Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Herveat RAMANANDAFY"'
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
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:
Herveat Ramanandafy, Solohery Jean Noël Ratsimbazafy, Mahefa Harilala Randrianarivony, Hitsy Andraina Razafindrazaka, Nainanirina Sylvain, Rova Malala Fandresena Randrianarisoa, Norosoa Eliane Sojandrimalala, Manoa Hariniaina Rakotoarisoa, Ainasalohimanana Marie Ymelda Randrianarisoa, Ida Marie Rahantamalala, Norotiana Stéphanie Andriamiharisoa, Andrianarivelo Solofo Ralamboson, Hanta Marie Danielle Vololontiana
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 71:199-202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffefc04141c3925ec0240353102e67fa
https://doi.org/10.1016/j.ancard.2022.05.001
https://doi.org/10.1016/j.ancard.2022.05.001
Autor:
Rova Malala Fandresena Randrianarisoa, Herveat Ramanandafy, Alexandre Mania, Hélène Monjanel, Sébastien Trouillier
Several observations have shown that patients with polycythemia have iron deficiency. Our objectives were to report the prevalence of iron deficiency, to evaluate the diagnostic performance of serum ferritin in polycythemia vera and to describe the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f076ab9d7ba2c1e763bd188b13ad6cc3
https://doi.org/10.20944/preprints202302.0467.v1
https://doi.org/10.20944/preprints202302.0467.v1
Autor:
Herveat RAMANANDAFY, léophonte samison Ramily, Raïssa Haingotiana Raharinoro, Fandresena sendrasoa, Lala Soavina Ramarozatovo, Hanta Marie Danielle Vololontiana, Rabenja Fahefantsoa Rapelanoro
A 24-year-old man had vascular purpuric infiltrated, associated elbows and knees’s polyarthralgia, and abdominal pain. The proteinuria was 0.73 g/24 h. Skin histology showed a lymphocytic vasculitis lesion and perivascular infiltrates, without fibr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c4a465a7c71593e3da0ae7cad0b0142
https://doi.org/10.22541/au.165034812.23043531/v1
https://doi.org/10.22541/au.165034812.23043531/v1
Autor:
Haritanjona Andriamiarintsoa, Herveat RAMANANDAFY, Koloina Randriantiana, Prosper Harinarivo Randrianarivelo, Emmylou Prisca Gabrielle Andrianah, Lova Hasina Ny Ony Narindra Rajaonarison, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana, Ahmad Ahmad
Spontaneous bilateral intra-orbital hematoma is a rare complication of sickle cell disease in children. Imaging examinations are of paramount importance in the diagnosis and condition the management in order to avoid complications that can compromise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57dfd69ae29fa9577ac79c6ed2c400c6
https://doi.org/10.22541/au.164293652.22372766/v1
https://doi.org/10.22541/au.164293652.22372766/v1
Autor:
Herveat, Ramanandafy, Solohery Jean Noël, Ratsimbazafy, Mahefa Harilala, Randrianarivony, Hitsy Andraina, Razafindrazaka, Nainanirina, Sylvain, Rova Malala Fandresena, Randrianarisoa, Norosoa Eliane, Sojandrimalala, Manoa Hariniaina, Rakotoarisoa, Ainasalohimanana Marie Ymelda, Randrianarisoa, Ida Marie, Rahantamalala, Norotiana Stéphanie, Andriamiharisoa, Andrianarivelo Solofo, Ralamboson, Hanta Marie Danielle, Vololontiana
Publikováno v:
Annales de cardiologie et d'angeiologie. 71(4)
Venous thrombosis of unusual sites is much rarer than in the lower limbs and requires a rigorous etiological approach. The objective was to describe the clinical and progressive peculiarities of unusual localization venous thrombosis as well as their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a3480783f6ae94166bc46bc9efcb9ae
https://pubmed.ncbi.nlm.nih.gov/35718550
https://pubmed.ncbi.nlm.nih.gov/35718550
Autor:
Herveat RAMANANDAFY, Princy Parfait Andriamahenina, Harison Michel Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Marcelle Razafimpihanina, Diamondra ombanjanahary Andriarimanga, Solohery Jean Noel Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana
Rendu Osler’s disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Rendu Osler’s disease was discovered during hypoxemia during an outbreak of SARS-Cov2.This was a 36-year-old woman with exertional dyspnea and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c9457d87182f64e524665cbf4f90817
https://doi.org/10.22541/au.163655519.92155116/v1
https://doi.org/10.22541/au.163655519.92155116/v1
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