Literature DB >> 25732363

Fatty acid 2-hydroxylase deficiency: clinical features and brain iron accumulation.

José Luiz Pedroso1, Benjamin W Handfas2, Agessandro Abrahão2, Fernando Kok2, Orlando G P Barsottini2, Acary S Bulle Oliveira2.   

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Year:  2015        PMID： 25732363     DOI： 10.1212/WNL.0000000000001316

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features.

Authors:  Faruk Incecik; Seyda Besen; Sevcan Tug Bozdogan
Journal:  Ann Indian Acad Neurol       Date:  2018 Oct-Dec       Impact factor: 1.383

Review 2.  Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.

Authors:  Felipe Franco da Graça; Thiago Junqueira Ribeiro de Rezende; Luiz Felipe Rocha Vasconcellos; José Luiz Pedroso; Orlando Graziani P Barsottini; Marcondes C França
Journal:  Front Neurol       Date:  2019-01-16       Impact factor: 4.003

3.  Leukodystrophy-Like Presentation in a Child: A Case of Hereditary Spastic Paraparesis-35.

Authors:  Kiruthiga Sugumar; Aakash Chandran Chidambaram; Jaikumar Govindaswamy Ramamoorthy; Tamil Selvan
Journal:  Ann Indian Acad Neurol       Date:  2022-03-25       Impact factor: 1.714
  3 in total

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