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pro vyhledávání: '"Giner Ayala, Alicia"'
Autor:
Giner-Ayala, Alicia1, Juana Angaroni, Celia1, Dodelson de Kremer, Raquel1, Dora Martínez, Lidia1,2
Publikováno v:
Journal of Clinical & Scientific Research. Oct-Dec2021, Vol. 10 Issue 4, p197-201. 5p.
Autor:
Angaroni, Celia J., de Kremer, Raquel Dodelson, Argaraña, Carlos E., Paschini-Capra, Ana E., Giner-Ayala, Alicia N., Pezza, Roberto J., Pan, Chi-Jiunn, Chou, Janice Y.
Publikováno v:
In Molecular Genetics and Metabolism 2004 83(3):276-279
Autor:
Dodelson De Kremer, Raquel, Paschini Capra, Ana, Bacman, Sandra, Argaraña, Carlos, Civallero, Gabriel, Kelley, Richard I., Guelbert, Norberto, Latini, Alexandra, Noher de Halac, Inés, Giner Ayala, Alicia, Johnston, Jennifer, Proujansky, Roy
Publikováno v:
Dodelson De Kremer, Raquel ORCID: https://orcid.org/0000-0003-4365-3661 , Paschini Capra, Ana, Bacman, Sandra ORCID: https://orcid.org/0000-0001-8701-6010 , Argaraña, Carlos ORCID: https://orcid.org/0000-0002-6169-3344 , Civallero, Gabriel, Kelley, Richard I. ORCID: https://orcid.org/0000-0001-9906-1345 , Guelbert, Norberto ORCID: https://orcid.org/0000-0003-3860-4750 , Latini, Alexandra ORCID: https://orcid.org/0000-0003-4255-3589 , Noher de Halac, Inés ORCID: https://orcid.org/0000-0003-2930-9282 , Giner Ayala, Alicia, Johnston, Jennifer and Proujansky, Roy (2001) Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation). American Journal of Medical Genetics, 99 (2). pp. 83-93. ISSN 0148-7299
An Argentine male child died at 4.5 years of age of a lethal mitochondrial disease associated with a MELAS mutation and a Barth syndrome-like presentation. The child had severe failure to thrive from the early months and for approximately two years t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2718::27f4868bc3979ab544de297014eaf576
http://pa.bibdigital.ucc.edu.ar/3930/
http://pa.bibdigital.ucc.edu.ar/3930/
Akademický článek
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Autor:
Kremer, Raquel Dodelson De, Paschini-Capra, Ana, Bacman, Sandra, Argaraña, Carlos, Civallero, Gabriel, Kelley, Richard I., Guelbert, Norberto, Latini, Alexandra, Halac, Inés Noher de, Giner-Ayala, Alicia, Johnston, Jennifer, Proujansky, Roy, Gonzalez, Iris, Depetris-Boldini, Catalina, Oller-Ramírez, Ana, Angaroni, Celia, Theaux, Ricardo A., Hliba, Ernesto, Juaneda, Ernesto
Publikováno v:
American Journal of Medical Genetics. Part A; 1 March 2001, Vol. 99 Issue: 2 p83-93, 11p