Literature DB >> 15654564

Chorea triggered by hyperglycemia in a maternally inherited diabetes and deafness (MIDD) patient with the A3243G mutation of mitochondrial DNA and basal ganglia calcification.

Ji-Hoon Kang, Sa-Yoon Kang, Jay-Chol Choi, Seong-Suk Lee, Ji-Soo Kim.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2005        PMID： 15654564     DOI： 10.1007/s00415-005-0600-y

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


× No keyword cloud information.
  9 in total

1.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Authors:  Y Goto; S Horai; T Matsuoka; Y Koga; K Nihei; M Kobayashi; I Nonaka
Journal:  Neurology       Date:  1992-03       Impact factor: 9.910

2.  A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutation.

Authors:  A Verma; C T Moraes; R T Shebert; W G Bradley
Journal:  Neurology       Date:  1996-05       Impact factor: 9.910

3.  Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation.

Authors:  M Arai; S Ohshima
Journal:  J Neurol       Date:  1997-07       Impact factor: 4.849

4.  Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.

Authors:  L M Lien; H C Lee; K L Wang; J C Chiu; H C Chiu; Y H Wei
Journal:  Acta Neurol Scand       Date:  2001-03       Impact factor: 3.209

Review 5.  Maternally inherited diabetes and deafness: a new diabetes subtype.

Authors:  J A Maassen; T Kadowaki
Journal:  Diabetologia       Date:  1996-04       Impact factor: 10.122

Review 6.  Presentation of striatal hyperintensity on T1-weighted MRI in patients with hemiballism-hemichorea caused by non-ketotic hyperglycemia: report of seven new cases and a review of literature.

Authors:  J J Lin; G Y Lin; C Shih; W C Shen
Journal:  J Neurol       Date:  2001-09       Impact factor: 4.849

7.  MR imaging and proton MR spectroscopy in A-to-G substitution at nucleotide position 3243 of leucine transfer RNA.

Authors:  J Bowen; T Richards; K Maravilla
Journal:  AJNR Am J Neuroradiol       Date:  1998-02       Impact factor: 3.825

8.  Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA.

Authors:  C T Moraes; F Ciacci; G Silvestri; S Shanske; M Sciacco; M Hirano; E A Schon; E Bonilla; S DiMauro
Journal:  Neuromuscul Disord       Date:  1993-01       Impact factor: 4.296

9.  Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.

Authors:  J M van den Ouweland; H H Lemkes; R C Trembath; R Ross; G Velho; D Cohen; P Froguel; J A Maassen
Journal:  Diabetes       Date:  1994-06       Impact factor: 9.461
  9 in total
  3 in total

1.  Hypoglycemia-induced hemichorea in a patient with Fahr's syndrome.

Authors:  George P Paraskevas; George S Vlachos; Sophia Vassilopoulou; Evangelos Anagnostou; Konstantinos Spengos; Vassilios Zis
Journal:  Neurol Sci       Date:  2012-04-24       Impact factor: 3.307

2.  Basal Ganglia Calcification with Tetanic Seizure Suggest Mitochondrial Disorder.

Authors:  Josef Finsterer; Barbara Enzelsberger; Adam Bastowansky
Journal:  Am J Case Rep       Date:  2017-04-09

3.  Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.

Authors:  Durjoy Lahiri; Vishal Madhukar Sawale; Subhadeep Banerjee; Souvik Dubey; Biman Kanti Roy; Shyamal Kumar Das
Journal:  J Med Case Rep       Date:  2019-03-06
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.