Zobrazeno 1 - 10 of 19 pro vyhledávání: '"Soumeya Siala, Gaigi"'
1
Congenital anomalies in Tunisia: Frequency and risk factors
Autor: Kaouther Nasri, A.M. Ben Hamida, Soumeya Siala Gaigi, Aida Masmoudi, N. Ben Jemaa, Raja Marrakchi, Meriem El Aloui
Publikováno v: Journal of Gynecology Obstetrics and Human Reproduction. 46:651-655
Background Despite the high risk of recurrence of congenital malformations, there are no well-accepted preventive measures in developing countries like Tunisia. It is recommended that thorough epidemiological studies of congenital anomalies in this c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e78ae84c0a152fee10a0c722d2644d1
https://doi.org/10.1016/j.jogoh.2017.05.006
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2
Syndrome de Neu-Laxova : rapport de trois cas et revue de la littérature
Autor: Nadia Boujelbene, M. B. Chanoufi, Mehdi Kehila, Aida Masmoudi, Soumeya Siala Gaigi, Reziga H, Sihem Darouich
Publikováno v: Annales de Pathologie. 36:235-244
Resume Introduction Le syndrome de Neu-Laxova (SNL) est un desordre polymalformatif, letal, autosomique recessif. Ses principales manifestations incluent un retard de croissance intra-uterin harmonieux severe, une dysmorphie faciale typique, une icht
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d6f540b98762841cfda55b8d3f5c6b0d
https://doi.org/10.1016/j.annpat.2016.04.004
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3
Maternal 25-hydroxyvitamin D level and the occurrence of neural tube defects in Tunisia
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f84172d7618f5493cd88ba2c08f04ae4
https://doi.org/10.1016/j.ijgo.2016.01.014
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4
Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents
Autor: Mehdi Ben Lassoued, Raja Marrakchi, Kaouther Nasri, Souhail Omar, Soumeya Siala Gaigi, Nadia Ben Jemaa, Mohamed Kacem Ben Fradj, Imen Mahjoubi, Moncef Feki, Riadh Jemaa, Safa Ben Wafi, Mariem Aloui, Fatma Midani, Mariem Soussi, Miryam Boulares, Amani Kallel, Abir Baara, Meriam Ben Halima
Publikováno v: Pathobiology : journal of immunopathology, molecular and cellular biology. 86(4)
Objective: This study aims to investigate the association of 5,10-methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) and methionine synthase reductase (MTRR A66G) gene polymorphisms with neural tube defects (NTDs) in a Tunisian population.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3ecf344de65027132175425bd31b36f
https://pubmed.ncbi.nlm.nih.gov/31238314
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5
A fetopathological and clinical study of the Dandy-Walker malformation and a literature review
Autor: Borislav Kitov, Tanya Kitova, Aida Masmoudi, Dalenda Chelli, Soumeya Siala Gaigi, Hristo Zhelyazkov, Denis Milkov
Publikováno v: Case Reports in Perinatal Medicine. 5:49-53
Aim: The Dandy-Walker malformation is a rare abnormality of the central nervous system pertaining to the group of cystic malformations. The frequency of occurrence of the malformation ranges from 1:800 to 35,000 live births. The aim of this study is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::351180eaec8ccab57ded0c40ee376c40
https://doi.org/10.1515/crpm-2015-0049
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6
Association of maternal homocysteine and vitamins status with the risk of neural tube defects in Tunisia: A case-control study
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cafcd94ce827140ffda9d25056d0b642
https://doi.org/10.1002/bdra.23418
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7
Correlation of trisomy 13 with atelencephalic aprosencephaly
Autor: Tanya Kitova, Borislav Kitov, Soumeya Siala Gaigi, Nahed Ben Cheikh
Publikováno v: Pteridines, Vol 26, Iss 1, Pp 37-40 (2015)
A rare phenotype-genotype correlation of atelencephalic aprosencephaly in a fetus with free trisomy 13 karyotype, obtained by pregnancy termination for holoprosencephaly during the 26th gestational week, is presented. Lack of cerebral hemispheres and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a41b125c02b68b3054e4c37f590eaf
https://doi.org/10.1515/pterid-2014-0016
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8
Fetopathological examination for the fetuses with Down syndrome in Tunisia: Epidemiological study and associated malformations
Autor: Dalenda Chelli, Habiba Chaâbouni, Dorra Zghal, Soumeya Siala Gaigi, Nadia Ben Jemaa, Meriem Sahraoui, Raja Marrakchi, Aida Masmoudi, Abdel Majid Ben Hamida, Meriem El Aloui, Kaouther Nasri
Publikováno v: Pathology, research and practice. 213(9)
Background For Down syndrome (DS), traditional epidemiological studies to determine the prevalence, cause, and clinical significance of the syndrome have been conducted over the last 100 years. In Tunisia, the current work is the first in-depth study
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50d52cb656a5da7cb6c4d5c5bf3f8899
https://pubmed.ncbi.nlm.nih.gov/28736088
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10
A fetus with meckel-gruber syndrome associated with isomerism
Autor: Denis Milkov, Kristina Kilova, Tanya Kitova, Borislav Kitov, Soumeya Siala Gaigi, Aida Masmoudi
Publikováno v: Open Medicine, Vol 9, Iss 3, Pp 481-484 (2014)
Abstract. Meckel-Gruber syndrome (MKS) is an autosomal recessive lethal malformation. As far as we know, the rate of incidence for the syndrome is 0.02 per 10,000 births. It is estimated that Meckel-Gruber syndrome accounts for 5% of all neural tube
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba381d2c07736e7f42f784060a3eb9cf
https://doi.org/10.2478/s11536-013-0304-0
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