Prenatal diagnosis of cytochrome c oxidase deficiency in cultured amniocytes is hazardous

1992 ◽  
Vol 12 (6) ◽  
pp. 548-549 ◽  
Author(s):  
Thomas Bourgeron ◽  
Dominique Chrétien ◽  
Agnès Rötig ◽  
Arnold Munnich ◽  
Pierre Rustin
Keyword(s):  
Prenatal Diagnosis ◽  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency

scholarly journals The new molecular p.M177T identified in two unrelated patients with clinical features of SCO2-dependent cytochrome c oxidase deficiency

2010 ◽  
Vol 1797 ◽  
pp. 52
Author(s):  
Sylwia Łuczak ◽  
Dorota Piekutowska-Abramczuk ◽  
Paweł Kowalski ◽  
Elżbieta Ciara ◽  
Dorota Jurkiewicz ◽  
...  
Keyword(s):  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Clinical Features ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency

Cytochrome c oxidase deficiency in menkes kinky hair disease

1983 ◽  
Vol 5 (6) ◽  
pp. 533-540 ◽  
Author(s):  
Mitsuo Maehara ◽  
Nobuaki Ogasawara ◽  
Naoki Mizutani ◽  
Kazuyoshi Watanabe ◽  
Sakae Suzuki
Keyword(s):  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency ◽  
Kinky Hair Disease ◽  
Menkes Kinky Hair Disease ◽  
Kinky Hair

Successful treatment of heart failure with enoximone in a patient with cytochrome c oxidase deficiency

1996 ◽  
Vol 155 (6) ◽  
pp. 525-525 ◽  
Author(s):  
A. Timnik ◽  
S. Mühlbauer ◽  
A. Merkenschlager ◽  
K. Reiter ◽  
W. Lindner ◽  
...  
Keyword(s):  
Heart Failure ◽  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Successful Treatment ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency

scholarly journals Cytochrome c Oxidase Deficiency in Human Posterior Cricoarytenoid Muscle

2011 ◽  
Vol 25 (4) ◽  
pp. 387-394 ◽  
Author(s):  
Cari M. Tellis ◽  
Clark Rosen ◽  
John M. Close ◽  
Michael Horton ◽  
J. Scott Yaruss ◽  
...  
Keyword(s):  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency ◽  
Posterior Cricoarytenoid Muscle ◽  
Posterior Cricoarytenoid

scholarly journals OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules

2010 ◽  
Vol 19 (15) ◽  
pp. 3043-3052 ◽  
Author(s):  
Patrick Yu-Wai-Man ◽  
Kamil S. Sitarz ◽  
David C. Samuels ◽  
Philip G. Griffiths ◽  
Amy K. Reeve ◽  
...  
Keyword(s):  
Cytochrome C ◽  
Cytochrome C Oxidase ◽  
Wild Type ◽  
Oxidase Deficiency ◽  
Cytochrome C Oxidase Deficiency
Sign in / Sign up

Export Citation Format

Share Document