Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Jens, Stahlschmidt"'
Autor:
Vanessa Daza-Cajigal, Adriana S. Albuquerque, Joanna Pearson, Jennifer Hinley, Andrew S. Mason, Jens Stahlschmidt, Adrian J. Thrasher, Vibhash Mishra, Jennifer Southgate, Siobhan O. Burns
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Inherited Primary Immunodeficiency (PID) disorders are associated with increased risk of malignancy that may relate to impaired antitumor immune responses or a direct role for PID germline mutations in tumorigenesis. We recently identified germline l
Externí odkaz:
https://doaj.org/article/f4a913741e234cc5acc5d4b3790636dc
Publikováno v:
Annales de Pathologie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19087956ee7159d44dcf0519fcd0eb6c
https://doi.org/10.1016/j.annpat.2023.05.005
https://doi.org/10.1016/j.annpat.2023.05.005
Publikováno v:
Diagnostic Histopathology. 28:470-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0beff5ad6085489c7c0698ad0286bb0
https://doi.org/10.1016/j.mpdhp.2022.08.008
https://doi.org/10.1016/j.mpdhp.2022.08.008
Autor:
Jens Stahlschmidt
Publikováno v:
Der Pathologe. 42:170-174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab019769d3b1e3ce0e76150b448ed07c
https://doi.org/10.1007/s00292-021-01025-5
https://doi.org/10.1007/s00292-021-01025-5
Autor:
Jennifer Hinley, Rosalind Duke, Jessica Jinks, Jens Stahlschmidt, David Keene, Raimondo M. Cervellione, Imran Mushtaq, Paolo De Coppi, Massimo Garriboli, Jennifer Southgate
Bladder exstrophy (BEX) is a rare developmental abnormality resulting in an open, exposed bladder plate. Although normal bladder urothelium is a mitotically quiescent barrier epithelium, histologic studies of BEX epithelia report squamous and prolife
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60fbc29f365a82a41404633f1354ed39
https://lirias.kuleuven.be/handle/20.500.12942/700525
https://lirias.kuleuven.be/handle/20.500.12942/700525
Autor:
Kavitha Jayaprakash, Sanjay Rajwal, Jens Stahlschmidt, Terry Humphrey, Helen Woodley, J Bernadette Moore, Eirini Kyrana
Publikováno v:
Liver.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9e81711d4f8e631c86fd90feb108a12
https://doi.org/10.1136/flgastro-2022-bspghan.67
https://doi.org/10.1136/flgastro-2022-bspghan.67
Autor:
Jens, Stahlschmidt
Publikováno v:
Der PathologeLiteratur. 42(Suppl 2)
Paediatric acute liver failure (PALF; also fulminant hepatic failure, fulminant hepatitis) is a critical clinical syndrome that is characterised by a sudden, rapid deterioration and disease progression in a usually previously healthy child. The patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e08d28d2d45619ca07a9f4eb45851a7a
https://pubmed.ncbi.nlm.nih.gov/34889991
https://pubmed.ncbi.nlm.nih.gov/34889991
Autor:
Dylan Lawless, David A. Parry, Rashida Anwar, Philip Wood, Jens Stahlschmidt, Anoop Mistry, Clive Carter, Sinisa Savic, Mark A. Hull, Gururaj Arumugakani
Publikováno v:
Journal of Clinical Immunology. 37:617-622
TTC7A deficiency typically causes severe gastrointestinal manifestations such as multiple intestinal atresia or early-onset inflammatory bowel disease. In some cases, this is associated with severe combined immunodeficiency. Partial loss-of-function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255e249f15146bb3a6329f836027f7e5
https://doi.org/10.1007/s10875-017-0427-1
https://doi.org/10.1007/s10875-017-0427-1
Publikováno v:
Journal of Pediatric Urology. 8:438-441
We report on two patients with urinary schistosomiasis, who both presented within a fortnight to our hospital with similar symptoms of persistent painless haematuria. Ultrasound, cystoscopic biopsies and histology were used to confirm diagnosis. Trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0dab1b5073ff1865eecab7aed98bb6e
https://doi.org/10.1016/j.jpurol.2011.11.008
https://doi.org/10.1016/j.jpurol.2011.11.008
Autor:
Jens Stahlschmidt, Peter E. Clayton, Christopher K. Bruce, Patricia McClean, Philippa B. Mills, Catherine P. K. Chong, A.S. Knisely, Paul Gissen
Publikováno v:
Journal of Inherited Metabolic Disease. 35:521-530
Born at 27 weeks gestation, a child of consanguineous parents of Pakistani origin required prolonged parenteral nutrition. She developed jaundice, with extensive fibrosis and architectural distortion at liver biopsy; jaundice resolved with supportive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e95776e4af42da255ee831066411138
https://doi.org/10.1007/s10545-011-9416-3
https://doi.org/10.1007/s10545-011-9416-3