Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting.

Literature DB >> 12905015

A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting.

Carmelo Damiano Salpietro¹, Silvana Briuglia, Maria Valeria Merlino, Chiara Di Bella, Luciana Rigoli.

Abstract

Entities: Disease Mutation

Mesh：

Substances：
DNA, Mitochondrial

Year: 2003 PMID： 12905015 DOI： 10.1007/s00431-003-1280-1

Source DB: PubMed Journal: Eur J Pediatr ISSN： 0340-6199 Impact factor: 3.183

× No keyword cloud information.

5 in total

1. Familial cyclic vomiting syndrome.

Authors: J Haan; E E Kors; M D Ferrari
Journal: Cephalalgia Date: 2002-09 Impact factor: 6.292

2. Cyclic vomiting syndrome and mitochondrial DNA mutations.

Authors: R G Boles; N Chun; D Senadheera; L J Wong
Journal: Lancet Date: 1997-11-01 Impact factor: 79.321

3. Sequence and organization of the human mitochondrial genome.

Authors: S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal: Nature Date: 1981-04-09 Impact factor: 49.962

Review 4. Mitochondrial disease and cyclic vomiting syndrome.

Authors: R G Boles; J C Williams
Journal: Dig Dis Sci Date: 1999-08 Impact factor: 3.199

Review 5. Cyclic vomiting syndrome: evolution in our understanding of a brain-gut disorder.

Authors: B U Li; J P Balint
Journal: Adv Pediatr Date: 2000

5 in total

12 in total

1. Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases.

Authors: Byung-Ok Choi; Jung Hee Hwang; Eun Min Cho; Eun Hye Jeong; Young Se Hyun; Hyeon Jeong Jeon; Ki Min Seong; Nam Soo Cho; Ki Wha Chung
Journal: Exp Mol Med Date: 2010-06-30 Impact factor: 8.718

2. A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa.

Authors: Maria Rachele Ceccarini; Vincenza Precone; Elena Manara; Stefano Paolacci; Paolo Enrico Maltese; Valentina Benfatti; Kristjana Dhuli; Kevin Donato; Giulia Guerri; Giuseppe Marceddu; Pietro Chiurazzi; Laura Dalla Ragione; Tommaso Beccari; Matteo Bertelli
Journal: Eat Weight Disord Date: 2021-11-25 Impact factor: 4.652

3. Recent concepts on cyclic vomiting syndrome in children.

Authors: Hye Ran Yang
Journal: J Neurogastroenterol Motil Date: 2010-04-27 Impact factor: 4.924

4. A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3.

Authors: Sheena Chew; Ravikumar Balasubramanian; Wai-Man Chan; Peter B Kang; Caroline Andrews; Bryn D Webb; Sarah E MacKinnon; Darren T Oystreck; Jessica Rankin; Thomas O Crawford; Michael Geraghty; Scott L Pomeroy; William F Crowley; Ethylin Wang Jabs; David G Hunter; Patricia E Grant; Elizabeth C Engle
Journal: Brain Date: 2013-01-31 Impact factor: 13.501

Review 10. The childhood migraine syndrome.

Authors: Ishaq Abu-Arafeh; Amy A Gelfand
Journal: Nat Rev Neurol Date: 2021-05-26 Impact factor: 42.937

A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting.

1. Familial cyclic vomiting syndrome.

2. Cyclic vomiting syndrome and mitochondrial DNA mutations.

3. Sequence and organization of the human mitochondrial genome.

Review 4. Mitochondrial disease and cyclic vomiting syndrome.

Review 5. Cyclic vomiting syndrome: evolution in our understanding of a brain-gut disorder.

1. Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases.

2. A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa.

3. Recent concepts on cyclic vomiting syndrome in children.

4. A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3.

5. Cyclic vomiting syndrome versus inborn errors of metabolism: A review with clinical recommendations.

6. Clinical and molecular features of two diabetes families carrying mitochondrial ND1 T3394C mutation.

7. The primary headaches: genetics, epigenetics and a behavioural genetic model.

8. Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.

9. ND2 mutation with minimal coenzyme-Q responsive manifestations.

Review 10. The childhood migraine syndrome.