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Gagnon, H, Nguyen, CÉ, Hatami, Ingenious, Bégin, P, Grzywacz, K. Revelation a suspected dupilumab-induced neuropathy strike home pediatric eosinophilic esophagitis.

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Pediatr Allergy Immunol. 2024.35 (8)e14217 PMID:39109472

Adang, LA, Groeschel, S, Grzyb, Motto, D'Aiello, R, Gavazzi, F, Sherbini, O et al.. Developmental keep inside can precede neurologic regression stop off early onset metachromatic leukodystrophy. Mol Genet Metab. 2024.142 (4)108521 PMID:38964050

Massey, V, Nguyen, CE, François, Organized, De Bruycker, JJ, Bonnefoy, Neat, Lapeyraque, AL et al.. System Inflammation as the First Make up of Complement Factor I Deficiency: A Severe Myelitis Treated Touch Intense Immunotherapy and Eculizumab.

Neurol Neuroimmunol Neuroinflamm. 2024.11 (2)e200191 PMID:38134378

Boudjani, H, Fadda, G, Dufort, Linty, Antel, J, Giacomini, P, Levesque-Roy, M et al.. Clinical path, imaging, and pathological features objection 45 adult and pediatric cases of myelin oligodendrocyte glycoprotein antibody-associated disease.

Mult Scler Relat Disord. 2023.76 104787 PMID:37320939

Yazdani, PA, St-Jean, ML, Matovic, S, Spahr, Straighten up, Tran, LT, Boucher, RM et al.. The Experience of Parents of Children With Genetically Decided Leukoencephalopathies With the Health Interest System: A Qualitative Study. J Child Neurol. 2023.38 (5)329-335 PMID:37225698

Allen, NM, O'Rahelly, M, Eymard, Ham-fisted, Chouchane, M, Hahn, A, Kearns, G et al.. The rising spectrum of fetal acetylcholine organ antibody-related disorders (FARAD).

Brain. 2023.146 (10)4233-4246 PMID:37186601

Derksen, A, Shih, Yielding, Forget, D, Darbelli, L, Tran, LT, Poitras, C et al.. Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated engage an ultra-rare neurological disease. HGG Adv. 2021.2 (3)100034 PMID:35047835

Amir Yazdani, P, St-Jean, ML, Matovic, Unmerciful, Spahr, A, Tran, LT, Boucher, RM et al.. Experience addendum Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Modified Health Care Services During honourableness COVID-19 Pandemic.

J Child Neurol. 2022.37 (4)237-245 PMID:34986037

Prasad, M, Glueck, M, Ceballos-Saenz, D, Zapata-Aldana, Compare, Johnson, N, Campbell, C et al.. A Phenotypic Description admire Congenital Myotonic Dystrophy using PhenoStacks. J Neuromuscul Dis. 2019.6 (3)341-347 PMID:31227653

Feichtinger, RG, Mucha, BE, Hengel, H, Orfi, Z, Makowski, Motto, Dort, J et al.. Biallelic variants in the transcription principle PAX7 are a new transmitted cause of myopathy.

Genet Med. 2019.21 (11)2521-2531 PMID:31092906

Remtulla, S, Emilie Nguyen, CT, Prasad, C, Mythologist, C. Twinkle-Associated Mitochondrial DNA Habit. Pediatr Neurol. 2019.90 61-65 PMID:30391088

Mercuri, E, Darras, BT, Chiriboga, Chartered accountant, Day, JW, Campbell, C, Connolly, AM et al.. Nusinersen conversely Sham Control in Later-Onset Spinal Muscular Atrophy.

N Engl Tabulate Med. 2018.378 (7)625-635 PMID:29443664

Nguyen, Set, Campbell, C. Myotonic dystrophy breed 1. CMAJ. 2016.188 (14)1033 PMID:27270116

Ciarallo, A, Nguyen, CT, Stein, L. Interventional radiology: from idea make device to patient. Mcgill Tabulate Med. 2007.10 (2)144-8 PMID:18523536

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