Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Julia Pytte"'
Autor:
Andrzej Karol Konopka, Anna Kasprzyk, Julia Pyttel, Lechosław Paweł Chmielik, Artur Niedzielski
Publikováno v:
Audiology Research, Vol 14, Iss 4, Pp 736-746 (2024)
APD (auditory processing disorders) is defined as difficulties in processing auditory stimuli within the central nervous system, with normative physical hearing and intellectual disabilities excluded. The scale of this phenomenon among children and a
Externí odkaz:
https://doaj.org/article/46e7254f28c54ff3886672308a0f8b54
Autor:
Frances Theunissen, Loren L. Flynn, Ryan S. Anderton, Frank Mastaglia, Julia Pytte, Leanne Jiang, Stuart Hodgetts, Daniel K. Burns, Ann Saunders, Sue Fletcher, Steve D. Wilton, Patrick Anthony Akkari
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
The underlying genetic and molecular mechanisms that drive amyotrophic lateral sclerosis (ALS) remain poorly understood. Structural variants within the genome can play a significant role in neurodegenerative disease risk, such as the repeat expansion
Externí odkaz:
https://doaj.org/article/7ee2c326248d4136b9a19c1947b39ca9
Autor:
Natasha Berthold, Julia Pytte, Cynthia M. Bulik, Monika Tschochner, Sarah E. Medland, Patrick Anthony Akkari
Publikováno v:
International Journal of Eating Disorders. 55:747-753
Anorexia nervosa (AN) is a devastating disorder with evidence of underexplored heritability. Twin and family studies estimate heritability (h
Autor:
Julia, Pytte, Loren L, Flynn, Ryan S, Anderton, Frank L, Mastaglia, Frances, Theunissen, Ian, James, Abigail, Pfaff, Sulev, Koks, Ann M, Saunders, Richard, Bedlack, Daniel K, Burns, Michael W, Lutz, Nailah, Siddique, Teepu, Siddique, Allen D, Roses, P Anthony, Akkari
Publikováno v:
Neurology: Genetics
Objective To test the hypothesis that rs573116164 will have disease-modifying effects in patients with superoxide dismutase 1 (SOD1) familial amyotrophic lateral sclerosis (fALS), we characterized rs573116164 within a cohort of 190 patients with fALS
Autor:
Frances Theunissen, Loren L. Flynn, Ryan S. Anderton, Frank Mastaglia, Julia Pytte, Leanne Jiang, Stuart Hodgetts, Daniel K. Burns, Ann Saunders, Sue Fletcher, Steve D. Wilton, Patrick Anthony Akkari
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 14 (2020)
Frontiers in Neuroscience, Vol 14 (2020)
The underlying genetic and molecular mechanisms that drive amyotrophic lateral sclerosis (ALS) remain poorly understood. Structural variants within the genome can play a significant role in neurodegenerative disease risk, such as the repeat expansion
Autor:
Abigail L Pfaff, Nailah Siddique, Richard Bedlack, Ian James, Sulev Kõks, Loren L. Flynn, Frances Theunissen, Allen D. Roses, P. Anthony Akkari, Ryan S. Anderton, Michael W. Lutz, Julia Pytte, Ann M. Saunders, Daniel K. Burns, Teepu Siddique, Frank L. Mastaglia
Publikováno v:
Neurology Genetics. 6:e470
ObjectiveTo test the hypothesis that rs573116164 will have disease-modifying effects in patients with superoxide dismutase 1 (SOD1) familial amyotrophic lateral sclerosis (fALS), we characterized rs573116164 within a cohort of 190 patients with fALS
Autor:
Teepu Siddique, Frank L. Mastaglia, Anthony Akkari, Richard Bedlack, Nailah Siddique, Ianthe Pitout, Loren L. Flynn, Ian James, Ryan S. Anderton, Leanne Jiang, Julia Pytte, Ann M. Saunders, Frances Theunissen
Publikováno v:
Neurology: Genetics
ObjectiveAs structural variations may underpin susceptibility to complex neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), the objective of this study was to investigate a structural variant (SV) within sequestosome 1 (SQSTM1).M