Zobrazeno 1 - 10
of 294
pro vyhledávání: '"Babakhouya A."'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 1, Pp 101-104 (2023)
Turner Syndrome (TS) is a genetic disorder caused by total or partial loss of an X chromosome. The isochromosome X (i(X)) is a known variant of TS, however, double i(X) is a very rare variant, reported very few times in the literature. We report on a
Externí odkaz:
https://doaj.org/article/0bdebe62e54e49079665cdf0b2e2eceb
Autor:
Elidrissi Errahhali, Manal, Elidrissi Errahhali, Mounia, Ramdani, Sara, Lhousni, Saida, Benajiba, Noufissa, Rkain, Maria, Babakhouya, Abdeladim, Elouali, Aziza, Ghanam, Ayad, Amrani, Rim, Messaoudi, Sahar, Ayyad, Anass, Oneib, Bouchra, Mimouni, Ahmed, Saadi, Hanane, Allaoui, Sanae, Ouarzane, Meryem, Guichet, Agnès, Charif, Majida, Boulouiz, Redouane, Bellaoui, Mohammed
Publikováno v:
In Archives de pédiatrie February 2024 31(2):112-116
Akademický článek
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Akademický článek
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Autor:
Ayad Ghanam, Aziza Elouali, Merouane Nour, Maria Rkain, Noufissa Benajiba, Abdeladim Babakhouya
Publikováno v:
Case Reports in Pediatrics, Vol 2022 (2022)
Bean syndrome (BS) or blue rubber bleb nevus syndrome is a rare clinical entity characterized by venous malformations mainly in the skin and digestive tract, whose hemorrhagic complications can be life threatening. We report a case of Bean syndrome i
Externí odkaz:
https://doaj.org/article/0c6a212b3ffa45b5817bf441ce19737d
Publikováno v:
Apollo Medicine, Vol 17, Iss 4, Pp 272-274 (2020)
Cholesteryl ester storage disease (CESD) in children is a rare anatomo-clinical entity, characterized by a secondary lysosomal accumulation and an autosomal recessive mutation in the LIPA gene, which results from a lysosomal acid lipase (LAL) deficie
Externí odkaz:
https://doaj.org/article/755ef849e93941f0b86febcced17c6dc
Autor:
Babakhouya, Naouel, Benammar, Souad, Hamitouche, Adh'ya-Eddine, Boudjemaa, Amel, Messaoud-Boureghda, Mohamed-Zine, Bachari, Khaldoun
Publikováno v:
Chemical Product & Process Modeling; Apr2024, Vol. 19 Issue 2, p297-314, 18p
Autor:
Belmokhtar, Karam Yahya, Cherkaoui, Imane, Lhousni, Saida, Elidrissi Errahhali, Mounia, Elidrissi Errahhali, Manal, Charif, Majida, Boulouiz, Redouane, Ouarzane, Meryem, Elouali, Aziza, Ghanam, Ayad, Babakhouya, Abdeladim, Rkain, Maria, Benajiba, Noufissa, Bellaoui, Mohammed
Publikováno v:
Molecular Syndromology; 2024, Vol. 15 Issue 2, p96-103, 8p
Publikováno v:
E3S Web of Conferences; 12/23/2023, Vol. 469, p1-15, 15p
Autor:
Zohair El Haddar, Aziza El Ouali, Ayad Ghanam, Maria Rkain, Noufissa Benajiba, Abdeladim Babakhouya
Publikováno v:
Case Reports in Pediatrics, Vol 2021 (2021)
Kawasaki disease (KD) is a vasculitis mostly seen in children aged less than 5 years. It can involve different organs and tissues. Its diagnosis is based on the clinical criteria of the American Heart Association (AHA). We report a case of a Moroccan
Externí odkaz:
https://doaj.org/article/9f49ed4945bb4251826623ca01c7c520