Search Results - "Jalila, El Bakkouri"
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Hematological and biochemical abnormalities associated with severe forms of COVID-19: A retrospective single-center study from Morocco
Published in PloS one (04-02-2021)“…Since December 2019, the coronavirus disease (COVID-19) pandemic has catapulted the world into a marked health crisis, with over 29 million cases and >930,000…”
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Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds
Published in Journal of clinical immunology (01-05-2023)“…Purpose The first molecular evidence of a monogenic predisposition to mycobacteria came from the study of Mendelian susceptibility to mycobacterial disease…”
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Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients
Published in Journal of clinical immunology (01-02-2023)“…Purpose Genetic testing provides great support to validate the clinical diagnosis of inborn errors of immunity (IEI). However, the high cost and advanced…”
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Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency
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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Primary Immunodeficiency Classification on Smartphone
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Clinical and serological correlation of systemic sclerosis in Moroccan patients
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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Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience
Published in Journal of clinical immunology (01-04-2021)“…Severe combined immunodeficiency (SCID) is a heterogeneous group of primary immunodeficiency diseases (PIDs) characterized by a lack of autologous T…”
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Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases
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
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
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
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
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
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
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
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
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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Human Genetic and Immunological Determinants of SARS-CoV-2 Infection and Multisystem Inflammatory Syndrome in Children
Published in Clinical and experimental immunology (19-07-2024)“…Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces pneumonia and acute respiratory failure in Coronavirus Disease 2019 (COVID-19) patients…”
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Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patients
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
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
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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