Username

Password

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Gil Tchernia

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Living Beings

Disorders

Concepts & Ideas

Physiology

Chemicals & Drugs

Procedures

Geographic Areas

France

Anatomy

Sign-in to see full Profile

Sign-in to see all Coauthors

Publications

TOP 3
Aguissa-Touré Almass-Houd; Da Costa Lydie; Leblanc Thierry; Tchernia Gil; Fribourg Sébastien; Gleizes Pierre-Emmanuel
[Diamond-Blackfan anemia reveals the dark side of ribosome biogenesis]
Crétien Aurore; Hurtaud Corinne; Moniz Hélène; Proust Alexis; Marie Isabelle; Wagner-Ballon Orianne; Choesmel Valérie; Gleizes Pierre-Emmanuel; Leblanc Thierry; Delaunay Jean; Tchernia Gil; Mohandas Narla; Da Costa Lydie
Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia.
Tchernia Gil; Bardakdjian Josiane; Lainé Agnés; Ly Aïcha; Orssaud Geneviève; Larnaudie Sylvie
[A center in Paris for screening and counselling sickle cell patients and carriers]

Sign-in to see all Publications

Sign in free and see...

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 visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Gil Tchernia (preview)

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

Flash Player Required

Sign-in to see more

All Publications

2009: Aguissa-Touré Almass-Houd; Da Costa Lydie; Leblanc Thierry; Tchernia Gil; Fribourg Sébastien; Gleizes Pierre-Emmanuel
[Diamond-Blackfan anemia reveals the dark side of ribosome biogenesis]
Médecine sciences : M/S 2009;25(1):69-76.
2008: Crétien Aurore; Hurtaud Corinne; Moniz Hélène; Proust Alexis; Marie Isabelle; Wagner-Ballon Orianne; Choesmel Valérie; Gleizes Pierre-Emmanuel; Leblanc Thierry; Delaunay Jean; Tchernia Gil; Mohandas Narla; Da Costa Lydie
Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia.
Haematologica 2008;93(11):1627-34.
2008: Tchernia Gil; Bardakdjian Josiane; Lainé Agnés; Ly Aïcha; Orssaud Geneviève; Larnaudie Sylvie
[A center in Paris for screening and counselling sickle cell patients and carriers]
Bulletin de l'Académie nationale de médecine 2008;192(7):1349-59; discussion 1359-60.
2008: Guitton C; Garçon L; Cynober T; Gauthier F; Tchernia G; Delaunay J; Leblanc T; Thuret I; Bader-Meunier B
[Hereditary spherocytosis: guidelines for the diagnosis and management in children]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2008;15(9):1464-73.
2008: Toye Ashley M; Williamson Rosalind C; Khanfar Moudji; Bader-Meunier Brigitte; Cynober Thérèse; Thibault Madeleine; Tchernia Gil; Déchaux Michèle; Delaunay Jean; Bruce Lesley J
Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A.
Blood 2008;111(11):5380-9.
2008: Alanio-Bréchot Cécile; Schischmanoff Pierre-Olivier; Fénéant-Thibault Madeleine; Cynober Thérèse; Tchernia Gil; Delaunay Jean; Garçon Loïc
Association between myeloid malignancies and acquired deficit in protein 4.1R: a retrospective analysis of six patients.
American journal of hematology 2008;83(4):275-8.
2008: Iolascon A; Camaschella C; Pospisilova D; Piscopo C; Tchernia G; Beaumont C
Natural history of recessive inheritance of DMT1 mutations.
The Journal of pediatrics 2008;152(1):136-9.
2007: Driss F; Tertian G; Becquemont L; Haddad B; Cynober T; Raphael M; Tchernia G
[Management of high risk pregnancy in sickle cell disease by a strategy of prophylactic red cell transfusion or automated red cell exchange]
Transfusion clinique et biologique : journal de la Société française de transfusion sanguine 2007;14(4):386-92.
2007: Proust Alexis; Guillet Benoît; Picard Capucine; de Saint Basile Geneviève; Pondarré Corinne; Tamary Hannah; Dreyfus Marie; Tchernia Gil; Fischer Alain; Delaunay Jean
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
Blood cells, molecules & diseases 2007;39(1):102-6.
2007: Beaurain Geneviève; Mathieu Flavie; Grootenboer Sabine; Fiquet Béatrice; Cynober Thérèse; Tchernia Gil; Delaunay Jean; Jeunemaitre Xavier
Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation.
European journal of haematology 2007;78(3):253-9.
2007: Choesmel Valérie; Bacqueville Daniel; Rouquette Jacques; Noaillac-Depeyre Jacqueline; Fribourg Sébastien; Crétien Aurore; Leblanc Thierry; Tchernia Gil; Da Costa Lydie; Gleizes Pierre-Emmanuel
Impaired ribosome biogenesis in Diamond-Blackfan anemia.
Blood 2007;109(3):1275-83.
2006: Gazda Hanna T; Grabowska Agnieszka; Merida-Long Lilia B; Latawiec Elzbieta; Schneider Hal E; Lipton Jeffrey M; Vlachos Adrianna; Atsidaftos Eva; Ball Sarah E; Orfali Karen A; Niewiadomska Edyta; Da Costa Lydie; Tchernia Gil; Niemeyer Charlotte; Meerpohl Joerg J; Stahl Joachim; Schratt Gerhard; Glader Bertil; Backer Karen; Wong Carolyn; Nathan David G; Beggs Alan H; Sieff Colin A
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
American journal of human genetics 2006;79(6):1110-8.
2006: Syfuss P-Y; Ciupea A; Brahimi S; Cynober T; Stewart G W; Grandchamp B; Beaumont C; Tchernia G; Delaunay J; Wagner J-C
Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis.
Clinical and laboratory haematology 2006;28(4):270-4.
2006: Saada Véronique; Cynober Thérèse; Brossard Yves; Schischmanoff Pierre Olivier; Sender Alfred; Cohen Henri; Delaunay Jean; Tchernia Gil
Incidence of hereditary spherocytosis in a population of jaundiced neonates.
Pediatric hematology and oncology 2006;23(5):387-97.
2006: Beaumont Carole; Delaunay Jean; Hetet Gilles; Grandchamp Bernard; de Montalembert Mariane; Tchernia Gil
Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload.
Blood 2006;107(10):4168-70.
2006: Faivre Laurence; Meerpohl Jörg; Da Costa Lydie; Marie Isabelle; Nouvel Christian; Gnekow Astrid; Bender-Götze Christine; Bauters Francis; Coiffier Bertand; Peaud Pierre-Yves; Rispal Patrick; Berrebi Alain; Berger Claire; Flesch Michel; Sagot Paul; Varet Bruno; Niemeyer Charlotte; Tchernia Gil; Leblanc Thierry
High-risk pregnancies in Diamond-Blackfan anemia: a survey of 64 pregnancies from the French and German registries.
Haematologica 2006;91(4):530-3.
2006: Guitton C; Ledeist F; Tchernia G; Bader-Meunier B
[Auto-immune hemolytic anemia and dyserythropoïesis as the presenting signs of Fas-deficient condition in 3 children]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2006;13(4):367-70.
2006: Arzouk Nadia; Snanoudj Renaud; Beauchamp-Nicoud Anne; Mourad Georges; Charpentier Bernard; Tchernia Gil; Durrbach Antoine
Parvovirus B19-induced anemia in renal transplantation: a role for rHuEPO in resistance to classical treatment.
Transplant international : official journal of the European Society for Organ Transplantation 2006;19(2):166-9.
2005: Chen S; Warszawski J; Bader-Meunier B; Tchernia G; Da Costa L; Marie I; Dommergues J P;
Diamond-blackfan anemia and growth status: the French registry.
The Journal of pediatrics 2005;147(5):669-73.
2005: Tamary Hannah; Dgany Orly; Proust Alexis; Krasnov Tatyana; Avidan Nili; Eidelitz-Markus Tal; Tchernia Gil; Geneviève David; Cormier-Daire Valérie; Bader-Meunier Brigitte; Ferrero-Vacher Corinne; Munzer Martine; Gruppo Ralph; Fibach Eithan; Konen Osnat; Yaniv Isaac; Delaunay Jean
Clinical and molecular variability in congenital dyserythropoietic anaemia type I.
British journal of haematology 2005;130(4):628-34.
2005: Bader-Meunier Brigitte; Leverger Guy; Tchernia Gil; Schischmanoff Olivier; Cynober Thérèse; Bernaudin Françoise; Leblanc Thierry; Munzer Martine; Roda Laurent; Soler Christine; Thuret Isabelle; Delaunay Jean
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2005;27(8):416-9.
2005: Kotb Rami; Pinganaud Caroline; Trichet Catherine; Lambotte Olivier; Dreyfus Marie; Delfraissy Jean-François; Tchernia Gil; Goujard Cécile
Efficacy of mycophenolate mofetil in adult refractory auto-immune cytopenias: a single center preliminary study.
European journal of haematology 2005;75(1):60-4.
2005: Proust Alexis; Guillet Benoît; Pellier Isabelle; Rachieru Petronela; Hoarau Cyrille; Claeyssens Ségolène; Léonard Claude; Charrier Sabine; Vainchenker William; Tchernia Gil; Delaunay Jean
Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
European journal of haematology 2005;75(1):54-9.
2005: Martinez-Duncker Ivan; Dupré Thierry; Piller Véronique; Piller Friedrich; Candelier Jean-Jacques; Trichet Catherine; Tchernia Gil; Oriol Rafael; Mollicone Rosella
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.
Blood 2005;105(7):2671-6.
2004: Beauchamp-Nicoud Anne; Da Costa Lydie; Proust Alexis; Rincé Patricia; Saker Safa; Tchernia Gil
Postmortem diagnosis of Diamond-Blackfan anemia.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2004;26(12):847-8.
2004: Chatr-Aryamontri Andrew; Angelini Mara; Garelli Emanuela; Tchernia Gil; Ramenghi Ugo; Dianzani Irma; Loreni Fabrizio
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia.
Human mutation 2004;24(6):526-33.
2004: Weller Sandra; Braun Moritz C; Tan Bruce K; Rosenwald Andreas; Cordier Corinne; Conley Mary Ellen; Plebani Alessandro; Kumararatne Dinakhanta S; Bonnet Damien; Tournilhac Olivier; Tchernia Gil; Steiniger Birte; Staudt Louis M; Casanova Jean-Laurent; Reynaud Claude-Agnès; Weill Jean-Claude
Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire.
Blood 2004;104(12):3647-54.
2004: Delaunay J; Nouyrigat V; Proust A; Schischmanoff P-O; Cynober T; Yvart J; Gaillard C; Danos O; Tchernia G
Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans.
British journal of haematology 2004;127(1):118-22.
2004: Tchernia Gil; Bader-Meunier Brigitte; Beauchamp-Nicoud Anne; Cynober Thérèse; Fénéant-Thibault Madeleine; Delaunay Jean
Congenital dyserythropoietic anemias.
The hematology journal : the official journal of the European Haematology Association / EHA 2004;5 Suppl 3():S191-4.
2003: Jaïs Xavier; Till Stephen J; Cynober Thérèse; Ioos Vincent; Garcia Gilles; Tchernia Gil; Dartevelle Philippe; Simonneau Gérald; Delaunay Jean; Humbert Marc
An extreme consequence of splenectomy in dehydrated hereditary stomatocytosis: gradual thrombo-embolic pulmonary hypertension and lung-heart transplantation.
Hemoglobin 2003;27(3):139-47.
2003: Zdebska Ewa; Bader-Meunier Brigitte; Schischmanoff Pierre-Olivier; Dupré Thierry; Seta Nathalie; Tchernia Gil; Koscielak Jerzy; Delaunay Jean
Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig.
Pediatric research 2003;54(2):224-9.
2003: Beauchamp-Nicoud Anne; Feneux Danielle; Bayle Chantal; Bernheim Alain; Léonard Claude; Koscielny Serge; Tchernia Gil; Bourhis Jean-Henri
Therapy-related myelodysplasia and/or acute myeloid leukaemia after autologous haematopoietic progenitor cell transplantation in a prospective single centre cohort of 221 patients.
British journal of haematology 2003;122(1):109-17.
2003: Da Costa Lydie; Tchernia Gil; Gascard Philippe; Lo Annie; Meerpohl Joerg; Niemeyer Charlotte; Chasis Joel-Anne; Fixler Jason; Mohandas Narla
Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology.
Blood 2003;101(12):5039-45.
2003: Grootenboer-Mignot Sabine; Crétien Aurore; Laurendeau Ingrid; Poissonnier Marie-Hélène; Doireau Valérie; Brossard Yves; Tchernia Gil; Cynober Thérèse; Delaunay Jean
Sub-lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnancies.
Prenatal diagnosis 2003;23(5):380-4.
2003: Da Costa Lydie; Narla Goutham; Willig Thiebaut-Noel; Peters Luanne L; Parra Marilyn; Fixler Jason; Tchernia Gil; Mohandas Narla
Ribosomal protein S19 expression during erythroid differentiation.
Blood 2003;101(1):318-24.
2003: Proust Alexis; Da Costa Lydie; Rince Patricia; Landois Anaely; Tamary Hannah; Zaizov Rina; Tchernia Gil; Delaunay Jean;
Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 gene.
The hematology journal : the official journal of the European Haematology Association / EHA 2003;4(2):132-6.
2002: Bader-Meunier Brigitte; Gabolde Martine; Casadevall Nicole; Seguin Guy; Tchernia Gil
Life-threatening complication of Rituximab in a child.
Haematologica 2002;87(12):ECR45.
2002: Martin Isabelle; Kriaa Fayçal; Proulle Valérie; Guillet Benoît; Kaplan Cécile; D'Oiron Roseline; Debré Marianne; Fressinaud Edith; Laurian Yyes; Tchernia Gil; Charpentier Bernard; Lambert Thierry; Dreyfus Marie
Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb-IIIa antibodies.
British journal of haematology 2002;119(4):991-7.
2002: Costa Lydie D A; Fixler Jason; Berets Olivier; Leblanc Thierry; Willig Thiebaut-Noel; Mohandas Narla; Tchernia Gil
Piebaldism in diamond-blackfan anaemia: a new phenotype?
British journal of haematology 2002;119(2):572.
2002: Delhommeau François; Vasseur-Godbillon Corinne; Leclerc Philippe; Schischmanoff Pierre-Olivier; Croisille Laure; Rince Patricia; Morinière Madeleine; Benz Edward J; Tchernia Gil; Tamagnini Gabriel; Ribeiro Leticia; Delaunay Jean; Baklouti Faouzi
A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells.
Blood 2002;100(7):2629-36.
2002: Roda Laurent; Pasche Jérôme; Fournier Alain; Terorotua Vaea; Wickramasinghe Sunitha N; Tamary Hannah; Schischmanoff Pierre Olivier; Tchernia Gil; Delaunay Jean
Congenital dyserythropoietic anemia, type 1, in a polynesian patient: response to interferon alpha2b.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2002;24(6):503-6.
2002: Diallo Dapa; Tchernia Gil
Sickle cell disease in Africa.
Current opinion in hematology 2002;9(2):111-6.
2001: Grootenboer S; Barro C; Cynober T; Olivier Schischmanoff P; Ayoubi J M; Tchernia G; Delaunay J; Pons J C
Dehydrated hereditary stomatocytosis: a cause of prenatal ascites.
Prenatal diagnosis 2001;21(13):1114-8.
2001: Guillet B; Kriaa F; Huysse M G; Proulle V; George C; Tchernia G; D'Oiron R; Laurian Y; Charpentier B; Lambert T; Dreyfus M
Protein A sepharose immunoadsorption: immunological and haemostatic effects in two cases of acquired haemophilia.
British journal of haematology 2001;114(4):837-44.
2001: Gazda H; Lipton J M; Willig T N; Ball S; Niemeyer C M; Tchernia G; Mohandas N; Daly M J; Ploszynska A; Orfali K A; Vlachos A; Glader B E; Rokicka-Milewska R; Ohara A; Baker D; Pospisilova D; Webber A; Viskochil D H; Nathan D G; Beggs A H; Sieff C A
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.
Blood 2001;97(7):2145-50.
2001: Croisille L; Tchernia G; Casadevall N
Autoimmune disorders of erythropoiesis.
Current opinion in hematology 2001;8(2):68-73.
2001: Guillet B; Tchernia G; Lambert T
[Hemophilia. Diagnosis, genetics, complications]
La Revue du praticien 2001;51(4):433-6.
2001: Da Costa L; Willig T N; Fixler J; Mohandas N; Tchernia G
Diamond-Blackfan anemia.
Current opinion in pediatrics 2001;13(1):10-5.
2001: Willig T B; Breton-Gorius J; Elbim C; Mignotte V; Kaplan C; Mollicone R; Pasquier C; Filipe A; Miélot F; Cartron J P; Gougerot-Pocidalo M A; Debili N; Guichard J; Dommergues J P; Mohandas N; Tchernia G
Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes--a new syndrome?
Blood 2001;97(3):826-8.
2001: Bader-Meunier B; Gauthier F; Archambaud F; Cynober T; Miélot F; Dommergues J P; Warszawski J; Mohandas N; Tchernia G
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.
Blood 2001;97(2):399-403.
2000: Dhermy D; Steen-Johnsen J; Bournier O; Hetet G; Cynober T; Tchernia G; Grandchamp B
Coinheritance of two alpha-spectrin gene defects in a recessive spherocytosis family.
Clinical and laboratory haematology 2000;22(6):329-36.
2000: Grootenboer S; Schischmanoff P O; Laurendeau I; Cynober T; Tchernia G; Dommergues J P; Dhermy D; Bost M; Varet B; Snyder M; Ballas S K; Ducot B; Babron M C; Stewart G W; Gasparini P; Iolascon A; Delaunay J
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24.
Blood 2000;96(7):2599-605.
2000: Parez N; Dommergues M; Zupan V; Chambost H; Fieschi J B; Delaunay J; Miélot F; Cramer E M; Dommergues J P; Wickramasinghe S N; Tchernia G
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy.
British journal of haematology 2000;110(2):420-3.
2000: Duval A; Feneux D; Sutton L; Tchernia G; Léonard C
Spurious monosomy 7 in leukemia due to centromeric heteromorphism.
Cancer genetics and cytogenetics 2000;119(1):67-9.
2000: Bader-Meunier B; Rieux-Laucat F; Croisille L; Yvart J; Mielot F; Dommergues J P; Ledeist F; Tchernia G
Dyserythropoiesis associated with a fas-deficient condition in childhood.
British journal of haematology 2000;108(2):300-4.
2000: Beauchamp-Nicoud A; Morle L; Lutz H U; Stammler P; Agulles O; Petermann-Khder R; Iolascon A; Perrotta S; Cynober T; Tchernia G; Delaunay J; Baudin-Creuza V
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG).
Haematologica 2000;85(1):19-24.
2000: Delhommeau F; Cynober T; Schischmanoff P O; Rohrlich P; Delaunay J; Mohandas N; Tchernia G
Natural history of hereditary spherocytosis during the first year of life.
Blood 2000;95(2):393-7.
2000: Tchernia G; Delhommeau F; Perrotta S; Cynober T; Bader-Meunier B; Nobili B; Rohrlich P; Salomon J L; Sagot-Bevenot S; del Giudice E M; Delaunay J; DeMattia D; Schischmanoff P O; Mohandas N; Iolascon A;
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(3):146-52.
1999: Willig T N; Draptchinskaia N; Dianzani I; Ball S; Niemeyer C; Ramenghi U; Orfali K; Gustavsson P; Garelli E; Brusco A; Tiemann C; Pérignon J L; Bouchier C; Cicchiello L; Dahl N; Mohandas N; Tchernia G
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression.
Blood 1999;94(12):4294-306.
1999: Willig T N; Niemeyer C M; Leblanc T; Tiemann C; Robert A; Budde J; Lambiliotte A; Kohne E; Souillet G; Eber S; Stephan J L; Girot R; Bordigoni P; Cornu G; Blanche S; Guillard J M; Mohandas N; Tchernia G
Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients. DBA group of Société d'Hématologie et d'Immunologie Pédiatrique (SHIP), Gesellshaft für Pädiatrische Onkologie und Hämatologie (GPOH), and the European Society for Pediatric Hematology and Immunology (ESPHI).
Pediatric research 1999;46(5):553-61.
1999: Beauchamp-Nicoud A; Schischmanoff P O; Alloisio N; Boivin P; Parsons S F; Mielot F; Tchernia G; Legrand A; Miraglia Del Giudice E; Gasparini P; Iolascon A; Wickramasinghe S N; Delaunay J
Suppression of CDA II expression in a homozygote.
British journal of haematology 1999;106(4):948-53.
1999: Bader-Meunier B; Miélot F; Breton-Gorius J; Cramer E; Guichard J; Landrieu P; Dommergues J P; Tchernia G
Hematologic involvement in mitochondrial cytopathies in childhood: a retrospective study of bone marrow smears.
Pediatric research 1999;46(2):158-62.
1999: Landau A; Castera L; Buffet C; Tertian G; Tchernia G
Acute autoimmune hemolytic anemia during interferon-alpha therapy for chronic hepatitis C.
Digestive diseases and sciences 1999;44(7):1366-7.
1999: Chiron M; Cynober T; Mielot F; Tchernia G; Croisille L
The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis.
Hematology and cell therapy 1999;41(3):113-6.
1999: Schischmanoff P O; Cynober T; Miélot F; Leclerc L; Vasseur-Godbillon C; Baudin-Creuza V; Magowan C; Yeung J; Mohandas N; Tchernia G; Delaunay J
Southeast Asian ovalocytosis in White persons.
Hemoglobin 1999;23(1):47-56.
1999: Marchand S; Tchernia G; Hiesse C; Tertian G; Cartron J; Kriaa F; Boubenider S; Goupy C; Lecointe D; Charpentier B
Human parvovirus B19 infection in organ transplant recipients.
Clinical transplantation 1999;13(1 Pt 1):17-24.
1999: Draptchinskaia N; Gustavsson P; Andersson B; Pettersson M; Willig T N; Dianzani I; Ball S; Tchernia G; Klar J; Matsson H; Tentler D; Mohandas N; Carlsson B; Dahl N
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.
Nature genetics 1999;21(2):169-75.
1998: Ajzenberg N; Dreyfus M; Kaplan C; Yvart J; Weill B; Tchernia G
Pregnancy-associated thrombocytopenia revisited: assessment and follow-up of 50 cases.
Blood 1998;92(12):4573-80.
1998: Willig T N; Pérignon J L; Gustavsson P; Gane P; Draptchinskaya N; Testard H; Girot R; Debré M; Stéphan J L; Chenel C; Cartron J P; Dahl N; Tchernia G
High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP).
Blood 1998;92(11):4422-7.
1998: Grootenboer S; Schischmanoff P O; Cynober T; Rodrigue J C; Delaunay J; Tchernia G; Dommergues J P
A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema.
British journal of haematology 1998;103(2):383-6.
1998: Gustavsson P; Garelli E; Draptchinskaia N; Ball S; Willig T N; Tentler D; Dianzani I; Punnett H H; Shafer F E; Cario H; Ramenghi U; Glomstein A; Pfeiffer R A; Goringe A; Olivieri N F; Smibert E; Tchernia G; Elinder G; Dahl N
Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity.
American journal of human genetics 1998;63(5):1388-95.
1998: Carella M; Stewart G; Ajetunmobi J F; Perrotta S; Grootenboer S; Tchernia G; Delaunay J; Totaro A; Zelante L; Gasparini P; Iolascon A
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).
American journal of human genetics 1998;63(3):810-6.
1998: Venencie P Y; Blanchet P; Mallet V; Chantome A; Quillard J; Croisille L; Lavabre C; Tchernia G; Bouchard P; Benoit G
[Pachydermoperiostosis with extramedullary hematopoiesis without myelofibrosis]
Annales de dermatologie et de vénéréologie 1998;125(3):193-5.
1998: Willig T N; Ball S E; Tchernia G
Current concepts and issues in Diamond-Blackfan anemia.
Current opinion in hematology 1998;5(2):109-15.
1997: Silveira P; Cynober T; Dhermy D; Mohandas N; Tchernia G
Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression.
American journal of clinical pathology 1997;108(4):391-9.
1997: Miélot F; Bader-Meunier B; Tchernia G; Dommergues J P
[Myelodysplasia in children and mitochondrial cytopathies]
Pathologie-biologie 1997;45(7):594-9.
1997: Gustavsson P; Willing T N; van Haeringen A; Tchernia G; Dianzani I; Donnér M; Elinder G; Henter J I; Nilsson P G; Gordon L; Skeppner G; van't Veer-Korthof L; Kreuger A; Dahl N
Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb.
Nature genetics 1997;16(4):368-71.
1997: Dhermy D; Galand C; Bournier O; Boulanger L; Cynober T; Schismanoff P O; Bursaux E; Tchernia G; Boivin P; Garbarz M
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.
British journal of haematology 1997;98(1):32-40.
1997: Bader-Meunier B; Tchernia G; Buisine J; Miélot F; Sommelet D; Dommergues J P
[Myelodysplastic syndromes in children, Groupe d'étude des myélodysplasies de l'enfant de la Société d'hématologie et d'immunologie pédiatrique (SHIP)]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1997;4(6):561-7.
1997: Castillo B; Cynober T; Bader-Meunier B; Gauthier F; Miélot F; Tchernia G; Dommergues J P
[Hereditary spherocytosis. Course and value of subtotal splenectomy]
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1997;4(6):515-20.
1997: Bader-Meunier B; Tchernia G; Miélot F; Fontaine J L; Thomas C; Lyonnet S; Lavergne J M; Dommergues J P
Occurrence of myeloproliferative disorder in patients with Noonan syndrome.
The Journal of pediatrics 1997;130(6):885-9.
1997: Gautier E; Bourhis J H; Bayle C; Cartron J; Pico J L; Tchernia G
Parvovirus B19 associated neutropenia. Treatment with Rh G-CSF.
Hematology and cell therapy 1997;39(2):85-7.
1997: Tchernia G; Bader-Meunier B; Berterottiere P; Eber S; Dommergues J P; Gauthier F
Effectiveness of partial splenectomy in hereditary spherocytosis.
Current opinion in hematology 1997;4(2):136-41.
1996: Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1996;319(10):913-9.
1996: Cynober T; Mohandas N; Tchernia G
Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity.
The Journal of laboratory and clinical medicine 1996;128(3):259-69.
1996: Tchernia G; Bader-Meunier B; Lavergne J M; Miélot F; Dommergues J P
Myelodysplasia in childhood may be a polyclonal disease.
Hematology and cell therapy 1996;38(4):325-30.
1996: Tertian G; Avalos M R; Léonard C; Lavergne J M; Misrahi M; Tchernia G
Additional translocation (9;12)(p13;q24.1) in newly diagnosed chronic myeloid leukemia: complete cytogenetic remission after interferon therapy.
Hematology and cell therapy 1996;38(3):269-73.
1996: Chasis J A; Coulombel L; McGee S; Lee G; Tchernia G; Conboy J; Mohandas N
Differential use of protein 4.1 translation initiation sites during erythropoiesis: implications for a mutation-induced stage-specific deficiency of protein 4.1 during erythroid development.
Blood 1996;87(12):5324-31.
1996: Bader-Meunier B; Miélot F; Tchernia G; Buisine J; Delsol G; Duchayne E; Lemerle S; Leverger G; de Lumley L; Manel A M
Myelodysplastic syndromes in childhood: report of 49 patients from a French multicentre study. French Society of Paediatric Haematology and Immunology.
British journal of haematology 1996;92(2):344-50.
1995: Ball S E; Tchernia G; Wranne L; Bastion Y; Bekassy N A; Bordigoni P; Debré M; Elinder G; Kamps W A; Lanning M
Is there a role for interleukin-3 in Diamond-Blackfan anaemia? Results of a European multicentre study.
British journal of haematology 1995;91(2):313-8.
1995: Magowan C; Coppel R L; Lau A O; Moronne M M; Tchernia G; Mohandas N
Role of the Plasmodium falciparum mature-parasite-infected erythrocyte surface antigen (MESA/PfEMP-2) in malarial infection of erythrocytes.
Blood 1995;86(8):3196-204.
1995: Tertian G; Misrahi M; Diallo D; Mielot F; Leonard C; Salmeron S; Tchernia G
Abnormal chromatin clumping in granulocytes in a case of Ph1-negative, BCR-ABL rearrangement positive, haematologically atypical chronic myeloid leukaemia (CML).
Nouvelle revue française d'hématologie 1995;37(4):245-7.
1994: Bader-Meunier B; Rötig A; Mielot F; Lavergne J M; Croisille L; Rustin P; Landrieu P; Dommergues J P; Munnich A; Tchernia G
Refractory anaemia and mitochondrial cytopathy in childhood.
British journal of haematology 1994;87(2):381-5.
1994: Bastion Y; Bordigoni P; Debré M; Girault D; Leblanc T; Tchernia G; Ball S; McGuckin C; Gordon-Smith E C; Békassy A
Sustained response after recombinant interleukin-3 in diamond blackfan anemia.
Blood 1994;83(2):617-8.
1993: Marfaing-Koka A; Boyer-Neumann C; Wolf M; Leroy-Matheron C; Cynober T; Tchernia G
Decreased protein S activity in sickle cell disease.
Nouvelle revue française d'hématologie 1993;35(4):425-30.
1993: Tchernia G; Morel-Kopp M C; Yvart J; Kaplan C
Neonatal thrombocytopenia and hidden maternal autoimmunity.
British journal of haematology 1993;84(3):457-63.
1993: Miélot F; Bader-Meunier B; Léonard C; Tchernia G
[Myelodysplastic syndromes in children]
La Revue du praticien 1993;43(11):1386-91.
1993: Rey C; Bader-Meunier B; Tertian G; Mielot F; Tchernia G; Yver A
Trilineage response to recombinant human granulocyte colony-stimulating factor administration in a patient with myelodysplastic syndrome.
American journal of hematology 1993;43(1):76-7.
1993: Tchernia G; Gauthier F; Mielot F; Dommergues J P; Yvart J; Chasis J A; Mohandas N
Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis.
Blood 1993;81(8):2014-20.
1993: Léonard C; Avalos M R; Miélot F; Poissonnier M; Dommergues J P; Lejeune J; Tchernia G
Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicism.
Cancer genetics and cytogenetics 1993;66(1):70-2.
1993: Conboy J G; Chasis J A; Winardi R; Tchernia G; Kan Y W; Mohandas N
An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
The Journal of clinical investigation 1993;91(1):77-82.
1992: Bader-Meunier B; Thollot F; Mielot F; Yvart J; Dommergues J P; Sommelet D; Tchernia G
[Regressive myelodysplastic syndromes in children. Committee on Childhood Myelodysplasia of the Society of Pediatric Hematology and Immunology]
Archives françaises de pédiatrie 1992;49(10):883-6.
1991: Cherin P; Brivet F; Tertian G; Dreyfus M; Barthélémy P; Dormont J; Tchernia G
[Recurrent thrombocytopenic thrombotic purpura associated to prostatic cancer. A case]
Presse médicale (Paris, France : 1983) 1991;20(23):1073-7.
1991: Garel D; Mielot F; Gaulard P; Quillard J; Dommergues J P; Tchernia G
Acute megakaryocytic leukemia (AMKL) with major myelofibrosis in an infant. Diagnosis by liver biopsy and response to treatment.
Nouvelle revue française d'hématologie 1991;33(1):5-8.
1989: Dommergues J P; Archambeaud M P; Ducot B; Gerval Y; Hiard C; Rossignol C; Tchernia G
[Iron deficiency and psychomotor development tests. Longitudinal study between 10 months and 4 years of age]
Archives françaises de pédiatrie 1989;46(7):487-90.
1989: Avalos M R; Léonard C; Mielot F; Tchernia G
Inactivated X chromosome fold in human leukemia and related clonal disorders.
Human genetics 1989;82(4):386-8.
1989: Tertian G; Tchernia G; Léonard C; Miélot F; Avalos M; Mirica C; Brivet F; Dommergues J P
Low-dose arabinosyl cytosine therapy of AML may be effective after failure of high or conventional doses.
Nouvelle revue française d'hématologie 1989;31(4):311-3.
1989: Archambeaud-Breton M P; Dommergues J P; Ducot B; Rossignol C; Yvart J; Tchernia G
Reevaluation of the utility of mean cell hemoglobin (MCH) screening in infants for iron deficiency.
Nouvelle revue française d'hématologie 1989;31(4):307-9.
1988: Coulombel L; Morardet N; Veber F; Leroy C; Mielot F; Fisher A; Teillet-Thiebaud F; Tchernia G; Griscelli C; Parmentier C
Granulopoietic differentiation in long-term bone marrow cultures from children with congenital neutropenia.
American journal of hematology 1988;27(2):93-8.
1987: Mielot F; Danel P; Boyer C; Coulombel L; Dommergues J P; Tchernia G; Larrieu M J
[Acquired deficiencies in antithrombin III and C protein during treatment with L-asparaginase]
Archives françaises de pédiatrie 1987;44(3):161-5.
1984: Dommergues J P; Breton M P; Ducot B; Yvart J; Rossignol C; Tchernia G
[Iron deficiency in infants. Study of risk factors]
Archives françaises de pédiatrie 1984;41(9):623-7.
1984: Coulombel L; Tchernia G; Mielot F; Mohandas N
Hemoglobin content of individual erythroblasts in hematopoietic dysplasia: marked heterogeneity at late stages of maturation.
Experimental hematology 1984;12(7):587-93.
1981: Tchernia G; Mielot F; Coulombel L; Mohandas N
Characterization of circulating erythroid progenitor cells in human newborn blood.
The Journal of laboratory and clinical medicine 1981;97(3):322-31.
1980: Morardet N; Mielot F; Tchernia G; Morel-Brossel S; Parmentier C
[Granulocyte progenitor cells (CFC) culture in the adult chronic idiopathic neutropenia. A study of 12 cases (author's transl)]
Nouvelle revue française d'hématologie 1980;22(2):125-34.

Sign-in to see more

Sign-in free and Explore the Exciting World of BiomedExperts:

NetworkView

Gil Tchernia

Research Profile (preview)

Living Beings

Disorders

Concepts & Ideas

Physiology

Chemicals & Drugs

Procedures

Geographic Areas

Anatomy

Network (preview)

Publications

Sign in free and see...

Visualized networks:

GeoTargeted Searches:

Research Profiles:

Geonetwork of Gil Tchernia (preview)

All Publications