Zobrazeno 1 - 10
of 213
pro vyhledávání: '"J.-M. Ziza"'
Autor:
G. Bart, V. Zeller, Y. Kerroumi, B. Heym, V. Meyssonnier, N. Desplaces, M. D. Kitzis, J. M. Ziza, S. Marmor
Publikováno v:
Journal of Bone and Joint Infection, Vol 5, Pp 110-117 (2020)
Introduction: Treatment of methicillin-resistant (MR) staphylococcal prosthetic joint infections (PJIs) remains a matter of discussion, with vancomycin-rifampin combination therapy being the preferred treatment for DAIR and one-stage exchange arthrop
Externí odkaz:
https://doaj.org/article/1ef54d762aec4bbdaa9108a127dd73c1
Autor:
G. Bart, V. Zeller, Y. Kerroumi, B. Heym, V. Meyssonnier, N. Desplaces, M. D. Kitzis, J. M. Ziza, S. Marmor
Publikováno v:
Journal of Bone and Joint Infection
Journal of Bone and Joint Infection, Vol 5, Pp 110-117 (2020)
Journal of Bone and Joint Infection, Vol 5, Pp 110-117 (2020)
Introduction: Treatment of methicillin-resistant (MR) staphylococcal prosthetic joint infections (PJIs) remains a matter of discussion, with vancomycin-rifampin combination therapy being the preferred treatment for DAIR and one-stage exchange arthrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47807814bc2591c4fedd051707377b7b
https://pubmed.ncbi.nlm.nih.gov/32566448
https://pubmed.ncbi.nlm.nih.gov/32566448
Autor:
O, Lidove, N, Belmatoug, R, Froissart, C, Lavigne, I, Durieu, K, Mazodier, C, Serratrice, C, Douillard, C, Goizet, P, Cathebras, G, Besson, Z, Amoura, A, Tazi, M, Gatfossé, S, Rivière, T, Sené, M T, Vanier, J-M, Ziza
Publikováno v:
La Revue de medecine interne. 38(5)
Acid sphingomyelinase deficiency (ASMD) is an autosomal recessive disease with a clinical spectrum ranging from a neurovisceral infantile form (Niemann-Pick disease type A) to a chronic visceral form also encountered in adults (Niemann-Pick disease t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1073af3a3ae9b893e3aa7762514833f
https://pubmed.ncbi.nlm.nih.gov/27884455
https://pubmed.ncbi.nlm.nih.gov/27884455
Publikováno v:
La Revue de medecine interne. 38(6)
Osteomalacia is associated with diffuse pain and multiple fractures and therefore, diagnosis and treatment of this condition are necessary. Clinicians should be aware of an uncommon mechanism of osteomalacia where hypophosphataemia is secondary to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fba1c2511b352ba5b4008a84299d3809
https://pubmed.ncbi.nlm.nih.gov/27659744
https://pubmed.ncbi.nlm.nih.gov/27659744
Publikováno v:
La Revue de Médecine Interne. 35:271-273
Resume Introduction Si le risque de neoplasie est clairement augmente dans les autres myosites inflammatoires comme la dermatomyosite et la polymyosite, il n’existe pas de preuve dans la litterature d’une association entre syndrome des antisynthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::666a42325d966edd9a12ccd84c11e9a9
https://doi.org/10.1016/j.revmed.2013.04.012
https://doi.org/10.1016/j.revmed.2013.04.012
Autor:
S-N, Tran Ba, O, Lidove, R, Dorent, M, Debauchez, P, Nataf, M, Delahousse, A, Karras, L, Azeroual, P, De Lentdecker, M P, Chauveheid, T, Sené, J-M, Ziza
Publikováno v:
La Revue de medecine interne. 38(2)
Fabry disease is a lysosomal storage disorder linked to an alpha-galactosidase A deficiency that can lead to heart and kidney failure. There is little data about the prognosis of patients who undergo a combined heart and kidney transplantation.Two br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e60339c3a6297afb0f76537cb0ebaa7a
https://pubmed.ncbi.nlm.nih.gov/27241078
https://pubmed.ncbi.nlm.nih.gov/27241078
Publikováno v:
Revue de Chirurgie Orthopédique et Réparatrice de l'Appareil Moteur. 92:47-54
Resume La prise en charge des arthrites septiques a connu dans les dernieres decennies deux grands tournants : l’apparition de l’antibiotherapie et le traitement arthroscopique. Les auteurs rapportent une revue retrospective de 78 dossiers issus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8664a67cece75f011594a7c6ca226790
https://doi.org/10.1016/s0035-1040(06)75963-3
https://doi.org/10.1016/s0035-1040(06)75963-3
Autor:
O, Lidove, L, Le Fèvre, N, Goasguen, M, Jamali, L, Vercellino, M, Garnier, M, Khellaf, N, Belmatoug, J-M, Ziza
Publikováno v:
La Revue de medecine interne. 36(9)
Acid sphingomyelinase deficiency leads to a severe infantile disease (Niemann-Pick disease type A) or an attenuated form of the disease encountered in adults (Niemann-Pick type B), including pulmonary fibrosis and splenomegaly.A 52-year-old man with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8db4b471a66c0deb7dfc0c89955aa41f
https://pubmed.ncbi.nlm.nih.gov/25479761
https://pubmed.ncbi.nlm.nih.gov/25479761
Autor:
E.-A. Hang-Korng, V. Zeller, P. Jacquenod, F. Koskas, A. Delcourt, J.-P. Brouland, N. Molinier, J.-M. Ziza
Publikováno v:
La Revue de Médecine Interne. 26:S304-S306
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1f9602893bebafdc3b1630352e328c0
https://doi.org/10.1016/s0248-8663(05)81294-9
https://doi.org/10.1016/s0248-8663(05)81294-9
Publikováno v:
La Revue de medecine interne. 35(6)
Acute necrosis of the esophagus, frequently referred to as black esophagus is a rare clinical entity.We here report a case of an acute necrosis of the esophagus secondary to hemodynamic compromise after total hip replacement. Past medical history of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f8f268e8c6d19efe6cd66113be6c97e
https://pubmed.ncbi.nlm.nih.gov/23947994
https://pubmed.ncbi.nlm.nih.gov/23947994