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of 33
pro vyhledávání: '"Fouad, Seghrouchni"'
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Autor:
Karima Sahmoudi, Hassan Abbassi, Nada Bouklata, Mohamed Nouredine El Alami, Abderrahmane Sadak, Christopher Burant, W. Henry Boom, Rajae El Aouad, David H. Canaday, Fouad Seghrouchni
Publikováno v:
BMC Immunology, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Lymph node tuberculosis (LNTB) is the most frequent extrapulmonary form of tuberculosis (TB). Studies of human tuberculosis at sites of disease are limited. LNTB provides a unique opportunity to compare local in situ and periphera
Externí odkaz:
https://doaj.org/article/0c9601eef7754e95b44728b5e7d83aa3
Autor:
Kamal El Bissati, Pauline Levigne, Joseph Lykins, El Bachir Adlaoui, Amina Barkat, Amina Berraho, Majda Laboudi, Bouchra El Mansouri, Azeddine Ibrahimi, Mohamed Rhajaoui, Fred Quinn, Manoradhan Murugesan, Fouad Seghrouchni, Jorge Enrique Gómez-Marín, François Peyron, Rima McLeod
Publikováno v:
Emerging Microbes and Infections, Vol 7, Iss 1, Pp 1-14 (2018)
Abstract Globally, congenital toxoplasmosis remains a significant cause of morbidity and mortality, and outbreaks of infection with T. gondii represent a significant, emerging public health burden, especially in the developing world. This parasite is
Externí odkaz:
https://doaj.org/article/7ab6020e27274c5eadce1a3ce0d22816
Cytometric analysis and clinical features in a Moroccan cohort with severe combined immunodeficiency
Autor:
Aicha El Allam, Sara El Fakihi, Hicham Tahoune, Karima Sahmoudi, Houria Bousserhane, Youssef Bakri, Naima El Hafidi, Fouad Seghrouchni
Publikováno v:
Human Antibodies. 30:67-77
Severe combined immunodeficiency (SCID) is a form of primary immunodeficiency disease (PID). It is characterized by a serious abnormality of the cellular and sometimes humoral system due to a deficiency in development of T cells, B cells and/or NK ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::839e6df2dab1fa8d59cda3662f916ca0
https://doi.org/10.3233/hab-211510
https://doi.org/10.3233/hab-211510
Publikováno v:
Cytometry Part A. 99:1102-1106
Multiple immunolabeling introduces high risks of interferences between fluorochromes. In an intend to analyze T cell clonality using CD3-APC Alexa750, CD4-Pac Blue, CD8-Krome Orange, CD56-PE-Cy7 and Vbeta clonotypes FITC and PE, we repeatedly observe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86607eb63ebce36cb109e264a0a8e30f
https://doi.org/10.1002/cyto.a.24342
https://doi.org/10.1002/cyto.a.24342
Autor:
Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui, Lamiae Belayachi, Naima El Hafidi, Houyam Hardizi, Elmostafa El Fahime, Naima Erreimi, Abdelhamid Barakat, Mohammed Khattab, Fouad Seghrouchni, Amine El Hassani
Publikováno v:
BioMed Research International.
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6629c4f900704ce4490b6c7d341067b
Autor:
Ahmed, Bouhouche, Yasmin, Tabache, Omar, Askander, Hicham, Charoute, Nada, Mesnaoui, Lamiae, Belayachi, Naima, El Hafidi, Houyam, Hardizi, Elmostafa, El Fahime, Naima, Erreimi, Abdelhamid, Barakat, Mohammed, Khattab, Fouad, Seghrouchni, Amine, El Hassani
Publikováno v:
BioMed research international. 2022
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa98e7b3587364832a77cf6901efd6b4
https://pubmed.ncbi.nlm.nih.gov/35281597
https://pubmed.ncbi.nlm.nih.gov/35281597
Autor:
Nada Bouklata, Philip Supply, Sanae Jaouhari, Reda Charof, Fouad Seghrouchni, Khalid Sadki, Youness El Achhab, Chakib Nejjari, Abdelkarim Filali-Maltouf, Ouafae Lahlou, Rajae El Aouad
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135695 (2015)
Standard 24-locus Mycobacterial Interspersed Repetitive Unit Variable Number Tandem Repeat (MIRU-VNTR) typing allows to get an improved resolution power for tracing TB transmission and predicting different strain (sub) lineages in a community.During
Externí odkaz:
https://doaj.org/article/80e88daecd8d4f648400b2f2ba89e110
Autor:
Mounia Qrafli, Youssef Amar, Jamaleddine Bourkadi, Jouda Ben Amor, Ghali Iraki, Youssef Bakri, Saaed Amzazi, Ouafae Lahlou, Fouad Seghrouchni, Rajae El Aouad, Khalid Sadki
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 1 (2014)
INTRODUCTION: Despite the medical progress in treatment. Tuberculosis (TB) continues to be a serious global health problem. A genome-wide linkage study identified a major susceptibility locus on chromosomal region 8q12-q13 in Moroccan TB patients. Th
Externí odkaz:
https://doaj.org/article/57783308876f428fa0cd552bc2c90df4
Autor:
Houria Bousserhane, Naima El Hafidi, Sara El Fakihi, Karima Sahmoudi, Hicham Tahoune, Fouad Seghrouchni, Youssef Bakri, Aicha El Allam
Publikováno v:
Human antibodies. 29(1)
The number of circulating lymphocytes is altered in a number of diseases including either increase (lymphocytosis) or decrease (lymphocytopenia). Therefore, the assessment of total blood lymphocyte numbers and the relative distribution of lymphocyte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaaf46b76a42766de38386566c082372
https://pubmed.ncbi.nlm.nih.gov/33252069
https://pubmed.ncbi.nlm.nih.gov/33252069