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Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.
Published in:
Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 102, doi. 10.1186/s13023-014-0183-8
By:
- Desplantes, Claire;
- Fremond, Marie Louis;
- Beaupain, Blandine;
- Luc Harousseau, Jean;
- Buzyn, Agnès;
- Pellier, Isabelle;
- Roques, Gaelle;
- Morville, Pierre;
- Paillard, Catherine;
- Bruneau, Julie;
- Pinson, Lucile;
- Jeziorski, Eric;
- Vannier, Jean Pierre;
- Picard, Capucine;
- Bellanger, Florence;
- Romero, Norma;
- de Pontual, Loïc;
- Lapillonne, Hélène;
- Lutz, Patrick;
- Bellanné Chantelot, Christine
Publication type:
Article
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.
Published in:
2014
By:
- Desplantes, Claire;
- Fremond, Marie Louise;
- Beaupain, Blandine;
- Harousseau, Jean Luc;
- Buzyn, Agnès;
- Pellier, Isabelle;
- Roques, Gaelle;
- Morville, Pierre;
- Paillard, Catherine;
- Bruneau, Julie;
- Pinson, Lucile;
- Jeziorski, Eric;
- Vannier, Jean Pierre;
- Picard, Capucine;
- Bellanger, Florence;
- Romero, Norma;
- de Pontual, Loïc;
- Lapillonne, Hélène;
- Lutz, Patrick;
- Chantelot, Christine Bellanné
Publication type:
Journal Article
Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome - a report from the SFCE & CCLG groups.
Published in:
British Journal of Haematology, 2017, v. 177, n. 1, p. 106, doi. 10.1111/bjh.14518
By:
- Shankar, Ananth G.;
- Roques, Gaelle;
- Kirkwood, Amy A.;
- Lambilliotte, Anne;
- Freund, Katja;
- Leblanc, Thierry;
- Hayward, Janis;
- Abbou, Samuel;
- Ramsay, Alan D.;
- Schmitt, Claudine;
- Gorde‐Grosjean, Stephanie;
- Pacquement, Hélène;
- Haouy, Stephanie;
- Boudjemaa, Sabah;
- Aladjidi, Nathalie;
- Hall, Georgina W.;
- Landman‐Parker, Judith
Publication type:
Article
Neurological findings and genetic alterations in patients with Kostmann syndrome and HAX1 mutations.
Published in:
Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1041, doi. 10.1002/pbc.24964
By:
- Roques, Gaëlle;
- Munzer, Martine;
- Barthez, Marie‐Anne Carpentier;
- Beaufils, Sandrine;
- Beaupain, Blandine;
- Flood, Terry;
- Keren, Boris;
- Bellanné‐Chantelot, Christine;
- Donadieu, Jean
Publication type:
Article

Found: 4

Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.

Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.

Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome - a report from the SFCE & CCLG groups.

Neurological findings and genetic alterations in patients with Kostmann syndrome and HAX1 mutations.