Jean Michaud
Affiliations: | Pathology and Laboratory Medicine | University of Ottawa, Ottawa, ON, Canada |
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"Jean Michaud"Bio:
UNIVERSITY OTTAWA
PATHOLOGY LAB MED DEPT
451 SMYTH RD 4155
OTTAWA, ON K1H8M5
Canada
Mean distance: 53433
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Publications
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| Bourque DK, Cloutier M, Kernohan KD, et al. (2019) Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis. American Journal of Medical Genetics. Part A |
| Joyal KM, Michaud J, van der Knaap MS, et al. (2019) Severe TUBB4A-Related Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum: Novel Neuropathological Findings. Journal of Neuropathology and Experimental Neurology. 78: 3-9 |
| Al Qawahmed R, Sawyer SL, Vassilyadi M, et al. (2018) Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 1093526618787736 |
| Lines MA, Ito Y, Kernohan KD, et al. (2017) Yunis-Varón syndrome caused by biallelic VAC14 mutations. European Journal of Human Genetics : Ejhg |
| Joseph JT, Innes AM, Smith AC, et al. (2014) Neuropathologic features of pontocerebellar hypoplasia type 6. Journal of Neuropathology and Experimental Neurology. 73: 1009-25 |
| Kalidindi N, Torres CH, Michaud J, et al. (2014) Primitive neuroectodermal tumor presenting with diffuse leptomeningeal involvement in a 55-year-old woman: a case report and brief summary of current diagnostic tests and treatment. Case Reports in Oncology. 7: 471-7 |
| Spence T, Sin-Chan P, Picard D, et al. (2014) CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entity. Acta Neuropathologica. 128: 291-303 |
| Buczkowicz P, Hoeman C, Rakopoulos P, et al. (2014) Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations. Nature Genetics. 46: 451-6 |
| Orr SL, Dos Santos MP, Jurencak R, et al. (2014) Central nervous system venulitis presenting as migraine. Headache. 54: 541-4 |
| Muzumdar D, Michaud J, Ventureyra EC. (2006) Primary giant congential infantile fibrosarcoma of the scalp: case report and review of literature. Child's Nervous System : Chns : Official Journal of the International Society For Pediatric Neurosurgery. 22: 300-4 |