| For: | Zeng HS, Zhang ZH, Hu Y, Zheng GL, Wang J, Zhang JW, Guo YX. Alagille syndrome associated with total anomalous pulmonary venous connection and severe xanthomas: A case report. World J Clin Cases 2022; 10(25): 8932-8938 [PMID: 36157644 DOI: 10.12998/wjcc.v10.i25.8932] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i25/8932.htm |
| Number | Citing Articles |
| 1 |
Priya Sharma, Deepti Abbey. Alagille Syndrome: Unraveling the Complexities of Genotype–Phenotype Relationships and Exploring Avenues for Improved Diagnosis and Treatment. Cell Biology International 2025; 49(5) doi: 10.1002/cbin.70009
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| 2 |
L. A. Levchenko, K. S. Zizyukina, T. Yu. Kravchenko, T. Lungu, A. A. Petrichenko, А. A. Gryaznova, A. Ya. Ilyina, H. A. Sarkisyan. Modern approaches to the management of children with Alagille syndrome. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 2025; 70(4) doi: 10.21508/1027-4065-2025-70-4-29-38
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| 3 |
Federico D'Antonio, María Teresa Politi, Ana Emilia Ruiz Mariani, Mariana del Rosario Fernández, Fausto José Ochoa Toro, Gladys Haydee Salgado, Diana Mariela Mouratian. Cardiovascular features of Alagille syndrome in hospitalized pediatric patients: a tertiary center experience. Progress in Pediatric Cardiology 2026; 82 doi: 10.1016/j.ppedcard.2026.101930
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| 4 |
Gustavo Dib Dangoni, Anne Caroline Barbosa Teixeira, Talita Ferreira Aguiar, Sofia Mizuho Miura Sugayama, Vicente Odone Filho, Débora Romeo Bertola, Ana Cristina Victorino Krepischi. A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation. Pediatric Blood & Cancer 2023; 70(7) doi: 10.1002/pbc.30311
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