Citation of this article
Corresponding Author of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (4115)
All Articles published online
|
May 21, 2009 (publication date) through Feb 15, 2025
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v15/i19/2412.htm |
| Number | Citing Articles |
| 1 |
Omid Vakili, Alireza Mafi, Morteza Pourfarzam. Liver Disorders Caused by Inborn Errors of Metabolism. Endocrine, Metabolic & Immune Disorders - Drug Targets 2024; 24(2): 194 doi: 10.2174/1871530323666230623120935
|
| 2 |
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; : 229 doi: 10.1007/978-2-8178-0046-2_14
|
| 3 |
C. Douillard, M.-C. Vantyghem, F. Maillot. Hypoglycémies métaboliques inhabituelles de l’adulte. Médecine des Maladies Métaboliques 2011; 5(4): 393 doi: 10.1016/S1957-2557(11)70272-3
|
| 4 |
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): 735 doi: 10.1016/j.ejps.2013.01.008
|
| 5 |
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): 142 doi: 10.5009/gnl20189
|
| 6 |
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: 1 doi: 10.1155/2014/713754
|
| 7 |
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): 137 doi: 10.1016/j.jadohealth.2018.07.014
|
| 8 |
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): 4969 doi: 10.3390/nu15234969
|
| 9 |
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): 136 doi: 10.14341/omet13052
|
| 10 |
|
| 11 |
Robert H. Lustig. Fructose: It’s “Alcohol Without the Buzz”. Advances in Nutrition 2013; 4(2): 226 doi: 10.3945/an.112.002998
|
| 12 |
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): 3394 doi: 10.3390/jcm13123394
|
| 13 |
Shanshan Liu, Hongyan Bai, Qian Sun, Weibing Zhang, Junhong Qian. Naphthalimide-based fluorescent photoinduced electron transfer sensors for saccharides. RSC Advances 2015; 5(4): 2837 doi: 10.1039/C4RA13414A
|
| 14 |
U. Wendel. Angeborene Stoffwechselkrankheiten bei Erwachsenen. 2014; : 193 doi: 10.1007/978-3-642-45188-1_21
|
| 15 |
Lalit Bharadia, Deepak Shivpuri. Non responsive celiac disease due to coexisting hereditary fructose intolerance. Indian Journal of Gastroenterology 2012; 31(2): 83 doi: 10.1007/s12664-012-0169-1
|
| 16 |
|
| 17 |
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): 295 doi: 10.1016/j.dld.2013.10.018
|
| 18 |
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
|
| 19 |
Esra Küpeli Akkol, Michael Aschner. The Role of Phytonutrients in Metabolic Disorders. 2022; : 3 doi: 10.1016/B978-0-12-824356-5.00004-7
|
| 20 |
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
|
| 21 |
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): 26 doi: 10.1186/1750-1172-7-26
|
| 22 |
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; : 31 doi: 10.2147/TACG.S401712
|
| 23 |
Wendy Marcason. Is Medical Nutrition Therapy (MNT) the Same for Hereditary vs Dietary Fructose Intolerance?. Journal of the American Dietetic Association 2010; 110(7): 1128 doi: 10.1016/j.jada.2010.05.016
|
| 24 |
Muthukumaran Ponnurangam, Seetharaman Balaji. Tune in to the terrific applications of turanose. European Food Research and Technology 2024; 250(2): 375 doi: 10.1007/s00217-023-04417-4
|