Renaud DL - Search Results

1

De Novo DNM1L Variant in a Teenager With Progressive Paroxysmal Dystonia and Lethal Super-refractory Myoclonic Status Epilepticus.

Ryan CS, Fine AL, Cohen AL, Schiltz BM, Renaud DL, Wirrell EC, Patterson MC, Boczek NJ, Liu R, Babovic-Vuksanovic D, Chan DC, Payne ET. Ryan CS, et al. Among authors: renaud dl. J Child Neurol. 2018 Sep;33(10):651-658. doi: 10.1177/0883073818778203. Epub 2018 Jun 7. J Child Neurol. 2018. PMID: 29877124 Free PMC article. Review.

2

Response to immunotherapy in a 20-month-old boy with anti-NMDA receptor encephalitis.

Wong-Kisiel LC, Ji T, Renaud DL, Kotagal S, Patterson MC, Dalmau J, Mack KJ. Wong-Kisiel LC, et al. Among authors: renaud dl. Neurology. 2010 May 11;74(19):1550-1. doi: 10.1212/WNL.0b013e3181dd41a1. Neurology. 2010. PMID: 20458074 Free PMC article. No abstract available.

3

Neuronal voltage-gated potassium channel complex autoimmunity in children.

Dhamija R, Renaud DL, Pittock SJ, McKeon A, Lachance DH, Nickels KC, Wirrell EC, Kuntz NL, King MD, Lennon VA. Dhamija R, et al. Among authors: renaud dl. Pediatr Neurol. 2011 Apr;44(4):275-81. doi: 10.1016/j.pediatrneurol.2010.10.015. Pediatr Neurol. 2011. PMID: 21397169

4

Internal Carotid Artery Pseudoaneurysm and Ischemic Stroke Secondary to Retropharyngeal and Parapharyngeal Abscess.

Ruff MW, Nasr DM, Klaas JP, Renaud DL. Ruff MW, et al. Among authors: renaud dl. J Child Neurol. 2017 Feb;32(2):230-236. doi: 10.1177/0883073816678556. Epub 2016 Nov 25. J Child Neurol. 2017. PMID: 27888269 Review.

5

Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis.

Lund TC, Miller WP, Eisengart JB, Simmons K, Pollard L, Renaud DL, Wenger DA, Patterson MC, Orchard PJ. Lund TC, et al. Among authors: renaud dl. Mol Genet Genomic Med. 2019 Jul;7(7):e00712. doi: 10.1002/mgg3.712. Epub 2019 May 21. Mol Genet Genomic Med. 2019. PMID: 31115173 Free PMC article.

6

Expansion of PURA-Related Phenotypes and Discovery of a Novel PURA Variant: A Case Report.

Boczek NJ, Macke EL, Kemppainen J, Klee EW, Renaud DL, Gavrilova RH. Boczek NJ, et al. Among authors: renaud dl. Child Neurol Open. 2020 Oct 14;7:2329048X20955003. doi: 10.1177/2329048X20955003. eCollection 2020 Jan-Dec. Child Neurol Open. 2020. PMID: 33117858 Free PMC article.

7

Pantothenate-kinase associated neurodegeneration (PKAN) "eye of the tiger" sign.

Renaud DL, Kotagal S. Renaud DL, et al. Pediatr Neurol. 2007 Jan;36(1):70-1. doi: 10.1016/j.pediatrneurol.2006.09.005. Pediatr Neurol. 2007. PMID: 17162204 No abstract available.

8

Magnetic resonance imaging findings in Alexander disease.

Matarese CA, Renaud DL. Matarese CA, et al. Among authors: renaud dl. Pediatr Neurol. 2008 May;38(5):373-4. doi: 10.1016/j.pediatrneurol.2008.01.004. Pediatr Neurol. 2008. PMID: 18410858 No abstract available.

9

Classical (type I) lissencephaly and Miller-Dieker syndrome.

Matarese CA, Renaud DL. Matarese CA, et al. Among authors: renaud dl. Pediatr Neurol. 2009 Apr;40(4):324-5. doi: 10.1016/j.pediatrneurol.2008.11.008. Pediatr Neurol. 2009. PMID: 19302951 No abstract available.

10

MRS is the test of choice for detecting and monitoring disorders of creatine metabolism.

Barger AV, Campeau NG, Port JD, Renaud DL. Barger AV, et al. Among authors: renaud dl. Pediatr Neurol. 2009 May;40(5):408-10. doi: 10.1016/j.pediatrneurol.2008.12.012. Pediatr Neurol. 2009. PMID: 19380084 No abstract available.

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