Literature DB >> 8295412

Molybdenum cofactor deficiency can mimic postanoxic encephalopathy.

H D Bakker1, N G Abeling, R ten Houten, J F van den Blij, W C Overweg-Plandsoen, R J Wanders, A H van Gennip.   

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Year:  1993        PMID： 8295412     DOI： 10.1007/BF00714290

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Attempt at treatment with tetrahydrobiopterin in combined deficiency of xanthine oxidase and sulphite oxidase.

Authors:  M Fujitaka; N Sakura; K Ueda; H Konishi; S Yoshida; T Yamasaki
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  Symmetrical thalamic lesions in infants.

Authors:  M Eicke; J Briner; U Willi; J Uehlinger; E Boltshauser
Journal:  Arch Dis Child       Date:  1992-01       Impact factor: 3.791
  2 in total
  2 in total

1.  The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile.

Authors:  A H van Gennip; N G Abeling; A E Stroomer; H Overmars; H D Bakker
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

2.  Delineating the phenotypic spectrum of sulfite oxidase and molybdenum cofactor deficiency.

Authors:  Albert L Misko; Ye Liang; Joshua B Kohl; Florian Eichler
Journal:  Neurol Genet       Date:  2020-07-14
  2 in total

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