The Seven STAT3-Related Hyper-IgE Syndromes von Fadil, Ilham, Ben-Ali, Meriem, Jeddane, Leila, Barbouche, Mohamed-Ridha, Bousfiha, Ahmed Aziz

Volltext

The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies von Bousfiha, Aziz, Jeddane, Leïla, Picard, Capucine, Ailal, Fatima, Bobby Gaspar, H., Al-Herz, Waleed, Chatila, Talal, Crow, Yanick J., Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M., Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Puck, Jennifer, Tang, Mimi L. K., Tangye, Stuart G., Torgerson, Troy R., Casanova, Jean-Laurent, Sullivan, Kathleen E.

Volltext

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations von Aadam, Zahra, Kechout, Nadia, Barakat, Abdelhamid, Chan, Koon-Wing, Ben-Ali, Meriem, Ben-Mustapha, Imen, Zidi, Fethi, Ailal, Fatima, Attal, Nabila, Doudou, Fatouma, Abbadi, Mohamed-Cherif, Kaddache, Chawki, Smati, Leila, Touri, Nabila, Chemli, Jalel, Gargah, Tahar, Brini, Ines, Bakhchane, Amina, Charoute, Hicham, Jeddane, Leila, El Atiqi, Sara, El Hafidi, Naïma, Hida, Mustapha, Saile, Rachid, Alj, Hanane Salih, Boukari, Rachida, Bejaoui, Mohamed, Najib, Jilali, Barbouche, Mohamed-Ridha, Lau, Yu-Lung, Mellouli, Fethi, Bousfiha, Ahmed Aziz

Volltext

The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies von Bousfiha, Aziz, Jeddane, Leïla, Al-Herz, Waleed, Ailal, Fatima, Casanova, Jean‐Laurent, Chatila, Talal, Conley, Mary Ellen, Cunningham‐Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Gaspar, H. Bobby, Holland, Steven M., Klein, Christoph, Nonoyama, Shigeaki, Ochs, Hans D., Oksenhendler, Eric, Picard, Capucine, Puck, Jennifer M., Sullivan, Kathleen E., Tang, Mimi L. K.

Volltext

Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience von Benhsaien, Ibtihal, Ailal, Fatima, El Bakkouri, Jalila, Jeddane, Leïla, Ouair, Hind, Admou, Brahim, Bouskraoui, Mohamed, Hbibi, Mohamed, Hida, Mustapha, Amenzoui, Naïma, Jouhadi, Zineb, El Hafidi, Naïma, Rada, Nouredine, Benajiba, Noufissa, Abilkassem, Rachid, Badou, Abdallah, Bousfiha, Ahmed Aziz

Volltext

Primary Immunodeficiency Classification on Smartphone von Jeddane, Leïla, Ouair, Hind, Benhsaien, Ibtihal, Bakkouri, Jalila El, Bousfiha, Ahmed Aziz

Volltext

Primary immunodeficiencies in highly consanguineous North African populations von Barbouche, Mohamed-Ridha, Galal, Nermeen, Ben-Mustapha, Imen, Jeddane, Leïla, Mellouli, Fethi, Ailal, Fatima, Bejaoui, Mohamed, Boutros, Jeanette, Marsafy, Aisha, Bousfiha, Ahmed Aziz

Volltext

Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM von Ouair Hind, Benhsaien Ibtihal, Jeddane Leila, Jalila, El Bakkouri, Elhafidi Naima, Rada Noureddine, Jilali, Najib, Ailal Fatima, Alj Hanane Salih, Bousfiha Ahmed Aziz

Volltext

Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds von Errami, Abderrahmane, Baghdadi, Jamila El, Ailal, Fatima, Benhsaien, Ibtihal, Bakkouri, Jalila El, Jeddane, Leila, Rada, Noureddine, Benajiba, Noufissa, Mokhantar, Khaoula, Ouazahrou, Kaoutar, Zaidi, Sanae, Abel, Laurent, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, Bousfiha, Ahmed Aziz

Volltext

The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity von Bousfiha, Aziz, Moundir, Abderrahmane, Tangye, Stuart G, Picard, Capucine, Jeddane, Leila, Al-Herz, Waleed, Rundles, Charlotte C, Franco, Jose Luis, Holland, Steven M, Klein, Christoph, Morio, Tomohiro, Oksenhendler, Eric, Puel, Anne, Puck, Jennifer, Seppanen, Mikko R.J, Somech, Raz, Su, Helen C, Sullivan, Kathleen E, Torgerson, Troy R, Meyts, Isabelle

Volltext

Genetic basis of common variable immunodeficiency: from common to variable von Allaoui, Abire, Mokhantar, Khaoula, Jeddane, Leila, Dehbi, Hind, Ailal, Fatima, Bousfiha, Ahmed Aziz, Elkabli, Hassan, Moudatir, Mina

Volltext

Genetic basis of common variable immunodeficiency: from common to variable von Allaoui, Abire, Mokhantar, Khaoula, Jeddane, Leila, Dehbi, Hind, Ailal, Fatima, Bousfiha, Ahmed Aziz, Elkabli, Hassan, Moudatir, Mina

Volltext

Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM von Ouair, Hind, Benhsaiene, Ibtihal, Jeddane, Leila, Bakkouri, Jalila El, Elhafidi, Naima, Rada, Noureddine, Najib, Jilali, Ailal, Fatima, Alj, Hanane Salih, Bousfiha, Ahmed Aziz

Volltext

Phénotypes de 126 patients HIES marocains selon Score NIH von Fadil, Ilham, Benhsaien, Ibtihal, El Bakkouri, Jalila, Jeddane, Leila, Benaajiba, Noufissa, Rada, Noureddine, Hbibi, Mohamed, Amenzoui, Naïma, Ben Miloud, Sara, Hida, Mustapha, Bouskraoui, Mohammed, El Fetoiki, Fatima-Zahra, Hali, Fouzia, Chiheb, Soumiya, Admou, Brahim, Casanova, Jean Laurent, Puel, Anne, Boisson, Bertrand, Beziat, Vivien, Ailal, Fatima, Bousfiha, Ahmed Aziz

Volltext

Clinical and immunological profile of 15 Moroccan patients with Hyper IgM syndrome von Ouair, Hind, Benhsaien, Ibtihal, Jeddane, Leila, El Bakkouri, Jalila, Elhafidi, Naima, Rada, Noureddine, Najib, Jilali, Ailal, Fatima, Alj, Hanane Salih, Bousfiha, Ahmed Aziz

Volltext

A-Project : a Training Program from ASID von Erwa, Nahla H. H., Jeddane, Leïla, Alao, Maroufou J., Esser, Monika, Dieye, Tandakha N., Chipeta, James, Bousfiha, Ahmed Aziz

Volltext