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Journal Abstract Search

115 related items for PubMed ID: 38465704

  • 1. Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities.
    Dange NS, Shah N, Oza C, Sharma J, Singhal J, Yewale S, Mondkar S, Ambike S, Khadilkar V, Khadilkar AV.
    J Pediatr Endocrinol Metab; 2024 May 27; 37(5):434-440. PubMed ID: 38465704
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  • 3. Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature.
    Simsek E, Simsek T, Tekgül S, Hosal S, Seyrantepe V, Aktan G.
    Acta Paediatr; 2003 May 27; 92(1):55-61. PubMed ID: 12650300
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  • 4. Lower Urinary Tract Dysfunction and Associated Pons Volume in Patients with Wolfram Syndrome.
    Rove KO, Vricella GJ, Hershey T, Thu MH, Lugar HM, Vetter J, Marshall BA, Austin PF.
    J Urol; 2018 Nov 27; 200(5):1107-1113. PubMed ID: 29883657
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  • 6. [Urinary disorders of Wolfram syndrome. Clinical and urodynamic analysis from 6 observations].
    Leroux C, Grasland M, Turmel N, Le Breton F, Chesnel C, Hentzen C, Amarenco G.
    Prog Urol; 2020 Mar 27; 30(4):205-208. PubMed ID: 31761518
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  • 7. An adolescent male with persistent urinary symptoms.
    Saha S, Sinha R.
    Pediatr Nephrol; 2024 Nov 27; 39(11):3209-3211. PubMed ID: 38842721
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  • 8. [Wolfram syndrome: clinical and genetic analysis in two sisters].
    Conart JB, Maalouf T, Jonveaux P, Guerci B, Angioi K.
    J Fr Ophtalmol; 2011 Oct 27; 34(8):543-6. PubMed ID: 21632151
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  • 11. The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family.
    Hong J, Zhang YW, Zhang HJ, Jia HY, Zhang Y, Ding XY, Zhou DY, Chen HP, Jiang XH, Cui B, Li XY, Ning G.
    Endocrine; 2009 Apr 27; 35(2):151-7. PubMed ID: 19160074
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  • 12. Wolfram syndrome: Portuguese research.
    Ferreras C, Gorito V, Pedro J, Ferreira S, Costa C, Santos Silva R, Castro Correia C.
    Endokrynol Pol; 2021 Apr 27; 72(4):353-356. PubMed ID: 34010437
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  • 15. Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis.
    Sherif M, Demirbilek H, Çayır A, Tahir S, Çavdarlı B, Demiral M, Cebeci AN, Vurallı D, Rahman SA, Unal E, Büyükyılmaz G, Baran RT, Özbek MN, Hussain K.
    J Clin Res Pediatr Endocrinol; 2021 Feb 26; 13(1):34-43. PubMed ID: 32938580
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  • 16. Wolfram syndrome in the Japanese population; molecular analysis of WFS1 gene and characterization of clinical features.
    Matsunaga K, Tanabe K, Inoue H, Okuya S, Ohta Y, Akiyama M, Taguchi A, Kora Y, Okayama N, Yamada Y, Wada Y, Amemiya S, Sugihara S, Nakao Y, Oka Y, Tanizawa Y.
    PLoS One; 2014 Feb 26; 9(9):e106906. PubMed ID: 25211237
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  • 17. Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
    Ghirardello S, Dusi E, Castiglione B, Fumagalli M, Mosca F.
    Ital J Pediatr; 2014 Sep 26; 40():76. PubMed ID: 25255707
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  • 18. A new mutation in WFS1 gene (C.1522-1523delTA, Y508fsX421) may be responsible for early appearance of clinical features of Wolfram syndrome and suicidal behaviour.
    Aluclu MU, Bahceci M, Tuzcu A, Arikan S, Gokalp D.
    Neuro Endocrinol Lett; 2006 Dec 26; 27(6):691-4. PubMed ID: 17187023
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  • 19. Molecular characterization of WFS1 in patients with Wolfram syndrome.
    van ven Ouweland JM, Cryns K, Pennings RJ, Walraven I, Janssen GM, Maassen JA, Veldhuijzen BF, Arntzenius AB, Lindhout D, Cremers CW, Van Camp G, Dikkeschei LD.
    J Mol Diagn; 2003 May 26; 5(2):88-95. PubMed ID: 12707373
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  • 20. Ophthalmic, systemic, and genetic characteristics of patients with Wolfram syndrome.
    Ustaoglu M, Onder F, Karapapak M, Taslidere H, Guven D.
    Eur J Ophthalmol; 2020 Sep 26; 30(5):1099-1105. PubMed ID: 30957632
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