Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Naziha Kaabechi"'
Autor:
Soumeya Siala Gaigi, Kaouther Nasri, Naziha Kaabechi, Moncef Feki, Mohamed Kacem Ben Fradj, Mariem Sahraoui, Raja Marrakchi, Aida Masmoudi
Publikováno v:
International Journal of Gynecology & Obstetrics. 134:131-134
To determine whether low vitamin D levels in pregnant women are associated with the occurrence of neural tube defects (NTDs) in Tunisia.In a prospective study, pregnant women were recruited at a center in Tunis between January 1, 2012, and December 3
Autor:
Mouna Tabebi, Ghada Ben Salah, Leila Keskes, Naziha Kaabechi, Fakhri Kallabi, Chahnez Triki, Hassen Kamoun, Emna Ellouz
Publikováno v:
Clinica Chimica Acta. 453:141-146
Introduction X-linked adrenoleukodystrophy is a neurodegenerative recessive disorder that affects the brain white matter and associated with adrenal insufficiency. It is characterized by an abnormal function of the peroxisomes, which leads to an accu
Autor:
Kaouther Nasri, Mariem Aloui, Raja Marrakchi, Mohamed Kacem Ben Fradj, Souhail Omar, Asma Touati, Aida Masmoudi, Soumeya Siala Gaigi, Michèle Véronique Elmay, Moncef Feki, Naziha Kaabechi, Nadia Ben Jemaa
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 103:1011-1020
Background This study was conducted to determine whether low folate and vitamin B12 levels, as well as high homocysteine levels in pregnant women are associated with neural tube defects (NTDs) in Tunisia. Methods A total of 75 NTDs pregnancies and 75
Autor:
Kaouther, Nasri, Mohamed Kacem, Ben Fradj, Asma, Touati, Mariem, Aloui, Nadia, Ben Jemaa, Aida, Masmoudi, Michèle Véronique, Elmay, Souhail, Omar, Moncef, Feki, Naziha, Kaabechi, Raja, Marrakchi, Soumeya Siala, Gaigi
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 103(12)
This study was conducted to determine whether low folate and vitamin B12 levels, as well as high homocysteine levels in pregnant women are associated with neural tube defects (NTDs) in Tunisia.A total of 75 NTDs pregnancies and 75 matched controls we
Autor:
I. Ben Ghorbel, Moncef Feki, J. Riadh, M.H. Houman, Amani Kallel, Naziha Kaabechi, M. Tougorti, M.K. Ben fradj
Publikováno v:
Annals of the Rheumatic Diseases. 75:1073.2-1073
Background Beyond its critical function in calcium homeostasis, vitamin D has recently been found to play an important role in the modulation of the immune/inflammation system. Increasing numbers of study have established that vitamin D insufficiency
Autor:
Sonia El Housaini, Radhouen Rachdi, Sarra Klai, Najiba Fekih-Mrissa, Brahim Nsiri, Nasredine Gritli, Naziha Kaabechi
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 22(5)
Our aim in this study was to investigate the association between elevated homocysteine levels and the two MTHFR polymorphisms, C677T and A1298C, with several pregnancy complications such as recurrent pregnancy loss, preeclampsia, placental abruption
Publikováno v:
Revue Neurologique. 170:A135-A136
Autor:
R. Rafrafi, Ameni Kallel, Imen Ayedi, W. Melki, Riadh Jomaa, Noomen Bouaziz, Oussama Sidhom, Moncef Feki, Naziha Kaabechi, Zouhaier El Hechmi
Publikováno v:
Psychiatry research. 179(1)
The existence of association between hyperhomocysteinaemia (HHC) and schizophrenia has been suggested by several recent studies. This study aimed to determine the prevalence of HHC and its main determinants, and sought a correlation with clinical fea
Publikováno v:
Annales d'Endocrinologie. 76:473
Background X-linked adrenoleukodystrophy (X-ALD; MIM #300100) is a neurodegenerative recessive disorder that affects the brain white matter and associated with adrenal insufficiency. It is characterized by an abnormal function of the peroxisomes, whi
Autor:
Chahnez Triki, Nadege Kamoun, Naziha Kaabechi, Hela Fourati, Faiza Fakhfakh, Emna Ellouz, Dhouha Chaari
Publikováno v:
Revue Neurologique. 171:A129
Introduction L’acidurie L-2-hydroxyglutarique (AL2OHG) est une maladie neurometabolique rare autosomique recessive liee a des mutations du gene L2HGDH. Elle est recemment decrite et reste encore mal connue. Objectifs Etudier le profil phenotypique