Parties d'ouvrages collectifs (1)
  1. 1. Sawaguchi, T., Franco, P., Kadhim, H., Mori, T., Ito, S., Taki, T., Sawaguchi, A., & Kahn, A. (2014). Sudden infant death syndrome from the perspective of arousal deficiency. In Sudden Infant Death Syndrome: From Pathophysiological Prospects (pp. 81-105). Springer Japan. doi:10.1007/978-4-431-54315-2_6
    2.   Articles dans des revues avec comité de lecture (64)
  2. 1. Catherine, J., Kadhim, H., Lambot, F., Liefferinckx, C., Meurant, V., & Otero Sanchez, L. (2022). Crohn’s disease-related ‘gastrocnemius myalgia syndrome’ successfully treated with infliximab: A case report. World Journal of Gastroenterology, 28(7), 755-762. doi:10.3748/wjg.v28.i7.755
  3. 2. Chevin, M., Sébire, G., Deltenre, P., & Kadhim, H. (2020). Necroptotic neuronal cell death in amyotrophic lateral sclerosis: A relevant hypothesis with potential therapeutic implication? Medical hypotheses, 144, 110295. doi:10.1016/j.mehy.2020.110295
  4. 3. Kadhim, H., Segers, V., Vilain, C., Désir, J., & D'Haene, N. (2017). First Report on Fetal Cerebral Polyglucosan Bodies in Mucopolysaccharidosis Type VII. Case reports in pediatrics, 2017, 9523427. doi:10.1155/2017/9523427
  5. 4. Sidiras, P., Vandergheynst, F., Verset, L., Kadhim, H., & Soyfoo, M. S. (2017). Dermatomyositis Associated with Sarcoidosis: Two Cases. European journal of case reports in internal medicine, 4(1). doi:10.12890/2016_000500
  6. 5. Specq, M. L., Bourgoin-Heck, M., Samson, N., Corbin, F., Gestreau, C., Richer, M., Kadhim, H., & Praud, J. P. (2016). Moderate hyperbilirubinemia alters neonatal cardiorespiratory control and induces inflammation in the nucleus tractus solitarius. Frontiers in physiology, 7(SEP), 437. doi:10.3389/fphys.2016.00437
  7. 6. Coppens, S., Koralkova, P., Aeby, A., Mojzikova, R., Deconinck, N., Kadhim, H., & van Wijk, R. (2016). Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency. Neuromuscular disorders, 26(3), 207-210. doi:10.1016/j.nmd.2015.11.008
  8. 7. Kadhim, H., Deltenre, P., Martin, J.-J., & Sébire, G. (2016). In-situ expression of Interleukin-18 and associated mediators in the human brain of sALS patients: Hypothesis for a role for immune-inflammatory mechanisms. Medical hypotheses, 86, 14-17. doi:10.1016/j.mehy.2015.11.022
  9. 8. Remiche, G., Kadhim, H., Abramowicz, M., Mavroudakis, N., Monnier, N., & Lunardi, J. (2015). A novel large deletion in the RYR1 gene in a Belgian family with late-onset and recessive core myopathy. Neuromuscular disorders, 25(5), 397-402. doi:10.1016/j.nmd.2015.01.016
  10. 9. Nachanakian, A., El-Helou, A., Alaywan, M., Hmaimess, G., Adem-Hachem, C., & Kadhim, H. (2015). Early modified functional hemispherectomy in a young infant with ohtahara syndrome and hemimegalencephaly. Journal of child neurology, 30(4), 522-526. doi:10.1177/0883073814539558
  11. 10. Votino, C., Cos Sanchez, T., Bessieres, B., Segers, V., Kadhim, H., Razavi, F., Condorelli, M., Votino, R., D'Ambrosio, V., & Jani, J. (2014). Minimally invasive fetal autopsy using ultrasound: a feasibility study. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.
  12. 11. Kadhim, H., Deltenre, P., Segers, V., & Sébire, G. (2012). Selective expression of a neuromodulatory cytokine (IL-2) in specific brainstem neurovegetative centers: A possible final common neuro-molecular pathway in dying patients. Medical hypotheses, 78(6), 793-795. doi:10.1016/j.mehy.2012.03.010
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