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3 in total

Review 1. Diseases of the mitochondrial DNA.

Authors: D C Wallace
Journal: Annu Rev Biochem Date: 1992 Impact factor: 23.643

2. Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Authors: M Zeviani; C Gellera; C Antozzi; M Rimoldi; L Morandi; F Villani; V Tiranti; S DiDonato
Journal: Lancet Date: 1991-07-20 Impact factor: 79.321

Review 3. Cardiomyopathy and abnormal mitochondrial function.

Authors: J Marin-Garcia; M J Goldenthal
Journal: Cardiovasc Res Date: 1994-04 Impact factor: 10.787

3 in total

4 in total

Review 1. Electron transport chain defects in heart failure.

Authors: Jordi Casademont; Oscar Miró
Journal: Heart Fail Rev Date: 2002-04 Impact factor: 4.214

Review 2. Metabolic cardiomyopathies.

Authors: B Guertl; C Noehammer; G Hoefler
Journal: Int J Exp Pathol Date: 2000-12 Impact factor: 1.925

3. A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis.

Authors: Sandrine Haut; Michèle Brivet; Guy Touati; Pierre Rustin; Sophie Lebon; Angela Garcia-Cazorla; Jean Marie Saudubray; Audrey Boutron; Alain Legrand; Abdelhamid Slama
Journal: Hum Genet Date: 2003-04-23 Impact factor: 4.132

4. Mitochondrial DNA Mutations and Rheumatic Heart Diseases.

Authors: Fatou Balla Wade; Marie Parsine Sall; Fatimata Mbaye; Mbacké Sembene
Journal: J Cardiovasc Dev Dis Date: 2019-10-11

4 in total