SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Garry Brown, Defects of thiamine transport and metabolism, Journal of Inherited Metabolic Disease, 2014, 37, 4, 577

    CrossRef

  2. 2
    M. Ramsi, C. Mowbray, G. Hartman, N. Pageler, Severe lactic acidosis and multiorgan failure due to thiamine deficiency during total parenteral nutrition, Case Reports, 2014, 2014, jun03 1, bcr2014205264

    CrossRef

  3. 3
    Mark Marinella, Nutrition and Bariatric Surgery, 2014,

    CrossRef

  4. 4
    Vikas Dua, Satya P. Yadav, Vijay Kumar, Afaq Ahmed Khan, Ratna Puri, Ishwar C. Verma, Sarah E. Flanagan, Sian Ellard, Anupam Sachdeva, Thiamine responsive megaloblastic anemia with a novel SLC19A2 mutation presenting with myeloid maturational arrest, Pediatric Blood & Cancer, 2013, 60, 7
  5. 5
    Charles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, Juergen Grulich-Henn, Abdelhadi M Habeb, Khalid Hussain, Renata Pomahacova, Krystyna Matyka, Mohamed Abdullah, Andrew T Hattersley, Sian Ellard, Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia, Pediatric Diabetes, 2012, 13, 4
  6. 6
    O. Bouyahia, M. Ouderni, F. Ben Mansour, N. Matoussi, F. Khaldi, Diabetic acido-ketosis revealing thiamine-responsive megaloblastic anemia, Annales d'Endocrinologie, 2009, 70, 6, 477

    CrossRef

  7. 7
    Anke K. Bergmann, Inderneel Sahai, Jill F. Falcone, Judy Fleming, Adam Bagg, Caterina Borgna-Pignati, Robin Casey, Luca Fabris, Elizabeth Hexner, Lulu Mathews, Maria Leticia Ribeiro, Klaas J. Wierenga, Ellis J. Neufeld, Thiamine-Responsive Megaloblastic Anemia: Identification of Novel Compound Heterozygotes and Mutation Update, The Journal of Pediatrics, 2009, 155, 6, 888

    CrossRef

  8. 8
    Mark A. Marinella, Anemia Following Roux-en-Y Surgery for Morbid Obesity: A Review, Southern Medical Journal, 2008, 101, 10, 1024

    CrossRef

  9. 9
    S. Kurtoglu, N. Hatipoglu, M. Keskin, M. Kendirci, M. Akcakus, Thiamine Withdrawal Can Lead to Diabetic Ketoacidosis in Thiamine Responsive Megaloblastic Anemia: Report of Two Siblings, Journal of Pediatric Endocrinology and Metabolism, 2008, 21, 4

    CrossRef

  10. 10
    A. S Alzahrani, E. Baitei, M. Zou, Y. Shi, Thiamine transporter mutation: an example of monogenic diabetes mellitus, European Journal of Endocrinology, 2006, 155, 6, 787

    CrossRef

  11. 11
    Christopher Ricketts, Jayne Minton, Jacob Samuel, Indra Ariyawansa, Jerry Wales, Ivan Lo, Timothy Barrett, Thiamine-responsive megaloblastic anaemia syndrome: Long-term follow-up and mutation analysis of seven families, Acta Paediatrica, 2006, 95, 1, 99

    CrossRef

  12. 12
    Christopher J. Ricketts, Jayne A. Minton, Jacob Samuel, Indra Ariyawansa, Jerry K. Wales, Ivan F. Lo, Timothy G. Barrett, Thiamine-responsive megaloblastic anaemia syndrome: Long-term follow-up and mutation analysis of seven families, Acta Paediatrica, 2006, 95, 1
  13. 13
    Alan Davidson, Patricia S Hartley, Peter Berman, Margaret H G Shuttleworth, Megaloblastic anaemia, diabetes and deafness in a 2-year-old child, Journal of Endocrinology, Metabolism and Diabetes of South Africa, 2005, 10, 2, 62

    CrossRef

  14. 14
    William H. Lagarde, Louis E. Underwood, Billie M. Moats-Staats, Ali S. Calikoglu, Novel mutation in the SLC19A2 gene in an African-American female with thiamine-responsive megaloblastic anemia syndrome, American Journal of Medical Genetics Part A, 2004, 125A, 3
  15. 15
    Kimihiko Oishi, George Diaz, Bruce Gelb, Thiamine, 2003,

    CrossRef

  16. 16
    Mehmet Akif Ozdemir, Mustafa Akcakus, Selim Kurtoglu, Tamer Gunes, Yasemin Altuner Torun, TRMA syndrome (thiamine-responsive megaloblastic anemia): a case report and review of the literature, Pediatric Diabetes, 2002, 3, 4
  17. 17
    Sami Gritli, Souheil Omar, Elena Tartaglini, Souha Guannouni, Judith C. Fleming, Mara P. Steinkamp, Charles I. Berul, Raouf Hafsia, Sarrah Baltagi-Ben Jilani, Ali Belhani, Mongi Hamdi, Ellis J. Neufeld, A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome, British Journal of Haematology, 2001, 113, 2
  18. 18
    Mouhab Ayas, Abdullah Al-Jefri, Mahmoud M. Mustafa, Mohamad Al-Mahr, Loubna Shalaby, Hassan Solh, Congenital sideroblastic anaemia successfully treated using allogeneic stem cell transplantation, British Journal of Haematology, 2001, 113, 4
  19. 19
    Timothy Geoffrey Barrett, Mitochondrial diabetes, DIDMOAD and other inherited diabetes syndromes, Best Practice & Research Clinical Endocrinology & Metabolism, 2001, 15, 3, 325

    CrossRef

  20. 20
    Ellis J. Neufeld, Judith C. Fleming, Elena Tartaglini, Mara P. Steinkamp, Thiamine-Responsive Megaloblastic Anemia Syndrome: A Disorder of High-Affinity Thiamine Transport, Blood Cells, Molecules, and Diseases, 2001, 27, 1, 135

    CrossRef

  21. 21
    Jacques Gardais, Dyshaemopoiesis in adults: a practical classification for diagnosis and management, Leukemia Research, 2000, 24, 8, 641

    CrossRef

  22. 22
    Tal Raz, Valentina Labay, Dana Baron, Raymonde Szargel, Yefim Anbinder, Tim Barrett, Wolfgang Rabl, Marcos B. Viana, Hanna Mandel, Andre Baruchel, Jean-Michel Cayuela, Nadine Cohen, The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families, Human Mutation, 2000, 16, 1
  23. 23
    F.M. Meire, M.M. Van Genderen, K. Lemmens, M.H. Ens-Dokkum, Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy, Ophthalmic Genetics, 2000, 21, 4, 243

    CrossRef

  24. 24
    Ewan R. Pearson, Andrew T. Hattersley, Monogenic Disorders of the β-Cell, International Textbook of Diabetes Mellitus,
  25. 25
    Quantitative Changes in Blood Cells,