Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Yamna Kriouile"'
Autor:
Filipa Curado, Sabine Rösner, Susanne Zielke, Gina Westphal, Ulrike Grittner, Volha Skrahina, Mohammed Alasel, Ahmad Mehmood Malik, Christian Beetz, Tobias Böttcher, Gal Barel, Ashish Prasad Sah, Tama Dinur, Nadeem Anjum, Quidad Ichraf, Yamna Kriouile, Zahra Hadipour, Fatemeh Hadipour, Shoshana Revel-Vilk, Claudia Cozma, Jörg Hartkamp, Huma Cheema, Ari Zimran, Peter Bauer, Arndt Rolfs
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2812 (2023)
Gaucher disease (GD) is a rare autosomal recessive disorder arising from bi-allelic variants in the GBA1 gene, encoding glucocerebrosidase. Deficiency of this enzyme leads to progressive accumulation of the sphingolipid glucosylsphingosine (lyso-Gb1)
Externí odkaz:
https://doaj.org/article/8bc45cefc4f4454f8ba12c3c3714514a
Autor:
Youssef El Kadiri, Ilham Ratbi, Fatima Zahra Laarabi, Yamna Kriouile, Abdelaziz Sefiani, Jaber Lyahyai
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)
Abstract Background Merosin-deficient congenital muscular dystrophy type 1A (MDC1A) is a rare autosomal recessive genetic condition caused by deleterious mutations in the LAMA2 gene encoding the laminin-α2 chain. It is the most frequent subtype of c
Externí odkaz:
https://doaj.org/article/1e269c2d80634cc7a78c86be9f9b1a76
Autor:
Naoual Nchinech, Afaf Elgharbi, Fatima Zahra Aglili, Yamna Kriouile, Yahia Cherrah, Asmaa Aaloui Mdaghri, Samira Serragui
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 89 (2019)
Dans notre pays, le recours aux recettes de médecine traditionnelle et aux produits cosmétiques artisanaux est très fréquent en raison du taux élevé d'analphabétisme, du faible pouvoir d'achat et du grand nombre d'herboristes. Le camphre est u
Externí odkaz:
https://doaj.org/article/91650878a7e84443bc098c1def725af2
Autor:
Thibault Vallet, Omar Elhamdaoui, Amina Berraho, Lalla Ouafae Cherkaoui, Yamna Kriouile, Chafiq Mahraoui, Nezha Mouane, Anne-Marie Pense-Lheritier, Fabrice Ruiz, Yahya Bensouda
Publikováno v:
Pharmaceutics, Vol 12, Iss 8, p 766 (2020)
Although knowledge on medicine acceptability remains fragmented, this multi-faceted concept has emerged as a key factor for compliance in pediatrics. In order to investigate the acceptability of medicines used in the University Medical Centre Ibn Sin
Externí odkaz:
https://doaj.org/article/b595fb8b671e46379aa13d914526a3a6
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 185 (2017)
INTRODUCTION: l'adrénoleucodystrophie liée à l'X (X-ALD) est une maladie neurodégénérative sévère, due à des mutations du gène ABCD1. Elle se manifeste par une atteinte du système nerveux central et périphérique, une insuffisance surrén
Externí odkaz:
https://doaj.org/article/c886d0ee4d9d4d44a6dff6d3a498f544
Publikováno v:
Türk Nöroloji Dergisi, Vol 24, Iss 3, Pp 283-284 (2018)
Externí odkaz:
https://doaj.org/article/cf3a2ded9b0043b6bdd27515e6177ff9
Publikováno v:
Saudi Journal of Medicine. 7:451-454
Introduction: The current global pandemic due to SARS-CoV-2 has resulted in a large literature on associated comorbidities, including diabetes. COVID 19 infection in a diabetic child can be complicated by severe ketoacidosis. The aim of this study is
Autor:
Keit Men Wong, Wayne M Jepsen, Stephanie Efthymiou, Vincenzo Salpietro, Meredith Sanchez-Castillo, Janice Yip, Yamna Kriouile, Susann Diegmann, Steffi Dreha-Kulaczewski, Janine Altmüller, Holger Thiele, Peter Nürnberg, Mehran Beiraghi Toosi, Javad Akhondian, Ehsan Ghayoor Karimiani, Hannah Hummel-Abmeier, Brenda Huppke, Henry Houlden, Jutta Gärtner, Reza Maroofian, Peter Huppke
Publikováno v:
Brain. 145:3022-3034
TAF8 is part of the transcription factor II D complex, composed of the TATA-binding protein and 13 TATA-binding protein–associated factors (TAFs). Transcription factor II D is the first general transcription factor recruited at promoters to assembl
Autor:
Nadia Mebrouk, Yasmine Lachkar, Aziza Bentalha, Latifa Chat, Yamna Kriouile, Asmaa Mdaghri Alaoui
Publikováno v:
International Journal of Innovative Research in Medical Science. 7:244-247
The Covid-19 infection disrupts various organs, including the liver, kidney, and nervous system. Common neurological symptoms of the Covid-19 infection include delirium, confusion, headache, and loss of sense of smell and taste. In rare cases it can
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Acute staphylococcal epidermolysis, also known as staphylococcal scalded skin syndrome (SSSS), in young children is caused by the release of exfoliative toxins A and B (ETA and/or ETB) from an initial outbreak which can be ear-nose-throat, conjunctiv