Browsing by Author "Guelbert, Norberto"

Now showing items 1-4 of 4

    • A novel CLN8 missense mutation underlies variant late infantile neuronal ceroid lipofuscinosis in Latin America 

      Pesaola, Favio; Sismondi, Inés Adriana; Guelbert, Norberto; Kohan, Romina; Carabelos, Noelia; Alonso, Graciela; Pons, Patricia; Oller Ramírez, Ana María; Noher de Halac, Rita Inés (2013)
      Neuronal ceroid lipofuscinosis (NCL), inheritedneurodegenerative diseases of all ages, presents with storage oflipofuscin-like lipopigments in cerebral neurons and peripheraltissues. Mutations in CLN8 gene causing epilepsy ...

    • Bone Diseases as the only clinical manifestation of gaucher disease type 

      Guelbert, Norberto; Robledo, Hugo; Becerra, Walter; Angaroni, Celia; Giner Ayala, Alicia; Ramírez Oller, Ana María; Dodelson Kremmer, Raquel (Sociedad Latinoamericana de Errores Innatos del Metabolismo y Pesquisa Neonatal, 2013)
      Gaucher disease (GD) is a lysosomal disease, due to the deficiency of Iˆ2-glucosidase, characterized by invol vement of hematopoietic organs such as the spleen, liver, bone marrow, lung, and bone. Bone is the second most ...

    • Neuronal ceroid lipofuscinosis type cln2: prevalent phenotypes and genotypes in Latin America 

      Sismondi, Inés Adriana; Guelbert, Norberto; Kohan, Romina; Carabelos, Noelia; Alonso, Graciela; Pons, Patricia; Oller Ramírez, Ana María; Noher de Halac, Rita Inés; Dodelson de Kremer, Raquel (2013)
      The Neuronal Ceroid Lipofuscinoses (NCLs), inherited neurodegenerative disorders, are the second most frequent group lysosomal pathologies (LP) of childhood. They are characterized by the pathological accumulation of ...

    • Urea cycle disorders: clinical, biochemical and genetic findings in agentinean patients 

      Laróvere, Laura; Silvera Ruiz, Silene; Arranz, José; Angaroni, Celia; Guelbert, Norberto; Antonozzi, Sandra; Bezard, Miriam; Dodelson de kremer, Raquel (2013)
      Urea cycle disorders (UCD) encompass several enzyme deficiencies with a wide clinical spectrum from asymptomatic to severe, mostly with cerebral damage. Objective: to communicate the autochthonous experience in the ...