Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Diego S, Fernández Romero"'
Publikováno v:
Medicina. 82(3)
Antibody deficiencies (AD) are characterized by low or absent immunoglobulin levels or the inability to develop a specific antibody response. They are classified in primary (PAD) when there is an intrinsic immune defect, or secondary (SAD) to other d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99be7f1674fc7f3a4d621363b098b1aa
https://pubmed.ncbi.nlm.nih.gov/35639056
https://pubmed.ncbi.nlm.nih.gov/35639056
Autor:
Ana Coraglia, Nora Galassi, Diego S. Fernández Romero, M. Cecilia Juri, Marta Felippo, Alejandro Malbrán, María M. E. de Bracco
Publikováno v:
Journal of Immunology Research, Vol 2016 (2016)
CD4+ T follicular helper cells (TFH) were assessed in adult patients with common variable immune deficiency (CVID) classified according to the presence of granulomatous disease (GD), autoimmunity (AI), or both GD and AI (Group I) or the absence of AI
Externí odkaz:
https://doaj.org/article/b9da62f1bdca488e9460c5e60964c135
Autor:
Sebastián Udry, Stephanie Morales Peréz, Cristina Belizna, Federico Aranda, Enrique Esteve-Valverde, Silvia Perés Wingeyer, Diego S Fernández-Romero, José O Latino, Gabriela de Larrañaga, Jaume Alijotas-Reig
Publikováno v:
Lupus. 31(3)
Objectives(1) To assess the clinical utility of the adjusted global antiphospholipid syndrome score (aGAPSS) to predict new obstetric events during follow-up in primary obstetric antiphospholipid syndrome (POAPS) patients under standard-of-care treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b128e03a01e3264d5d0369ebd37bdf89
https://pubmed.ncbi.nlm.nih.gov/35157809
https://pubmed.ncbi.nlm.nih.gov/35157809
Autor:
Ana Laura, López, Julie, Niemela, Jennifer, Stoddard, María Virginia, Paolini, Sergio, Rosenzweig, Diego S, Fernández Romero
Publikováno v:
Medicina. 81(6)
Germline gain-of-function (GOF) mutation of the signal transducer and activator of transcription 3 (STAT3) gene causes a disease clinically characterized by a significant lymphoproliferation, including lymphadenopathy and/or hepatosplenomegaly, as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b83a807f4d5ab5ddb86d7b01e189c22a
https://pubmed.ncbi.nlm.nih.gov/34875609
https://pubmed.ncbi.nlm.nih.gov/34875609
Autor:
María V. Paolini, Silvia Danielian, Emma Prieto, María Fernanda Tami, Matías M. Oleastro, Diego S. Fernández Romero
Publikováno v:
Medicina (Buenos Aires), Vol 78, Iss 2, Pp 123-126 (2018)
WHIM syndrome is a primary autosomal dominant immuno deficiency due to CXCR4 mutations characterized by mucocutaneous warts, hypogammaglobulinemia, recurrent bacterial infections and myelokathesis. Treatment consists in prophylactic antibiotics, immu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::bd2f245b4fa88f4d5f24bad668fb20d8
http://www.medicinabuenosaires.com/PMID/29659363.pdf
http://www.medicinabuenosaires.com/PMID/29659363.pdf
Publikováno v:
Medicina. 76(6)
Most studies about treatment of inflammatory myopathies consist of cross-sectional analyses that do not assess long-term efficacy. In the present study we describe the follow-up of seven patients with inflammatory myopathies, 5 polymyositis and 2 der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d869ab403be459d49cc772dd49b18c34
https://pubmed.ncbi.nlm.nih.gov/27959849
https://pubmed.ncbi.nlm.nih.gov/27959849
Publikováno v:
Medicina (Buenos Aires), Vol 73, Iss 2, Pp 119-126 (2013)
Las vasculitis asociadas a anticuerpos anti-citoplasma de neutrófilos (ANCA) comprenden a un grupo de enfermedades caracterizadas por la inflamación de la pared de pequeños vasos. Analizamos las características epidemiológicas y clínicas en una
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::9b09171ba7a03ff0492ebd6ec52f5d4b
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000200004&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000200004&lng=en&tlng=en
Publikováno v:
Medicina. 76(2)
X-linked agammaglobulinemia (XLA) is characterized by absent or severely reduced B cells, low or undetectable immunoglobulin levels and clinically by extracellular bacterial infections which mainly compromise the respiratory tract as well as recurren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::022b9a7f6072b7f790f62b9272bfb88e
https://pubmed.ncbi.nlm.nih.gov/27135842
https://pubmed.ncbi.nlm.nih.gov/27135842
Publikováno v:
Medicina (Buenos Aires), Vol 72, Iss 2, Pp 119-123 (2012)
El angioedema hereditario (HAE) es una enfermedad rara, autosómica dominante, caracterizada por episodios que comprometen la piel, el tracto gastrointestinal y la laringe. Tiene una mortalidad histórica por asfixia del 15 al 50%. Es producida por l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::8e95192b3050a6413c946de91be51406
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802012000200006&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802012000200006&lng=en&tlng=en