Identification of differentially expressed genes in microarray data in a principal component space

Por Ospina, Luis, López-Kleine, Liliana
Publicado em 2013

Anti-inflammatory effects of the gorgonian Pseudopterogorgia elisabethae collected at the Islands of Providencia and San Andrés (SW Caribbean)

Por Correa, Hebelin, Valenzuela, Alba Lucia, Ospina, Luis Fernando, Duque, Carmenza
Publicado em 2009

Susceptibility of Porphyromonas gingivalis and Streptococcus mutans to Antibacterial Effect from Mammea americana

Por Herrera Herrera, Alejandra, Franco Ospina, Luis, Fang, Luis, Díaz Caballero, Antonio
Publicado em 2014

Visual disorders with psychostimulants: A paediatric case report

Por Soyer, Julie, Jean-Louis, Jennifer, Ospina, Luis H, Bélanger, Stacey Ageranioti, Bussières, Jean-François, Kleiber, Niina
Publicado no Paediatr Child Health (2019)

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms

Por Damaj, Lena, Lupien-Meilleur, Alexis, Lortie, Anne, Riou, Émilie, Ospina, Luis H, Gagnon, Louise, Vanasse, Catherine, Rossignol, Elsa
Publicado no Eur J Hum Genet (2015)

A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect

Por Bellerose, Jenny, Neugnot-Cerioli, Mathilde, Bédard, Karine, Brunel-Guitton, Catherine, Mitchell, Grant A., Ospina, Luis H., Beauchamp, Miriam H.
Publicado no JIMD Rep (2015)

Folk medicine in the northern coast of Colombia: an overview

Por Gómez-Estrada, Harold, Díaz-Castillo, Fredyc, Franco-Ospina, Luís, Mercado-Camargo, Jairo, Guzmán-Ledezma, Jaime, Medina, José Domingo, Gaitán-Ibarra, Ricardo
Publicado em 2011

Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population

Por Srour, Myriam, Schwartzentruber, Jeremy, Hamdan, Fadi F., Ospina, Luis H., Patry, Lysanne, Labuda, Damian, Massicotte, Christine, Dobrzeniecka, Sylvia, Capo-Chichi, José-Mario, Papillon-Cavanagh, Simon, Samuels, Mark E., Boycott, Kym M., Shevell, Michael I., Laframboise, Rachel, Désilets, Valérie, Maranda, Bruno, Rouleau, Guy A., Majewski, Jacek, Michaud, Jacques L.
Publicado em 2012

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104

Por Srour, Myriam, Hamdan, Fadi F., McKnight, Dianalee, Davis, Erica, Mandel, Hanna, Schwartzentruber, Jeremy, Martin, Brissa, Patry, Lysanne, Nassif, Christina, Dionne-Laporte, Alexandre, Ospina, Luis H., Lemyre, Emmanuelle, Massicotte, Christine, Laframboise, Rachel, Maranda, Bruno, Labuda, Damian, Décarie, Jean-Claude, Rypens, Françoise, Goldsher, Dorith, Fallet-Bianco, Catherine, Soucy, Jean-François, Laberge, Anne-Marie, Maftei, Catalina, Boycott, Kym, Brais, Bernard, Boucher, Renée-Myriam, Rouleau, Guy A., Katsanis, Nicholas, Majewski, Jacek, Elpeleg, Orly, Kukolich, Mary K., Shalev, Stavit, Michaud, Jacques L.
Publicado no Am J Hum Genet (2015)