| Year |
Citation |
Score |
| 2019 |
Bourque DK, Cloutier M, Kernohan KD, Bareke E, Grynspan D, Michaud J, Boycott KM. 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. PMID 30838783 DOI: 10.1002/Ajmg.A.61076 |
0.309 |
|
| 2019 |
Joyal KM, Michaud J, van der Knaap MS, Bugiani M, Venkateswaran S. Severe TUBB4A-Related Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum: Novel Neuropathological Findings. Journal of Neuropathology and Experimental Neurology. 78: 3-9. PMID 30476126 DOI: 10.1093/Jnen/Nly105 |
0.31 |
|
| 2018 |
Al Qawahmed R, Sawyer SL, Vassilyadi M, Qin W, Boycott KM, Michaud J. 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. PMID 30103666 DOI: 10.1177/1093526618787736 |
0.321 |
|
| 2017 |
Lines MA, Ito Y, Kernohan KD, Mears W, Hurteau-Miller J, Venkateswaran S, Ward L, Khatchadourian K, McClintock J, Bhola P, Campeau PM, Boycott KM, Michaud J, van Kuilenburg AB, et al. Yunis-Varón syndrome caused by biallelic VAC14 mutations. European Journal of Human Genetics : Ejhg. PMID 28635952 DOI: 10.1038/Ejhg.2017.99 |
0.306 |
|
| 2014 |
Joseph JT, Innes AM, Smith AC, Vanstone MR, Schwartzentruber JA, Bulman DE, Majewski J, Daza RA, Hevner RF, Michaud J, Boycott KM. Neuropathologic features of pontocerebellar hypoplasia type 6. Journal of Neuropathology and Experimental Neurology. 73: 1009-25. PMID 25289895 DOI: 10.1097/Nen.0000000000000123 |
0.312 |
|
| 2014 |
Kalidindi N, Torres CH, Michaud J, Zwicker JC. 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. PMID 25202261 DOI: 10.1159/000365414 |
0.309 |
|
| 2014 |
Spence T, Sin-Chan P, Picard D, Barszczyk M, Hoss K, Lu M, Kim SK, Ra YS, Nakamura H, Fangusaro J, Hwang E, Kiehna E, Toledano H, Wang Y, Shi Q, ... ... Michaud J, et al. CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entity. Acta Neuropathologica. 128: 291-303. PMID 24839957 DOI: 10.1007/S00401-014-1291-1 |
0.313 |
|
| 2014 |
Buczkowicz P, Hoeman C, Rakopoulos P, Pajovic S, Letourneau L, Dzamba M, Morrison A, Lewis P, Bouffet E, Bartels U, Zuccaro J, Agnihotri S, Ryall S, Barszczyk M, Chornenkyy Y, ... ... Michaud J, et al. Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations. Nature Genetics. 46: 451-6. PMID 24705254 DOI: 10.1038/Ng.2936 |
0.301 |
|
| 2014 |
Orr SL, Dos Santos MP, Jurencak R, Michaud J, Miller E, Doja A. Central nervous system venulitis presenting as migraine. Headache. 54: 541-4. PMID 23879203 DOI: 10.1111/Head.12188 |
0.326 |
|
| 2006 |
Muzumdar D, Michaud J, Ventureyra EC. 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. PMID 16133274 DOI: 10.1007/S00381-005-1199-0 |
0.319 |
|
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