Search Results - "Coste, E"

Hepatitis E Virus‐Induced Neurological Symptoms in a Kidney‐Transplant Patient with Chronic Hepatitis by Kamar, N., Izopet, J., Cintas, P., Garrouste, C., Uro‐Coste, E., Cointault, O., Rostaing, L.

“…It has been shown that hepatitis E virus (HEV) may be responsible for chronic hepatitis in solid‐organ transplant patients. It has also been suggested that HEV…”
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Molecular and clinical diversity in primary central nervous system lymphoma by Hernández-Verdin, I., Kirasic, E., Wienand, K., Mokhtari, K., Eimer, S., Loiseau, H., Rousseau, A., Paillassa, J., Ahle, G., Lerintiu, F., Uro-Coste, E., Oberic, L., Figarella-Branger, D., Chinot, O., Gauchotte, G., Taillandier, L., Marolleau, J.-P., Polivka, M., Adam, C., Ursu, R., Schmitt, A., Barillot, N., Nichelli, L., Lozano-Sánchez, F., Ibañez-Juliá, M.-J., Peyre, M., Mathon, B., Abada, Y., Charlotte, F., Davi, F., Stewart, C., de Reyniès, A., Choquet, S., Soussain, C., Houillier, C., Chapuy, B., Hoang-Xuan, K., Alentorn, A.

“…Primary central nervous system lymphoma (PCNSL) is a rare and distinct entity within diffuse large B-cell lymphoma presenting with variable response rates…”
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Vocal-fold leukoplakia and dysplasia. Mini-review by the French Society of Phoniatrics and Laryngology (SFPL) by Garrel, R., Uro Coste, E., Costes-Martineau, V., Woisard, V., Atallah, I., Remacle, M.

“…Vocal-fold leukoplakia and dysplasia are together designated “epithelial hyperplastic laryngeal lesions” (EHLL). Work-up and follow-up are founded on optical…”
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Use of fluorescent in‐situ hybridisation in salivary gland cytology: A powerful diagnostic tool by Evrard, S. M., Meilleroux, J., Daniel, G., Basset, C., Lacoste‐Collin, L., Vergez, S., Uro‐Coste, E., Courtade‐Saidi, M.

“…Objective Salivary gland cytology is challenging because it includes a diversity of lesions and a wide spectra of tumours. Recently, it has been reported that…”
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A French retrospective study on clinical outcome in 102 choroid plexus tumors in children by Siegfried, A., Morin, S., Munzer, C., Delisle, M. B., Gambart, M., Puget, S., Maurage, C. A., Miquel, C., Dufour, C., Leblond, P., André, N., Branger, D. Figarella, Kanold, J., Kemeny, J.-L., Icher, C., Vital, A., Coste, E. Uro, Bertozzi, A. I.

“…The aim of this study was to review and describe therapeutic approaches in children with choroid plexus tumor (CPT) based on a nationwide series. The World…”
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Cytopathological analysis of salivary gland cancer: REFCOR recommendations by the formal consensus method by Courtade-Saïdi, M., Uro-Coste, E., Vergez, S., Verillaud, B., Pham Dang, N., Chabrillac, E., Fakhry, N., Bigorgne, C., Costes-Martineau, V.

“…To determine the indications for fine-needle cytology and the modalities of frozen section pathological analysis in the management of salivary gland cancer…”
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Characteristics of IDH-mutant gliomas with non-canonical IDH mutation by Poetsch, L., Bronnimann, C., Loiseau, H., Frénel, J. S., Siegfried, A., Seizeur, R., Gauchotte, G., Cappellen, D., Carpentier, C., Figarella-Branger, D., Eimer, S., Meyronet, D., Ducray, F.

“…Background Approximately 10% of IDH -mutant gliomas harbour non-canonical IDH mutations (non- p.R132H IDH1  and IDH2 mutations). Objective The aim of this…”
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Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part I: Primary treatment of pleomorphic adenoma by Vergez, S., Fakhry, N., Cartier, C., Kennel, T., Courtade-Saidi, M., Uro-Coste, E., Varoquaux, A., Righini, C.-A., Malard, O., Mogultay, P., Thariat, J., Tronche, S., Garrel, R., Chevalier, D.

“…The authors present the guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL) for the diagnosis and treatment of pleomorphic…”
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Removal of eriochrome black T from aqueous solution using coffee husk as bioadsorbent by Almeida Amancio, Nathan, E Colpa, Poliana Coste, Guardabaxo, Cíntia Moda Salatino, Silva, Carla Beatriz, Da Silva, Leandro Gustavo

“…The eriochrome black T dye belongs to the azo dye class and is often used as an indicator in complexometric titrations and as a fiber dye in industrial…”
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Subventricular zones: new key targets for glioblastoma treatment by Khalifa, J, Tensaouti, F, Lusque, A, Plas, B, Lotterie, J-A, Benouaich-Amiel, A, Uro-Coste, E, Lubrano, V, Cohen-Jonathan Moyal, E

“…We aimed to identify subventricular zone (SVZ)-related prognostic factors of survival and patterns of recurrence among patients with glioblastoma. Forty-three…”
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Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma by Vande Perre, P., Siegfried, A., Corsini, C., Bonnet, D., Toulas, C., Hamzaoui, N., Selves, J., Chipoulet, E., Hoffmann, J. S., Uro-Coste, E., Guimbaud, R.

“…Germline mutations of the POLE gene are responsible for polymerase proofreading-associated polyposis syndrome (PPAP). These mutations were hypothesised to…”
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Special ways of managing with neurodegenerative disease at home as seen by a mobile team of the Aquitaine serious disability network, HLA33 by Coste, E

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Guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL), part II: Management of recurrent pleomorphic adenoma of the parotid gland by Malard, O., Thariat, J., Cartier, C., Chevalier, D., Courtade-Saidi, M., Uro-Coste, E., Garrel, R., Kennel, T., Mogultay, P., Tronche, S., Varoquaux, A., Righini, C.A., Vergez, S., Fakhry, N.

“…The authors present the guidelines of the French Society of Otorhinolaryngology–Head and Neck Surgery (SFORL) for the management of recurrent pleomorphic…”
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Evidence for BRAF V600E and H3F3A K27M double mutations in paediatric glial and glioneuronal tumours by Nguyen, Anh Tuan, Colin, Carole, Nanni-Metellus, Isabelle, Padovani, Laetitia, Maurage, Claude-Alain, Varlet, Pascale, Miquel, Catherine, Uro-Coste, Emmanuelle, Godfraind, Catherine, Lechapt-Zalcman, Emmanuelle, Labrousse, François, Gauchotte, Guillaume, Silva, Karen, Jouvet, Anne, Figarella-Branger, Dominique

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Antenatal screening of small for gestational age: Impact on obstetrical management and neonatal outcomes in case of trial of labor after 37 weeks by Coste, E., Crequit, S., Dabi, Y., Tataru, C., Redel, D., Rota, M., Haddad, B., Lecarpentier, E.

“…Antenatal screening of small fetuses for gestational age (SGA) is a public health challenge. The aim of this study is to assess the obstetrical management and…”
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PO-0647: Subventricular zones: new key targets for glioblastoma treatment by Khalifa, J, Tensaouti, F, Lusque, A, Plas, B, Lotterie, J.A, Uro-Coste, E, Lubrano, V, Moyal, E. Cohen-Jonathan

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Atherosclerosis severity in patients with familial hypercholesterolemia: The role of T and B lymphocytes by Fonzar, Waleria T., Fonseca, Francisco A., Fonseca, Henrique A., Silva, Tuany P., Rodrigues, Alfredo A., Teixeira, Daniela, Ishimura, Mayari E., Coste, Maria E., França, Carolina N., Bianco, Henrique T., Gidlund, Magnus, Morais, Rafael L., Bittencourt, Clarissa A., Fonzar, Carlos A., Sant’Anna, Viviane A., Maugeri, Ieda L., Pesquero, Joao B., Izar, Maria C.

“…Familial hypercholesterolemia (FH) is characterized by lifelong exposure to high LDL-c concentrations and premature atherosclerotic cardiovascular disease;…”
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Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in the Ferritin Light Polypeptide Gene by VIDAL, R, GHETTI, B, TAKAO, M, BREFEL-COURBON, C, URO-COSTE, E, GLAZIER, B S, SIANI, V, BENSON, M D, CALVAS, P, MIRAVALLE, L, RASCOL, O, DELISLE, M B

“…Abnormal accumulation of ferritin was found to be associated with an autosomal dominant slowly progressing neurodegenerative disease clinically characterized…”
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Congenital neuromuscular diseases with neonatal respiratory failure excluding myotonic dystrophy type 1 and infantile spinal muscular atrophy. Diagnosis strategy according to a 19-child series by Raignoux, J, Walther-Louvier, U, Espil, C, Berthomieu, L, Uro-Coste, E, Rivier, F, Cances, C

“…Apart from spinal muscular atrophy (SMA) and myotonic dystrophy type 1 (DM1), congenital neuromuscular diseases with early neonatal symptoms mean diagnostic…”
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Efficiency of targeted NGS on myopathies and muscular dystrophy genes: Importance of an optimized strategy of capture, sequencing, bioinformatic analyses and multidisciplinary approach for variants detection and interpretation by Zenagui, R, Lacourt, D, Juntas-Morales, R, Sole, G, Cances, C, River, F, Renard, D, Walther-Louvier, U, Ferrer-Monasterio, X, Espil, C, Arné-Bes, M, Cintas, P, Uro-Coste, E, Martin Negrier, M, Rigau, V, Bieth, E, Goizet, C, Claustres, M, Koenig, M, Cossee, M

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