Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Laila, Bouguenouch"'
Autor:
Mohamed Hssaini, Sana Abourazzak, Ihsane El Otmani, Mohamed Ahakoud, Amina Ameli, Laila Bouguenouch, Hicham Bekkari
Publikováno v:
Endocrine Connections, Vol 13, Iss 10, Pp 1-10 (2024)
Background: Differences/disorders of sex development (DSD) encompass a wide range of conditions. Their clinical spectrum and etiological diagnosis have not been reported in Moroccan patients. Aims: The study aims to highlight the clinical spectrum, e
Externí odkaz:
https://doaj.org/article/c3a23ca68f05438994ee994e45daac26
Autor:
Chaimae Samtal, Laila Bouguenouch, Nabil Ismaili, Marwa El Baldi, Badreddine El Makhzen, Karima El Rhazi, Mohammed Mzyiene, Moulay Hassan Farih, Karim Ouldim, Hassan Ghazal, Hicham Bekkari
Publikováno v:
African Journal of Urology, Vol 30, Iss 1, Pp 1-7 (2024)
Abstract Background Prostate cancer stands as the most frequently diagnosed cancer among men globally, with over 600,000 new cases annually. In-depth epidemiological studies play a pivotal role in delineating the unique characteristics of specific po
Externí odkaz:
https://doaj.org/article/c75f914080234db68d0f66c3a59991bd
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:
Sara Boukansa, Ismail Mouhrach, Fatima El Agy, Laila Bouguenouch, Mounia Serraj, Bouchra Amara, Yassine Ouadnouni, Mohamed Smahi, Badreeddine Alami, Nawfel Mellas, Zineb Benbrahim, Hinde El Fatemi
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background In the current treatment landscape for non-small cell lung cancers, epidermal growth factor receptor-tyrosine kinase inhibitors have emerged as a well-established treatment option for patients with advanced or metastatic disease.
Externí odkaz:
https://doaj.org/article/557016738b5a4fe6a39d79fded5b97ba
Autor:
Sara Boukansa, Ismail Mouhrach, Fatima El Agy, Sanae El Bardai, Laila Bouguenouch, Mounia Serraj, Bouchra Amara, Yassine Ouadnouni, Mohamed Smahi, Badreeddine Alami, Nawfel Mellas, Zineb Benbrahim, Hinde El Fatemi
Publikováno v:
PLoS ONE, Vol 19, Iss 6 (2024)
Externí odkaz:
https://doaj.org/article/14238232cc884837b825c82d09b48d4e
Autor:
Fatima El Agy PhD, Sanae El Bardai PhD, Sara Boukansa PhD, Laila Bouguenouch MD, Zineb Benbrahim MD, Khalid Mazaz MD, El Bachir Benjelloun MD, Abdelmalek Ousadden MD, Karim Ouldim MD, Sidi Adil Ibrahimi MD, Laila Chbani MD
Publikováno v:
Cancer Control, Vol 31 (2024)
Purpose To date, only a few studies have investigated the role of molecular alterations in cancer recurrence. This exploratory study aimed to evaluate the impact of molecular alterations on the time and site of recurrence in patients with stage I–I
Externí odkaz:
https://doaj.org/article/2d55f33f694b4b0f8b062cd052c6ff0e
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Background: Over 200 pathogenic variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with cystic fibrosis (CF)—the most prevalent autosomal recessive disease globally, the p.Phe508del variant being the most
Externí odkaz:
https://doaj.org/article/0ff911f5b88a4d31824ff44e792c5fe1
Autor:
Meriame Abbassi, Hanane Sayel, Nadia Senhaji, Said Trhanint, Hanane Bay Bay, Laila Bouguenouch, Fatima Zahra Mernisi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Xeroderma pigmentosum (XP) is a rare autosomal recessive skin disorder characterized by hyperpigmentation, premature skin aging, ocular and cutaneous photosensitivity with increased risk of skin tumors. XP is caused by mutations i
Externí odkaz:
https://doaj.org/article/5c5e91126bd44e1fba166f7c3cd899e8
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100065- (2023)
Externí odkaz:
https://doaj.org/article/c3047a6bada6400c822d8c1cf7c3a28b
Autor:
Abdelhamid Bouramtane, Hajar El Azami El Idrissi, Mohamed Ahakoud, Badreddine Elmakhzen, Ahmed Lazraq, Laila Bouguenouch, Karim Ouldim
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100066- (2023)
Externí odkaz:
https://doaj.org/article/f286aef9318a416bb52e1d23cc0d4751