FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Despina Moshous

Research Profile

Disorders

Living Beings

Chemicals & Drugs

Physiology

Anatomy

Co-author Network

Publications

TOP 3
Nizar Mahlaoui; Cécile Mignot; Despina Moshous; Bénédicte Neven; Isabelle Pellier; Capucine Picard; Chrystèle Bilhou-Nabéra; Stéphane Blanche; Marina Cavazzana-Calvo; Geneviève de Saint Basile; Jean-Philippe Jais; Alain Fischer
Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome.
Fabian Hauck; Sébastien Heritier; Claire Hivroz; Nathalie Lambert; Sylvain Latour; Annick Lim; Zosia Maciorowski; Emmanuel Martin; Despina Moshous; Stéphane Blanche; Nicole Brousse; Isabelle Callebaut; Alain Fischer; Stéphane Gerart; Pierre Quartier; Clotilde Randriamampita; Frédéric Rieux-Laucat; Jean Soulier; Fabien Touzot; André Veillette; Capucine Picard
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency.
Jennifer Heimall; Michael Keller; Barbara Ariue; Rebecca H Buckley; Nancy Bunin; Jean-Pierre De Villartay; Blythe H Devlin; Elizabeth A McCarthy; Donna McDonald-McGinn; Despina Moshous; Suhag Parikh; Rushani Saltzman; Elaine Zakai; M Louise Markert
Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Despina Moshous (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Nizar Mahlaoui; Cécile Mignot; Despina Moshous; Bénédicte Neven; Isabelle Pellier; Capucine Picard; Chrystèle Bilhou-Nabéra; Stéphane Blanche; Marina Cavazzana-Calvo; Geneviève de Saint Basile; Jean-Philippe Jais; Alain Fischer
Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome.
Blood 2013;121(9):1510-6.
2012: Fabian Hauck; Sébastien Heritier; Claire Hivroz; Nathalie Lambert; Sylvain Latour; Annick Lim; Zosia Maciorowski; Emmanuel Martin; Despina Moshous; Stéphane Blanche; Nicole Brousse; Isabelle Callebaut; Alain Fischer; Stéphane Gerart; Pierre Quartier; Clotilde Randriamampita; Frédéric Rieux-Laucat; Jean Soulier; Fabien Touzot; André Veillette; Capucine Picard
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency.
The Journal of allergy and clinical immunology 2012;130(5):1144-1152.e11.
2012: Jennifer Heimall; Michael Keller; Barbara Ariue; Rebecca H Buckley; Nancy Bunin; Jean-Pierre De Villartay; Blythe H Devlin; Elizabeth A McCarthy; Donna McDonald-McGinn; Despina Moshous; Suhag Parikh; Rushani Saltzman; Elaine Zakai; M Louise Markert
Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.
Journal of clinical immunology 2012;32(5):1141-4.
2012: Simon T Cliffe; Christian Gilissen; Erik-Jan Kamsteeg; Gérard Lefranc; Robert Lindeman; André Megarbané; Siraj Misbah; Despina Moshous; Peck Y Ong; Umaimainthan Palendira; Janine Reichenbach; Ezia Ruga; Uli Salzer; Polina Stepensky; Santi Suryani; Stuart G Tangye; Antonino Trizzino; Brynn K Wainstein; Melanie Wong; John B Ziegler; Mario Abinun; Carlo Akatcherian; Danielle T Avery; Donald B Bloch; Michael F Buckley; Joseph A Church; Tony Roscioli
Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndrome.
The Journal of allergy and clinical immunology 2012;130(3):735-742.e6.
2012: Fabien Touzot; Virginie Verkarre; Stéphane Blanche; Marina Cavazzana-Calvo; Anne Crucis-Armengaud; Liliane Dal Cortivo; Pierre Frange; Salima Hacein-Bey-Abina; Sébastien Héritier; Sophie Kaltenbach; Annick Lim; Despina Moshous; Capucine Picard; Alain Fischer
Massive expansion of maternal T cells in response to EBV infection in a patient with SCID-Xl.
Blood 2012;120(9):1957-9.
2012: Pierre Frange; Despina Moshous; Christine Rouzioux; Florence Veber; Véronique Avettand-Fenoel; Stéphane Blanche; Nelly Briand; Marie-Laure Chaix
CCR5 antagonists: a therapeutic option in HIV-1 perinatally infected children experiencing virologic failure?
AIDS (London, England) 2012;26(13):1673-7.
2012: Kumaran Deiva; A Fischer; Nizar Mahlaoui; Yann Mikaeloff; Despina Moshous; F Beaudonnet; S Blanche; Guillaume Caridade; Geneviève de Saint Basile; Marc Tardieu
CNS involvement at the onset of primary hemophagocytic lymphohistiocytosis.
Neurology 2012;78(15):1150-6.
2012: Angelo Paci; Aurélie Pétain; Gilles Vassal; Zeinab D Abdi; Nathalie Bleyzac; Sophie Broutin; Jean-Hugues Dalle; Claire Galambrun; Véronique Kemmel; Despina Moshous; Bénédicte Neven; Laurent Nguyen
Pharmacokinetic behavior and appraisal of intravenous busulfan dosing in infants and older children: the results of a population pharmacokinetic study from a large pediatric cohort undergoing hematopoietic stem-cell transplantation.
Therapeutic drug monitoring 2012;34(2):198-208.
2012: Juliana F Fernandes; Alain Fischer; Wilhelm Friedrich; H Bobby Gaspar; Andrew R Gennery; Eliane Gluckman; Michael Grimley; Tayfun Gungor; Krzysztof Kalwak; Myriam Labopin; Paul Landais; Despina Moshous; Bénédicte Neven; Fulvio Porta; Vanderson Rocha; Ansgar Schulz; Mary A Slatter; Pierre Taupin; Paul Veys; Donna Wall; Mouhab Ayas; Yves Bertrand; Stéphane Blanche; Carmen M S Bonfim; Marina Cavazzana-Calvo; Ka Wah Chan; Cristina Diaz de Heredia; Wolfram Ebell
Transplantation in patients with SCID: mismatched related stem cells or unrelated cord blood?
Blood 2012;119(12):2949-55.
2012: Alessandra Pangrazio; Claire Schlack; Ansgar Schulz; D Strina; Ashok Vellodi; Paul Veys; Paolo Vezzoni; Anna Villa; Luca Zammataro; Barbara Cassani; Robert Chiesa; Julie Crockett; Anne Durandy; Angela Duthie; Alain Fischer; Matteo M Guerrini; Miep H Helfrich; Uwe Kornak; Nadia Lo Iacono; Veronica Marrella; David J Mellis; Despina Moshous; Cristina Sobacchi
RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012;27(2):342-51.
2011: Despina Moshous; Capucine Picard; Tania Roskams; Felipe Suarez; Jaan Toelen; Carine Wouters; Christine Bodemer; Kris De Boeck; Marianne Debré; Antoine Deschildre; Sylvie Fraitag; Carl E I Janssen; Isabelle Meyts; Alain Fischer
Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbs.
The Journal of allergy and clinical immunology 2011;128(4):847-53.
2011: Pierre Frange; Nizar Mahlaoui; Despina Moshous; Christine Rouzioux; Florence Veber; Véronique Avettand-fenoel; Stéphane Blanche; Nelly Briand; Marie-Laure Chaix
Lopinavir/ritonavir-based antiretroviral therapy in human immunodeficiency virus type 1-infected naive children: rare protease inhibitor resistance mutations but high lamivudine/emtricitabine resistance at the time of virologic failure.
The Pediatric infectious disease journal 2011;30(8):684-8.
2010: Jérôme Cros; Nicolas Cagnard; kevin woollard; Natacha Patey; Shen-Ying Zhang; Brigitte Senechal; Anne Puel; Subhra K Biswas; Despina Moshous; Capucine Picard; Jean-Philippe jais; David D'Cruz; Jean-Laurent Casanova; Céline Trouillet; Frederic Geissmann
Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors.
Immunity 2010;33(3):375-86.
2010: Felix Meissner; Reinhard A Seger; Despina Moshous; Alain Fischer; Janine Reichenbach; Arturo Zychlinsky
Inflammasome activation in NADPH oxidase defective mononuclear phagocytes from patients with chronic granulomatous disease.
Blood 2010;116(9):1570-3.
2009: Jana Pachlopnik Schmid; Despina Moshous; Nathalie Boddaert; Bénédicte Neven; Liliane Dal Cortivo; Marc Tardieu; Marina Cavazzana-Calvo; Stéphane Blanche; Geneviève de Saint Basile; Alain Fischer
Hematopoietic stem cell transplantation in Griscelli syndrome type 2: a single-center report on 10 patients.
Blood 2009;114(1):211-8.
2009: Bénédicte Neven; Sandrine Leroy; Hélène Decaluwe; Françoise Le Deist; Capucine Picard; Despina Moshous; Nizar Mahlaoui; Marianne Debré; Jean-Laurent Casanova; Liliane Dal Cortivo; Yoann Madec; Salima Hacein-Bey-Abina; Geneviève de Saint Basile; Jean-Pierre De Villartay; Stéphane Blanche; Marina Cavazzana-Calvo; Alain Fischer
Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency.
Blood 2009;113(17):4114-24.
2008: Salima Hacein-Bey-Abina; Alexandrine Garrigue; Gary P Wang; Jean Soulier; Annick Lim; Estelle Morillon; Emmanuelle Clappier; Laure Caccavelli; Eric Delabesse; Kheira Beldjord; Vahid Asnafi; Elizabeth Macintyre; Liliane Dal Cortivo; Isabelle Radford; Nicole Brousse; François Sigaux; Despina Moshous; Julia Hauer; Arndt Borkhardt; Bernd H Belohradsky; Uwe Wintergerst; Maria C Velez; Lily Leiva; Ricardo Sorensen; Nicolas Wulffraat; Stéphane Blanche; Frederic D Bushman; Alain Fischer; Marina Cavazzana-Calvo
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1.
The Journal of clinical investigation 2008;118(9):3132-42.
2007: Despina Moshous; Oliver Feyen; Petra Lankisch; Klaus Schwarz; Jörg Schaper; Marion Schneider; Dagmar Dilloo; Hans-Jürgen Laws; Bernd C Schwahn; Tim Niehues
Primary necrotizing lymphocytic central nervous system vasculitis due to perforin deficiency in a four-year-old girl.
Arthritis and rheumatism 2007;56(3):995-9.
2006: Dietke Buck; Despina Moshous; Régina de Chasseval; Yunmei Ma; Françoise Le Deist; Marina Cavazzana-Calvo; Alain Fischer; Jean-Laurent Casanova; Michael R Lieber; Jean-Pierre De Villartay
Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.
European journal of immunology 2006;36(1):224-35.
2004: Catherine Poinsignon; Régina de Chasseval; Sebastien Soubeyrand; Despina Moshous; Alain Fischer; Robert J G Haché; Jean-Pierre De Villartay
Phosphorylation of Artemis following irradiation-induced DNA damage.
European journal of immunology 2004;34(11):3146-55.
2004: Françoise Le Deist; Catherine Poinsignon; Despina Moshous; Alain Fischer; Jean-Pierre De Villartay
Artemis sheds new light on V(D)J recombination.
Immunological reviews 2004;200():142-55.
2004: Catherine Poinsignon; Despina Moshous; Isabelle Callebaut; Régina de Chasseval; Isabelle Villey; Jean-Pierre De Villartay
The metallo-beta-lactamase/beta-CASP domain of Artemis constitutes the catalytic core for V(D)J recombination.
The Journal of experimental medicine 2004;199(3):315-21.
2003: Despina Moshous; Isabelle Callebaut; Régina de Chasseval; Catherine Poinsignon; Isabelle Villey; Alain Fischer; Jean-Pierre De Villartay
The V(D)J recombination/DNA repair factor artemis belongs to the metallo-beta-lactamase family and constitutes a critical developmental checkpoint of the lymphoid system.
Annals of the New York Academy of Sciences 2003;987():150-7.
2003: Despina Moshous; Christophe Pannetier; Régina de Chasseval Rd; Françoise le Deist Fl; Marina Cavazzana-Calvo; Serge Romana; Elizabeth Macintyre; Danielle Canioni; Nicole Brousse; Alain Fischer; Jean-Laurent Casanova; Jean-Pierre de Villartay
Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis.
The Journal of clinical investigation 2003;111(3):381-7.
2002: Isabelle Callebaut; Despina Moshous; Jean-Paul Mornon; Jean-Pierre De Villartay
Metallo-beta-lactamase fold within nucleic acids processing enzymes: the beta-CASP family.
Nucleic acids research 2002;30(16):3592-601.
2002: Lanying Li; Despina Moshous; Yungui Zhou; Junhua Wang; Gang Xie; Eduardo Salido; Diana Hu; Jean-Pierre De Villartay; Morton J Cowan
A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans.
Journal of immunology (Baltimore, Md. : 1950) 2002;168(12):6323-9.
2001: Barbara Corneo; Despina Moshous; Tayfun Güngör; Nico M Wulffraat; P Philippet; Françoise Le Deist; Alain Fischer; Jean-Pierre De Villartay
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome.
Blood 2001;97(9):2772-6.
2001: Despina Moshous; Isabelle Callebaut; Régina de Chasseval; Barbara Corneo; Marina Cavazzana-Calvo; Françoise Le Deist; Ilhan Tezcan; Ozden Sanal; Y Bertrand; N Philippe; Alain Fischer; Jean-Pierre De Villartay
Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.
Cell 2001;105(2):177-86.
2000: Barbara Corneo; Despina Moshous; Isabelle Callebaut; Régina de Chasseval; Alain Fischer; Jean-Pierre De Villartay
Three-dimensional clustering of human RAG2 gene mutations in severe combined immune deficiency.
The Journal of biological chemistry 2000;275(17):12672-5.
2000: Despina Moshous; L Li; R Chasseval; N Philippe; Nada Jabado; Morton J Cowan; Alain Fischer; Jean-Pierre De Villartay
A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.
Human molecular genetics 2000;9(4):583-8.
1998: N Nicolas; Despina Moshous; Marina Cavazzana-Calvo; D Papadopoulo; Régina de Chasseval; Françoise Le Deist; Alain Fischer; Jean-Pierre De Villartay
A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency.
The Journal of experimental medicine 1998;188(4):627-34.