Zobrazeno 1 - 9 of 9 pro vyhledávání: '"MESH : Agammaglobulinemia"'
1
Helicobacter bilis-Associated Suppurative Cholangitis in a Patient with X-Linked Agammaglobulinemia
Autor: Agnès Ferroni, Justine Dautremer, Nicolas Degand, Julie Bruneau, Fanny Lanternier, Marc Lecuit, Olivier Hermine, Olivier Lortholary, Stéphane Blanche, Benoit Pilmis, Xavier Nassif
Publikováno v: Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2017, 37 (7), pp.727-731. ⟨10.1007/s10875-017-0437-z⟩
Journal of Clinical Immunology, 2017, 37 (7), pp.727-731. ⟨10.1007/s10875-017-0437-z⟩
International audience; Helicobacter bilis is a commensal bacterium causing chronic hepatitis and colitis in mice. In humans, enterohepatic Helicobacter spp. are associated with chronic hepatobiliary diseases. Purpose : We aimed at understanding the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9eb2e8086949878575690fec8cc7f9
https://hal-pasteur.archives-ouvertes.fr/pasteur-02449154
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2
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
Autor: Hicham Charoute, Jalel Chemli, Nabila Attal, Leila Jeddane, Yu-Lung Lau, Sara El Atiqi, Rachid Saile, Ahmed Aziz Bousfiha, Chawki Kaddache, Imen Ben-Mustapha, Fethi Mellouli, Naima El Hafidi, Mohamed Bejaoui, Hanane Salih Alj, Nabila Touri, Zahra Aadam, Leila Smati, Rachida Boukari, Mustapha Hida, Fatouma Doudou, Mohamed-Cherif Abbadi, Tahar Gargah, I. Brini, Fatima Ailal, J. Najib, Amina Bakhchane, Mohamed-Ridha Barbouche, Meriem Ben-Ali, Nadia Kechout, Koon-Wing Chan, Fethi Zidi, Abdelhamid Barakat
Publikováno v: Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2016, 36 (3), pp.187-194. ⟨10.1007/s10875-016-0251-z⟩
International audience; X-linked agammagobulinemia (XLA) is a primary immunodeficiency caused by Bruton's tyrosine kinase (BTK) gene defect. XLA patients have absent or reduced number of peripheral B cells and a profound deficiency in all immunoglobu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59c0300b0273e49851f2567f39a41c29
https://hal-riip.archives-ouvertes.fr/pasteur-01374987
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3
Study on 43 patients with lymphoma and a « Common Variable Immunodeficiency (CVID) – like » disorder
Autor: Allain, Vincent
Publikováno v: Médecine humaine et pathologie. 2017
In patients with a diagnosis of Common Variable Immunodeficiency (CVID), about 5% will develop a lymphomaduring the course of the disease. Little is known about the characteristics of these patients and lymphomas. Todate, lymphoma remains an exclusio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2592::715bff89de05ed6e7717af4f3637aaff
https://dumas.ccsd.cnrs.fr/dumas-02474488/document
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5
Next-Generation Sequencing for Diagnosis and Tailored Therapy: A Case Report of Astrovirus-Associated Progressive Encephalitis
Autor: Nizar Mahlaoui, Marie-Louise Frémond, Marine Dumarest, Capucine Picard, C. Hébert, Philippe Pérot, Guilhem Cros, Nicole Corre-Catelin, Isabelle Desguerre, Marc Eloit, Stéphane Blanche, Danielle Seilhean, Marc Lecuit, E. Muth, Bénédicte Neven
Publikováno v: Journal of the Pediatric Infectious Diseases Society
Journal of the Pediatric Infectious Diseases Society, Oxford University Press 2015, 4 (3), pp.e53-e57. ⟨10.1093/jpids/piv040⟩
Journal of the Pediatric Infectious Diseases Society, 2015, 4 (3), pp.e53-e57. ⟨10.1093/jpids/piv040⟩
International audience; A boy with X-linked agammaglobulinemia experienced progressive global motor decline, cerebellar syndrome, and epilepsy. All standard polymerase chain reactions for neurotropic viruses were negative on cerebrospinal fluid and b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8145214fd7ba2df80da6ed45cf5581d3
https://hal-pasteur.archives-ouvertes.fr/pasteur-02452610/document
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6
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia
Autor: Julien Beauté, Pierre Galanaud, Pauline Brosselin, Capucine Picard, Romain Micol, Samer Kayal, Jean-Claude Lecron, Isabelle Pellier, Olivier Lambotte, Raphaele Nove-Josserand, Fabrice Monpoux, Nizar Mahlaoui, Fanny Lanternier, Stéphane Blanche, Anne Durandy, Caroline Thomas, Kamila Kebaili, Felipe Suarez, Marie-Alexandra Alyanakian, Pierre Teira, Olivier Lortholary, Yasmine Dudoit, Olivier Join-Lambert, Ioannis Theodorou, Alain Fischer, Alexandra Salmon, Marie-Dominique Tabone, Olivier Hermine, Marc Lecuit, Marianne Debré, Nathalie Aladjidi, Fabienne Dulieu, Gael Mouillot, Agathe Masseau, Eric Oksenhendler, Hélène Coignard-Biehler, Vincent Barlogis, Gaelle Obenga
Publikováno v: Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology, Elsevier, 2012, 129 (3), pp.770-7. ⟨10.1016/j.jaci.2011.09.047⟩
Journal of Allergy and Clinical Immunology, 2012, 129 (3), pp.770-7. ⟨10.1016/j.jaci.2011.09.047⟩
Journal of Allergy and Clinical Immunology; Vol 129
Journal of Allergy and Clinical Immunology, Elsevier, 2012, 129 (3), pp.770-7. 〈10.1016/j.jaci.2011.09.047〉
International audience; BACKGROUND: Primary immunoglobulin deficiencies lead to recurrent bacterial infections of the respiratory tract and bronchiectasis, even with adequate immunoglobulin replacement therapy. It is not known whether patients able t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::142bcb598c96274464176295bd1e8116
https://hal.archives-ouvertes.fr/hal-00796444
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7
Nucleotide variation in Sabin type 2 poliovirus from an immunodeficient patient with poliomyelitis
Autor: Valentina Donati, Javier Martin, Stefano Fiore, R. Vivarelli, Paolo Balestri, Francis Delpeyroux, Alessandro Plebani, Gabriele Buttinelli, Anna Rosa Soresina, Jill Marturano, Lucia Fiore
Publikováno v: Journal of General Virology
Journal of General Virology, Microbiology Society, 2003, 84 (Pt 5), pp.1215-21. ⟨10.1099/vir.0.18974-0⟩
Journal of General Virology, 2003, 84 (Pt 5), pp.1215-21. ⟨10.1099/vir.0.18974-0⟩
The molecular and antigenic properties of a Sabin-like type 2 poliovirus, isolated from the stool samples of a 2-year-old agammaglobulinaemic child who developed paralysis 1 year after receiving the third dose of oral poliovirus vaccine, were analyse
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ccbc45501d1de35285667d1e608d61
https://doi.org/10.1099/vir.0.18974-0
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8
Granulomatous disease in CVID: retrospective analysis of clinical characteristics and treatment efficacy in a cohort of 59 patients
Autor: Boursiquot, Jean-Nicolas, Gérard, Laurence, Malphettes, Marion, Fieschi, Claire, Galicier, Lionel, Boutboul, David, Borie, Raphael, Viallard, Jean-François, Soulas-Sprauel, Pauline, Berezne, Alice, Jaccard, Arnaud, Hachulla, Eric, Haroche, Julien, Schleinitz, Nicolas, Têtu, Laurent, Oksenhendler, Eric, Renseigné, Non
Publikováno v: Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2013, 33 (1), pp.84-95. ⟨10.1007/s10875-012-9778-9⟩
International audience; BACKGROUND: Granulomatous disease (GD) will develop in a subset of patients with common variable immunodeficiency (CVID). Little is known about the efficacy of therapeutic agents used for treating this disorder. OBJECTIVE: To
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96fa632007e1c7119856bf5859393b0f
https://hal.archives-ouvertes.fr/hal-00945425
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9
Leukocyte analysis from WHIM syndrome patients reveals a pivotal role for GRK3 in CXCR4 signaling
Autor: Olivier Hermine, Françoise Baleux, Bernard Lagane, Julie Harriague, Lysiane Klemm, Karl Balabanian, Françoise Bachelerie, Angélique Levoye, Fernando Arenzana-Seisdedos
Publikováno v: Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2008, 10, pp.1172-1183
Journal of Clinical Investigation, American Society for Clinical Investigation, 2008, 118 (3), pp.1074-84. ⟨10.1172/JCI33187⟩
Journal of Clinical Investigation, 2008, 118 (3), pp.1074-84. ⟨10.1172/JCI33187⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2008, 118 (3), pp.1074-84. 〈10.1172/JCI33187〉
International audience; Leukocytes from individuals with warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome, a rare immunodeficiency, and bearing a wild-type CXCR4 ORF (WHIM(WT)) display impaired CXCR4 internalization and des
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::654ee31884a581ba7a718c265f938511
https://doi.org/10.1172/jci33187
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