincent  (1)
Brachet, Cécile (1)
De Bilderling, Georges (1)
Farhat, Nesrine  (1)
Main Referenced Keywords
central hypoventilation (1); dysautonomia (1); Endocrinology, Diabetes and Metabolism (1); familial CPP (1); genetics of puberty (1);
Main Referenced Disciplines
Genetics & genetic processes (2)
Pediatrics (1)

Publications (total 3)

The most downloaded
257 downloads
HARVENGT, J., GERNAY, C., Mastouri, M., FARHAT, N., LEBRETHON, M.-C., Seghaye, M.-C., & Bours, V. (2020). ROHHAD(NET) Syndrome: Systematic review of the clinical timeline and recommendations for diagnosis and prognosis. Journal of Clinical Endocrinology and Metabolism. doi:10.1210/clinem/dgaa247 https://hdl.handle.net/2268/247972

The most cited

30 citations (Scopus®)

HARVENGT, J., GERNAY, C., Mastouri, M., FARHAT, N., LEBRETHON, M.-C., Seghaye, M.-C., & Bours, V. (2020). ROHHAD(NET) Syndrome: Systematic review of the clinical timeline and recommendations for diagnosis and prognosis. Journal of Clinical Endocrinology and Metabolism. doi:10.1210/clinem/dgaa247 https://hdl.handle.net/2268/247972

Gernay, C., Brachet, C., Boros, E., Tenoutasse, S., Libioulle, C., & Heinrichs, C. (17 November 2022). Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty. Journal of the Endocrine Society, 7 (1), 168. doi:10.1210/jendso/bvac168
Peer Reviewed verified by ORBi

HARVENGT, J., GERNAY, C., Mastouri, M., FARHAT, N., LEBRETHON, M.-C., Seghaye, M.-C., & Bours, V. (2020). ROHHAD(NET) Syndrome: Systematic review of the clinical timeline and recommendations for diagnosis and prognosis. Journal of Clinical Endocrinology and Metabolism. doi:10.1210/clinem/dgaa247
Peer reviewed

GERNAY, C., Vanden Brande, L., & De Bilderling, G. (10 March 2016). Acute pancreatitis as initial presentation for hereditary spherocytosis: A case report [Poster presentation]. 44th Annual Congress BVK-SBP, Bruxelles, Belgium.

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