Zobrazeno 1 - 10
of 136
pro vyhledávání: '"Arti, Nanda"'
Autor:
Ludmila Perelygina, Raeesa Faisthalab, Emily Abernathy, Min-hsin Chen, LiJuan Hao, Lionel Bercovitch, Diana K. Bayer, Lenora M. Noroski, Michael T. Lam, Maria Pia Cicalese, Waleed Al-Herz, Arti Nanda, Joud Hajjar, Koen Vanden Driessche, Shari Schroven, Julie Leysen, Misha Rosenbach, Philipp Peters, Johannes Raedler, Michael H. Albert, Roshini S. Abraham, Hemalatha G. Rangarjan, David Buchbinder, Lisa Kobrynski, Anne Pham-Huy, Julie Dhossche, Charlotte Cunningham Rundles, Anna K. Meyer, Amy Theos, T. Prescott Atkinson, Amy Musiek, Mehdi Adeli, Ute Derichs, Christoph Walz, Renate Krüger, Horst von Bernuth, Christoph Klein, Joseph Icenogle, Fabian Hauck, Kathleen E. Sullivan
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Rubella virus (RuV) has recently been found in association with granulomatous inflammation of the skin and several internal organs in patients with inborn errors of immunity (IEI). The cellular tropism and molecular mechanisms of RuV persistence and
Externí odkaz:
https://doaj.org/article/42a46da9868e480f8c8f79db28a8fb27
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Background and ObjectivesReports on skin manifestations in inborn errors of immunity (IEI) are based on retrospective analysis, small series, or isolated case reports. The present prospective study aimed to determine the spectrum of skin manifestatio
Externí odkaz:
https://doaj.org/article/b71fab1370a0415d985d46731e901a9c
Publikováno v:
Pediatric Dermatology. 40:547-550
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4742b7a603c79ff933bf0bf150559042
https://doi.org/10.1111/pde.15211
https://doi.org/10.1111/pde.15211
Publikováno v:
Pediatric Dermatology. 40:370-372
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d67f8796380f9029a0b2e73a78b4b5b
https://doi.org/10.1111/pde.15171
https://doi.org/10.1111/pde.15171
Publikováno v:
Clinical and Experimental Dermatology. 48:149-151
We report a 16-year-old adolescent girl with Down syndrome who developed a slowly progressive papulonodular eruption in the inguinal area. Skin biopsy for histopathology showed foci of bony trabeculae with osteoblasts and calcium deposition in the de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f85ca2bcb7a0aa132f752475bf8bc1b
https://doi.org/10.1093/ced/llac032
https://doi.org/10.1093/ced/llac032
Publikováno v:
Pediatric Dermatology. 39:650-652
CEDNIK syndrome is a rare autosomal recessive syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and keratoderma of which 25 cases from 19 families have been reported to date. It is a progressive neurodegenerative disorder caused
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58fe494e9a7100409da8e844dd7ad23e
https://doi.org/10.1111/pde.14961
https://doi.org/10.1111/pde.14961
Publikováno v:
Pediatric Dermatology. 38:50-57
BACKGROUND Autoimmune bullous diseases (AIBD) are rare among children. The data describing the overall spectrum and prognosis of pediatric AIBD (pAIBD) are scarce, and there are no established treatment guidelines. OBJECTIVES The present study examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ecacb7efd23706fd8ace78e5c77d914
https://doi.org/10.1111/pde.14368
https://doi.org/10.1111/pde.14368
Autor:
Daphna Weissglas-Volkov, Ofer Sarig, J. Mohamad, Alon Peled, Eli Sprecher, N. Malchin, Noam Shomron, Kiril Malovitski, M. Pavlovsky, John A. McGrath, Rashida Pramanik, Arti Nanda
Publikováno v:
Experimental Dermatology. 29:742-748
Autosomal recessive congenital ichthyosis (ARCI) manifests with generalized scaling often associated with generalized erythema. Mutations in at least 13 different genes have been reported to cause ARCI. Acral peeling skin syndrome (APSS) is a rare au
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd94f60662cf6ab27d1e533dee1e3ca6
https://doi.org/10.1111/exd.14140
https://doi.org/10.1111/exd.14140
Publikováno v:
Pediatric dermatologyREFERENCES. 39(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33abf1d5471f23c6ae093597d9ba3e17
https://pubmed.ncbi.nlm.nih.gov/36206214
https://pubmed.ncbi.nlm.nih.gov/36206214
Publikováno v:
Dermatology online journal. 27(11)
TP63-related disorders comprise a group of six overlapping autosomal dominant (AD) syndromes caused by heterozygous pathogenic variants in the tumor protein p63 gene (TP63). The present report describes the identification of heterozygous de novo path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e31d4524704a312d82a436c60ce305d
https://pubmed.ncbi.nlm.nih.gov/35130400
https://pubmed.ncbi.nlm.nih.gov/35130400