Researcher profile · Semantic Scholar

L. Lehwald

h-index: 7
Works: 20
Citations: 419

Most-cited papers

Neurologic Consequences of Preterm Birth
Margie A. Ream, L. Lehwald
2018Current Neurology and Neuroscience Reports200 citations
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Management Strategies for CLN2 Disease.
Ruth E. Williams, Heather R. Adams, M. Blohm, J. Cohen-Pfeffer +22 more
2017Pediatric Neurology106 citations Open access
Semantic Scholar
Intracerebroventricular Cerliponase Alfa for Neuronal Ceroid Lipofuscinosis Type 2 Disease: Clinical Practice Considerations From US Clinics.
E. C. de los Reyes, L. Lehwald, Erika F. Augustine, E. Berry-Kravis +14 more
2020Pediatric Neurology27 citations Open access
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Cerliponase Alfa for the Treatment of Atypical Phenotypes of CLN2 Disease: A Retrospective Case Series
E. Wibbeler, Raymond Y. Wang, E. C. de los Reyes, N. Specchio +12 more
2020Journal of Child Neurology16 citations Open access
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Neuronal Ceroid Lipofuscinosis and Associated Sleep Abnormalities.
L. Lehwald, Rachael Pappa, S. Steward, E. C. de los Reyes
2016Pediatric Neurology16 citations
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Isolated sympathetic failure with autoimmune autonomic ganglionopathy.
P. Fischer, P. Sandroni, S. Pittock, Co-burn J. Porter +2 more
2010Pediatric Neurology16 citations
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Negative effect of treatment with mGluR5 negative allosteric modulator AFQ056 on blood biomarkers in young individuals with Fragile X syndrome
D. Protic, E. Breeze, Guadalupe Mendoza, Marwa Zafarullah +19 more
2024SAGE Open Medicine7 citations Open access
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Primary Diffuse Leptomeningeal Gliomatosis
G. Jicha, Janel N. Glantz, M. Clarke, L. Lehwald +7 more
2009European Neurology7 citations
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Accepted Manuscript Management strategies for CLN 2 disease
Ruth E. Williams, Heather R. Adams, M. Blohm, L. Jessica +27 more
20175 citations
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Single-dose AAV9-CLN6 gene transfer slows the decline in motor and language function in variant late infantile neuronal ceroid lipofuscinosis 6: Interim results from phase 1/2 trial
E. C. de los Reyes, S. Aylward, K. Meyer, L. Lehwald +8 more
20214 citations
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Sleep disturbance in pediatric intracranial hypertension
Alexandra B. Kornbluh, Katherine L. Thompson, Gada Mcmahen, David L. Rogers +3 more
2020Journal of Clinical Sleep Medicine (JCSM)4 citations Open access
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Novel LMNA mutation in a patient with progeroid phenotype
L. Lehwald, D. Renaud, N. Campeau, D. Babovic-Vuksanovic
2007Journal of Pediatric Neurology online4 citations
Semantic Scholar
Single-dose AAV9-CLN6 gene transfer stabilizes motor and language function in CLN6-type Batten disease: Interim results from the first clinical gene therapy trial
E. C. de los Reyes, K. Meyer, L. Lehwald, C. Albright +4 more
20203 citations
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Atlas of inherited metabolic diseases, third edition
L. Lehwald
2013Neurology3 citations
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NEUROLOGY OF THE NEONATE
L. Lehwald, Laurel A. Slaughter
20121 citations
Semantic Scholar
Intracerebroventricular cerliponase alfa for CLN2 disease: Clinical practice considerations from US clinics
Raymond Y. Wang, E. C. de los Reyes, L. Lehwald, Erika F. Augustine +14 more
20200 citations
Semantic Scholar
Sleep Disturbances in Pediatric Intracranial Hypertension (P5.6-058)
Alexandra B. Kornbluh, Katherine Thompson, Gada Mcmahen, Shawn C. Aylward +1 more
2019Neurology0 citations
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Book Review: Neonatal Seizures: Current Management and Future Challenges
L. Lehwald
2017Journal of Child Neurology0 citations
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Expert opinion on the management of CLN2 disease
A. Schulz, Heather R. Adams, M. Blohm, J. Cohen-Pfeffer +21 more
20160 citations
Semantic Scholar
SLEEP DISTURBANCE IN PEDIATRIC CHRONIC DAILY HEADACHE PATIENTS
L. Lehwald, K. Mack
20060 citations
Semantic Scholar

N. Specchio

×4

Ruth E. Williams×3

Heather R. Adams×3

M. Blohm×3

J. Denecke×3

C. Fairhurst×3

M. Frazier×3

Annamaria Kofler×3