Literature DB >> 16491382

Efficacious vitamin E treatment in a child with ataxia with isolated vitamin E deficiency.

Laura Doria-Lamba1, Elisa De Grandis, Elisabetta Cristiani, Isabella Fiocchi, Luciano Montaldi, Paolo Grosso, Cinzia Gellera.   

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Year:  2006        PMID： 16491382     DOI： 10.1007/s00431-006-0085-4

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  6 in total

Review 1.  Hereditary vitamin-E deficiency.

Authors:  N Gordon
Journal:  Dev Med Child Neurol       Date:  2001-02       Impact factor: 5.449

Review 2.  Ataxia with isolated vitamin E deficiency: case report and review of the literature.

Authors:  J M Aparicio; A Bélanger-Quintana; L Suárez; D Mayo; J Benítez; M Díaz; H Escobar
Journal:  J Pediatr Gastroenterol Nutr       Date:  2001-08       Impact factor: 2.839

3.  Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families.

Authors:  L Cavalier; K Ouahchi; H J Kayden; S Di Donato; L Reutenauer; J L Mandel; M Koenig
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

4.  Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.

Authors:  S Gabsi; N Gouider-Khouja; S Belal; M Fki; M Kefi; I Turki; M Ben Hamida; H Kayden; R Mebazaa; F Hentati
Journal:  Eur J Neurol       Date:  2001-09       Impact factor: 6.089

5.  Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.

Authors:  C Mariotti; C Gellera; M Rimoldi; R Mineri; G Uziel; G Zorzi; D Pareyson; G Piccolo; D Gambi; S Piacentini; F Squitieri; R Capra; B Castellotti; S Di Donato
Journal:  Neurol Sci       Date:  2004-07       Impact factor: 3.307

6.  Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Authors:  C Ben Hamida; N Doerflinger; S Belal; C Linder; L Reutenauer; C Dib; G Gyapay; A Vignal; D Le Paslier; D Cohen
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330
  6 in total
  6 in total

1.  Mammalian diseases of phosphatidylinositol transfer proteins and their homologs.

Authors:  Aaron H Nile; Vytas A Bankaitis; Aby Grabon
Journal:  Clin Lipidol       Date:  2010-12-01

Review 2.  Vitamin E in renal therapeutic regiments.

Authors:  Mohamed Alaa Thabet; James C M Chan
Journal:  Pediatr Nephrol       Date:  2006-09-21       Impact factor: 3.714

Review 3.  Ataxia with vitamin E deficiency: update of molecular diagnosis.

Authors:  I Di Donato; S Bianchi; A Federico
Journal:  Neurol Sci       Date:  2010-05-13       Impact factor: 3.307

4.  Pedigree analysis and exclusion of alpha-tocopherol transfer protein (TTPA) as a candidate gene for neuroaxonal dystrophy in the American Quarter Horse.

Authors:  C J Finno; T Famula; M Aleman; R J Higgins; J E Madigan; D L Bannasch
Journal:  J Vet Intern Med       Date:  2012-11-27       Impact factor: 3.333

5.  Ataxia with vitamin e deficiency in norway.

Authors:  Areej Elkamil; Krisztina K Johansen; Jan Aasly
Journal:  J Mov Disord       Date:  2015-01-13

6.  Natural and Synthetic α-Tocopherol Modulate the Neuroinflammatory Response in the Spinal Cord of Adult Ttpa-null Mice.

Authors:  Katherine M Ranard; Matthew J Kuchan; Janice M Juraska; John W Erdman
Journal:  Curr Dev Nutr       Date:  2021-02-12
  6 in total

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