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2004, Bibliothèque de droit privé, ISBN 9782275024448, Volume t. 410, xvii, 436
Book
The New England Journal of Medicine, ISSN 0028-4793, 04/2012, Volume 366, Issue 15, pp. 1371 - 1381
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2015, Volume 47, Issue 11, pp. 1334 - 1340
Juvenile myelomonocytic leukemia (JMML) is a rare and severe myelodysplastic and myeloproliferative neoplasm of early childhood initiated by germline or... 
LYSINE 27 | COMPLEX | MULTIPLE MECHANISMS | NRAS MUTATION | GENETICS & HEREDITY | MYELOID MALIGNANCIES | RHO-GTPASES | DETECTABLE CLONAL MOSAICISM | CANCER | NERVE SHEATH TUMORS | SOMATIC MUTATIONS | ras Proteins - genetics | Leukemia, Myelomonocytic, Juvenile - metabolism | Polycomb Repressive Complex 2 - genetics | Humans | Leukemia, Myeloid - genetics | Transcriptome | Child, Preschool | ras Proteins - metabolism | Infant | Male | Phosphatidylinositol 3-Kinases - metabolism | Protein Subunits - metabolism | DNA Copy Number Variations | Female | Acetylation | Leukemia, Myelomonocytic, Juvenile - genetics | Child | Protein Subunits - genetics | Acute Disease | Gene Regulatory Networks - genetics | Signal Transduction - genetics | Disease Progression | Phosphatidylinositol 3-Kinases - genetics | Microscopy, Confocal | Leukemia, Myeloid - metabolism | Survival Analysis | Histones - metabolism | Mutation | Methylation | Polycomb Repressive Complex 2 - metabolism | Sequence Analysis, DNA - methods | Gene mutations | Leukemia in children | Development and progression | Genetic aspects | Identification and classification | Health aspects | Myeloproliferative disorders | Laboratories | Colonies & territories | Genomes | Kinases | Patients | Data bases | Proteins | Studies | Archives & records | Acquisitions & mergers | Tumors | Cancer | Life Sciences | Genetics
Journal Article
Journal Article
Blood, ISSN 0006-4971, 07/2018, Volume 132, Issue 4, pp. 351 - 361
Adolescent and young adult (AYA) patients with acute lymphoblastic leukemia (ALL) are recognized as a unique population with specific characteristics and... 
KINASE INHIBITOR THERAPY | ALLOGENEIC TRANSPLANTATION | TEENAGERS | RISK | PEDIATRIC PROTOCOL | MUTATIONS | BLINATUMOMAB | HEMATOLOGY | MINIMAL RESIDUAL DISEASE | CANCER | CHEMOTHERAPY | Index Medicus | Abridged Index Medicus
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2013, Volume 14, Issue 13, pp. e609 - e620
Summary Neonatal cancer is rare and comprises a heterogeneous group of neoplasms with substantial histological diversity. Almost all types of paediatric cancer... 
Hematology, Oncology and Palliative Medicine | MESENCHYMAL TUMOR | TRANSIENT MYELOPROLIFERATIVE DISORDER | INTERNATIONAL-SOCIETY | ONCOLOGY | JUVENILE MYELOMONOCYTIC LEUKEMIA | 1ST YEAR | RISK | FETAL | PRENATAL-DIAGNOSIS | BRAIN-TUMORS | CHILDREN | Neoplasms - etiology | Retinoblastoma - therapy | Soft Tissue Neoplasms - diagnosis | Humans | Liver Neoplasms - therapy | Neoplasms - diagnosis | Neuroblastoma - therapy | Maternal Exposure | Neoplasms, Germ Cell and Embryonal - diagnosis | Kidney Neoplasms - diagnosis | Congenital Abnormalities - diagnosis | Neoplasms - complications | Neoplasms - therapy | Neoplasms - genetics | Delivery, Obstetric | Female | Retinoblastoma - diagnosis | Infant, Newborn | Kidney Neoplasms - therapy | Soft Tissue Neoplasms - therapy | Diagnosis, Differential | Genetic Predisposition to Disease | Prenatal Diagnosis | Leukemia - therapy | Central Nervous System Neoplasms - therapy | Neuroblastoma - diagnosis | Interdisciplinary Communication | Liver Neoplasms - diagnosis | Ultrasonography, Prenatal | Urogenital Neoplasms - therapy | Leukemia - diagnosis | Disease Management | Neoplasms - pathology | Central Nervous System Neoplasms - diagnosis | Neoplasms, Germ Cell and Embryonal - therapy | Urogenital Neoplasms - diagnosis | Infants (Newborn) | Genetic disorders | Sarcoma | Pregnant women | Leukemia | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2018, Volume 378, Issue 5, pp. 439 - 448
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 09/2015, Volume 33, Issue 27, pp. 2938 - 2948
Journal Article
Medicine (United States), ISSN 0025-7974, 07/2012, Volume 91, Issue 4, pp. e1 - e19
Autosomal dominant deficiency of signal transducer and activator of transcription 3 (STAT3) is the main genetic etiology of hyper-immunoglobulin (Ig) E... 
MEDICINE, GENERAL & INTERNAL | JOBS-SYNDROME | TRANSCRIPTION 3 | HYPERIMMUNOGLOBULIN-E SYNDROME | INVASIVE FUNGAL DISEASE | RECURRENT INFECTION | ANTIBODY-RESPONSES | CHRONIC MUCOCUTANEOUS CANDIDIASIS | COLD STAPHYLOCOCCAL ABSCESSES | SIGNAL TRANSDUCER | BONE-RESORPTION | Job Syndrome - immunology | Phosphorylation | Age Distribution | Job Syndrome - genetics | Humans | Middle Aged | Pneumonia, Bacterial - etiology | Child, Preschool | Infant | Male | Incidence | Skin Diseases, Bacterial - etiology | Young Adult | Eczema - epidemiology | Skin Diseases, Bacterial - epidemiology | DNA Mutational Analysis | STAT3 Transcription Factor - deficiency | Adult | Female | Respiratory Tract Infections - etiology | Genetic Predisposition to Disease - epidemiology | Child | Infant, Newborn | STAT3 Transcription Factor - genetics | Databases, Factual | Severity of Illness Index | France - epidemiology | Cross-Sectional Studies | Risk Assessment | Signal Transduction | Pneumonia, Bacterial - epidemiology | Eczema - etiology | Job Syndrome - epidemiology | Staphylococcal Infections - epidemiology | Job Syndrome - complications | Adolescent | Immunocompromised Host - genetics | Survival Analysis | Sex Distribution | Heterozygote | Respiratory Tract Infections - epidemiology | Staphylococcal Infections - etiology | Gene mutations | Causes of | Physiological aspects | Immunological deficiency syndromes | ACHOO syndrome | Genetic aspects | Research | Genetic transcription | T cells | Life Sciences | Genetics | Immunology
Journal Article