Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Amira Moussa"'
Autor:
Ibtihel Benhaj Mbarek, Saoussen Mdimeg, Amira Moussa, Dorsaf Zellama, Hayat Kaarout, Jaouida Abdelmoula, Abdellatif Achour, Saoussen Abroug, Asma Omezzine, Ali Bouslama
Publikováno v:
BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background Primary hyperoxaluria type 1 (PH1), is a rare and heterogeneous disease and one of major causes of renal insufficiency in Tunisia, caused by mutations in the AGXT gene. 33-34InsC mutation, was mainly described in children with a s
Externí odkaz:
https://doaj.org/article/e40e3b56fdbf46a18874d849d350f2fe
Autor:
Hayet Kaarout, Jalel Chemli, Abdellatif Achour, Amira Moussa, Asma Omezzine, Saoussen Abroug, Ali Bouslama, Geneviéve Souche, Sabra Aloui, Saoussen M'dimegh, Ibtihel M'barek, Cécile Aquaviva-bourdain, Sameh Mabrouk
Publikováno v:
Annals of Human Genetics. 81:1-10
Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal alanine:glyoxylate aminotransferase (AGT). PH1 is a clinically and genetically hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff396de0b8279edb0a1bca82e8aed24b
https://doi.org/10.1111/ahg.12178
https://doi.org/10.1111/ahg.12178
Autor:
Amira Moussa, Sana Samet, Ali Bouslama, Nourhene Khayati, Mariem Ammar, Omezzine Asma, Sana Ben Amor
Publikováno v:
Revue Neurologique. 177:S89
Introduction L’hyperhomocysteinemie (HHCy) est un facteur de risque cardiovasculaire independant implique dans les accidents vasculaires cerebraux (AVC) ischemiques. Parmi ses etiologies, on trouve les carences vitaminiques B et la mutation C677 T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cad745227e855d0feb441cdc6aceac2
https://doi.org/10.1016/j.neurol.2021.02.285
https://doi.org/10.1016/j.neurol.2021.02.285
Autor:
Ons Fekih, Afifa Koubaa, Ibtihel B hajMbarek, Med-Fadhel Najjar, Haithem Hamdouni, Fadoua Neffati, Asma Omezzine, Marwa Ajmi, Sonia Triki, Ali Bouslama, Amira Moussa
Publikováno v:
Clinical laboratory. 63(3)
BACKGROUND The aim of this study was to evaluate the association of ACE, angiotensinogen (AGT) and angiotensin II receptor type I (AGTR1) polymorphisms with diabetic nephropathy (DN) in Tunisians. METHODS The study population comprised 236 type 2 dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a079fe492eb005d49f47ae6c1231be8
https://pubmed.ncbi.nlm.nih.gov/28271690
https://pubmed.ncbi.nlm.nih.gov/28271690
Autor:
Saoussen Mdimeg, Hayat Kaarout, Ali Bouslama, Abdellatif Achour, Asma Omezzine, Amira Moussa, Ibtihel M'barek, Jaouida Abdelmoula, Saoussen Abroug, Dorsaf Zellama
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)
BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)
Background Primary hyperoxaluria type 1 (PH1), is a rare and heterogeneous disease and one of major causes of renal insufficiency in Tunisia, caused by mutations in the AGXT gene. 33-34InsC mutation, was mainly described in children with a severe cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3566973080fdac5a975fb662e7f53ae9
https://pubmed.ncbi.nlm.nih.gov/28619084
https://pubmed.ncbi.nlm.nih.gov/28619084
Autor:
Saoussen, M'dimegh, Asma, Omezzine, Ibtihel, M'barek, Amira, Moussa, Sameh, Mabrouk, Hayet, Kaarout, Geneviéve, Souche, Jalel, Chemli, Sabra, Aloui, Cécile, Aquaviva-Bourdain, Abdellatif, Achour, Saoussen, Abroug, Ali, Bouslama
Publikováno v:
Annals of human genetics. 81(1)
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal alanine:glyoxylate aminotransferase (AGT). PH1 is a clinically and genetically heterogeneous dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2f45f3905d4b4a7e4b5f1affd326d23
https://pubmed.ncbi.nlm.nih.gov/27935012
https://pubmed.ncbi.nlm.nih.gov/27935012
Autor:
Kaouther Kchok, Naoufel Nabli, Nabila Ben Rejeb, R. Belkahla, Asma Omezzine, Lamia Rebhi, Ahmed Ben Abdelaziz, Essia Boughzala, Imen Boumaiza, Ali Bouslama, Ibtihel Ben HadjMbarek, Amira Moussa, Jihène Rejeb, Slim Kacem
Publikováno v:
Molecular Biology Reports. 39:9893-9901
Lipoprotein lipase (LPL) is the rate-limiting enzyme in the hydrolysis of triglyceride-rich lipoprotein particles (Chylomicrons and very-low-density lipoprotein). LPL polymorphisms’ effects on lipids and coronary artery disease are controversial am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9244e4b0520e7c093b73ae018c95c9e
https://doi.org/10.1007/s11033-012-1856-9
https://doi.org/10.1007/s11033-012-1856-9
Autor:
Benjamin Kuhar, Olga V. Savinova, Konstantinos Damiris, Maria M. Plummer, José Luis Millán, Daniel J Moussouros, Lawrence Markel, Amira Moussa, Afshan Tabassum, Matthew A. Cascio, Jes Kuruvilla, Slava Gitelman, JoseYnigo Villanueva, Ashna Mehra, Jennifer Behbodikhah, Alexander Ogden, Muhddesa Lakhana, Gregg D. Blumberg, Muhammad Ahsan
Publikováno v:
Gastroenterology. 154:S-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ff1b8113918c8466347e7786518df05
https://doi.org/10.1016/s0016-5085(18)31103-x
https://doi.org/10.1016/s0016-5085(18)31103-x
Autor:
Lobna Bouacida, Ali Bouslama, Ons Achour, Jihène Rejeb, Nabila Ben Rejeb, Dorsaf Zellama, Amira Moussa, Sahbi Elmtaoua, Abdellatif Achour, Asma Omezzine, Imene Boumaiza
Publikováno v:
Journal of nephrology. 29(5)
Hyperhomocysteinaemia, an independent risk factor for cardiovascular diseases, is common in hemodialysis patients (HD) and particularly in those homozygous for polymorphism of the 5,10‐methylenetetrahydrofolate reductase (MTHFR) gene. B vitamins su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be37436fefc0f1fd1b9d170c2f1b30bf
https://pubmed.ncbi.nlm.nih.gov/26559681
https://pubmed.ncbi.nlm.nih.gov/26559681
Autor:
Asma Omezzine, Ahmed Ben Abdelaziz, Nabila Ben Rejeb, Amira Moussa, Lamia Rebhi, Essia Boughzala, Jihène Rejeb, Slim Kacem, Ali Bouslama, Imen Boumaiza
Publikováno v:
Biochemical genetics. 52(5-6)
Haptoglobin (Hp) polymorphism generates three common human genotypes (Hp1-1, Hp2-1, and Hp2-2), having functional differences, related to the risk of development of cardiovascular diseases. These functions are a consequence of hemoglobin binding that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e4299ef89124e6fc46bfeac625e7aea
https://pubmed.ncbi.nlm.nih.gov/24535155
https://pubmed.ncbi.nlm.nih.gov/24535155