Search Results - "Jalila, El Bakkouri"

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    Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency by El Kettani, Assiya, Ouair, Hind, Marnissi, Farida, El Bakkouri, Jalila, Chevalier, Rémi, Lorenzo, Lazaro, Kholaiq, Halima, Béziat, Vivien, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Bousfiha, Ahmed Aziz

    Published in Viruses (05-09-2024)
    “…Epidermodysplasia verruciformis (EV) is a rare genodermatosis caused by β-human papillomaviruses (HPV) in immunodeficient patients. EV is characterized by flat…”
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    Journal Article
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    Clinical and serological correlation of systemic sclerosis in Moroccan patients by Ouazahrou, Kaoutar, El Bakkouri, Jalila, Souali, Manal, Jeddane, Leila, Mokhantar, Khaoula, Errami, Abderrahmane, El Kabli, Hassan, Bousfiha, Ahmed Aziz, Echchilali, Khadija

    Published in Rheumatology advances in practice (2023)
    “…Abstract Objective SSc is a CTD characterized by excessive fibrosis of the skin and internal organs, along with microvascular damage, and is often associated…”
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    Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases by Refaat, Marwa, Oujane, Chaymae, Kholaiq, Halima, Aadam, Zahra, Errami, Abderrahmane, Baghad, Bouchra, Boussetta, Soufiane

    Published in Egyptian Journal of Medical Human Genetics (13-11-2024)
    “…Background Innate immune deficiencies can impair both cellular and humoral immune responses. In contrast, other immune functions may appear normal, leading to…”
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    Exploring inflammatory markers of COVID-19 severity in Moroccans by Drissi Bourhanbour, Asmaa, Kattra, Aziza Bachir, Aissaoui, Ouissal, Ouair, Hind, Benzekri, Driss, Kholaiq, Halima, Charra, Boubaker, Jalila, El Bakkouri, Bousfiha, Ahmed Aziz

    Published in Scientific African (01-06-2024)
    “…The global impact of the SARS-CoV-2-induced COVID-19 pandemic has reached Morocco. Early identification of factors contributing to severity is imperative for…”
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    Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM by Ouair Hind, Benhsaien Ibtihal, Jeddane Leila, Jalila, El Bakkouri, Elhafidi Naima, Rada Noureddine, Jilali, Najib, Ailal Fatima, Alj Hanane Salih, Bousfiha Ahmed Aziz

    Published in The Pan African medical journal (19-04-2017)
    “…Le Syndrome hyper IgM est un déficit immunitaire héréditaire bien connu, décrit pour la première fois en 1961. Il est causé par un défaut au niveau des…”
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    HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity by El Kettani, Assiya, Ailal, Fatima, El Bakkouri, Jalila, Zerouali, Khalid, Béziat, Vivien, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Bousfiha, Ahmed Aziz

    Published in Pathogens (Basel) (29-07-2022)
    “…Patients with inborn errors of immunity (IEI) are prone to develop infections, either due to a broad spectrum of pathogens or to only one microbe. Since skin…”
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    Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases by Benhsaien, Ibtihal, Ailal, Fatima, Elazhary, Khadija, El bakkouri, Jalila, Badou, Abdallah, Bousfiha, Ahmed Aziz

    Published in Case reports in immunology (07-01-2021)
    “…Severe combined immunodeficiency (SCID) comprises a heterogeneous group of inherited immunologic disorders with profound defects in cellular and humoral…”
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    Atypical Cutaneous Viral Infections Reveal an Inborn Error of Immunity in 8 Patients by El Kettani, Assiya, Ailal, Fatima, Marnissi, Farida, Hali, Fouzia, El Bakkouri, Jalila, Benhsaien, Ibtihal, Le Voyer, Tom, Guèye, Mame Sokhna, Chevalier, Rémi, Chiheb, Soumiya, Zerouali, Khalid, Jouanguy, Emmanuelle, Casanova, Jean-Laurent, Bousfiha, Ahmed Aziz

    Published in Microorganisms (Basel) (04-05-2023)
    “…Unusual viral skin infections might be the first clinical manifestation in children with an inborn error of immunity (IEI). We performed a prospective study…”
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    A laboratory-based study of COVID-19 in Casablanca, Morocco by Diawara, Idrissa, Benrahma, Houda, Meskaouni, Nida, Rahoui, Jalila, Moujid, Fatima-Zahra, Jaras, Khadija, Benmessaoud, Rachid, Arouro, Khadija, Aadam, Zahra, Nahir, Salma, Aouzal, Zineb, Elguazzar, Hajar, Jeddan, Leila, Rida, Hind, Ousti, Fadoua, Bakkouri, Jalila E., Smyej, Imane, Nejjari, Chakib

    Published in Journal of public health in Africa (31-12-2021)
    “…Given the spread of coronavirus disease 2019 (COVID-19) and its impact on human health, laboratory confirmation of diagnosis is essential. This study examined…”
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    Syndrome lymphoprolifératif avec autoimmunité: à propos d’un cas by Youssif, Houda Ben, Ailal, Fatima, Benhsaien, Ibtihal, Bakkouri, Jalila El, Jeddane, Laila, Maani, Khadija El, Bousfiha, Ahmed Aziz

    Published in The Pan African medical journal (07-10-2022)
    “…Le syndrome lymphoprolifératif avec autoimmunité (ALPS) est un trouble hériditaire rare de l´homéostasie lymphocytaire, résultant de mutations dans la voie…”
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    Le déficit immunitaire humoral: mieux le connaître pour mieux le prendre en charge by El Bakkouri, Jalila, Aadam, Zahra, Ailal, Fatima, Alj, Hanane Salih, Bousfiha, Ahmed Aziz

    Published in The Pan African medical journal (04-08-2014)
    “…Les déficits immunitaires humoraux (DIH) sont des maladies hétérogènes allant des formes asymptomatiques rencontrés lors des déficits sélectifs en…”
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    Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patients by Mokhantar, Khaoula, Allaoui, Abir, Ailal, Fatima, Bakkouri, Jalila El, Ouazahrou, Kaoutar, Errami, Abderrahmane, Bousfiha, Ahmed Aziz, Moudatir, Mina

    Published in Qatar medical journal (31-05-2023)
    “…Objective: Common variable immunodeficiency (CVID) is a complex inborn error of humoral immunity with complications of both infectious and non-infectious…”
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    Autoimmune lymphoproliferative syndrome: a case report by Youssif, Houda Ben, Ailal, Fatima, Benhsaien, Ibtihal, Bakkouri, Jalila El, Jeddane, Laila, Maani, Khadija El, Bousfiha, Ahmed Aziz

    Published in The Pan African medical journal (2022)
    “…Autoimmune lymphoproliferative syndrome (ALPS) is a rare genetic disorder of lymphocyte homeostasis, resulting from mutations in the Fas apoptotic pathway. It…”
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    Orientation diagnostic devant une neutropénie héréditaire de l’enfant : Revue narrative de la littérature by Kasmi, Zakaria, El Bakkouri, Jalila, Ailal, Fatima, Oukkache, Bouchra, Donadieu, Jean, Bousfiha, Ahmed Aziz

    Published in Tunisie Medicale (01-07-2023)
    “…A l’ère de la génomique l’orientation devant une neutropénie héréditaire nécessite encore et d’abord une bonne analyse clinique et cytologique. La trentaine de…”
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