Literature DB >> 26830281

Celiac Disease Presenting with Biotinidase Deficiency and Paraplegia.

Sahin Erdol1, Halil Saglam2, Tanju Ozkan Basarır2, Mehmet Sait Okan2.   

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Year:  2016        PMID： 26830281     DOI： 10.1007/s12098-015-1974-1

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Worldwide survey of neonatal screening for biotinidase deficiency.

Authors:  B Wolf
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 2.  Clinical issues and frequent questions about biotinidase deficiency.

Authors:  Barry Wolf
Journal:  Mol Genet Metab       Date:  2010-01-11       Impact factor: 4.797

3.  Delayed-onset profound biotinidase deficiency.

Authors:  B Wolf; R J Pomponio; K J Norrgard; I T Lott; E R Baumgartner; T Suormala; V T Ramaekers; T Coskun; A Tokatli; I Ozalp; J Hymes
Journal:  J Pediatr       Date:  1998-02       Impact factor: 4.406

4.  Biotinidase deficiency: a treatable leukoencephalopathy.

Authors:  S Grünewald; M P Champion; J V Leonard; J Schaper; A A M Morris
Journal:  Neuropediatrics       Date:  2004-08       Impact factor: 1.947

5.  Profound biotinidase deficiency in a child with predominantly spinal cord disease.

Authors:  Aziza K Chedrawi; Ayman Ali; Zuhair N Al Hassnan; Muhammad Faiyaz-Ul-Haque; Barry Wolf
Journal:  J Child Neurol       Date:  2008-07-21       Impact factor: 1.987
  5 in total

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