| For: | Yasawy MI, Folsch UR, Schmidt WE, Schwend M. Adult hereditary fructose intolerance. World J Gastroenterol 2009; 15(19): 2412-2413 [PMID: 19452588 DOI: 10.3748/wjg.15.2412] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v15/i19/2412.htm |
| Number | Citing Articles |
| 1 |
Min Soo Kim, Jin Soo Moon, Man Jin Kim, Moon-Woo Seong, Sung Sup Park, Jae Sung Ko. Hereditary Fructose Intolerance Diagnosed in Adulthood. Gut and Liver 2021; 15(1) doi: 10.5009/gnl20189
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| 2 |
Rajat Kumar Shah, Sajjad Ahmed Khan, Bijita Aryal, Aakash Khatiwada, Binita Gurubacharya, Shamin Parajuli. Unmasking Hereditary Fructose Intolerance: Turning a Rare Diagnosis Into a Path for Healing. Clinical Case Reports 2025; 13(12) doi: 10.1002/ccr3.71654
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| 3 |
Santhosh Kumar Yasam, Joice Kuzhipalayil Joseph, Senthilkumar Rajagopal. Handbook of Synthetic Biology. 2026; doi: 10.1007/978-981-95-3957-4_41
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| 4 |
Prisca Da Lozzo, Andrea Magnolato, Irene Del Rizzo, Fabio Sirchia, Irene Bruno, Egidio Barbi. When Long-Lasting Food Selectivity Leads to an Unusual Genetic Diagnosis: A Case Report. Journal of Adolescent Health 2019; 64(1) doi: 10.1016/j.jadohealth.2018.07.014
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| 5 |
Fabiana Zingone, Luisa Bertin, Daria Maniero, Michela Palo, Greta Lorenzon, Brigida Barberio, Carolina Ciacci, Edoardo Vincenzo Savarino. Myths and Facts about Food Intolerance: A Narrative Review. Nutrients 2023; 15(23) doi: 10.3390/nu15234969
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| 6 |
Robert H. Lustig. Fructose: It’s “Alcohol Without the Buzz”. Advances in Nutrition 2013; 4(2) doi: 10.3945/an.112.002998
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| 7 |
U. Wendel. Angeborene Stoffwechselkrankheiten bei Erwachsenen. 2014; doi: 10.1007/978-3-642-45188-1_21
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| 8 |
Lalit Bharadia, Deepak Shivpuri. Non responsive celiac disease due to coexisting hereditary fructose intolerance. Indian Journal of Gastroenterology 2012; 31(2) doi: 10.1007/s12664-012-0169-1
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| 9 |
Mustafa Kılıç, Esra Sayar, Suzan İcil, Abdullah Sezer. Genotypic and Phenotypic Characteristics of Turkish Patients with Hereditary Fructose Intolerance. Molecular Syndromology 2026; doi: 10.1159/000551573
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| 10 |
Esra Küpeli Akkol, Michael Aschner. The Role of Phytonutrients in Metabolic Disorders. 2022; doi: 10.1016/B978-0-12-824356-5.00004-7
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| 11 |
Sumit Kumar Singh, Moinak Sen Sarma. Hereditary fructose intolerance: A comprehensive review. World Journal of Clinical Pediatrics 2022; 11(4): 321-329 doi: 10.5409/wjcp.v11.i4.321
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| 12 |
Claire Douillard, Karine Mention, Dries Dobbelaere, Jean-Louis Wemeau, Jean-Marie Saudubray, Marie-Christine Vantyghem. Hypoglycaemia related to inherited metabolic diseases in adults. Orphanet Journal of Rare Diseases 2012; 7(1) doi: 10.1186/1750-1172-7-26
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| 13 |
Teng-San Hsieh, Yu-Hou Yu, Zhen-Fan You, Rong-Jiun Sheu, Jin-Pei Deng, Chung-Shan Yu. Alditols in complex with boronophenylalanine for improving aqueous solubility for boron neutron capture therapy. RSC Pharmaceutics 2026; 3(1) doi: 10.1039/D5PM00180C
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| 14 |
Wendy Marcason. Is Medical Nutrition Therapy (MNT) the Same for Hereditary vs Dietary Fructose Intolerance?. Journal of the American Dietetic Association 2010; 110(7) doi: 10.1016/j.jada.2010.05.016
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| 15 |
Muthukumaran Ponnurangam, Seetharaman Balaji. Tune in to the terrific applications of turanose. European Food Research and Technology 2024; 250(2) doi: 10.1007/s00217-023-04417-4
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| 16 |
Omid Vakili, Alireza Mafi, Morteza Pourfarzam. Liver Disorders Caused by Inborn Errors of Metabolism. Endocrine, Metabolic & Immune Disorders - Drug Targets 2024; 24(2) doi: 10.2174/1871530323666230623120935
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| 17 |
Pascale De Lonlay, Sandrine Dubois, Vassili Valayannopoulos, Eliane Depondt, Chris Ottolenghi, Daniel Rabier. Prise en charge médicale et diététique des maladies héréditaires du métabolisme. 2013; doi: 10.1007/978-2-8178-0046-2_14
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| 18 |
C. Douillard, M.-C. Vantyghem, F. Maillot. Hypoglycémies métaboliques inhabituelles de l’adulte. Médecine des Maladies Métaboliques 2011; 5(4) doi: 10.1016/S1957-2557(11)70272-3
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| 19 |
Gavin Halbert, Moira Elliott, Steven Ford, Lindsay Dick, Elke Schmidt. Improved pharmaceutical stability of a boronphenylalanine mannitol formulation for boron neutron capture therapy. European Journal of Pharmaceutical Sciences 2013; 48(4-5) doi: 10.1016/j.ejps.2013.01.008
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| 20 |
Manuela Scorza, Ausilia Elce, Federica Zarrilli, Renato Liguori, Felice Amato, Giuseppe Castaldo. Genetic Diseases That Predispose to Early Liver Cirrhosis. International Journal of Hepatology 2014; 2014 doi: 10.1155/2014/713754
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| 21 |
M. Yu. Yukina, E. A. Troshina, N. F. Nuralieva, S. V. Popov, N. G. Mokrysheva. Congenital disorders of glucose metabolism in adults with nondiabetic hypoglycemia. Obesity and metabolism 2024; 21(2) doi: 10.14341/omet13052
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| 22 |
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| 23 |
Leszek Garbowski, Marzena Walasek, Rafał Firszt, Ewelina Chilińska-Kopko, Paulina Błażejewska-Gała, Daniel Popielnicki, Zofia Dzięcioł-Anikiej. A Case Study of a Rare Disease (Fructosemia) Diagnosed in a Patient with Abdominal Pain. Journal of Clinical Medicine 2024; 13(12) doi: 10.3390/jcm13123394
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| 24 |
Shanshan Liu, Hongyan Bai, Qian Sun, Weibing Zhang, Junhong Qian. Naphthalimide-based fluorescent photoinduced electron transfer sensors for saccharides. RSC Advances 2015; 5(4) doi: 10.1039/C4RA13414A
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| 25 |
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| 26 |
Pietro Vajro, Lorenza Ferrante, Selvaggia Lenta, Claudia Mandato, Marcello Persico. Management of adults with paediatric-onset chronic liver disease: Strategic issues for transition care. Digestive and Liver Disease 2014; 46(4) doi: 10.1016/j.dld.2013.10.018
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| 27 |
Martha Catalina Morales-Alvarez, Maria Laura Ricardo-Silgado, Hernan Nicolas Lemus, Deyanira González-Devia, Carlos O Mendivil. Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3′ untranslated region of the aldolase B gene. SAGE Open Medical Case Reports 2019; 7 doi: 10.1177/2050313X18823098
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| 28 |
Ninna Karsbæk Senftleber, Stina Ramne, Ida Moltke, Marit Eika Jørgensen, Anders Albrechtsen, Torben Hansen, Mette K Andersen. Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future Perspectives. The Application of Clinical Genetics 2023; doi: 10.2147/TACG.S401712
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