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Clinical and Translational Allergy|April 17, 2019
Correction to: Dissociating polysensitization and multimorbidity in children and adults from a Polish general population cohortFilip Raciborski, Jean Bousquet, Andrzej Namysłowski, et al.
The New England Journal of Medicine|May 3, 2023
Reappraisal of Idiopathic CD4 Lymphocytopenia at 30 YearsAndrea Lisco, Ana M Ortega-Villa, Harry Mystakelis, et al.
Human Mutation|March 4, 2020
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
Clinical and Translational Allergy|February 23, 2019
Dissociating polysensitization and multimorbidity in children and adults from a Polish general population cohortFilip Raciborski, Jean Bousquet, Jean Bousqet, et al.
Human Molecular Genetics|September 8, 2021
Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humansNicole J Van Bergen, Katrina M Bell, Kirsty Carey, et al.
Genome Research|July 21, 2016
Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the youngD Nicole R Methner, Steven E Scherer, Katherine Welch, et al.
JPGN Reports|May 19, 2023
Hemosuccus Pancreaticus Following Acute Pancreatitis in a 12-years-old Boy Secondary to Pancreatic Pseudoaneurysm Treated With Endovascular Coil EmbolizationChristiana Ekezie, Kara G Gill, Patrick R Pfau, et al.
Human Mutation|November 10, 2020
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10Guy Helman, Alison G Compton, Daniella H Hock, et al.
Otolaryngologia Polska = the Polish Otolaryngology|December 17, 2009
Prevalence of rhinitis in Polish population according to the ECAP (Epidemiology of Allergic Disorders in Poland) studyBolesław Samoliński, Adam J Sybilski, Filip Raciborski, et al.
Frontiers in Immunology|March 6, 2023
Case report: Discovery of a de novo FAM111B pathogenic variant in a patient with an APECED-like clinical phenotypeElise M N Ferré, Yunting Yu, Vasileios Oikonomou, et al.
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