Search Results - "Touri, Nabila"

An algerian three-month-old infant with juvenile myelomonocytic leukemia and noonan syndrome: a case report and review of literature by Nora, Boukouira, Sabrinel, Ferrache Wiam, Yassamine, Ouerdane, Touri, Nabila Souad, Samira, Guemghar, Abdulrazzak, Mohammed, Jobran, Afnan W. M., Keiji, Leila

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Algerian Registry for Inborn Errors of Immunity in Children: Report of 887 Children (1985–2021) by Yagoubi, Abdelghani, Tahiat, Azzeddine, Touri, Nabila Souad, Ladj, Mohamed Samir, Drali, Ouardia, Belaid, Brahim, Mohand-Oussaid, Ayda, Dehimi, Abdelhak, Belbouab, Reda, Ferhani, Yacine, Melzi, Souhila, Guedouar, Assia, Hakem, Saliha, Khemici, Ouardia, Inouri, Yacine, Meddour, Yanis, Dib, Saadeddine, Mansouri, Zohra, Iddir, Samir, Boufersaoui, Abderrahmane, Boudiaf, Houda, Bouhdjila, Abderrachid, Ibsaine, Ouardia, Maouche, Hachemi, Dahlouk, Djazia, Mekki, Azzedine, Bioud, Belkacem, Bouzerar, Zair, Zeroual, Zoulikha, Benhassine, Fadila, Bekkat-Berkani, Dahila, Naamoune, Soumeya, Salah, Samir Sofiane, Chaib, Samia, Attal, Nabila, Bensaadi, Nadia, Bouchair, Nadira, Cherif, Nacira, Kedji, Leila, Bendeddouche, Salih, Atif, Mohamed Lamine, Djenouhat, Kamel, Kechout, Nadia, Djidjik, Reda, Benhalla, Keltoum Nafissa, Smati, Leila, Boukari, Rachida

“…Introduction Inborn errors of immunity (IEI) represent a heterogeneous large group of genetic disorders characterized by susceptibility of affected individuals…”
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X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations by 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

“…Purpose X-linked agammagobulinemia (XLA) is a primary immunodeficiency caused by Bruton’s tyrosine kinase ( BTK ) gene defect. XLA patients have absent or…”
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Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey by Alzyoud, Raed, El-Kholy, Nermeen, Arab, Yousra, Choueiter, Nadine, Harahsheh, Ashraf S., Aselan, Adnan Salem, Kotby, Alyaa, Bouaziz, Asma, Salih, Aso F., Abushhaiwia, Awatif, Alahmadi, Fahad, Agha, Hala M., Elmarsafawy, Hala M., Alrabte, Hanifa, Al-Saloos, Hesham, Boudiaf, Houda, Hijazi, Issa, Bouayed, Kenza, Al Senaidi, Khalfan Salim, Boughammoura, Lamia, Jalal, Maryam, Ladj, Mohamed S., Abu-Shukair, Mohammed E., ElGanzoury, Mona M., Hammadouche, Nacera, Elsamman, Nora, Mouawad, Pierre, Boukari, Rachida, Benalikhoudja, Nassiba, Jdour, Salima, Abu Al-Saoud, Sima Y., Touri, Soued Nabila, Kammoun, Thouraya, Fitouri, Zohra, Dahdah, Nagib

“…Kawasaki Disease (KD) is still the most common acquired heart disease in children below the age of five years; it has been well described in the developed…”
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