Search Results - "Pagnier, A."

A Large National Cohort of French Patients With Chronic Recurrent Multifocal Osteitis by Wipff, J., Costantino, F., Lemelle, I., Pajot, C., Duquesne, A., Lorrot, M., Faye, A., Bader‐Meunier, B., Brochard, K., Despert, V., Jean, S., Grall‐Lerosey, M., Marot, Y., Nouar, D., Pagnier, A., Quartier, P., Job‐Deslandre, C.

“…Objective To document more fully the characteristics of chronic recurrent multifocal osteomyelitis (CRMO) in pediatric patients, to collect data on the…”
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Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema by Deroux, A., Boccon‐Gibod, I., Fain, O., Pralong, P., Ollivier, Y., Pagnier, A., Djenouhat, K., Du‐Thanh, A., Gompel, A., Faisant, C., Launay, D., Bouillet, L.

“…Summary Hereditary angioedema (HAE) is a rare disease associated with either a quantitative or qualitative deficiency in C1‐inhibitor (C1‐INH) or normal…”
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Standard-Risk Medulloblastoma Treated by Adjuvant Chemotherapy Followed by Reduced-Dose Craniospinal Radiation Therapy: A French Society of Pediatric Oncology Study by OYHARCABAL-BOURDEN, V, KALIFA, C, NEUENSCHWANDER, S, VINCHON, M, BOURS, D, MOSSERI, V, LE GALES, C, RUCHOUX, M, CARRIE, C, DOZ, F, GENTET, J. C, FRAPPAZ, D, EDAN, C, CHASTAGNER, P, SARIBAN, E, PAGNIER, A, BABIN, A, PICHON, F

“…The primary objective of this study was to decrease the late effects of prophylactic radiation without reducing survival in standard-risk childhood…”
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Shortened apheresis-based extra-corporeal photochemotherapy for acute refractory GVHD in children: a prospective study by Sauret, A, Rabiau, N, Rochette, E, Grèze, V, Halle, P, Ouachée, M, Dalle, J-H, Seror, E, Serraz, D, Yakouben, K, Adjaoud, D, Pagnier, A, Marie-Cardine-Bobbia, A, Oudot, C, Curtillet, C, Poirée, M, Kanold, J, Merlin, E

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Malignant infantile osteopetrosis: Case report of a 5-month-old boy by Ledemazel, J, Plantaz, D, Pagnier, A, Girard, P, Lasfargue, M, Hullo, E, Dietrich, K, Collet, C, Moshous, D

“…Malignant infantile osteopetrosis is a rare congenital disease characterized by a dysfunction of osteoclasts followed by an abnormal bone densification. We…”
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Treatment of high risk medulloblastomas in children above the age of 3 years: A SFOP study by Verlooy, J., Mosseri, V., Bracard, S., Tubiana, A. Lellouch, Kalifa, C., Pichon, F., Frappaz, D., Chastagner, P., Pagnier, A., Bertozzi, A.-I., Gentet, J.C., Sariban, E., Rialland, X., Edan, C., Bours, D., Zerah, M., Le Gales, C., Alapetite, C., Doz, F.

“…Improvement of EFS of children older than 3 years with high risk medulloblastoma. Between 1993 and 1999, 115 patients (3–18 years, mean 8 years) with high risk…”
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Mendelian susceptibility to mycobacterial disease: a case report of disseminated infection due to Mycobacterium avium by Darleguy, A, Bost-Bru, C, Pagnier, A, Plantaz, D, Piolat, C, Nugues, F, Picard, C

“…Mendelian susceptibility to mycobacterial disease (MSMD) is a rare genetic syndrome that predisposes patients to infections caused by weakly virulent…”
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Severe HPA-15b related neonatal alloimmune thrombocytopenia by Moncharmont, P, Courvoisier, S, Pagnier, A, Cotta, L, Debillon, T, Rigal, D

“…The HPA‐15 platelet (PLT) group was recently described. Severe neonatal thrombocytopenia due to alloimmunization by HPA‐15b has very rarely been observed. A…”
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Chronic pain in cryopyrin-associated periodic syndrome: A retrospective French study in 133 patients by Houx, L, Guennoc, X, Kone-Paut, I, Hacchulla, E, Quartier, P, Grateau, G, Hamidou, M, Pagnier, A, Neven, B, Cuisset, L, Remy-Neris, O, Devauchelle, V

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Lymphohistiocytic activation syndrome and Burkholderia cepacia complex infection in a child revealing chronic granulomatous disease and chromosomal integration of the HHV-6 genome by Araujo, A, Pagnier, A, Frange, P, Wroblewski, I, Stasia, M-J, Morand, P, Plantaz, D

“…Chronic granulomatous disease (GCD) is characterized by severe infections, notably with Burkholderia cepacia complex (BCC). GCD is rarely complicated by…”
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Hodgkin disease and autoimmunity in children: 11 case reports by Jarrassé, C, Pagnier, A, Edan, C, Landman-Parker, J, Mazingue, F, Mansuy, L, Bertrand, Y, Paillard, C, Pellier, I, Margueritte, G, Plantaz, D

“…The association of lymphoma and autoimmune manifestations has been predominantly studied in adults affected by non-Hodgkin lymphoma. Few publications exist in…”
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Mineralocorticoid deficiency in post-operative cerebral salt wasting by Papadimitriou, Dimitrios T, Spiteri, Anne, Pagnier, Anne, Bayle, Monique, Mischalowski, Mariana Bohns, Bourdat, Guylhène, Passagia, Jean-Guy, Plantaz, Dominique, Bost, Michel, Garnier, Philippe E

“…Acute hyponatremia, following neurosurgery, results from inappropriate antidiuretic hormone secretion (SIADH) or cerebral salt wasting (CSW). CSW is due to…”
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Syndrome de susceptibilité mendélienne aux infections mycobactériennes : à propos d’un cas d’infection disséminée à Mycobacterium avium by Darleguy, A., Bost-Bru, C., Pagnier, A., Plantaz, D., Piolat, C., Nugues, F., Picard, C.

“…Le syndrome de susceptibilité mendélienne aux infections mycobactériennes (SSMIM) est un syndrome génétique rare prédisposant aux infections à des…”
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Les douleurs chroniques dans le syndrome périodique associé à la cryopyrine : étude rétrospective française de 133 patients by Houx, L, Guennoc, X, Kone-Paut, I, Hacchulla, E, Quartier, P, Grateau, G, Hamidou, M, Pagnier, A, Neven, B, Cuisset, L, Remy-Neris, O, Devauchelle, V

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Syndrome d'activation lymphohistiocytaire associé à une infection à Burkholderia cepacia complex chez un nourrisson révélant une granulomatose septique et une intégration génomique du virus HHV-6 by ARAUIO, A, PAGNIER, A, FRANGE, P, WROBLEWSKI, I, STASIA, M.-J, MORAND, P, PLANTAZ, D

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Décompensation tardive d'une maladie d'Imerslund-Grasbëck by Eitenschenck, L., Armari-Alla, C., Plantaz, D., Pagnier, A., Ducros, V.

“…La maladie d'Imerslund–Gräsbeck est une maladie récessive autosomique caractérisée par une anémie mégaloblastique par carence en vitamine B12 et une…”
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Efficacy and safety of crizotinib in ALK-positive systemic anaplastic large cell lymphoma in children, adolescents and adult patients: results of the French AcSe-crizotinib trial by Brugières, L, Cozic, N, Houot, R, Rigaud, C, Sibon, D, Arfi-Rouche, J, Bories, P, Cottereau, AS, Delmer, A, Ducassou, S, Garnier, N, Lamant, L, Leruste, A, Millot, F, Moalla, S, Morschhauser, F, Nolla, M, Pagnier, A, Reguerre, Y, Renaud, L, Schmitt, A, Simonin, M, Verschuur, A, Hoog Labouret, N, Mahier Ait Oukhatar, C, Vassal, G

“…The French phase II AcSé-crizotinib trial aimed to evaluate the safety and efficacy of crizotinib in patients with ALK, ROS1 and MET-driven malignancies…”
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Maladie de Hodgkin et auto-immunité chez l’enfant : à propos de 11 observations by Jarrassé, C., Pagnier, A., Edan, C., Landman-Parker, J., Mazingue, F., Mansuy, L., Bertrand, Y., Paillard, C., Pellier, I., Margueritte, G., Plantaz, D.

“…L’association de lymphomes, principalement non hodgkiniens, et de manifestations auto-immunes a surtout été étudiée chez l’adulte. Les publications concernant…”
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114 - ALK INHIBITORS SAFETY PROFILE IN PEDIATRIC PATIENTS TREATED FOR AN ALK-POSITIVE ANAPLASTIC LARGE CELL LYMPHOMA: REAL LIFE EXPERIENCE AMONG A FRENCH COHORT by d’Hautefeuille, C., Abbou, S., El-Gourari-Miaz, L., Lambilliotte, A., Renard, C., Landman-Parker, J., Gourdon, S., Metayer, L., Leblanc, T., Pacquement, H., Rabian, F., Verschuur, A., Brasme, J., Millot, F., Pagnier, A., Buchbinder, N., Rorhlich, P., Minard-Colin, V., Brugières, L., Ducassou, S., Rigaud, C.

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ALK INHIBITORS SAFETY PROFILE IN PEDIATRIC PATIENTS TREATED FOR AN ALK-POSITIVE ANAPLASTIC LARGE CELL LYMPHOMA: REAL LIFE EXPERIENCE AMONG A FRENCH COHORT by d’Hautefeuille, C., Abbou, S., El-Gourari-Miaz, L., Lambilliotte, A., Renard, C., Landman-Parker, J., Gourdon, S., Metayer, L., Leblanc, T., Pacquement, H., Rabian, F., Verschuur, A., Brasme, J., Millot, F., Pagnier, A., Buchbinder, N., Rorhlich, P., Minard-Colin, V., Brugières, L., Ducassou, S., Rigaud, C.

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