Publications by authors named "Henry Rivera"

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Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene.
Elena Martín-Hernández, María Teresa García-Silva, Pilar Quijada-Fraile, María Elena Rodríguez-García, Henry Rivera

Pediatr Dev Pathol· May 2019

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Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome.
Aitor Delmiro, Henry Rivera, María Teresa García-Silva, Inés García-Consuegra, Elena Martín-Hernández

Hum Mutat· December 2013

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A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome.
Henry Rivera, Elena Martín-Hernández, Aitor Delmiro, María Teresa García-Silva, Pilar Quijada-Fraile

BMC Nephrol· September 2013

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[Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia].
Ignacio J Posada, María Esther Gallardo, Cristina Domínguez, Henry Rivera, Ana Cabello

Med Clin (Barc)· October 2010

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An analysis of falls experienced by older adult patients diagnosed with cancer.
Janine A Overcash, Henry R Rivera, Jill Van Schaick

Oncol Nurs Forum· September 2010

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Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency.
María Morán, Lorena Marín-Buera, M Carmen Gil-Borlado, Henry Rivera, Alberto Blázquez

Hum Mutat· August 2010

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Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch.
Henry Rivera, Begoña Merinero, Mercedes Martinez-Pardo, Ignacio Arroyo, Pedro Ruiz-Sala

Mitochondrion· June 2010

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Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report.
Raquel Montero, Jose A Sánchez-Alcázar, Paz Briones, Aleix Navarro-Sastre, Ester Gallardo, Henry Rivera

Clin Biochem· May 2009

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Depression symptoms in cancer caregivers.
Henry R Rivera

Clin J Oncol Nurs· April 2009

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Physical performance evaluation of older cancer patients: a preliminary study.
Janine A Overcash, Henry R Rivera

Crit Rev Oncol Hematol· December 2008

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OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.
Patrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, Maria Esther Gallardo, Belén Bornstein, Henry Rivera

Brain· February 2008

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Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase.
Henry Rivera, Alberto Blázquez, Julián Carretero, José C Alvarez-Cermeño, Y Campos

Neuromuscul Disord· October 2007

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Immunophenotype characteristics of peripheral blood mononuclear leukocytes of chronic idiopathic urticaria patients.
Jenny V Garmendia, Mercedes Zabaleta, Oscar Aldrey, Henry Rivera, Juan B De Sanctis

Invest Clin· December 2006

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Hypodense eosinophils: characterization of surface molecule expression.
Angela Conesa, Paolo Tassinari, Henry Rivera, Juan B De Sanctis, Nicolás Bianco

Allergy Asthma Proc· November 2002

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