Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hervéat Ramanandafy"'
Autor:
Herveat Ramanandafy, Finaritra Princy Parfait Andriamahenina, Michel Harison Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Razafimpihanina, Diamondra Andriarimanga, Jean Noêl Solohery Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana
Publikováno v:
Clinical Case Reports, Vol 10, Iss 1, Pp n/a-n/a (2022)
Abstract Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The prese
Externí odkaz:
https://doaj.org/article/9a261cb40b4f4f1ea2aaed621bbe9345
Autor:
Rova Malala Fandresena Randrianarisoa, Hervéat Ramanandafy, Alexandre Mania, Assia Djelloul Benelhadj, Mélissa Clément, Lara Sabbagh, Pierre Vernet, Hélène Monjanel, Sébastien Trouillier
Publikováno v:
Clinical Case Reports, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract A 75‐year‐old man with an aortic bioprosthesis was admitted with polyarthritis in a non‐febrile setting. Blood cultures were positive for Listeria monocytogenes. The diagnosis of Listeria endocarditis and spondylodiscitis was evoked. T
Externí odkaz:
https://doaj.org/article/8c2f641b9ae34a5d918b7bd865a873bb
Autor:
Rova Malala Fandresena Randrianarisoa, Herveat Ramanandafy, Alexandre Mania, Hélène Monjanel, Sébastien Trouillier
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTIntroduction Several observations have shown that patients with polycythemia have iron deficiency. Our objectives were to report the prevalence of iron deficiency and to evaluate the diagnostic performance of serum ferritin in polycythemia ve
Externí odkaz:
https://doaj.org/article/aebc43b6829d494d8f36aa1143a88bb9
Autor:
Haritanjona Andriamiarintsoa, Herveat Ramanandafy, Orlando Andoniaina Andriamiadanalisoa, Koloina Randriantianarisoa, Prosper Harinarivo Randrianarivelo, Emmylou Prisca Gabrielle Andrianah, Lova Hasina Ny Ony Narindra Rajaonarison, Léa Raobela, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana, Ahmad Ahmad
Publikováno v:
Clinical Case Reports, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Spontaneous bilateral intraorbital hematoma is a rare complication of sickle cell disease in children. Imaging examinations are of paramount importance in the diagnosis and conditioning of the management processes in order to avoid complicat
Externí odkaz:
https://doaj.org/article/fe5148332f3e462d9ad609eb92f705fb