Literature DB >> 33380711

Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions.

Josef Finsterer1.   

Abstract

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Year:  2020        PMID： 33380711      PMCID： PMC8061596          DOI： 10.4103/ijmr.IJMR_1039_19

Source DB:  PubMed          Journal:  Indian J Med Res        ISSN： 0971-5916            Impact factor:   2.375


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  5 in total

1.  Complex multisystem phenotype associated with the mitochondrial DNA m.5522G>A mutation.

Authors:  Claudia Nesti; Anna Rubegni; Deborah Tolomeo; Jacopo Baldacci; Denise Cassandrini; Francesca D'Amore; Filippo M Santorelli
Journal:  Neurol Sci       Date:  2019-04-01       Impact factor: 3.307

Review 2.  Genetic Counselling for Maternally Inherited Mitochondrial Disorders.

Authors:  Joanna Poulton; Josef Finsterer; Patrick Yu-Wai-Man
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

3.  Lactate stress testing in 155 patients with mitochondriopathy.

Authors:  Josef Finsterer; Erika Milvay
Journal:  Can J Neurol Sci       Date:  2002-02       Impact factor: 2.104

4.  A descriptive pilot study of mitochondrial mutations & clinical phenotype in fibromyalgia syndrome.

Authors:  Sumita Danda; Blessy Mariam Thomas; G Paramasivam; Raji Thomas; John Mathew; Debashish Danda
Journal:  Indian J Med Res       Date:  2019-01       Impact factor: 2.375

Review 5.  Lipid Myopathies.

Authors:  Elena Maria Pennisi; Matteo Garibaldi; Giovanni Antonini
Journal:  J Clin Med       Date:  2018-11-23       Impact factor: 4.241
  5 in total
  1 in total

1.  Authors' response.

Authors:  S Danda; B M Thomas; G Paramshivam; Raji Thomas; John Mathew; D Danda
Journal:  Indian J Med Res       Date:  2020-10       Impact factor: 2.375
  1 in total

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