A thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia von Mamoune, Asmaa, Bahuau, Michel, Hamel, Yamina, Serre, Valérie, Pelosi, Michele, Habarou, Florence, Nguyen Morel, Marie-Ange, Boisson, Bertrand, Vergnaud, Sabrina, Viou, Mai Thao, Nonnenmacher, Luc, Piraud, Monique, Nusbaum, Patrick, Vamecq, Joseph, Romero, Norma, Ottolenghi, Chris, Casanova, Jean-Laurent, de Lonlay, Pascale

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Progressive Development of PTH Resistance in Patients With Inactivating Mutations on the Maternal Allele of GNAS von Usardi, Alessia, Mamoune, Asmaa, Nattes, Elodie, Carel, Jean-Claude, Rothenbuhler, Anya, Linglart, Agnès

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Acute rhabdomyolysis von De Lonlay, Pascale, Mamoune, Asmaa, Hamel, Yamina, Bahuau, Michel, Vergnaud, Sabrina, Piraud, Moniqu, Lallemand, Lætitia, Nguyen More, Marie-Ange, Vio, Mai Thao, Romero, Norma Beatriz

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Acute rhabdomyolysis and inflammation von Hamel, Yamina, Mamoune, Asmaa, Mauvais, François-Xavier, Habarou, Florence, Lallement, Laetitia, Romero, Norma Beatriz, Ottolenghi, Chris, de Lonlay, Pascale

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Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase von Soreze, Yohan, Boutron, Audrey, Habarou, Florence, Barnerias, Christine, Nonnenmacher, Luc, Delpech, Hélène, Mamoune, Asmaa, Chrétien, Dominique, Hubert, Laurence, Bole-Feysot, Christine, Nitschke, Patrick, Correia, Isabelle, Sardet, Claude, Boddaert, Nathalie, Hamel, Yamina, Delahodde, Agnès, Ottolenghi, Chris, de Lonlay, Pascale

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Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts von Michot, Caroline, Mamoune, Asmaa, Vamecq, Joseph, Viou, Mai Thao, Hsieh, Lu-Sheng, Testet, Eric, Lainé, Jeanne, Hubert, Laurence, Dessein, Anne-Frédérique, Fontaine, Monique, Ottolenghi, Chris, Fouillen, Laetitia, Nadra, Karim, Blanc, Etienne, Bastin, Jean, Candon, Sophie, Pende, Mario, Munnich, Arnold, Smahi, Asma, Djouadi, Fatima, Carman, George M., Romero, Norma, de Keyzer, Yves, de Lonlay, Pascale

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Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia von Michot, Caroline, Hubert, Laurence, Romero, Norma B., Gouda, Amr, Mamoune, Asmaa, Mathew, Suja, Kirk, Edwin, Viollet, Louis, Rahman, Shamima, Bekri, Soumeya, Peters, Heidi, McGill, James, Glamuzina, Emma, Farrar, Michelle, von der Hagen, Maya, Alexander, Ian E., Kirmse, Brian, Barth, Magalie, Laforet, Pascal, Benlian, Pascale, Munnich, Arnold, JeanPierre, Marc, Elpeleg, Orly, Pines, Ophry, Delahodde, Agnès, de Keyzer, Yves, de Lonlay, Pascale

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Successful treatment of congenital hyperinsulinism with long-acting release octreotide von Le Quan Sang, Kim-Hanh, Arnoux, Jean-Baptiste, Mamoune, Asmaa, Saint-Martin, Cécile, Bellanné-Chantelot, Christine, Valayannopoulos, Vassili, Brassier, Anais, Kayirangwa, Honorine, Barbier, Valérie, Broissand, Christine, Fabreguettes, Jean-Roch, Charron, Brigitte, Thalabard, Jean-Christophe, de Lonlay, Pascale

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Calpain-2 as a target for limiting prostate cancer invasion von MAMOUNE, Asmaa, LUO, Jian-Hua, LAUFFENBURGER, Douglas A, WELLS, Alan

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Cloning and characterization of a novel transcription factor involved in cellular proliferation arrest : PATF von CRISANTI, Patricia, RAGUENEZ, Gilda, BLANCHER, Christine, NERON, Bertrand, MAMOUNE, Asmaa, OMRI, Boubaker

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A Thermolabile Aldolase A Mutant Causes Fever-Induced Recurrent Rhabdomyolysis without Hemolytic Anemia: e1004711 von Mamoune, Asmaa, Bahuau, Michel, Hamel, Yamina, Serre, Valérie, Pelosi, Michele, Habarou, Florence, Morel, Marie-Ange Nguyen, Boisson, Bertrand, Vergnaud, Sabrina, Viou, Mai Thao, Nonnenmacher, Luc, Piraud, Monique, Nusbaum, Patrick, Vamecq, Joseph, Romero, Norma, Ottolenghi, Chris, Casanova, Jean-Laurent, Lonlay, Pascale de

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DU145 human prostate carcinoma invasiveness is modulated by urokinase receptor (uPAR) downstream of epidermal growth factor receptor (EGFR) signaling von Mamoune, Asmaa, Kassis, Jareer, Kharait, Sourabh, Kloeker, Susanne, Manos, Elisabeth, Jones, David A, Wells, Alan

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Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase von Soreze, Yohan, Boutron, Audrey, Habarou, Florence, Barnerias, Christine, Nonnenmacher, Luc, Delpech, Hñlène, Mamoune, Asmaa, Chrñtien, Dominique, Hubert, Laurence, Bole-Feysot, Christine, Nitschke, Patrick, Correia, Isabelle, Sardet, Claude, Boddaert, Nathalie, Hamel, Yamina, Delahodde, Agnès, Ottolenghi, Chris, de Lonlay, Pascale

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Autoantibodies to CD45 in Systemic Lupus Erythematosus von Mamoune, Asmâa, Saraux, Alain, Delaunay, Jean-Louis, Le Goff, Paul, Youinou, Pierre, Le Corre, Rozenn

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Острый рабдомиолиз von de Lonlay, Pascale, Mamoune, Asmaa, Hamel, Yamina, Bahuau, Michel, Vergnaud, Sabrina, Piraud, Monique, Lallemand, Lætitia, Marie-Ange Ngu Nguyen Morel, Mai Thao Viou, Romero, Norma Beatriz, Piraud, Moniqu, Marie-Ange Nguyen More, Mai Thao Vio

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