Results 31 to 40 of about 2,267,031 (171)

Post-Acute Sequelae Patients with Severe COVID-19 History Show a Prolonged Inflammatory, Vascular Injury Pattern. [PDF]

Eur J Immunol
Long‐COVID or post‐acute sequelae of COVID‐19 syndrome (PASC) patients with previous severe COVID‐19 ICU history prior vaccination display sustained significant changes in their immune profile at both the cellular and the inflammatory level, revealing signatures of persistent inflammation and endothelial injury.
Ruhl L, Pink I, Chichelnitskiy E, Drick N, Sauer A, Boblitz L, Beushausen K, Keil J, Ullrich AL, Schmidt J, Hoeper MM, Welte T, Kühne JF, Falk CS.   +13 more
europepmc   +2 more sources

Defective apoptosis of peripheral-blood lymphocytes in hyper-IgD and periodic fever syndrome. [PDF]

, 2007
Hereditary periodic fever syndromes are characterized by incapacitating attacks of fever and generalized inflammation. While the mutated genes for the major syndromes in this group are known, the pathogenesis remains unclear. The aim of this study was to
Heerde, W.L. van, Bodar, E.J., Drenth, J.P.H., Simon, A., Meer, J.W.M. van der, Hilst, J.C.H. van der   +5 more
core   +1 more source

Variability in fricative production of young people with Down's syndrome : an EPG analysis [PDF]

, 2007
Speech production in Down's syndrome is highly variable, with particular problems arising from complex articulations such as fricatives. In this paper, EPG analysis is used to study the variation in the production of the fricatives /s/ and /sh/ in 6 ...
Hardcastle, William, Hardcastle, William J., Hardcastle, William J, McCann, Joanne, Wood, Sara, Wishart, Jennifer, Timmins, Claire   +6 more
core   +3 more sources

Table_1_Case Report: Comorbid Hyper-IgD Syndrome and Hidradenitis Suppurativa – A New Syndromic Form of HS? A Report of Two Cases.docx

, 2022
Hidradenitis Suppurativa (HS) is a chronic suppurative disease of the pilosebaceous unit. The current model of HS pathophysiology describes the condition as the product of hyperkeratinisation and inflammation at the hair follicular unit.
Agnes Duquesne (12755411), Dillon Mintoff (12281000), Elie Cogan (9227888), Philippe Guillem (12755405), Mariam Kabbani (12755408), Virginie Vlaeminck-Guillem (428280), Farida Benhadou (10915383)   +6 more
core   +1 more source

Autoinflammatory Syndromes in the Practice of Pediatrician

Zdorovʹe Rebenka, 2014
В обзорной статье предоставлены информация, характеристика, определение и классификация заболеваний, которые были отнесены к отдельной нозологической группе и названы аутовоспалительными заболеваниями или синдромами (АВС).
S.N. Nedelskaya, I.A. Zhilenko, A.S. Merezhko, A.V. Shapran   +3 more
doaj   +1 more source

Hyper-programming in Java [PDF]

, 2011
Hyper-programming is a technology only available in persistent systems since hyper-program source contains both text and links to persistent objects. A hyper-programming system has already been prototyped in the persistent programming language Napier88 ...
Zirintsis, E, Dunstan, VS, Morrison, Ronald, Kirby, Graham Njal Cameron   +3 more
core   +2 more sources

Effects of Anakinra on Health-Related Quality of Life in a Patient with 1129G>A/928G>A Mutations in MVK Gene and Heterozygosity for the Mutation 2107C>A in CIAS1 Gene

Frontiers in Pediatrics, 2017
Mevalonate kinase deficiency impairs several aspects of the patient’s quality of life, thus early diagnosis and treatment are required to improve health-related quality of life (HRQOL).
Gianluigi Laccetta, Maria Tutera, Mario Miccoli, Rita Consolini   +3 more
doaj   +1 more source

Aberrant expression of costimulatory molecules in splenocytes of the mevalonate kinase-deficient mouse model of human hyper-IgD syndrome (HIDS). [PDF]

J Inherit Metab Dis, 2012
Objective We sought to determine the activation status and proliferative capacities of splenic lymphocyte populations from a mevalonate kinase-deficient mouse model of hyper-IgD syndrome (HIDS).
Hager EJ, Piganelli JD, Tse HM, Gibson KM.   +3 more
europepmc   +2 more sources

Neonatal Hepatitis as First Manifestation of Hyperimmunoglobulinemia D Syndrome

Case Reports in Pediatrics, 2014
Hyper IgD syndrome (HIDS) is a rare metabolic autoinflammatory syndrome characterised by recurrent febrile episodes, accompanied by various inflammatory symptoms.
Marie-Louise von Linstow, Vibeke Rosenfeldt   +1 more
doaj   +1 more source

Establishment of pediatric reference ranges for circulating naïve and memory T and B cell subsets guided by the human immunophenotyping consortium standardization initiative: A large, single center U.S. experience

Cytometry Part B: Clinical Cytometry, EarlyView.
Abstract Our knowledge of the immune system continues to expand at a rapid pace, and this coupled with technological advances now enables us to interrogate both the breadth and the depth of the immune response at levels without precedent. This has also facilitated rapidly integrating some of this carefully vetted knowledge into clinical practice ...
Aaruni Khanolkar, Aisha Ahmed
wiley   +1 more source