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Search Results - Dupre, Bobby
Search Results - Dupre, Bobby
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Fibromyalgia: can online cognitive behavioral therapy help?
by
Menga, Gwendoline
,
Ing, Sharon
,
Khan, Omar
,
Dupre, Bobby
,
Dornelles, Adriana C
,
Alarakhia, Anika
,
Davis, William
,
Zakem, Jerald
,
Webb-Detiege, Tamika
,
Scopelitis, Eve
,
Quinet, Robert
Published in
The Ochsner journal
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A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
by
Ng, Bobby G.
,
Sosicka, Paulina
,
Fenaille, François
,
Harroche, Annie
,
Vuillaumier-Barrot, Sandrine
,
Porterfield, Mindy
,
Xia, Zhi-Jie
,
Wagner, Shannon
,
Bamshad, Michael J.
,
Vergnes-Boiteux, Marie-Christine
,
Cholet, Sophie
,
Dalton, Stephen
,
Dell, Anne
,
Dupré, Thierry
,
Fiore, Mathieu
,
Haslam, Stuart M.
,
Huguenin, Yohann
,
Kumagai, Tadahiro
,
Kulik, Michael
,
McGoogan, Katherine
,
Michot, Caroline
,
Nickerson, Deborah A.
,
Pascreau, Tiffany
,
Borgel, Delphine
,
Raymond, Kimiyo
,
Warad, Deepti
,
Flanagan-Steet, Heather
,
Steet, Richard
,
Tiemeyer, Michael
,
Seta, Nathalie
,
Bruneel, Arnaud
,
Freeze, Hudson H.
Published in
American journal of human genetics
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Long-Term Follow-up Study after Lentiviral Hematopoietic Stem/Progenitor Cell Gene Therapy for Wiskott - Aldrich Syndrome
by
Magnani, Alessandra
,
Semeraro, Michaela
,
ADAM, Frédéric
,
Booth, Claire
,
Dupre, Loic
,
Morris, Emma C
,
Gabrion, Aurélie
,
Roudaut, Cecile
,
Borgel, Delphine
,
Toubert, Antoine
,
Clave, Emmanuel
,
Abdo, Chrystelle
,
Gorochov, Guy
,
Petermann, Rachel
,
Guiot, Mélanie
,
Miyara, Makoto
,
Moshous, Despina
,
Magrin, Elisa
,
Denis, Adeline
,
Suarez, Felipe
,
Lagresle-Peyrou, Chantal
,
Doto, Aoife
,
Everett, John K.
,
Trinquand, Amélie
,
Guisset, Marianne
,
Xu-Bayford, Jin Hua
,
Hacein-Bey-Abina, Salima
,
Kauskot, Alexandre
,
Elfeky, Reem
,
Rivat, Christine
,
Abbas, Sarah
,
Gaspar, Bobby H
,
Macintyre, Elizabeth A.
,
Picard, Capucine
,
Bushman, Frederic D.
,
Galy, Anne
,
Fischer, Alain
,
Six, Emmanuelle
,
Thrasher, Adrian J.
,
Cavazzana, Marina
Published in
Blood
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Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings
by
Wilson, Matthew P.
,
Garanto, Alejandro
,
Pinto e Vairo, Filippo
,
Ng, Bobby G.
,
Ranatunga, Wasantha K.
,
Ventouratou, Marina
,
Baerenfaenger, Melissa
,
Huijben, Karin
,
Thiel, Christian
,
Ashikov, Angel
,
Keldermans, Liesbeth
,
Souche, Erika
,
Vuillaumier-Barrot, Sandrine
,
Dupré, Thierry
,
Michelakakis, Helen
,
Fiumara, Agata
,
Pitt, James
,
White, Susan M.
,
Lim, Sze Chern
,
Gallacher, Lyndon
,
Peters, Heidi
,
Rymen, Daisy
,
Witters, Peter
,
Ribes, Antonia
,
Morales-Romero, Blai
,
Rodríguez-Palmero, Agustí
,
Ballhausen, Diana
,
de Lonlay, Pascale
,
Barone, Rita
,
Janssen, Mirian C.H.
,
Jaeken, Jaak
,
Freeze, Hudson H.
,
Matthijs, Gert
,
Morava, Eva
,
Lefeber, Dirk J.
Published in
American journal of human genetics
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