Literature DB >> 8884577

Magnetic resonance imaging in lactic acidosis.

M S van der Knaap1, C Jakobs, J Valk.   

Abstract

Mitochondrial defects, defects in gluconeogenesis, and biotin-responsive multiple carboxylase deficiency are disorders characterized by primary lactic acidosis. In this review, characteristic findings in magnetic resonance imaging (MRI) of the brain, as related to histopathological abnormalities, are described for the different disorders and the diagnostic value of the MRI findings is discussed. Inborn errors of metabolism with primary lactic acidosis should be considered in particular when MRI shows lesions similar to or reminiscent of effects of focal or generalized hypoxia-ischaemia, or when MRI shows signs of chronic neurodegeneration, but rarely in cases with predominantly white-matter changes.

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Year:  1996        PMID: 8884577     DOI: 10.1007/bf01799114

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


  49 in total

1.  Isolated and combined deficiencies of the alpha-keto acid dehydrogenase complexes.

Authors:  B H Robinson; K Chun; N Mackay; G Otulakowski; R Petrova-Benedict; H Willard
Journal:  Ann N Y Acad Sci       Date:  1989       Impact factor: 5.691

Review 2.  Disorders of lysosomes, peroxisomes, and mitochondria.

Authors:  B E Kendall
Journal:  AJNR Am J Neuroradiol       Date:  1992 Mar-Apr       Impact factor: 3.825

3.  Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenetic speculations.

Authors:  R Van Coster; A Lombres; D C De Vivo; T L Chi; W E Dodson; S Rothman; E J Orrechio; W Grover; G T Berry; J F Schwartz
Journal:  J Neurol Sci       Date:  1991-07       Impact factor: 3.181

4.  Magnetic resonance imaging in MELAS syndrome.

Authors:  L Rosen; S Phillips; D Enzmann
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

5.  Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency.

Authors:  L T Wong; A G Davidson; D A Applegarth; J E Dimmick; M G Norman; J R Toone; G Pirie; J Wong
Journal:  Pediatr Res       Date:  1986-03       Impact factor: 3.756

6.  [Familial leukoencephalopathy associated with congenital lactic acidosis].

Authors:  E Farkas-Bargeton; F Goutières; J M Richardet; S Thieffry; H E Brissaud
Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

Review 7.  Fumarase deficiency: two siblings with enlarged cerebral ventricles and polyhydramnios in utero.

Authors:  A M Remes; H Rantala; J K Hiltunen; J Leisti; A Ruokonen
Journal:  Pediatrics       Date:  1992-04       Impact factor: 7.124

8.  MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.

Authors:  L Medina; T L Chi; D C DeVivo; S K Hilal
Journal:  AJNR Am J Neuroradiol       Date:  1990 Mar-Apr       Impact factor: 3.825

9.  Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and a response to acetazolamide.

Authors:  I R Livingstone; D Gardner-Medwin; R J Pennington
Journal:  J Neurol Sci       Date:  1984-04       Impact factor: 3.181

10.  Mitochondrial disorders: analysis of their clinical and imaging characteristics.

Authors:  A J Barkovich; W V Good; T K Koch; B O Berg
Journal:  AJNR Am J Neuroradiol       Date:  1993 Sep-Oct       Impact factor: 3.825

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  6 in total

Review 1.  Clinical mitochondrial genetics.

Authors:  P F Chinnery; N Howell; R M Andrews; D M Turnbull
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

2.  Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.

Authors:  Doris D M Lin; Thomas O Crawford; Peter B Barker
Journal:  AJNR Am J Neuroradiol       Date:  2003-01       Impact factor: 3.825

Review 3.  Neuroimaging of mitochondrial disease.

Authors:  Russell P Saneto; Seth D Friedman; Dennis W W Shaw
Journal:  Mitochondrion       Date:  2008-05-23       Impact factor: 4.160

4.  Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiency.

Authors:  J P Harpey; D Heron; M Prudent; C Charpentier; P Rustin; G Ponsot; V Cormier-Daire
Journal:  J Inherit Metab Dis       Date:  1998-10       Impact factor: 4.982

Review 5.  The in-depth evaluation of suspected mitochondrial disease.

Authors:  Richard H Haas; Sumit Parikh; Marni J Falk; Russell P Saneto; Nicole I Wolf; Niklas Darin; Lee-Jun Wong; Bruce H Cohen; Robert K Naviaux
Journal:  Mol Genet Metab       Date:  2008-02-01       Impact factor: 4.797

6.  Evidence of Brain Alterations in Noncerebral Falciparum Malaria.

Authors:  Sanjib Mohanty; Praveen K Sahu; Rajyabardhan Pattnaik; Megharay Majhi; Sameer Maharana; Jabamani Bage; Akshaya Mohanty; Anita Mohanty; Martin Bendszus; Catriona Patterson; Himanshu Gupta; Arjen M Dondorp; Lukas Pirpamer; Angelika Hoffmann; Samuel C Wassmer
Journal:  Clin Infect Dis       Date:  2022-08-24       Impact factor: 20.999

  6 in total

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