Child Neurology: Zellweger syndrome

le Lee, Paul R., Raymond, Gerald V.
Foilsithe 2013

Clinical Reasoning: A 56-year-old man with progressive spasticity

le Dhamija, Radhika, Raymond, Gerald V., Gavrilova, Ralitza
Foilsithe 2013

Auditory function in adrenomyeloneuropathy

le Pillion, Joseph P., Moser, Hugo W., Raymond, Gerald V.
Foilsithe 2008

X-linked Adrenoleukodystrophy: The Role of Contrast-enhanced MR Imaging in Predicting Disease Progression

le Melhem, Elias R., Loes, Daniel J., Georgiades, Christos S., Raymond, Gerald V., Moser, Hugo W.
Foilsithe in AJNR Am J Neuroradiol (2000)

Cerebral Spinal Fluid levels of Cytokines are elevated in Patients with Metachromatic Leukodystrophy

le Thibert, Kathryn A., Raymond, Gerald V., Tolar, Jakub, Miller, Weston P., Orchard, Paul J., Lund, Troy C.
Foilsithe in Sci Rep (2016)

Cerebrospinal Fluid Matrix Metalloproteinases Are Elevated in Cerebral Adrenoleukodystrophy and Correlate with MRI Severity and Neurologic Dysfunction

le Thibert, Kathryn A., Raymond, Gerald V., Nascene, David R., Miller, Weston P., Tolar, Jakub, Orchard, Paul J., Lund, Troy C.
Foilsithe 2012

Elevated cerebral spinal fluid biomarkers in children with mucopolysaccharidosis I-H

le Raymond, Gerald V., Pasquali, Marzia, Polgreen, Lynda E., Dickson, Patricia I., Miller, Weston P., Orchard, Paul J., Lund, Troy C.
Foilsithe in Sci Rep (2016)

A Hierarchical Bayesian Approach for Combining Pharmacokinetic/Pharmacodynamic Modeling and Phase IIa Trial Design in Orphan Drugs: Treating Adrenoleukodystrophy with Lorenzo’s Oil...

le Basu, Cynthia, Ahmed, Mariam A., Kartha, Reena V., Brundage, Richard C., Raymond, Gerald V., Cloyd, James C., Carlin, Bradley P.
Foilsithe in J Biopharm Stat (2016)

Newborn Screening for X-Linked Adrenoleukodystrophy

le Moser, Ann B., Jones, Richard O., Hubbard, Walter C., Tortorelli, Silvia, Orsini, Joseph J., Caggana, Michele, Vogel, Beth H., Raymond, Gerald V.
Foilsithe in Int J Neonatal Screen (2016)

QUANTITATIVE MAGNETIZATION TRANSFER CHARACTERISTICS OF THE HUMAN CERVICAL SPINAL CORD IN VIVO: APPLICATION TO ADRENOMYELONEUROPATHY

le Smith, Seth A., Golay, Xavier, Fatemi, Ali, Mahmood, Asif, Raymond, Gerald V., Moser, Hugo W., van Zijl, Peter C. M., Stanisz, Greg J.
Foilsithe 2009

Neurocognitive Trajectory of Boys Who Received a Hematopoietic Stem Cell Transplant at an Early Stage of Childhood Cerebral Adrenoleukodystrophy

le Pierpont, Elizabeth I., Eisengart, Julie B., Shanley, Ryan, Nascene, David, Raymond, Gerald V., Shapiro, Elsa G., Ziegler, Rich S., Orchard, Paul J., Miller, Weston P.
Foilsithe in JAMA Neurol (2017)

Association between APOE4 and biomarkers in cerebral adrenoleukodystrophy

le Orchard, Paul J., Markowski, Todd W., Higgins, LeeAnn, Raymond, Gerald V., Nascene, David R., Miller, Weston P., Pierpont, Elizabeth I., Lund, Troy C.
Foilsithe in Sci Rep (2019)

Failure of intrathecal allogeneic mesenchymal stem cells to halt progressive demyelination in two boys with cerebral adrenoleukodystrophy

le Gupta, Ashish, Orchard, Paul J., Miller, Weston P., Nascene, Dave R., Raymond, Gerald V., Loes, Daniel J., McKenna, David H., Lund, Troy C.
Foilsithe in Stem Cells Transl Med (2020)

A model‐based approach to assess the exposure–response relationship of Lorenzo's oil in adrenoleukodystrophy

le Ahmed, Mariam A., Kartha, Reena V., Brundage, Richard C., Cloyd, James, Basu, Cynthia, Carlin, Bradley P., Jones, Richard O., Moser, Ann B., Fatemi, Ali, Raymond, Gerald V.
Foilsithe in Br J Clin Pharmacol (2016)

Post‐transplant adaptive function in childhood cerebral adrenoleukodystrophy

le Pierpont, Elizabeth I., McCoy, Erin, King, Kelly E., Ziegler, Rich S., Shanley, Ryan, Nascene, David, Raymond, Gerald V., Phelan, Rachel, Lund, Troy C., Orchard, Paul J., Miller, Weston P.
Foilsithe in Ann Clin Transl Neurol (2018)

MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If

le Schenk, Barbara, Imbach, Timo, Frank, Christian G., Grubenmann, Claudia E., Raymond, Gerald V., Hurvitz, Haggit, Raas-Rotschild, Annick, Luder, Anthony S., Jaeken, Jaak, Berger, Eric G., Matthijs, Gert, Hennet, Thierry, Aebi, Markus
Foilsithe 2001

Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines

le Braverman, Nancy E., Raymond, Gerald V., Rizzo, William B., Moser, Ann B., Wilkinson, Mark E., Stone, Edwin M., Steinberg, Steven J., Wangler, Michael F., Rush, Eric T., Hacia, Joseph G., Bose, Mousumi
Foilsithe in Mol Genet Metab (2015)

Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy

le Turk, Bela R., Theisen, Benjamin E., Nemeth, Christina L., Marx, Joel S., Shi, Xiaohai, Rosen, Melissa, Jones, Richard O., Moser, Ann B., Watkins, Paul A., Raymond, Gerald V., Tiffany, Carol, Fatemi, Ali
Foilsithe in JAMA Neurol (2017)

MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If

le Schenk, Barbara, Imbach, Timo, Frank, Christian G., Grubenmann, Claudia E., Raymond, Gerald V., Hurvitz, Haggit, Raas-Rotschild, Annick, Luder, Anthony S., Jaeken, Jaak, Berger, Eric G., Matthijs, Gert, Hennet, Thierry, Aebi, Markus, Jaeken, Jaak
Foilsithe 2003

Newborn Screening for X-linked Adrenoleukodystrophy: Further evidence high throughput screening is feasible

le Theda, Christiane, Gibbons, Katy, DeFor, Todd E., Donohue, Pamela K., Golden, W. Christopher, Kline, Antonie D., Gulamali-Majid, Fizza, Panny, Susan R., Hubbard, Walter C., Jones, Richard O., Liu, Anita K., Moser, Ann B., Raymond, Gerald V.
Foilsithe 2013