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Renaud, Deborah
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1

Childhood apraxia of speech, oral motor apraxia, and veloph..:

Davis, Jessica M. ; Renaud, Deborah L.
Annals of the Child Neurology Society.  1 (2023)  4 - p. 327-328 , 2023
Link: https://doi.org/10.1002/..
 
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2

Pediatric leukodystrophies:

, In: Advances in Magnetic Resonance Technology and Applications; Imaging Neuroinflammation,
Renaud, Deborah L. - p. 405-424 , 2023
Link: https://doi.org/10.1016/..
 
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3

Beta-Mannosidosis Is a Cause of Hypomyelination:

Renaud, Deborah L.
Pediatric Neurology.  140 (2023)  - p. 76-77 , 2023
Link: https://doi.org/10.1016/..
 
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4

Stable Leukoencephalopathy in a Patient WithACTA2-Associate..:

Bieber, David ; Port, John D. ; Renaud, Deborah L.
Neurology.  99 (2022)  8 - p. 338-340 , 2022
Link: https://doi.org/10.1212/..
 
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5

Treatment of Low Cerebrospinal Fluid 5-Methyltetrahydrofola..:

Renaud, Deborah L.
Pediatric Neurology.  114 (2021)  - p. 9-10 , 2021
Link: https://doi.org/10.1016/..
 
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6

Expanding the phenotype of ASXL3‐related syndrome: A compre..:

Schirwani, Schaida ; Albaba, Shadi ; Carere, Deanna Alexis...
American Journal of Medical Genetics Part A.  185 (2021)  11 - p. 3446-3458 , 2021
Link: https://doi.org/10.1002/..
 
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7

Biallelic variants in KARS1 are associated with neurodevelo..:

Lin, Sheng-Jia ; Vona, Barbara ; Barbalho, Patricia G....
Genetics in Medicine.  23 (2021)  10 - p. 1933-1943 , 2021
Link: https://doi.org/10.1038/..
 
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8

Neuropsychological Functioning in Alexander Disease: A Case..:

Kirsch, Alexandra C. ; McCall, Dana M. ; Lange, Hadley...
Child Neurology Open.  8 (2021)  - p. 2329048X2110486 , 2021
Link: https://doi.org/10.1177/..
 
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9

Pseudopapilledema in Cockayne syndrome:

Brodsky, Michael C. ; Renaud, Deborah L.
American Journal of Ophthalmology Case Reports.  22 (2021)  - p. 101035 , 2021
Link: https://doi.org/10.1016/..
 
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10

Expansion of PURA-Related Phenotypes and Discovery of a Nov..:

Boczek, Nicole J. ; Macke, Erica L. ; Kemppainen, Jennifer...
Child Neurology Open.  7 (2020)  - p. 2329048X2095500 , 2020
Link: https://doi.org/10.1177/..
 
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11

Expanding the clinical and phenotypic heterogeneity associa..:

Blackburn, Patrick R. ; Schultz, Matthew J. ; Lahner, Carrie A....
Annals of Clinical and Translational Neurology.  7 (2020)  6 - p. 1013-1028 , 2020
Link: https://doi.org/10.1002/..
 
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12

Complex I Deficiency due to a Nuclear Mitochondrial DNA Mut..:

Mehta, Dev ; Mansukhani, Sasha ; Whealy, Mark...
Neurology.  94 (2020)  15_supplement - p. , 2020
Link: https://doi.org/10.1212/..
 
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13

Developmental delay, coarse facial features, and epilepsy i..:

Gupta, Aditi ; Ewing, Sarah A. ; Renaud, Deborah L....
Clinical Case Reports.  7 (2019)  4 - p. 632-637 , 2019
Link: https://doi.org/10.1002/..
 
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14

Targeted gene approach with biochemical assay confirms ABCD..:

Mauermann, Michelle L. ; Niu, Zhiyv ; Renaud, Deborah L....
Neuromuscular Disorders.  29 (2019)  2 - p. 146-149 , 2019
Link: https://doi.org/10.1016/..
 
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15

Biochemical and clinical response after umbilical cord bloo..:

Lund, Troy C. ; Miller, Weston P. ; Eisengart, Julie B....
Molecular Genetics & Genomic Medicine.  7 (2019)  7 - p. , 2019
Link: https://doi.org/10.1002/..
 
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