Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation von Cuchet-Lourenço, Delphine, Eletto, Davide, Wu, Changxin, Plagnol, Vincent, Papapietro, Olivier, Curtis, James, Ceron-Gutierrez, Lourdes, Bacon, Chris M, Hackett, Scott, Alsaleem, Badr, Maes, Mailis, Gaspar, Miguel, Alisaac, Ali, Goss, Emma, AlIdrissi, Eman, Siegmund, Daniela, Wajant, Harald, Kumararatne, Dinakantha, AlZahrani, Mofareh S, Arkwright, Peter D, Abinun, Mario, Doffinger, Rainer, Nejentsev, Sergey

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Enteroendocrine Dysfunction in Two Saudi Sisters von Ahmed, Amna Basheer M., Alsaleem, Badr M. Rasheed

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Tricho-hepato-enteric syndrome: Retrospective multicenter experience in Saudi Arabia von Alsaleem, Badr, Hasosah, Mohammed, Ahmed, Amna, Al Hatlani, Maher, Alanazi, Aziz, Al-Hussaini, Abdulrahman, Asery, Ali, Alghamdi, Khalid, AlRuwaithi, Muhanad, Khormi, Musa, Al Sarkhy, Ahmed, Alshamrani, Ali

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Viral dysbiosis in children with new-onset celiac disease von El Mouzan, Mohammad, Assiri, Asaad, Al Sarkhy, Ahmed, Alasmi, Mona, Saeed, Anjum, Al-Hussaini, Abdulrahman, AlSaleem, Badr, Al Mofarreh, Mohammad

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Diagnostic delay of pediatric inflammatory bowel disease in Saudi Arabia von El Mouzan, Mohammad, AlSaleem, Badr, Hasosah, Mohammed, Al-Hussaini, Abdulrahman, Al Anazi, Aziz, Saadah, Omar, Al Sarkhy, Ahmed, Al Mofarreh, Mohammad, Assiri, Asaad

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KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon von Almannai, Mohammed, AlAbdi, Lama, Maddirevula, Sateesh, Alotaibi, Maha, Alsaleem, Badr M., Aljadhai, Yaser I., Alsaif, Hessa S., Abukhalid, Musaad, Alkuraya, Fowzan S

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Fungal Dysbiosis in Children with Celiac Disease von El Mouzan, Mohammad, Al-Hussaini, Abdulrahman, Fanelli, Brian, Assiri, Asaad, AlSaleem, Badr, Al Mofarreh, Mohammad, Al Sarkhy, Ahmed, Alasmi, Mona

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Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics von Maddirevula, Sateesh, Kuwahara, Hiroyuki, Ewida, Nour, Shamseldin, Hanan E., Patel, Nisha, Alzahrani, Fatema, AlSheddi, Tarfa, AlObeid, Eman, Alenazi, Mona, Alsaif, Hessa S., Alqahtani, Maha, AlAli, Maha, Al Ali, Hatoon, Helaby, Rana, Ibrahim, Niema, Abdulwahab, Firdous, Hashem, Mais, Hanna, Nadine, Monies, Dorota, Derar, Nada, Alsagheir, Afaf, Alhashem, Amal, Alsaleem, Badr, Alhebbi, Hamoud, Wali, Sami, Umarov, Ramzan, Gao, Xin, Alkuraya, Fowzan

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Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects von Janecke, Andreas R., Liu, Xiaoqin, Adam, Rüdiger, Punuru, Sumanth, Viestenz, Arne, Strauß, Valeria, Laass, Martin, Sanchez, Elizabeth, Adachi, Roberto, Schatz, Martha P., Saboo, Ujwala S., Mittal, Naveen, Rohrschneider, Klaus, Escher, Johanna, Ganesh, Anuradha, Al Zuhaibi, Sana, Al Murshedi, Fathiya, AlSaleem, Badr, Alfadhel, Majid, Al Sinani, Siham, Alkuraya, Fowzan S., Huber, Lukas A., Müller, Thomas, Heidelberger, Ruth, Janz, Roger

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Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea von Alsaleem, Badr M. Rasheed, Ahmed, Amna Basheer M., Fageeh, Musa Ahmad

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Unusual Manifestation of Ulcerative Colitis von Ahmed, Amna Basheer M., Alsaleem, Badr M. Rasheed

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Outcome of biliary atresia among Saudi children: A tertiary care center experience von Holdar, Sinan, Alsaleem, Badr, Asery, Ali, Al-Hussaini, Abdulrahman

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Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene von Ahmed, Amna Basheer M., Alsaleem, Badr M. Rasheed

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Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure von Al-Hussaini, Abdulrahman, MD, Faqeih, Eissa, MD, El-Hattab, Ayman W., MD, Alfadhel, Majid, Asery, Ali, MD, Alsaleem, Badr, MD, Bakhsh, Eman, MD, Ali, Ashraf, MD, Alasmari, Ali, MD, Lone, Khurram, MD, Nahari, Ahmed, MD, Eyaid, Wafaa, MD, Al Balwi, Mohammed, MD, Craig, Kate, PhD, Butterworth, Anna, BSc, He, Langping, PhD, Taylor, Robert W., PhD, FRCPath

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Corrigendum to “Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene” von Ahmed, Amna Basheer M., Alsaleem, Badr M. Rasheed

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Clinical, Biochemical, and Molecular Characterization of Neonatal-Onset Dubin-Johnson Syndrome in a Large Case Series From the Arabs von Al-Hussaini, Abdulrahman, AlSaleem, Badr, AlHomaidani, Hamad, Asery, Ali, Alruwaithi, Muhanad, Alameer, Mohammed, Afashah, Waleed, Salman, Bashir Muhammed, Almontashiri, Naif

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Use of oral iron in managing iron deficiency anemia in children with intestinal failure von Alsaleem, Badr, Albanyan, Nora, Alamer, Ahmad, Asdaq, Syed Mohammed Basheeruddin, Mohzari, Yahya, Alrahili, Mohannad M., Albasheer, Amna B., Alrashed, Ahmed A., Alamri, Abdulhakeem S., Alsanie, Walaa F., Alhomrani, Majid

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Liver Failure Among Young Saudi Infants: Etiology, Clinical Presentation, and Outcome von Lone, Khurram Sadiq, AlSaleem, Badr, Asery, Ali, Bashir, Muhammed Salman, Al-Hussaini, Abdulrahman

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Liver Failure Among Young Saudi Infants: Etiology, Clinical Presentation, and Outcome von Lone, Khurram Sadiq, AlSaleem, Badr, Asery, Ali, Bashir, Muhammed Salman, Al-Hussaini, Abdulrahman

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Liver Failure Among Young Saudi Infants von Lone, Khurram Sadiq, AlSaleem, Badr, Asery, Ali, Bashir, Muhammed Salman, Al‐Hussaini, Abdulrahman

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