Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Kerkeni, E.
Sakka, R.
Sfar, S.
Bouaziz, S.
Ghedira, N.
Ameur, K. Ben
Hmida, H. Ben
Chioukh, F.-Z.
Ghédira, E.S.
Gribaa, M.
and
Monastiri, K.
2015.
Sanjad-Sakati syndrome in a Tunisian child.
Archives de Pédiatrie,
Vol. 22,
Issue. 9,
p.
951.
Janati, A. Bruce
ALGhasab, Naif Saad
Umair, Muhammad
FazelHaq
Osman, Aboubaker
Sammour, Mohammad
Ahmed, AmalAbdulgadir
Ghorbel, Sofiane
Alshammeri, Hesse
Aldaife, Maram
Abdollah, Ahmad
and
ALMubaddel, Afnan Ibrahim
2018.
Lennox-Gastaut syndrome associated with dysgenesis of corpus callosum.
Annals of Clinical Neurophysiology,
Vol. 20,
Issue. 1,
p.
36.
Bashar, Masharib
Taimur, Muhammad
Amreek, FNU
Sayeed, Khalid A
and
Tahir, Amber
2020.
Endocrinological Manifestations of Sanjad-Sakati Syndrome.
Cureus,
Aminzadeh, Majid
Galehdari, Hamid
Shariati, Gholamreza
Malekpour, Nasrin
and
Ghandil, Pegah
2020.
Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad–Sakati syndrome.
Jornal de Pediatria,
Vol. 96,
Issue. 1,
p.
60.
Aminzadeh, Majid
Galehdari, Hamid
Shariati, Gholamreza
Malekpour, Nasrin
and
Ghandil, Pegah
2020.
Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad‐Sakati syndrome.
Jornal de Pediatria (Versão em Português),
Vol. 96,
Issue. 1,
p.
60.
Alghamdi, Sara
2022.
Oral Facial Manifestations of Sanjad–Sakati Syndrome: A Literature Review.
Children,
Vol. 9,
Issue. 4,
p.
448.
Zhou, Yang
and
Tong, Chenglin
2024.
Spontaneous intracranial hypotension in a patient without corpus callosum: A case report.
Medicine,
Vol. 103,
Issue. 30,
p.
e39090.