Zobrazeno 1 - 10
of 193
pro vyhledávání: '"presymptomatic diagnosis"'
Autor:
Fengle Zhu, Zhenzhu Su, Alireza Sanaeifar, Anand Babu Perumal, Mostafa Gouda, Ruiqing Zhou, Xiaoli Li, Yong He
Publikováno v:
Engineering, Vol 22, Iss , Pp 171-184 (2023)
Plant pathogens continuously impair agricultural yields and food security. Therefore, the dynamic characterization of early pathogen progression is crucial for disease monitoring and presymptomatic diagnosis. Hyperspectral imaging (HSI) has great pot
Externí odkaz:
https://doaj.org/article/acc58e4eecf44ca5b75a5d799d119380
Akademický článek
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Autor:
Mahya Dezfouli, Sofia Bergström, Lillemor Skattum, Hassan Abolhassani, Maja Neiman, Monireh Torabi-Rahvar, Clara Franco Jarava, Andrea Martin-Nalda, Juana M. Ferrer Balaguer, Charlotte A. Slade, Anja Roos, Luis M. Fernandez Pereira, Margarita López-Trascasa, Luis I. Gonzalez-Granado, Luis M. Allende-Martinez, Yumi Mizuno, Yusuke Yoshida, Vanda Friman, Åsa Lundgren, Asghar Aghamohammadi, Nima Rezaei, Manuel Hernández-Gonzalez, Ulrika von Döbeln, Lennart Truedsson, Toshiro Hara, Shigeaki Nonoyama, Jochen M. Schwenk, Peter Nilsson, Lennart Hammarström
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
The clinical outcomes of primary immunodeficiencies (PIDs) are greatly improved by accurate diagnosis early in life. However, it is not common to consider PIDs before the manifestation of severe clinical symptoms. Including PIDs in the nation-wide ne
Externí odkaz:
https://doaj.org/article/f39438c83a124a7b99700d19394fcd89
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2005 Oct 01. 102(41), 14854-14859.
Externí odkaz:
https://www.jstor.org/stable/4143406
Akademický článek
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Autor:
Dezfouli, Mahya, Bergström, Sofia, Skattum, Lillemor, Abolhassani, Hassan, Neiman, Maja, Torabi-Rahvar, Monireh, Franco Jarava, Clara, Martin-Nalda, Andrea, Ferrer Balaguer, Juana M., Slade, Charlotte A, Roos, Anja, Fernández Pereira, Luis M, López-Trascasa, Margarita, González-Granado, Luis I, Allende-Martinez, Luis M, Mizuno, Yumi, Yoshida, Yusuke, Friman, Vanda, Lundgren, Åsa, Aghamohammadi, Asghar, Rezaei, Nima, Hernández-Gonzalez, Manuel, Döbeln, Ulrika von, Truedsson, Lennart, Hara, Toshiro, Nonoyama, Shigeaki, Schwenk, Jochen M, Nilsson, Peter, Hammarström, Lennart
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
Universidad Camilo José Cela (UCJC)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Immunology
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Universidad Camilo José Cela (UCJC)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Frontiers in Immunology
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
The clinical outcomes of primary immunodeficiencies (PIDs) are greatly improved by accurate diagnosis early in life. However, it is not common to consider PIDs before the manifestation of severe clinical symptoms. Including PIDs in the nation-wide ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7d6dec0003cee26547878d7443771ae3
http://hdl.handle.net/10486/693039
http://hdl.handle.net/10486/693039
Autor:
Shigeo Takashima, Hiroki Kawai, Nobuyuki Shimozawa, Kazuo Kubota, Kenji E. Orii, Megumi Ogawa, Hideo Sasai, Hidenori Ohnishi
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 58, p 58 (2021)
International Journal of Neonatal Screening
International Journal of Neonatal Screening
We established a diagnostic system for adrenoleukodystrophy (ALD) and peroxisomal disorders (PD) over 35 years ago in Japan, and have diagnosed 237 families with ALD and more than 100 cases of PD other than ALD using biochemical and molecular analyse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043c6a7d1a6d7da31c2cb516676c37f0
https://www.mdpi.com/2409-515X/7/3/58
https://www.mdpi.com/2409-515X/7/3/58
Autor:
Massimo Martinelli, Francesca Cammarota, Andrea Cerasuolo, Erasmo Miele, Francesca Duraturo, Annamaria Staiano, Paola Izzo, Marina De Rosa
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 8201, p 8201 (2020)
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 8201, p 8201 (2020)
Peutz&ndash
Jeghers Syndrome (PJS) is an autosomal dominant pre-cancerous disorder caused in 80&ndash
90% of cases by germline mutations in the tumor suppressor gene STK11. We performed a genetic test of the STK11 gene in two Italian young
Jeghers Syndrome (PJS) is an autosomal dominant pre-cancerous disorder caused in 80&ndash
90% of cases by germline mutations in the tumor suppressor gene STK11. We performed a genetic test of the STK11 gene in two Italian young
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7dc9051e30e7d7fd2a449d21d086a33
Why research the genetic status of members of a family affected by a hereditary disease andreveal this information to them, particularly when there is no treatment available? On whatbasis does the individual at risk make the decision of whether or no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::19037723c2d40985a81e05f2e3fda6b5
https://hal-mines-paristech.archives-ouvertes.fr/hal-03040870
https://hal-mines-paristech.archives-ouvertes.fr/hal-03040870
Akademický článek
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