Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Amira Nasri"'
Autor:
Fatma, Laatar, Imen, Kacem, Amira, Nasri, Mouna, Ben Djebara, Amina, Gargouri, Riadh, Gouider
Publikováno v:
La Tunisie medicale. 95(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0054939d42074831308f362d52da9623
https://pubmed.ncbi.nlm.nih.gov/29878297
https://pubmed.ncbi.nlm.nih.gov/29878297
Autor:
Boutheina, Ben Amou, Imen, Kacem, Amira, Nasri, Mouna, Ben Djebara, Youssef, Sidhom, Amina, Gargouri, Riadh, Gouider
Publikováno v:
La Tunisie medicale. 94(8-9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e92bbedb9c26671b47b8c78042698f1f
https://pubmed.ncbi.nlm.nih.gov/28603832
https://pubmed.ncbi.nlm.nih.gov/28603832
Autor:
Fatma Nabli, Ghada El Euch-Fayache, Yosr Bouhlal, Monia B. Hammer, Amira Nasri, Houda Nehdi, Fayçal Hentati, Wieme Maamouri-Hicheri, Dalel Saidi, Rim Amouri
Publikováno v:
Diagnostic molecular pathology : the American journal of surgical pathology, part B. 21(4)
Ataxia with oculomotor apraxia type 2 (AOA2) is a recently described autosomal recessive cerebellar ataxia caused by mutations in the SETX gene. It is a rare monogenic disease characterized by progressive cerebellar ataxia, oculomotor apraxia, axonal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d09d869480537be0a10810a2668c020
https://pubmed.ncbi.nlm.nih.gov/23111195
https://pubmed.ncbi.nlm.nih.gov/23111195
Publikováno v:
Humanities & Social Sciences Communications; 5/11/2023, Vol. 10 Issue 1, p1-10, 10p
Autor:
Hammer, Monia Benhamed, El Euch-Fayache, Ghada, Nehdi, Houda, Saidi, Dalel, Nasri, Amira, Nabli, Fatma, Bouhlal, Yosr, Maamouri-Hicheri, Wieme, Hentati, Fayçal, Amouri, Rim
Publikováno v:
Diagnostic Molecular Pathology; Dec2012, Vol. 21 Issue 4, p241-245, 5p