Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Abdelhafid Natiq"'
Autor:
Hinde El Mouhi, Meriame Abbassi, Meryem Jalte, Abdelhafid Natiq, Laila Bouguenouch, Sana Chaouki
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 67-82 (2024)
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy, is a severe epileptic syndrome affecting children, with an incidence of 1/22,000 to 1/49,900 live births annually. Characterized by resistant and prolonged seizures, it o
Externí odkaz:
https://doaj.org/article/8bf80ad138e640d29c02084f77c3bf97
Autor:
Fatima Ouboukss, Zhour El Amrani, Hicham Bouchahta, Ilham Ratbi, Aziza Sbiti, Thomas Liehr, Abdelaziz Sefiani, Abdelhafid Natiq
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: The majority of small supernumerary marker chromosomes (sSMCs) are derived from one single chromosome. Complex sSMCs, on the other hand, consist of genetic material derived from more than one, normally two chromosomes. Complex sSMCs inv
Externí odkaz:
https://doaj.org/article/d41a9bacfd38469f92632042d1f9a6a3
Autor:
Luis A. Méndez-Rosado, Norma de León-Ojeda, Alina García, Frenny Sheth, Asmaa Gaadi, Ahmed Aziz Bousfiha, Mouna Lehlimi, Abdelhafid Natiq, Oxana S. Kurinnaia, Svetlana G. Vorsanova, Ivan Iourov, Dagmar Huhle, Thomas Liehr
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-8 (2022)
Abstract Background DiGeorge syndrome (DGS), caused by a deletion del(22)(q11.2q11.2), is the most frequently observed microdeletion syndrome. There is a vast clinical heterogeneity in DGS, and several studies suggested also heterogeneity of clinical
Externí odkaz:
https://doaj.org/article/1d14f5e89b2c49e4aece3d936bbec468
Autor:
Hasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, Thomas Liehr, Hind Dehbi, Latifa Loukhmas, Fatima Chegdani
Publikováno v:
Leukemia Research Reports, Vol 14, Iss , Pp 100217- (2020)
Cytogenetic and iFISH plays a major part in the diagnosis of the MM and have an important prognostic significance.10–15% of patients with amyloidosis will also have multiple myeloma (MM). Few studies have addressed the clinical and cytogenetic feat
Externí odkaz:
https://doaj.org/article/79b6edd44a2b4de29cc55211c35bea79
Publikováno v:
The Pan African Medical Journal, Vol 13, Iss 38 (2012)
INTRODUCTION: Le but de cette étude était de présenter les premiers résultats de diagnostic anténatal de la trisomie 21 par la technique d'hybridation in situ en fluorescence (FISH) au Maroc et discuter son intérêt dans le diagnostic rapide de
Externí odkaz:
https://doaj.org/article/d0302481a02348b2bb611e275263add3
Autor:
Zhour, El Amrani, Siham Chafai, Elalaoui, Wafae, Jdioui, Aziza, Sbiti, Ilham, Ratbi, Thomas, Liehr, Abdelaziz, Sefiani, Abdelhafid, Natiq
Publikováno v:
Ophthalmic Genetics. 43:689-692
Retinoblastoma (RB) is the most common malignant intraocular tumor in children; it affects their eyes often even prenatally. RB may be sporadic or familial, due to germinal mutation in RB1 gene or by abnormal chromosomal abnormalities involving RB1 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116ef3f73d02ab1c6b2a94bd26b5e174
https://doi.org/10.1080/13816810.2022.2083183
https://doi.org/10.1080/13816810.2022.2083183
Autor:
Hamdaoui Hasna, Abdelhafid Natiq, Oumaima Benlarroubia, Faiza CHBEL, Rajaa Chahboun, jihane Toughza, Afaf Lamzouri
Cup Like acute myeloid leukemia is the rarest form of children leukemia. We present a case of Cup Like Acute Myeloid Leukemia (AML) with t(4;12) (q12;p13) associated with two other clones t(1;16)(q12;q24) and t(12;13)(p13;q13). Cytogenetic and iFISH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b79f0629d5e33205b8f23b956668ca
https://doi.org/10.22541/au.166661107.77254644/v1
https://doi.org/10.22541/au.166661107.77254644/v1
Autor:
Mustafa Zakaria, Marcuse F. Steven, Abdelhafid Natiq, Noureddine Louanjli, Mohammed Zarqaoui, Wassym R. Senhaji
Publikováno v:
OALib. :1-13
This review article demonstrates and shows the embryo transfer process in ART treatment; It also compares different embryo transfer timing and days to evaluate the pregnancy and implantation rates with day three versus day five embryo and day five ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fa9ea4796c7547ed363796e0891a1e4
https://doi.org/10.4236/oalib.1107322
https://doi.org/10.4236/oalib.1107322
Autor:
Modou M. Mbaye, Aya Al-Ibraheemi, Mohamed Zarqaoui, Mustafa Zakaria, Wassym R. Senhaji, Mohamed Ennaji, Romaissa Boutiche, Noureddine Louanjli, Abdelhafid Natiq
Publikováno v:
OALib. :1-11
The impact of progesterone on pregnancy and supporting embryo implantation prior embryo transfer in IVF treatment have been well studied and several studies proved and demonstrated the positive impact of P4 on pregnancy. However, this impact can be i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81d279c25f686c87c8bf71c8a1ef899c
https://doi.org/10.4236/oalib.1107414
https://doi.org/10.4236/oalib.1107414
Autor:
Mustafa Zakaria, Aya Al-ibraheemi, Mohamed Ennaji, Wassym R. Senhaji, Abdelhafid Natiq, Romaissa Boutiche, Modou M. Mbaye, Mohamed Zarqaoui, Muhjah F. Hassan, Hayder A. Mossa, Noureddine Louanjli
Publikováno v:
Gynecology & Reproductive Health. 5
Sperm DNA fragmentation is common in infertile male. Besides, sperm DNA integrity is essential for fertilization and healthy offspring development. Numerous genetic and environmental elements are associated with impacting sperm DNA integrity negative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80defcbf6308f3ba98ac60182d64afc8
https://doi.org/10.33425/2639-9342.1159
https://doi.org/10.33425/2639-9342.1159