Zobrazeno 1 - 10
of 6 517
pro vyhledávání: '"hypogammaglobulinemia"'
Autor:
Chiara Russo, Malgorzata Mikulska, Emanuele Delfino, Federica Toscanini, Laura Mezzogori, Riccardo Schiavoni, Claudia Bartalucci, Emanuele Angelucci, Giulia Bartalucci, Massimiliano Gambella, Anna Maria Raiola, Paola Morici, Francesca Crea, Silvia Chiola, Silvia Daniela Morbelli, Anna Marchese, Matteo Bassetti
Publikováno v:
Infectious Diseases and Therapy, Vol 13, Iss 10, Pp 2179-2193 (2024)
Abstract Mycoplasma hominis can be a part of human urogenital tract microbiome, and it is a frequent cause of urogenital infections. In rare cases, it can also cause extragenital infections, especially in immunocompromised patients. In this case seri
Externí odkaz:
https://doaj.org/article/cfeba45bfb9249f8897dafc3269267cb
Publikováno v:
Медицинская иммунология, Vol 26, Iss 5, Pp 1001-1008 (2024)
We present a unique clinical case of an atypical hemolytic-uremic syndrome in a child. The mutation in exon 6 of the CD46 gene (chr1:207940532G>C) leads to a homozygous or hemizygous missense substitution. An 8-year-old girl was urgently hospitalized
Externí odkaz:
https://doaj.org/article/02d3b3e256dd44118b5b234ba3d543a2
Publikováno v:
Biomedical Papers, Vol 168, Iss 2, Pp 167-176 (2024)
Background. RTX, an anti-CD20 monoclonal antibody, added to chemotherapy has proven to be effective in children and adolescents with high-grade, high-risk and matured non-Hodgkin lymphoma. RTX leads to prompt CD19+ B lymphocyte depletion. However, de
Externí odkaz:
https://doaj.org/article/12e3a8a9174d4c269d0e5e672ef1062d
Autor:
Cristina Frias Sartorelli de Toledo Piza, Carolina Sanchez Aranda, Dirceu Solé, Stephen Jolles, Antonio Condino-Neto
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
PurposeCalculated globulin (CG, total protein minus albumin levels) correlate well with IgG levels and has been proposed as a suitable screening method for individuals with primary antibody deficiencies (PADs). We aimed to show the correlation of CG
Externí odkaz:
https://doaj.org/article/b1b3f5c1de9540eca1dc7fb6bf4b2c6e
Analysis of rare genetic variants in All of Us cohort patients with common variable immunodeficiency
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Common variable immunodeficiency (CVID) is a group of genetic disorders involving more than a dozen genetic loci and characterized by a deficiency in specific antibody isotypes leading to poor immune responses and recurrent infection. CVID affects ap
Externí odkaz:
https://doaj.org/article/0b2a077a62264057a8ec2241c8696863
Autor:
Amanda Salih, Amanda Brown, Amanda Grimes, Sana Hasan, Manuel Silva-Carmona, Leyat Tal, Joud Hajjar
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Common variable immunodeficiency (CVID) can be complicated by granulomatous disease, often granulomatous lymphocytic interstitial lung disease (GLILD). Granulomatous interstitial nephritis represents an atypical presentation in pediatrics. Our patien
Externí odkaz:
https://doaj.org/article/d83633cbb3684891930bdd7c4818fb9a
Publikováno v:
Immunological Medicine, Pp 1-3 (2024)
Kabuki syndrome (KS) is a genetic disorder caused by gene mutations in either lysine-specific methyltransferase 2D (KMT2D) or lysine demethylase 6A (KDM6A). This congenital disorder exhibits characteristic facial features, developmental delays in psy
Externí odkaz:
https://doaj.org/article/78444e0b3f1b489a88c07806b4d6b9f0
Autor:
Yoji Uejima, Satoshi Sato
Publikováno v:
Immunological Medicine, Vol 47, Iss 2, Pp 106-109 (2024)
AbstractCongenital Myotonic Dystrophy (CMD) is an autosomal dominant hereditary disease caused by mutations in the dystrophia myotonica protein kinase gene. Patients with CMD often exhibit low immunoglobulin (Ig) G levels. While Ig replacement therap
Externí odkaz:
https://doaj.org/article/76d431fa43074ff3b9308a8ef558e89d
Autor:
Justin J. Y. Kim, Liz Dennett, Maria B. Ospina, Anne Hicks, Harissios Vliagoftis, Adil Adatia
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-13 (2024)
Abstract Purpose Immunoglobulin replacement therapy is a standard treatment for patients with antibody production deficiencies, which is of interest in patients with chronic obstructive pulmonary disease (COPD). This systematic review, registered wit
Externí odkaz:
https://doaj.org/article/d48a511902d14e708356cfe46282e5c2
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