Search Results - "Fossé, Q."

Defective exercise-related expiratory muscle recruitment in patients with PHOX2B mutations: A clue to neural determinants of the congenital central hypoventilation syndrome by Laveneziana, P., Fossé, Q., Bret, M., Patout, M., Dudoignon, B., Llontop, C., Morélot-Panzini, C., Cayetanot, F., Bodineau, L., Straus, C., Similowski, T.

“…The human congenital central hypoventilation syndrome (CCHS) is caused by mutations in the PHOX2B (paired-like homeobox 2B) gene. Genetically engineered PHOX2B…”
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Alemtuzumab‐induced immune‐mediated thrombotic thrombocytopenic purpura: A newly described drug‐related autoimmune disease by Bourdin, V., Fossé, Q., Lambotte, O., Joly, B., Coppo, P., Anguel, N., Labeyrie, C.

“…Summary Immune‐mediated thrombotic thrombocytopenic purpura (iTTP) is a rare and life‐threatening disease that may result from drug exposure. We report a case…”
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Severe community-acquired Capnocytophaga leadbetteri pneumonia in a HIV-infected patient by Fossé, Q., Flateau, C., Gomart, C., Decousser, J.W., Gallien, S.

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