Of the importance of the clinical phenotypes in the interpretation of the studies dealing with Fabry disease

por Mauhin, Wladimir, Lidove, Olivier, Benveniste, Olivier
Publicado 2019

Fabry nephropathy: 5 years of enzyme replacement therapy—a short review

por Barbey, Frédéric, Lidove, Olivier, Schwarting, Andreas
Publicado 2008

Interstitial lung disease in lysosomal storage disorders

por Borie, Raphaël, Crestani, Bruno, Guyard, Alice, Lidove, Olivier
Publicado 2021

Prevalence of Cancer in Acid Sphingomyelinase Deficiency

por Mauhin, Wladimir, Levade, Thierry, Vanier, Marie T., Froissart, Roseline, Lidove, Olivier
Publicado 2021

Disease manifestations and burden of illness in patients with acid sphingomyelinase deficiency (ASMD)

por McGovern, Margaret M., Avetisyan, Ruzan, Sanson, Bernd-Jan, Lidove, Olivier
Publicado 2017

Streptococcal and Staphylococcus aureus prosthetic joint infections: are they really different?

por Kherabi, Yousra, Zeller, Valérie, Kerroumi, Younes, Meyssonnier, Vanina, Heym, Beate, Lidove, Olivier, Marmor, Simon
Publicado 2022

Cutibacterium acnes Prosthetic Joint Infections: Is Rifampicin-Combination Therapy Beneficial?

por Saltiel, Grégoire, Meyssonnier, Vanina, Kerroumi, Younes, Heym, Beate, Lidove, Olivier, Marmor, Simon, Zeller, Valérie
Publicado 2022

Pseudomonas aeruginosa prosthetic joint-infection outcomes: Prospective, observational study on 43 patients

por Prié, Héloïse, Meyssonnier, Vanina, Kerroumi, Younes, Heym, Beate, Lidove, Olivier, Marmor, Simon, Zeller, Valérie
Publicado 2022

Strong increase of leukocyte apha‐galactosidase A activity in two male patients with Fabry disease following oral chaperone therapy

por Lamari, Foudil, Mauhin, Wladimir, Koraichi, Fairouz, Khrouf, Walid, Bordet, Celine, London, Jonathan, Lidove, Olivier, Charron, Philippe
Publicado 2019

Coagulation disorders during treatment with cefazolin and rifampicin: rare but dangerous

por Kouki, Ines, Montagner, Clémence, Mauhin, Wladimir, London, Jonathan, Lazard, Thierry, Grimbert, Sylvie, Zeller, Valérie, Lidove, Olivier
Publicado 2021

Acid Sphingomyelinase Deficiency: Sharing Experience of Disease Monitoring and Severity in France

por Mauhin, Wladimir, Borie, Raphaël, Dalbies, Florence, Douillard, Claire, Guffon, Nathalie, Lavigne, Christian, Lidove, Olivier, Brassier, Anaïs
Publicado 2022

Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1

por Stirnemann, Jérôme, Rose, Christian, Serratrice, Christine, Dalbies, Florence, Lidove, Olivier, Masseau, Agathe, Pers, Yves-Marie, Baron, Camille, Belmatoug, Nadia
Publicado 2015

Prevalence of Raynaud Phenomenon and Nailfold Capillaroscopic Abnormalities in Fabry Disease: A Cross-Sectional Study

por Deshayes, Samuel, Auboire, Laurent, Jaussaud, Roland, Lidove, Olivier, Parienti, Jean-Jacques, Triclin, Nathalie, Imbert, Bernard, Bienvenu, Boris, Aouba, Achille
Publicado 2015

Semen and male genital tract characteristics of patients with Fabry disease: the FERTIFABRY multicentre observational study

por Papaxanthos-Roche, Aline, Maillard, Aline, Chansel-Debordeaux, Lucie, Albert, Martine, Patrat, Catherine, Lidove, Olivier, Germain, Dominique P., Perez, Paul, Lacombe, Didier
Publicado 2019

Coagulation Parameters in Adult Patients With Type-1 Gaucher Disease

por Serratrice, Christine, Cherin, Patrick, Lidove, Olivier, Noel, Esther, Masseau, Agathe, Leguy-Seguin, Vanessa, Jaussaud, Roland, Marie, Isabelle, Lavigne, Christian, Maillot, Francois
Publicado 2019

Parsing Fabry Disease Metabolic Plasticity Using Metabolomics

por Ducatez, Franklin, Mauhin, Wladimir, Boullier, Agnès, Pilon, Carine, Pereira, Tony, Aubert, Raphaël, Benveniste, Olivier, Marret, Stéphane, Lidove, Olivier, Bekri, Soumeya, Tebani, Abdellah
Publicado 2021

Do clinical guidelines facilitate or impede drivers of treatment in Fabry disease?

por Hughes, Derralynn A., Aguiar, Patrício, Lidove, Olivier, Nicholls, Kathleen, Nowak, Albina, Thomas, Mark, Torra, Roser, Vujkovac, Bojan, West, Michael L., Feriozzi, Sandro
Publicado 2022

Cardiac device implantation in Fabry disease: A retrospective monocentric study

por Sené, Thomas, Lidove, Olivier, Sebbah, Joel, Darondel, Jean-Marc, Picard, Hervé, Aaron, Laurent, Fain, Olivier, Zenone, Thierry, Joly, Dominique, Charron, Philippe, Ziza, Jean-Marc
Publicado 2016

Recommendations for clinical monitoring of patients with acid sphingomyelinase deficiency (ASMD)

por Wasserstein, Melissa, Dionisi-Vici, Carlo, Giugliani, Roberto, Hwu, Wuh-Liang, Lidove, Olivier, Lukacs, Zoltan, Mengel, Eugen, Mistry, Pramod K., Schuchman, Edward H., McGovern, Margaret
Publicado 2018

Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency

por McGovern, Margaret M., Dionisi-Vici, Carlo, Giugliani, Roberto, Hwu, Paul, Lidove, Olivier, Lukacs, Zoltan, Eugen Mengel, Karl, Mistry, Pramod K., Schuchman, Edward H., Wasserstein, Melissa P.
Publicado 2017