Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Houda Nassih"'
Autor:
Soumia Nachate, Mouad El Mouhtadi, Yousra Zouine, Mohamed Amine Haouane, Mohamed Amine Azami, Mohamed Oulad Saiad, Dounia Basraoui, Hicham Jalal, Houda Nassih, Rabiy Elqadiry, Aicha Bourrahouat, Imane Ait Sab, Awatif El Hakkouni
Publikováno v:
Annals of Pediatric Surgery, Vol 19, Iss 1, Pp 1-10 (2023)
Abstract Background Invasive aspergillosis (IA) is one of the rarest opportunistic fungal infections and has increased in frequency worldwide in recent years. It is a life-threatening infection associated with high mortality rates. Invasive pulmonary
Externí odkaz:
https://doaj.org/article/bb825367ef0e41418b7a779b41b6e602
Autor:
Houda Nassih PhD, Sara Belghmaidi PhD, Rabiy El Qadiry PhD, Ibtissam Hajji PhD, Aicha Bourrahouat PhD, Abdeljalil Moutaouakil PhD, Imane Ait Sab PhD
Publikováno v:
Global Pediatric Health, Vol 9 (2022)
There is a global concern about children presenting with inflammatory syndrome with variable clinical features during the ongoing COVID-19 pandemic. This paper reports the first pediatric case of bilateral serous retinal detachment and conjunctival h
Externí odkaz:
https://doaj.org/article/a3c41caddaa44ff5ac402d88c91b6a11
Publikováno v:
Global Pediatric Health, Vol 9 (2022)
We report the case of a child who had tuberculosis associated with nephrotic syndrome. In this case, it was difficult to identify if the renal involvement was due to renal infection with mycobacterium tuberculosis, the consequence of nephrotoxicity o
Externí odkaz:
https://doaj.org/article/685dd5831c0c4fd6b485db25dc475f44
Publikováno v:
Case Reports in Hematology, Vol 2022 (2022)
Rosai–Dorfman disease (RDD) is a rare and benign nonLangerhans cell histiocytosis. RDD commonly affects children and young adults typically presenting with massive, painless, and bilateral cervical lymphadenopathy. Extranodal involvement is present
Externí odkaz:
https://doaj.org/article/991ad02539b6446fa294a284514f99e2
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 5, Pp 351-353 (2021)
We report the case of a 4-year-old boy with protein-losing enteropathy, leading to severe malnutrition. Associated thrombotic microangiopathic features made diagnosis difficult and challenging.
Externí odkaz:
https://doaj.org/article/d4831dfcc6f1401487d2d63769b90aae
Autor:
Houda Nassih, Fatimzehra El Hanafi, Safa Elalaoui, Rabiy El Qadiry, Aicha Bourahouat, Imane Ait Sab
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 166 (2020)
Scabies is very common among children. It is often a harmless infectious disease, responding well to antiparasitic medication. Nevertheless, severe forms can occur in immunocompromised populations like newborns and infants. We report a unique case of
Externí odkaz:
https://doaj.org/article/873a0331d7a5469b86c834449d698586
Publikováno v:
Journal of Neonatology. 35:262-264
Isolated thrombocytopenia is a common finding in neonates and infants. Physicians should rule out infection at first. Meanwhile, neonatal lupus erythematosus is classically revealed by cutaneous and cardiac manifestations. Hematological involvement i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa0495eeedce4c104d42a3d48a466ae5
https://doi.org/10.1177/09732179211045008
https://doi.org/10.1177/09732179211045008
Autor:
Miloud Hammoud, Es-said Sabir, Imane Assiri, Karima Lafhal, Samira Najeh, Imane ait Saab, Aicha Bourrahouat, Rabiy Elqadiry, Houda Nassih, My Ahmed Elamiri, Fadl Mrabih Rabou Maoulainine, Nadia Elidriss Slitine, Fatiha Bennaoui, Mounir Bourrous, Alice M.S. Rodrigues, Didier Stien, Soumia Mrhar, Nourddine Rada, Mohammed Bouskraoui, Fdil Naima
Publikováno v:
Molecular Genetics and Metabolism. 138:107138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498199c7b24ad01bcb3d0bd8e254ff1e
https://doi.org/10.1016/j.ymgme.2022.107138
https://doi.org/10.1016/j.ymgme.2022.107138
Publikováno v:
Rheumatology. 60
Background Neonatal lupus is a rare condition linked to the maternal-fetal transmission of maternal anti-SSA and/or anti-SSB antibodies, more rarely anti-U1-RNP. The most frequent clinical manifestations are cardiac and cutaneous, more rarely hematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::323892ad5ef0625f68434ced8c28c1b3
https://doi.org/10.1093/rheumatology/keab722.086
https://doi.org/10.1093/rheumatology/keab722.086
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 5, Pp 351-353 (2021)
Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons
We report the case of a 4-year-old boy with protein-losing enteropathy, leading to severe malnutrition. Associated thrombotic microangiopathic features made diagnosis difficult and challenging.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6d95c6b5d1719728f70ba1bb1b0188e
http://www.jiaps.com/article.asp?issn=0971-9261
http://www.jiaps.com/article.asp?issn=0971-9261