日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Burden of Congenital Hypothyroidism Without Newborn Screening: Clinical and Cognitive Findings from a Multicenter Study in Algeria

未进行新生儿筛查的先天性甲状腺功能减退症的负担:阿尔及利亚一项多中心研究的临床和认知发现

Djermane, Adel; Ouarezki, Yasmine; Boulesnane, Kamelia; Kherra, Sakina; Bouferoua, Fadila; Bessahraoui, Mimouna; Selim, Nihad; Djahlat, Larbi; Mohammedi, Kahina; Bouziane Nedjadi, Karim; Abes, Hakima; Bensalah, Meriem; Lograb, Dyaeddine; Abdelaziz, Foued; Douiri, Dalila; Djebari, Soumia; Demdoum, Mohamed Seghir; Rouabeh, Nadira; Oussalah, Meriem; Van Vliet, Guy; Ladjouze, Asmahane

Inborn Errors of Immunity in Algerian Children and Adults: A Single-Center Experience Over a Period of 13 Years (2008-2021)

阿尔及利亚儿童和成人先天性免疫缺陷:单中心13年(2008-2021年)经验

Belaid, Brahim; Lamara Mahammed, Lydia; Drali, Ouardia; Oussaid, Aida Mohand; Touri, Nabila Souad; Melzi, Souhila; Dehimi, Abdelhak; Berkani, Lylia Meriem; Merah, Fatma; Larab, Zineb; Allam, Ines; Khemici, Ouarda; Kirane, Sonya Yasmine; Boutaba, Mounia; Belbouab, Reda; Bekkakcha, Hadjira; Guedouar, Assia; Chelali, Abdelhakim; Baamara, Brahim; Noui, Djamila; Baaziz, Hadda; Rezak, Radia; Azzouz, Sidi Mohamed; Aichaoui, Malika; Moktefi, Assia; Benhatchi, Redha Mohamed; Oussalah, Meriem; Benaissa, Naila; Laredj, Amel; Bouchetara, Assia; Adria, Abdelkader; Habireche, Brahim; Tounsi, Noureddine; Dahmoun, Fella; Touati, Rabah; Boucenna, Hamza; Bouferoua, Fadila; Sekfali, Lynda; Bouhafs, Nadjet; Aboura, Rawda; Kherra, Sakina; Inouri, Yacine; Dib, Saadeddine; Medouri, Nawel; Khelfaoui, Noureddine; Redjedal, Aicha; Zelaci, Amara; Yahiaoui, Samah; Medjadj, Sihem; Touhami, Tahar Khelifi; Kadi, Ahmed; Amireche, Fouzia; Frada, Imane; Houasnia, Shahrazed; Benarab, Karima; Boubidi, Chahynez; Ferhani, Yacine; Benalioua, Hayet; Sokhal, Samia; Benamar, Nadia; Aggoune, Samira; Hadji, Karima; Bellouti, Asma; Rahmoune, Hakim; Boutrid, Nada; Okka, Kamelia; Ammour, Assia; Saadoune, Houssem; Amroun, Malika; Belhadj, Hayet; Ghanem, Amina; Abbaz, Hanane; Boudrioua, Sana; Zebiche, Besma; Ayad, Assia; Hamadache, Zahra; Ouaras, Nassima; Achour, Nassima; Bouchair, Nadira; Boudiaf, Houda; Bekkat-Berkani, Dahila; Maouche, Hachemi; Bouzrar, Zahir; Aissat, Lynda; Ibsaine, Ouardia; Bioud, Belkacem; Kedji, Leila; Dahlouk, Djazia; Bensmina, Manoubia; Radoui, Abdelkarim; Bessahraoui, Mimouna; Bensaadi, Nadia; Mekki, Azzeddine; Zeroual, Zoulikha; Chan, Koon-Wing; Leung, Daniel; Tebaibia, Amar; Ayoub, Soraya; Mekideche, Dalila; Gharnaout, Merzak; Casanova, Jean Laurent; Puel, Anne; Lau, Yu Lung; Cherif, Nacira; Ladj, Samir; Smati, Leila; Boukari, Rachida; Benhalla, Nafissa; Djidjik, Reda

Hypogonadism in Prader-Willi syndrome from birth to adulthood: a 28-year experience in a single centre

普拉德-威利综合征患者从出生到成年的性腺功能减退:单中心28年经验

Kherra, Sakina; Forsyth Paterson, Wendy; Cizmecioglu, Filiz Mine; Jones, Jeremy Huw; Kourime, Mariam; Elsedfy, Heba Hassan; Tawfik, Sameh; Kyriakou, Andreas; Shaikh, Mohamad Guftar; Donaldson, Malcolm David Cairns

Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

普拉德-威利综合征的新生儿特征;出生后第一周内进行诊断的必要性

Çizmecioğlu, Filiz Mine; Jones, Jeremy Huw; Paterson, Wendy Forsyth; Kherra, Sakina; Kourime, Mariam; McGowan, Ruth; Shaikh, M Guftar; Donaldson, Malcolm

Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation

与 ESR1 功能丧失突变相关的家族性多发性雌激素不敏感症

Bernard, Valérie; Kherra, Sakina; Francou, Bruno; Fagart, Jérôme; Viengchareun, Say; Guéchot, Jérôme; Ladjouze, Asmahane; Guiochon-Mantel, Anne; Korach, Kenneth S; Binart, Nadine; Lombès, Marc; Christin-Maitre, Sophie