Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rebecca, Shiffman"'
Autor:
Simon S. Rabinowitz, Eduardo Bonilla, Michelangelo Mancuso, David Otaegui, Karen Thompson, Rebecca Shiffman, Michio Hirano, Pilar Camaño, Salvatore DiMauro, Sabrina Sacconi, Leonardo Salviati, Annette Feigenbaum, Claire M. Wilson, Alberto Marina, Tuan Vu, Ali Naini
Publikováno v:
Annals of Neurology. 52:311-317
Mitochondrial DNA depletion syndrome is a clinically heterogeneous group of disorders characterized by a reduction in mitochondrial DNA copy number. The recent discovery of mutations in the deoxyguanosine kinase (dGK) gene in patients with the hepato
Autor:
Arul Veerappan, Zoila Velastegui, Manonmani Arul, Theodore Hale, Daniel W. Skupski, Jimmy Nguyen, Rebecca Shiffman, Benamanahalli K. Rajegowda, Ray Mercado
Publikováno v:
Journal of Perinatal Medicine. 39
Objective: To evaluate whether National Institute of Child Health and Human Health and Development (NICHD) fetal heart rate categories were predictive of neonatal survival in periviable pregnancies. Methods: We reviewed the charts of 57 infants deliv
Autor:
Leonardo, Salviati, Sabrina, Sacconi, Michelangelo, Mancuso, David, Otaegui, Pilar, Camaño, Alberto, Marina, Simon, Rabinowitz, Rebecca, Shiffman, Karen, Thompson, Claire M, Wilson, Annette, Feigenbaum, Ali B, Naini, Michio, Hirano, Eduardo, Bonilla, Salvatore, DiMauro, Tuan H, Vu
Publikováno v:
Annals of neurology. 52(3)
Mitochondrial DNA depletion syndrome is a clinically heterogeneous group of disorders characterized by a reduction in mitochondrial DNA copy number. The recent discovery of mutations in the deoxyguanosine kinase (dGK) gene in patients with the hepato
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 67:297-300