Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Yessine, Amri"'
Autor:
Latifa Chkioua, Houda El Fissi, Yessine Amri, Chayma Sahli, Fadoua Bouzid, Hela Boudabous, Neji Tbib, Salima Ferchichi, Taieb Massoud, Najat Alif, Sandrine Laradi, Hassen Ben Abdennebi
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Mucopolysaccharidosis type I is a lysosomal storage disease resulting from a deficiency in alpha-L-iduronidase (IDUA), which causes the accumulation of partially degraded dermatan sulfate and heparan sulfate. This retrospective st
Externí odkaz:
https://doaj.org/article/15bce9b578064770b9c19476d24d775b
Autor:
Sarra Tombari, Yessine Amri, Yosra Hasni, Sondess Hadj Fredj, Yesmine Salem, Salima Ferchichi, Leila Essaddam, Taieb Messaoud, Rym Dabboubi
Publikováno v:
Heliyon, Vol 10, Iss 14, Pp e34947- (2024)
Introduction: Growth Hormone Deficiency (GHD) is a rare disease marked by a complete or partial reduction in the production of growth hormone. Vitamin D deficiency is frequent and may be associated with several pathologies. However, the association b
Externí odkaz:
https://doaj.org/article/01af9c3f89184630bb3f14d3ea0c7f2c
Autor:
Ben Bnina, Amène1,2 (AUTHOR), Yessine, Amri3,4 (AUTHOR) amri.yessine@yahoo.com, El Bahri, Yasmine1,5 (AUTHOR), Chouchene, Saoussen2,6 (AUTHOR), Ben Lazrek, Nada1 (AUTHOR), Mimouna, Mariem1 (AUTHOR), Mlika, Zeineb1 (AUTHOR), Messoudi, Aziza1 (AUTHOR), Zellama, Dorsaf5,7 (AUTHOR), Sahtout, Wissal5,7 (AUTHOR), Bouatay, Amina1,2 (AUTHOR)
Publikováno v:
BMC Medical Genomics. 2/29/2024, Vol. 17 Issue 1, p1-14. 14p.
Publikováno v:
Applications in Engineering Science, Vol 16, Iss , Pp 100153- (2023)
Background: The determination of area tumor presents the chief challenge in brain tumor therapy and assessment. Without ionizing radiation, the medical Magnetic Resonance Imaging (MRI) tool has appeared as an essential diagnostic technique for brain
Externí odkaz:
https://doaj.org/article/ed925285b2f240b988127d84228631c6
Autor:
Latifa Chkioua, Yessine Amri, Chayma Sahli, Ferdawes Ben Rhouma, Amel Ben Chehida, Neji Tebib, Taieb Messaoud, Hassen Ben Abdennebi, Sandrine Laradi
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 15, Iss 1, Pp 1-7 (2023)
Abstract Background Glycogen storage disease type 1b (GSD1b) is an autosomal recessive lysosomal storage disease caused by defective glucose-6-phosphate transporter encoded by SLC37A4 leading to the accumulation of glycogen in various tissues. The hi
Externí odkaz:
https://doaj.org/article/5c3a8d027fbc4cf9ba800c73837901e7
Autor:
Latifa Chkioua, Yessine Amri, Chaima Saheli, Wassila Mili, Sameh Mabrouk, Imen Chabchoub, Hela Boudabous, Wissem Ben Azzouz, Hadhami Ben Turkia, Salima Ferchichi, Neji Tebib, Taieb Massoud, Mohamed Ghorbel, Sandrine Laradi
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly as
Externí odkaz:
https://doaj.org/article/719f2484eacd45bd80f7b8a19e31bbfd
Autor:
Latifa Chkioua, Yessine Amri, Chayma Saheli, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Messaoud, Neji Tebib, Sandrine Laradi
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-11 (2021)
Abstract Background Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-l-fucosidase (FUCA1) activity, leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues. Clinical f
Externí odkaz:
https://doaj.org/article/05e8d5831c2b44aab94c8e7c13743974
Autor:
Taher Mahmoud, Chaima Sahli, Sondess Hadj Fredj, Yessine Amri, Rim Othmani, Ghaber S. Mohamed, Ekhtelbenina Zein, Taieb Messaoud
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few studies have been conducted on hemoglobinopathies in Mauritania. Therefore, the aim of
Externí odkaz:
https://doaj.org/article/6382c27ae37a4ff2b7770ed6b61bdab7
Autor:
Yessine Amri, Sana Aboulkacem, Rym Dabboubi, Manel Ayoub, Oussema Lamine, Mariem Othmani, Zied Aouni, Taieb Messaoud, Chakib Mazigh
Publikováno v:
Annales de Biologie Clinique. 81:204-209
Autor:
Latifa Chkioua, Yessine Amri, Sahli Chaima, Ferdawes Fenni, Hela Boudabous, Hadhami Ben Turkia, Taieb Messaoud, Neji Tebib, Sandrine Laradi
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/92ffcb6638d14c009fa5b4e80550f66f