Brigitte Bader-Meunier researcher
Bader-Meunier, Brigitte, 19..-...., médecin
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Bader-Meunier, Brigitte
Bader-Meunier, B. (Brigitte)
VIAF ID: 44476863 (Personal)
Permalink: http://viaf.org/viaf/44476863
Preferred Forms
4xx's: Alternate Name Forms (6)
Works
| Title | Sources |
|---|---|
| Accès aux soins et parcours diagnostique des patients atteints d'arthrite juvénile idiopathique |
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| Access to pediatric rheumatology care and diagnostic pathway in Juvenile idiopathic arthritis (JIA). |
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| Atteintes abdominales dans le lupus erythémateux disséminé de l'enfant |
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| Clinical and molecular characterisation of type I interferonopathies |
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| COMPLICATIONS ET SEQUELLES NEUROLOGIQUES DES LEUCEMIES AIGUES LYMPHOBLASTIQUES DE L'ENFANT ; ANALYSE SUR UNE POPULATION DE 79 PATIENTS |
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| Dyserythropoïèse acquise et anémie hémolytique auto-immune : à propos de 6 cas pédiatriques |
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| Efficacité et tolérance des agents biologiques dans les rhumatismes inflammatoires à début juvénile dans les essais cliniques randomisés et les études observationnelles |
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| Efficacité et tolérance d'un traitement de première ligne par corticoïdes et méthotrexate dans la dermatomyosite juvénile : une étude de cohorte rétrospective |
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| Efficacy and safety of biological agents in juvenile inflammatory rheumatic diseases : from randomized clinical trials and observational studies. |
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| Evolution à l’âge adulte du lupus érythémateux systémique à début pédiatrique |
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| FORME SYSTEMIQUE D'ARTHRITE CHRONIQUE JUVENILE : MISE EN EVIDENCE DE FORMES PARTICULIERES A PROPOS DE 23 OBSERVATIONS ET REVUE DE LA LITTERATURE |
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| Long-term outcomes in adult patients with childhood-onset systemic lupus erythematosus. |
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| Maladies inflammatoires en pédiatrie, 2012: |
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| Maltraitance à enfants et adolescents |
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| Médecine de l'adolescent |
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| [Misdiagnosis of venous thrombosis in childhood] |
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| MODALITES DE PRISE EN CHARGE ET DEVENIR AU LONG TERME D'ENFANTS HOSPITALISES POUR MAUVAIS TRAITEMENTS : A PROPOS DE 54 CAS OBSERVES EN PEDIATRIE GENERALE (DES PEDIATRIE) |
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| Monocentric cohort of systemic onset juvenile idiopathic arthritis (SoJIA) patients diagnosed between 1985 and 2005 : a study on 114 patients. |
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| Mutation in MMP2 gene may result in scleroderma-like skin thickening |
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| [Myelodysplasia in children and mitochondrial cytopathies] |
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| Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis |
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| [Neural sarcoidosis in children. A case report] |
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| [Neuro-cognitive sequelae during acute lymphoblastic leukemia in children] |
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| New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children |
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| [New treatments for systemic diseases] |
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| Noninfectious febrile inflammatory syndromes in children: diagnosis and usefulness of diagnostic procedures |
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| [Nutritional anemia in children] |
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| Occurrence of inflammatory bowel disease during treatment of juvenile idiopathic arthritis with etanercept: a French retrospective study. |
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| Paediatric Castleman disease: report of seven cases and review of the literature. |
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| Pediatric systemic lupus erythematosus and human parvovirus B19 infection |
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| Pharmacokinetics of mycophenolate mofetil in children with lupus and clinical findings in favour of therapeutic drug monitoring |
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| Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry. |
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| [Practical management of neutropenia in children |
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| Présentation clinique et prise en charge des varicelles hospitalisées en pédiatrie générale entre octobre 1997 et décembre 2002 au Kremlin Bicêtre |
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| Presentations and outcomes of juvenile dermatomyositis patients admitted to intensive care units |
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| Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia? |
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| Prolonged fever in a big child |
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| PW03-016 – Blau prospective cohort study: articular outcomes. |
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| Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis. |
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| Recombinant human G-CSF (Lenograstim) for infectious complications in glycogen storage disease type Ib. Report of 7 cases |
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| Recommandations pour la prise en charge des formes oligoarticulaire et polyarticulaires |
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| [Regressive myelodysplastic syndromes in children. Committee on Childhood Myelodysplasia of the Society of Pediatric Hematology and Immunology] |
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| Retroperitonal fibrosis and lymphoma in a 15-year-old boy |
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| [Rheumatic diseases in children] |
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| Safety and efficacy of rituximab in systemic lupus erythematosus: results from 136 patients from the French AutoImmunity and Rituximab registry |
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| Safety, effectiveness, and pharmacokinetics of adalimumab in children with polyarticular juvenile idiopathic arthritis aged 2 to 4 years |
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| SCINTIGRAPHIE RENALE A L'ACIDE DIMERCAPTOSUCCINIQUE ET DOPPLER ENERGIE DANS LE DIAGNOSTIC DE PYELONEPHRITE AIGUE CHEZ L'ENFANT |
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| [Screening and management of cardiovascular risk factors in systemic lupus erythematosus: Recommendations for clinical practice based on the literature and expert opinion]. |
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| Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register |
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| Self-healing juvenile cutaneous mucinosis: Clinical and histopathologic findings of 9 patients: The relevance of long-term follow-up. |
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| Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity |
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| [Severe autoimmune immunoglobulin A hemolytic anemia in a 10-month-old infant] |
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| Severe early-onset colitis revealing mevalonate kinase deficiency. |
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| Severe hematological side effects following Rituximab therapy in children |
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| SHARE – workpackage 5: evidence-based recommendations for diagnosis and treatment of kawasaki disease and henoch schönlein purpura. |
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| The skin manifestations must not be neglected in auto-inflammatory syndromes. |
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| LA SPLENECTOMIE SUB-TOTALE D'INDICATION HEMATOLOGIQUE : A PROPOS DE 36 CAS |
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| Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey |
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| Steroid treatment in children with sickle-cell disease |
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| Syndrome d'Evans : étude rétrospective de la société d'hématologie et d'immunologie pédiatrique (36 cas) |
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| Systemic-onset juvenile rheumatoid arthritis and ANCA-associated glomerulonephritis. |
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| Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature |
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| LES TENTATIVES DE SUICIDE DE L'ENFANT AGE DE MOINS DE 13 ANS : ANALYSE RETROSPECTIVE DE 11 CAS D'ENFANTS HOSPITALISES EN SERVICE DE PEDIATRIE GENERALE |
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| THROMBOPENIES AUTO-IMMUNES CHRONIQUES DE L'ENFANT : ETUDE RETROSPECTIVE SUR 59 CAS |
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| Thrombotic microangiopathy and Purtscher-like retinopathy as a rare presentation of juvenile dermatomyositis |
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| Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome). |
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| [Tolerance of biological agents in children] |
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| [Transverse leukonychia and anti-leukemia chemotherapy] |
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| Treatment of hemophagocytic lymphohistiocytosis with cyclosporin A and steroids in a boy with lysinuric protein intolerance |
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| Trilineage response to recombinant human granulocyte colony-stimulating factor administration in a patient with myelodysplastic syndrome |
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| Type I interferon-mediated autoinflammation due to DNase II deficiency |
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| Unusual clinical expression and long survival of a pseudouridylate synthase (PUS1) mutation into adulthood |
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| Varicella-associated pancytopenia |
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| Vasculopathy-related clinical and pathological features are associated with severe juvenile dermatomyositis. |
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| Visceral leishmaniasis in a patient with systemic juvenile arthritis treated by IL-1RA agonist (Anakinra) |
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