Tuberous Sclerosis Complex: Genetic counselling and perinatal follow-up

Autor: Touraine, R. ^*, Hauet, Q., Harzallah, I., Baruteau, A.-E.

Publikováno v: In Archives de pédiatrie December 2022 29(5) Supplement

Effectiveness of simulation-based communication training for cardio pediatricians in announcing congenital heart disease diagnosis in children: A randomized controlled trial (SIMUL - CHD)

Autor: Padovani, P., Hauet, Q., Lefort, B., Letellier, M., Bergé, M., Amedro, P., Baruteau, A.E.

Publikováno v: In Archives of Cardiovascular Diseases Supplements September 2023 15(4):292-292

Bilateral Aneurysm of the Internal Jugular Vein Associated with Menkes Disease: Diagnosis, Risk Factors and Management

Autor: Bonnet Jb, Piloquet H, Hauet Q, Barth M, Kuster A, Gautier A, Pistorius Ma, Moizard Mp

Publikováno v: Journal of Vascular Medicine and Surgery 06 (03), 1-4. (2015)
Journal of Vascular Medicine & Surgery
Journal of Vascular Medicine & Surgery, 2015, 03 (06), pp.1-4. ⟨10.4172/2329-6925.1000235⟩

International audience; Menkes disease is a rare genetic disease due to an abnormality in copper metabolism. Clinical picture mainly includes neurological and cutaneous symptoms, and may present vascular complications. We report two cases of bilatera

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36e2582b63790d6952c5663faf3d1738
https://doi.org/10.4172/2329-6925.1000235

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