Search Results - Sahin, Mustafa

  • Showing 1 - 7 results of 7
Refine Results
  1. 1
    Cover Image

    Clinical and molecular outcomes from the 5-Year natural history study of SSADH deficiency, a model metabolic neurodevelopmental disorder by Tokatly Latzer, Itay (Author) , Roullet, Jean-Baptiste (Author) , Afshar-Saber, Wardiya (Author) , Lee, Henry H. C. (Author) , Bertoldi, Mariarita (Author) , McGinty, Gabrielle E. (Author) , DiBacco, Melissa L. (Author) , Arning, Erland (Author) , Tsuboyama, Melissa (Author) , Rotenberg, Alexander (Author) , Opladen, Thomas (Author) , Jeltsch, Kathrin (Author) , García-Cazorla, Àngels (Author) , Julià-Palacios, Natalia (Author) , Gibson, K. Michael (Author) , Sahin, Mustafa (Author) , Pearl, Phillip L. (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  2. 2
    Cover Image

    The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15 by Saffari, Afshin (Author) , Kellner, Melanie (Author) , Jordan, Catherine (Author) , Rosengarten, Helena (Author) , Mo, Alisa (Author) , Zhang, Bo (Author) , Strelko, Oleksandr (Author) , Neuser, Sonja Anna (Author) , Davis, Marie Y (Author) , Yoshikura, Nobuaki (Author) , Futamura, Naonobu (Author) , Takeuchi, Tomoya (Author) , Nabatame, Shin (Author) , Ishiura, Hiroyuki (Author) , Tsuji, Shoji (Author) , Aldeen, Huda Shujaa (Author) , Cali, Elisa (Author) , Rocca, Clarissa (Author) , Houlden, Henry (Author) , Efthymiou, Stephanie (Author) , Assmann, Birgit (Author) , Yoon, Grace (Author) , Trombetta, Bianca A (Author) , Kivisäkk, Pia (Author) , Eichler, Florian (Author) , Nan, Haitian (Author) , Takiyama, Yoshihisa (Author) , Tessa, Alessandra (Author) , Santorelli, Filippo M (Author) , Sahin, Mustafa (Author) , Blackstone, Craig (Author) , Yang, Edward (Author) , Schüle-Freyer, Rebecca (Author) , Ebrahimi-Fakhari, Darius (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  3. 3
    Cover Image

    Blended phenotype of Silver-Russell Syndrome and SPG50 caused by maternal isodisomy of chromosome 7 by Ziegler, Marvin (Author) , Russell, Bianca E. (Author) , Eberhardt, Kathrin (Author) , Geisel, Gregory (Author) , D'Amore, Angelica (Author) , Sahin, Mustafa (Author) , Kornblum, Harley I. (Author) , Ebrahimi-Fakhari, Darius (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  4. 4
    Cover Image

    Impaired mitochondrial dynamics and mitophagy in neuronal models of tuberous sclerosis complex by Ebrahimi-Fakhari, Darius (Author) , Saffari, Afshin (Author) , Wahlster, Lara (Author) , Di Nardo, Alessia (Author) , Turner, Daria (Author) , Lewis, Tommy L. (Author) , Conrad, Christopher (Author) , Rothberg, Jonathan M. (Author) , Lipton, Jonathan O. (Author) , Kölker, Stefan (Author) , Hoffmann, Georg F. (Author) , Han, Min-Joon (Author) , Polleux, Franck (Author) , Sahin, Mustafa (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  5. 5
    Cover Image

    Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism by Ebrahimi-Fakhari, Darius (Author) , Saffari, Afshin (Author) , Wahlster, Lara (Author) , Lu, Jenny (Author) , Byrne, Susan (Author) , Hoffmann, Georg F. (Author) , Jungbluth, Heinz (Author) , Sahin, Mustafa (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  6. 6
    Cover Image

    Autism and the synapse: emerging mechanisms and mechanism-based therapies by Ebrahimi-Fakhari, Darius (Author) , Sahin, Mustafa (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  7. 7
    Cover Image

    Parkinson's disease: a disorder of axonal mitophagy? by Ebrahimi-Fakhari, Darius (Author) , Wahlster, Lara (Author) , Sahin, Mustafa (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:

Search Tools: