Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Hazim Kadhim"'
Autor:
Hazim Kadhim
Publikováno v:
مجلة الآداب, Iss 145 (2023)
يهدف هذا البحث إلى الكشف عن التباين المكاني لزراعة أشجار النخيل في محافظة بابل، وتعد زراعة أشجار النخيل من أهم الأنشطة الزراعية البارزة
Externí odkaz:
https://doaj.org/article/15c9db582a9a437ba02da6dae3ceecd9
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
We report on the detection of discordant inclusions in the brain of a 25-week female fetus with a very rare lysosomal storage disease, namely, Sly disease (mucopolysaccharidosis (MPS) type VII), presenting with nonimmune hydrops fetalis. Besides vacu
Externí odkaz:
https://doaj.org/article/f8f7411a1ba049fa9c1afb280c95cbe2
Autor:
Paschalis Sidiras, Frédéric Vandergheynst, Laurine Verset, Hazim Kadhim, Muhammad Shahnawaz Soyfoo
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 4, Iss 1 (2017)
Dermatomyositis (DM) and sarcoidosis are two idiopathic systemic disorders. Reports of patients with both conditions are extremely rare. Here we describe two patients who presented with DM and DM-associated antibodies, and later developed biopsy-prov
Externí odkaz:
https://doaj.org/article/91f82e55a123432b8731bae407fc534d
Autor:
Marie-Laure Specq, Mélisande Bourgoin-Heck, Nathalie Samson, François Corbin, Christian Gestreau, Maxime Richer, Hazim Kadhim, Jean-Paul Praud
Publikováno v:
Frontiers in Physiology, Vol 7 (2016)
Hyperbilirubinemia (HB) occurs in 90% of preterm newborns. Moderate HB can induce acute neurological disorders while severe HB has been linked to a higher incidence of apneas of prematurity. The present study aimed to test the hypothesis that even mo
Externí odkaz:
https://doaj.org/article/873b6c0aada644a1a86b943184f55840
Autor:
Hazim Kadhim, Eliane El-Howayek, Sandra Coppens, Jennifer Duff, Ana Topf, Jean-Paul Kaleeta, Paolo Simoni, Grammatina Boitsios, Gauthier Remiche, Volker Straub, Catheline Vilain, Nicolas Deconinck
Publikováno v:
Neuromuscular Disorders. 33:410-416
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1feec5c0a4df156cfb661155323534a1
https://doi.org/10.1016/j.nmd.2023.03.007
https://doi.org/10.1016/j.nmd.2023.03.007
Autor:
Julien Catherine, Hazim Kadhim, Frédéric Lambot, Claire Liefferinckx, Virginie Meurant, Lukas Otero Sanchez
Publikováno v:
World Journal of Gastroenterology. 28:755-762
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6c2607a685589d3e57b90b445c81946
https://doi.org/10.3748/wjg.v28.i7.755
https://doi.org/10.3748/wjg.v28.i7.755
Autor:
Marie Rivera-Zengotita, Alison M. Barnard, Sanna Puusepp, Anna Łusakowska, Ros Quinlivan, Margherita Milone, Isabelle Draper, Katherine R. Chao, Erica L. Macke, Mait Nigul, Teepu Siddique, Vijay S. Ganesh, Sander Pajusalu, Nicolas Deconinck, Sanna Gudmundsson, Masashi Ogasawara, Sandra Donkervoort, Christine C. Bruels, Glenn A. Walter, Ehsan Ghayoor Karimiani, Christina A. Pacak, Reza Maroofian, Sabine Costagliola, Julia K. Goodrich, Anne H. O’Donnell-Luria, Mehran Beiraghi Toosi, Sandra Coppens, Yao Meng, Lynn Pais, Henry Houlden, Eleina M. England, Rasha El Sherif, Anne Boland-Auge, Bertold Schrank, Volker Straub, Gisèle Bonne, Catheline Vilain, Payam Mohassel, Tanya Stojkovic, Isabelle Nelson, Ichizo Nishino, Stefan Nicolau, Anna Kostera-Pruszczyk, Ben Weisburd, Jean-François Deleuze, Enzo Cohen, Michael G. Hanna, Hazim Kadhim, Peter B. Kang, Dorianmarie Vargas-Franco, Penny A. Handford, Katrin Õunap, Pilvi Ilves, Ana Töpf, Carsten G. Bönnemann, Brendan C. Lanpher, Eric W. Klee, Andreas Hahn
Publikováno v:
The American Journal of Human Genetics
Am J Hum Genet
Am J Hum Genet
JAG2 encodes the Notch ligand Jagged2. The conserved Notch signaling pathway contributes to the development and homeostasis of multiple tissues, including skeletal muscle. We studied an international cohort of 23 individuals with genetically unsolved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de5cf77949f159f13e3db961570ab30b
https://doi.org/10.1016/j.ajhg.2021.03.020
https://doi.org/10.1016/j.ajhg.2021.03.020
Autor:
Alexis Dembour, Anne Destrée, Marie Deprez, Hazim Kadhim, Deniz Karadurmus, Olivier Froment, Nicolas Deconinck, Damien Lederer
Publikováno v:
European Journal of Medical Genetics, Vol. 65, no.4, p. 104469 (2022)
Pathogenic variants in the genes encoding for the ASC1 complex were recently reported in patients with congenital fractures, joint contractures, neonatal hypotonia and respiratory distress. Here we report two male children with biallelic TRIP4 pathog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72f1efd02d810b204fab12a2e4949827
https://pubmed.ncbi.nlm.nih.gov/35276412
https://pubmed.ncbi.nlm.nih.gov/35276412
Publikováno v:
Medical hypotheses. 144
Necroptosis is emerging among possible mechanisms underlying cell death in neurodegenerative diseases. In this line, we hypothesize that necroptosis might be implicated in neuronal cell death in amyotrophic lateral sclerosis (ALS). To support this hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac5593362b0aa5ac9c3c72d78ba91e77
https://pubmed.ncbi.nlm.nih.gov/33254488
https://pubmed.ncbi.nlm.nih.gov/33254488
Publikováno v:
Medical hypotheses
Recent studies reported over-expression of a cytokine (Interleukin (IL)-18) in the serum of sporadic amyotrophic lateral sclerosis (sALS) patients. Here, we report on the first-time detection of in-situ expression of activated IL-18 in the human brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::034537a514f4f9d77792180859a6087f
https://doi.org/10.1016/j.mehy.2015.11.022
https://doi.org/10.1016/j.mehy.2015.11.022