Enfermedad CLN8 congénita de lipofuscinosis neuronal ceroidea: un nuevo fenotipo von Pesaola, Favio, Kohan, Romina, Cismondi, Inés Adriana, Guelbert, Norberto, Pons, Patricia, Oller Ramírez, Ana María, Noher de Halac, Inés

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The neuronal ceroid lipofuscinoses program: A translational research experience in Argentina von Kohan, Romina, Pesaola, Favio, Guelbert, Norberto, Pons, Patricia, Oller-Ramírez, Ana María, Rautenberg, Gisela, Becerra, Adriana, Sims, Katherine, Xin, Winnie, Cismondi, Inés Adriana, de Halac, Inés Noher

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Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder von Cismondi, Inés Adriana, Kohan, Romina, Adams, Heather, Bond, Mike, Brown, Rachel, Cooper, Jonathan D., de Hidalgo, Perla K., Holthaus, Sophia-Martha Kleine, Mole, Sara E., Mugnaini, Julia, de Ramirez, Ana María Oller, Pesaola, Favio, Rautenberg, Gisela, Platt, Frances M., de Halac, Inés Noher

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Gerstmann-Sträussler-Scheinker Syndrome with Variable Phenotype in a New Kindred with PRNP-P102L Mutation von Riudavets, Miguel A., Sraka, María Alejandra, Schultz, Marcelo, Rojas, Estefanía, Martinetto, Horacio, Begué, Christian, de Halac, Inés Noher, Poleggi, Anna, Equestre, Michele, Pocchiari, Maurizio, Sevlever, Gustavo, Taratuto, Ana Lía

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Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis von Fietz, Michael, AlSayed, Moeenaldeen, Burke, Derek, Cohen-Pfeffer, Jessica, Cooper, Jonathan D., Dvořáková, Lenka, Giugliani, Roberto, Izzo, Emanuela, Jahnová, Helena, Lukacs, Zoltan, Mole, Sara E., Noher de Halac, Ines, Pearce, David A., Poupetova, Helena, Schulz, Angela, Specchio, Nicola, Xin, Winnie, Miller, Nicole

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Neuronal ceroid lipofuscinosis type CLN2: A new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America von Kohan, Romina, Carabelos, María Noelia, Xin, Winnie, Sims, Katherine, Guelbert, Norberto, Cismondi, Inés Adriana, Pons, Patricia, Alonso, Graciela Irene, Troncoso, Mónica, Witting, Scarlet, Pearce, David A., Dodelson de Kremer, Raquel, Oller-Ramírez, Ana María, Noher de Halac, Inés

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Palmitoyl Protein Thioesterase1 (PPT1) and Tripeptidyl Peptidase-I (TPP-I) are expressed in the human saliva. A reliable and non-invasive source for the diagnosis of infantile ( CL... von Kohan, Romina, Halac, Inés Noher de, Anzolini, Verónica Tapia, Cismondi, Adriana, Ramírez, Ana María Oller, Capra, Ana Paschini, Kremer, Raquel Dodelson de

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Natural History of Neuronal Ceroid Lipofuscinosis Type 6, Late Infantile Disease von O'Neal, Matthew, Noher de Halac, Ines, Aylward, Shawn C., Yildiz, Vedat, Zapanta, Bianca, Abreu, Nicolas, de los Reyes, Emily

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G erstmann‐ S träussler‐ S cheinker Syndrome with Variable Phenotype in a New Kindred with PRNP ‐ P102L Mutation von Riudavets, Miguel A., Sraka, María Alejandra, Schultz, Marcelo, Rojas, Estefanía, Martinetto, Horacio, Begué, Christian, de Halac, Inés Noher, Poleggi, Anna, Equestre, Michele, Pocchiari, Maurizio, Sevlever, Gustavo, Taratuto, Ana Lía

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Congenital CLN8 disease of neuronal ceroid lipofuscinosis: a novel phenotype von Pesaola, F, Kohan, R, Cismondi, I A, Guelbert, N, Pons, P, Oller-Ramirez, A M, Noher de Halac, I

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Expert recommendations for the laboratory diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Diagnostic algorithm and best practice guidelines for a timely diagnosi... von Giugliani, Roberto, Fietz, Michael, Al-Sayed, Moeenaldeen, Burke, Derek, Cohen-Pfeffer, Jessica, Cooper, Jonathan D., de Halac, Ines Noher, Dvořáková, Lenka, Izzo, Emanuela, Jahnová, Helena, Lukacs, Zoltan, Mole, Sara, Pearce, David, Schulz, Angela, Specchio, Nicola, Xin, Winnie, Miller, Nicole

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Valuation of exfoliative cytology as prediction factor in oral mucosa lesions von Brunotto, Mabel, Zárate, Ana María, Cismondi, Adriana, Fernández, María del Carmen, Noher de Halac, Rita Inés

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Distribution of pectins in the pollen apertures of Oenothera hookeri.velans ster/+ster von Noher de Halac, I, Cismondi, I A, Rodriguez-Garcia, M I, Famá, G

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Different Patterns of Callose Wall Formation during Megasporogenesis in Two Species of Oenothera (Onagraceae) von de Halac, Inés Noher, Harte, Cornelia

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Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation) von De Kremer, Raquel Dodelson, Paschini-Capra, Ana, Bacman, Sandra, Argaraña, Carlos, Civallero, Gabriel, Kelley, Richard I., Guelbert, Norberto, Latini, Alexandra, de Halac, Inés Noher, Giner-Ayala, Alicia, Johnston, Jennifer, Proujansky, Roy, Gonzalez, Iris, Depetris-Boldini, Catalina, Oller-Ramírez, Ana, Angaroni, Celia, Theaux, Ricardo A., Hliba, Ernesto, Juaneda, Ernesto

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Histoenzymology of oxidases and dehydrogenases in peripheral blood lymphocytes and monocytes for the study of mitochondrial oxidative phosphorylation von Noher de Halac, I, Bacman, S R, de Kremer, R D

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Genetics and development of morphological and physiological characters of male sterility in Oenothera von Noher de Halac, I, Harte, C

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Organogenesis of anther-derived calluses in long-term cultures of Oenothera hookeri de Vries von Martinez, L.D. (Universidad Nacional de Cordoba (Argentina). Centro de Microscopia Electronica), Noher de Halac, I

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Fine structure of nucellar cells during development of the embryo sac in Oenothera biennis L von Noher de Halac, I

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Pollen ontogenesis in Oenothera: a comparison of genotypically normal anthers with the male-sterile mutant sterilis von Noher de Halac, I, Cismondi, I.A, Harte, C

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