Search Results - "Celma Nos, Ferran"

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases by Celma Nos, Ferran, Hernández, Gonzalo, Ferrer-Cortès, Xènia, Hernandez-Rodriguez, Ines, Navarro-Almenzar, Begoña, Fuster, José Luis, Bermúdez Cortés, Mar, Pérez-Montero, Santiago, Tornador, Cristian, Sanchez, Mayka

“…Hereditary hyperferritinemia-cataract syndrome (HHCS) is a rare disease characterized by high serum ferritin levels, congenital bilateral cataracts, and the…”
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S289: PPP1R1B BINDS IRON REGULATORY PROTEINS AND MODULATES IRON CELLULAR CONTENT by Calvo López, Laura, Hernández, Gonzalo, Celma Nos, Ferran, Sanchez, Mayka

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ERK MAPK signaling pathway inhibition as a potential target to prevent autophagy alterations in Spinal Muscular Atrophy motoneurons by Sansa, Alba, Miralles, Maria P., Beltran, Maria, Celma-Nos, Ferran, Calderó, Jordi, Garcera, Ana, Soler, Rosa M.

“…Spinal Muscular Atrophy (SMA) is a severe genetic neuromuscular disorder that occurs in childhood and is caused by misexpression of the survival motor neuron…”
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Control of Systemic Iron Homeostasis by the 3’ Iron‐Responsive Element of Divalent Metal Transporter 1 in Mice by Tybl, Elisabeth, Gunshin, Hiromi, Gupta, Sanjay, Barrientos, Tomasa, Bonadonna, Michael, Celma Nos, Ferran, Palais, Gael, Karim, Zoubida, Sanchez, Mayka, Andrews, Nancy C., Galy, Bruno

“…Supplemental Digital Content is available in the text…”
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Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases by Celma Nos, Ferran, Hernández, Gonzalo, Ferrer-Cortès, Xènia, Hernandez-Rodriguez, Ines, Navarro-Almenzar, Begoña, Fuster, José Luis, Bermúdez Cortés, Mar, Pérez-Montero, Santiago, Tornador, Cristian, Sanchez, Mayka

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