Literature DB >> 19149282

The clinical spectrum of mitochondrial genetic disorders.

Matthew A Kirkman1, Patrick Yu-Wai-Man, Patrick F Chinnery.   

Abstract

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Year:  2008        PMID： 19149282      PMCID： PMC4954398          DOI： 10.7861/clinmedicine.8-6-601

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN： 1470-2118            Impact factor:   2.659


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  5 in total

1.  Some physicochemical properties of hemoglobin-manitoba (alpha2 102Ser replaced by Arg (G9) beta2).

Authors:  R N Wrightstone; L L Smith; J B Wilson; F Vella; T H Huisman
Journal:  Biochim Biophys Acta       Date:  1975-12-15

Review 2.  Biochemical diagnosis of mitochondrial disorders.

Authors:  Richard J T Rodenburg
Journal:  J Inherit Metab Dis       Date:  2010-05-04       Impact factor: 4.982

Review 3.  How to spot mitochondrial disease in adults.

Authors:  Michael J Keogh; Patrick F Chinnery
Journal:  Clin Med (Lond)       Date:  2013-02       Impact factor: 2.659

4.  Rhodamine-based sensor for real-time imaging of mitochondrial ATP in living fibroblasts.

Authors:  Diego de la Fuente-Herreruela; Vicente Gónzalez-Charro; Víctor G Almendro-Vedia; María Morán; Miguel Ángel Martín; M Pilar Lillo; Paolo Natale; Iván López-Montero
Journal:  Biochim Biophys Acta Bioenerg       Date:  2017-09-22       Impact factor: 3.991

Review 5.  Genetic manipulation for inherited neurodegenerative diseases: myth or reality?

Authors:  Patrick Yu-Wai-Man
Journal:  Br J Ophthalmol       Date:  2016-03-21       Impact factor: 4.638
  5 in total

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