Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Farid, Keramatian"'
Autor:
Elham Jaberi, Casey Turk, Frank J. Steemers, Abolfazl Moghadam, Jian-Bing Fan, Masoud Soleimani, Gholam Ali Shahidi, Farid Keramatian, Elahe Elahi, Ehsan Arefian, Brandy Klotzle, Shahriar Nafissi, Mohsen Karimi Arzenani, Mohammad Rohani
Publikováno v:
Movement Disorders. 31:1004-1011
Background We aimed to identify the genetic cause of neurological disease in an Iranian family whose manifestations include symptoms of parkinsonism and cognitive dysfunction. Methods Clinical data on the patients were gathered by interviews with par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9501700090ba7c481372c8301461d85d
https://doi.org/10.1002/mds.26627
https://doi.org/10.1002/mds.26627
Autor:
Elham, Jaberi, Mohammad, Rohani, Gholam Ali, Shahidi, Shahriar, Nafissi, Ehsan, Arefian, Masoud, Soleimani, Abolfazl, Moghadam, Mohsen Karimi, Arzenani, Farid, Keramatian, Brandy, Klotzle, Jian-Bing, Fan, Casey, Turk, Frank, Steemers, Elahe, Elahi
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 31(7)
We aimed to identify the genetic cause of neurological disease in an Iranian family whose manifestations include symptoms of parkinsonism and cognitive dysfunction.Clinical data on the patients were gathered by interviews with parents, neurological e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb83f710523c9f1c201272515c756d02
https://pubmed.ncbi.nlm.nih.gov/29143421
https://pubmed.ncbi.nlm.nih.gov/29143421
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.
Autor:
Jaberi, Elham, Rohani, Mohammad, Shahidi, Gholam Ali, Nafissi, Shahriar, Arefian, Ehsan, Soleimani, Masoud, Moghadam, Abolfazl, Arzenani, Mohsen Karimi, Keramatian, Farid, Klotzle, Brandy, Fan, Jian‐Bing, Turk, Casey, Steemers, Frank, Elahi, Elahe, Fan, Jian-Bing
Publikováno v:
Movement Disorders; Jul2016, Vol. 31 Issue 7, p1004-1011, 9p
Publikováno v:
Movement Disorders; Jul2016, Vol. 31 Issue 7, pn/a-N.PAG, 2p