XX Ovarian Dysgenesis Is Caused by a PSMC3IP/ HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription von Zangen, David, Kaufman, Yotam, Zeligson, Sharon, Perlberg, Shira, Fridman, Hila, Kanaan, Moein, Abdulhadi-Atwan, Maha, Abu Libdeh, Abdulsalam, Gussow, Ayal, Kisslov, Irit, Carmel, Liran, Renbaum, Paul, Levy-Lahad, Ephrat

Volltext

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity von Faingelernt, Yaniv, Hershkovitz, Eli, Abu‐Libdeh, Bassam, Abedrabbo, Amal, Abu‐Rmaileh Amro, Sara, Zarivach, Raz, Zangen, David, Lavi, Eran, Haim, Alon, Parvari, Ruti, Abu‐Libdeh, Abdulsalam

Volltext

Eligibility for growth hormone therapy in children born small for gestational age is substantially lower than expected von Lavi, Eran, Shafrir, Asher, Halloun, Rana, Basel, Itai, Eventov Friedman, Smadar, Abu‐Libdeh, Abdulsalam, Shoob, Hanna, Stein‐Zamir, Chen, Zangen, David Haim

Volltext

Growth hormone therapy for children with Duchenne muscular dystrophy and glucocorticoid induced short stature von Lavi, Eran, Cohen, Amitay, Libdeh, Abdulsalam Abu, Tsabari, Reuven, Zangen, David, Dor, Talya

Volltext

Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy von Abu Libdeh, Abdulsalam, Levy-Khademi, Floris, Abdulhadi-Atwan, Maha, Bosin, Emily, Korner, Mira, White, Perrin C, Zangen, David H

Volltext

Propionic acidemia mimicking diabetic ketoacidosis von Dweikat, Imad M, Naser, Enas N, Abu Libdeh, Abdulsalam I, Naser, Osama J, Abu Gharbieh, Najwan N, Maraqa, Nizar F, Abu Libdeh, Bassam Y

Volltext

Combined Gestational Age- and Birth Weight–Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia von Pode-Shakked, Naomi, Blau, Ayala, Pode-Shakked, Ben, Tiosano, Dov, Weintrob, Naomi, Eyal, Ori, Zung, Amnon, Levy-Khademi, Floris, Tenenbaum-Rakover, Yardena, Zangen, David, Gillis, David, Pinhas-Hamiel, Orit, Loewenthal, Neta, de Vries, Liat, Landau, Zohar, Rachmiel, Mariana, Abu-Libdeh, Abdulsalam, Eliakim, Alon, Strich, David, Koren, Ilana, German, Alina, Sack, Joseph, Almashanu, Shlomo

Volltext

Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation von Molho-Pessach, Vered, Ramot, Yuval, Mogilevsky, Maxim, Cohen-Daniel, Leonor, Eisenstein, Eli M, Abu-Libdeh, Abdulsalam, Siam, Ihab, Berger, Michael, Karni, Rotem, Zlotogorski, Abraham

Volltext

RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1 von Abu-Libdeh, Bassam, Jhujh, Satpal S, Dhar, Srijita, Sommers, Joshua A, Datta, Arindam, Longo, Gabriel Mc, Grange, Laura J, Reynolds, John J, Cooke, Sophie L, McNee, Gavin S, Hollingworth, Robert, Woodward, Beth L, Ganesh, Anil N, Smerdon, Stephen J, Nicolae, Claudia M, Durlacher-Betzer, Karina, Molho-Pessach, Vered, Abu-Libdeh, Abdulsalam, Meiner, Vardiella, Moldovan, George-Lucian, Roukos, Vassilis, Harel, Tamar, Brosh, Jr, Robert M, Stewart, Grant S

Volltext

Lessons Learned From COVID-19 Lockdown: An ASPED/MENA Study on Lifestyle Changes and Quality of Life During Ramadan Fasting in Children and Adolescents Living With Type 1 Diabetes von Babiker, Amir, Elbarbary, Nancy Samir, Alaqeel, Bothainah, Al Noaim, Khalid, Al Yaarubi, Saif, Al-Abdulrazzaq, Dalia, Al-Kandari, Hessa, Alkhayyat, Haya, Odeh, Rasha, Babiker, Omer, Abu-Libdeh, Abdulsalam, Aljohani, Amal, Al Abdul Salam, Noof, Al-Juailla, Fatima, Masuadi, Emad, Deeb, Asma, Weissberg-Benchell, Jill, Gregory, Alice M., Hassanein, Mohamed, Al Alwan, Ibrahim

Volltext

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence von Abdulhadi-Atwan, Maha, Bushman, Jeremy, Bushmann, Jeremy, Tornovsky-Babaey, Sharona, Perry, Avital, Abu-Libdeh, Abdulsalam, Glaser, Benjamin, Shyng, Show-Ling, Zangen, David H

Volltext

9 Monogenic diabetes: the Palestinian experience von Abu-Libdeh, Abdulsalam

Volltext

Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village von Rowlands, Amanda, Deeb, Asma, Ladjouze, Asmahane, Hamza, Rasha T, Musa, Salwa A, Raza, Jamal, Jennane, Farida, Abu-Libdeh, Abdulsalam, Chanoine, Jean-Pierre, Fadila, Bouferoua, Hana, Delileche, Larbi, Djahlat, Mustapha, Noumi, Alkhayyat, Haya, Douksie, Abdourahman, Rabbani, Ali, Al-Jumaili, Ali, Odeh, Rasha, Alkandari, Hessa, Tfayli, Hala, Abusrewil, Suleiman, Ghawil, Millad, senani, Aisha Al, Abu-Libdeh, Abdulsalam, Alkhalaf, Fawziya, Habeb, Abdelhadi, Ahmad, Noman, Elshareef, Omer, Abdullah, Mohamed, Al-Hassan, Olivia, Karah, Dima, Hachicha, Mongia, Alshakka, Mohammed

Volltext

Familial Autosomal Recessive Renal Tubular Acidosis: Importance of Early Diagnosis von Vivante, Asaf, Lotan, Danny, Pode-Shakked, Naomi, Landau, Daniel, Svec, Peter, Nampoothiri, Sheela, Verma, Ishwar, Abu-Libdeh, Abdulsalam, Bockenhauer, Detlef, Dekel, Benjamin, Anikster, Yair

Volltext

Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield von Rips, Jonathan, Halstuk, Orli, Fuchs, Adina, Lang, Ziv, Sido, Tal, Gershon-Naamat, Shiri, Abu-Libdeh, Bassam, Edvardson, Simon, Salah, Somaya, Breuer, Oded, Hadhud, Mohamad, Eden, Sharon, Simon, Itamar, Slae, Mordechai, Damseh, Nadirah S., Abu-Libdeh, Abdulsalam, Eskin-Schwartz, Marina, Birk, Ohad S., Varga, Julia, Schueler-Furman, Ora, Rosenbluh, Chaggai, Elpeleg, Orly, Yanovsky-Dagan, Shira, Mor-Shaked, Hagar, Harel, Tamar

Volltext

Retraction Notice to “Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation” von Molho-Pessach, Vered, Ramot, Yuval, Mogilevsky, Maxim, Cohen-Daniel, Leonor, Eisenstein, Eli M., Abu-Libdeh, Abdulsalam, Siam, Ihab, Berger, Michael, Karni, Rotem, Zlotogorski, Abraham

Volltext

Global Emergencies in Child Health: Challenges and Solutions—Viewpoint and Recommendations from the European Paediatric Association and the International Pediatric Association von Thacker, Naveen, Hasanoglu, Enver, Dipesalema, Joel, Namazova-Baranova, Leyla, Pulungan, Aman, Alden, Errol, Abu-Libdeh, Abdulsalam, Díaz, Juan José, Hoey, Hilary, Kyne, Louise, Vural, Mehmet, Riestra, Sergio, Camcıoğlu, Yıldız, Mujkic, Aida, Carrasco-Sanz, Angel, Pettoello-Mantovani, Massimo

Volltext

Wolfram Syndrome-2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review von Ateya, Rania, Ciecierega, Thomas, Abusamra, Muttaz, Abuawwad, Motee, Abu-Libdeh, Abdulsalam, Sultan, Mutaz

Volltext

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and inc... von Weinberg-Shukron, Ariella, Abu-Libdeh, Abdulsalam, Zhadeh, Fouad, Carmel, Liran, Kogot-Levin, Aviram, Kamal, Lara, Kanaan, Moien, Zeligson, Sharon, Renbaum, Paul, Levy-Lahad, Ephrat, Zangen, David

Volltext

GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome von Danielpur, Liron, Sohn, Yang-Sung, Karmi, Ola, Fogel, Chen, Zinger, Adar, Abu-Libdeh, Abdulsalam, Israeli, Tal, Riahi, Yael, Pappo, Orit, Birk, Ruth, Zangen, David H, Mittler, Ron, Cabantchik, Zvi-Ioav, Cerasi, Erol, Nechushtai, Rachel, Leibowitz, Gil

Volltext