Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report.

Authors: Kasmi, Zakaria, Ain El Hayat, Imane, Aadam, Zahra, Errami, Abderrahmane, Benhsaien, Ibtihal, EL Bakkouri, Jalila, Ben Sabbahia, Dalal, Atrassi, Meryem, Bousfiha, Ahmed Aziz, Ailal, Fatima

Source: BMC Medical Genomics; 2/4/2025, Vol. 18 Issue 1, p1-7, 7p

Subject Terms: GLYCOGEN storage disease, GRANULOCYTE-colony stimulating factor, GENETIC variation, SYMPTOMS, METABOLIC disorders

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families

Authors: Ben-Ali, Meriem, Kechout, Nadia, Mekki, Najla, Yang, Jing, Chan, Koon Wing, Barakat, Abdelhamid, Aadam, Zahra, Gamara, Jouda, Gargouri, Lamia, Largueche, Beya, BelHadj-Hmida, Nabil, Nedri, Amel, Ameur, Houcine Ben, Mellouli, Fethi, Boukari, Rachida, Bejaoui, Mohamed, Bousfiha, Aziz, Ben-Mustapha, Imen, Lau, Yu-Lung, Barbouche, Mohamed-Ridha

Source: Journal of clinical immunology. 40(1):96-104

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100164400714.0x000001&indx=1&recIds=ETOCvdc_100164400714.0x000001

Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report.

Authors: Kasmi, Zakaria, Ain El Hayat, Imane, Aadam, Zahra, Errami, Abderrahmane, Benhsaien, Ibtihal, EL Bakkouri, Jalila, Ben Sabbahia, Dalal, Atrassi, Meryem, Bousfiha, Ahmed Aziz, Ailal, Fatima

Source: BMC Medical Genomics; 2/3/2025, Vol. 18 Issue 1, p1-1, 1p

Subject Terms: GLYCOGEN storage disease, MEDICAL genomics, HYPERCALCEMIA

A laboratory-based study of COVID-19 in Casablanca, Morocco.

Authors: Diawara, Idrissa, Benrahma, Houda, Nida, Meskaouni, Rahoui, Jalila, Moujid, Fatima-Zahra, Jaras, Khadija, Benmessaoud, Rachid, Arouro, Khadija, Aadam, Zahra, Nahir, Salma, Aouza, Zineb, Elguezzar, Hajar, Jeddan, Leila, Rida, Hind, Ousti, Fadoua, El Bakkouri, Jalila, Smyej, Imane, Nejjari, Chakib

Source: Journal of Public Health in Africa; 2021, Vol. 12 Issue 2, p30-34, 5p

Subject Terms: CORONAVIRUS diseases, REVERSE transcriptase polymerase chain reaction, COVID-19, COVID-19 pandemic

Geographic Terms: CASABLANCA (Morocco), MOROCCO

Le déficit immunitaire humoral: mieux le connaître pour mieux le prendre en charge.

Authors: El Bakkouri, Jalila^1,2, Aadam, Zahra³, Ailal, Fatima^2,4, Alj, Hanane Salih³, Bousfiha, Ahmed Aziz^2,4

Source: Pan African Medical Journal. 2014, Vol. 18, p1-14. 14p.

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Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases.

Authors: Refaat, Marwa¹ (AUTHOR) Refaat.marwa71@gmail.com, Oujane, Chaymae¹ (AUTHOR), Kholaiq, Halima¹ (AUTHOR), Aadam, Zahra¹ (AUTHOR), Errami, Abderrahmane¹ (AUTHOR), Baghad, Bouchra^1,2 (AUTHOR), Boussetta, Soufiane¹ (AUTHOR), El Kettani, Assiya^1,3 (AUTHOR), Benhsaien, Ibtihal^1,3 (AUTHOR), Ailal, Fatima^1,3 (AUTHOR), Bourhanbour, Asmaa Drissi^1,4 (AUTHOR), El Bakkouri, Jalila^1,4 (AUTHOR), Bousfiha, Ahmed Aziz^1,3 (AUTHOR)

Source: Egyptian Journal of Medical Human Genetics. 11/13/2024, Vol. 25 Issue 1, p1-12. 12p.

Subject Terms: *PRIMARY immunodeficiency diseases, *MYCOBACTERIAL diseases, *LYMPHOCYTE subsets, *BACTERIAL diseases, *HERPES simplex virus

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Exploring the landscape of congenital and idiopathic neutropenia in Moroccan children: a comprehensive retrospective analysis.

Authors: Kasmi, Zakaria, Chihi, Milouda, Aadam, Zahra, Ouair, Hind, Drissi Bourhanbour, Asmaa, EL Bakkouri, Jalila, Benhsaien, Ibtihal, Bousfiha, Ahmed Aziz, Ailal, Fatima

Source: Immunologic Research; Dec2025, Vol. 73 Issue 1, p1-13, 13p

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