These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 20153672)

  • 1. Two unusual clinical and radiological presentations of biotinidase deficiency.
    Mc Sweeney N; Grunewald S; Bhate S; Ganesan V; Chong WK; Hemingway C
    Eur J Paediatr Neurol; 2010 Nov; 14(6):535-8. PubMed ID: 20153672
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biotinidase deficiency: a treatable genetic disorder in the Saudi population.
    Joshi S; al-Essa MA; Archibald A; Ozand PT
    East Mediterr Health J; 1999 Nov; 5(6):1213-7. PubMed ID: 11924114
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biotinidase deficiency presenting as recurrent myelopathy in a 7-year-old boy and a review of the literature.
    Raha S; Udani V
    Pediatr Neurol; 2011 Oct; 45(4):261-4. PubMed ID: 21907891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biotinidase deficiency: novel mutations and their biochemical and clinical correlates.
    Wolf B; Jensen KP; Barshop B; Blitzer M; Carlson M; Goudie DR; Gokcay GH; Demirkol M; Baykal T; Demir F; Quary S; Shih LY; Pedro HF; Chen TH; Slonim AE
    Hum Mutat; 2005 Apr; 25(4):413. PubMed ID: 15776412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A girl with spastic tetraparesis associated with biotinidase deficiency.
    Komur M; Okuyaz C; Ezgu F; Atici A
    Eur J Paediatr Neurol; 2011 Nov; 15(6):551-3. PubMed ID: 21571559
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel imaging findings in two cases of biotinidase deficiency-a treatable metabolic disorder.
    Bhat MD; Bindu PS; Christopher R; Prasad C; Verma A
    Metab Brain Dis; 2015 Oct; 30(5):1291-4. PubMed ID: 26037171
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of partial biotinidase deficiency associated with autism.
    Zaffanello M; Zamboni G; Fontana E; Zoccante L; Tatò L
    Child Neuropsychol; 2003 Sep; 9(3):184-8. PubMed ID: 13680408
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnosis, treatment and follow-up in four children with biotinidase deficiency from Pakistan.
    Afroze B; Wasay M
    J Coll Physicians Surg Pak; 2013 Nov; 23(10):823-5. PubMed ID: 24169397
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Profound biotinidase deficiency in a child with predominantly spinal cord disease.
    Chedrawi AK; Ali A; Al Hassnan ZN; Faiyaz-Ul-Haque M; Wolf B
    J Child Neurol; 2008 Sep; 23(9):1043-8. PubMed ID: 18645204
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Biotinidase deficiency: a treatable leukoencephalopathy.
    Grünewald S; Champion MP; Leonard JV; Schaper J; Morris AA
    Neuropediatrics; 2004 Aug; 35(4):211-6. PubMed ID: 15328559
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biotinidase deficiency presenting as Neuromyelitis Optica Spectrum Disorder.
    Shah S; Khan N; Lakshmanan R; Lewis B; Nagarajan L
    Brain Dev; 2020 Nov; 42(10):762-766. PubMed ID: 32741581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biotinidase deficiency should be considered in individuals exhibiting myelopathy with or without and vision loss.
    Wolf B
    Mol Genet Metab; 2015 Nov; 116(3):113-8. PubMed ID: 26358973
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Audiologic findings in children with biotinidase deficiency in Turkey.
    Genc GA; Sivri-Kalkanoğlu HS; Dursun A; Aydin HI; Tokatli A; Sennaroglu L; Belgin E; Wolf B; Coşkun T
    Int J Pediatr Otorhinolaryngol; 2007 Feb; 71(2):333-9. PubMed ID: 17161472
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of mutations causing biotinidase deficiency.
    Pindolia K; Jordan M; Wolf B
    Hum Mutat; 2010 Sep; 31(9):983-91. PubMed ID: 20556795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biotinidase deficiency in childhood.
    Venkataraman V; Balaji P; Panigrahi D; Jamal R
    Neurol India; 2013; 61(4):411-3. PubMed ID: 24005734
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biotinidase deficiency with hypertonia as unusual feature.
    Rathi N; Rathi M
    Indian Pediatr; 2009 Jan; 46(1):65-7. PubMed ID: 19179722
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reversal of brain atrophy with biotin treatment in biotinidase deficiency.
    Bousounis DP; Camfield PR; Wolf B
    Neuropediatrics; 1993 Aug; 24(4):214-7. PubMed ID: 8232780
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome.
    Battini R; Olivieri G; Milone R; Mazio F; Scalise R; Verdolotti T; Primiano G; Genovese O; Mercuri E; Servidei S
    Brain Dev; 2020 Jun; 42(6):457-461. PubMed ID: 32209270
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.
    Coşkun T; Tokatli A; Ozalp I
    Turk J Pediatr; 1994; 36(4):267-78. PubMed ID: 7825232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Biotinidase deficiency and eye].
    Mrugacz M; Bakunowicz-Łazarczyk A; Sredzińska-Kita D
    Klin Oczna; 2002; 104(3-4):293-4. PubMed ID: 12608322
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.