Výsledky vyhledávání - "Matthew J Schultz"

Akademický článek

Anterior Cruciate Ligament Stump Elongation Technique for Anterior Cruciate Ligament Restoration

Autor: Matthew J. Schultz, D.O., A.T.C., Hannah R. Popper, D.O., Sean McMillan, D.O.

Publikováno v: Arthroscopy Techniques, Vol 13, Iss 12, Pp 103140- (2024)

There is renewed interest in anterior cruciate ligament (ACL) preservation techniques. Prior studies have shown good outcomes and low failure rates with ACL preservation in patients with good tissue quality and more proximal tears. We describe a tech

Externí odkaz: https://doaj.org/article/c3544f753ea74d85951f528a9bfa4a45

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Akademický článek

Microporous dermal-mimetic electrospun scaffolds pre-seeded with fibroblasts promote tissue regeneration in full-thickness skin wounds.

Autor: Paul P Bonvallet, Matthew J Schultz, Elizabeth H Mitchell, Jennifer L Bain, Bonnie K Culpepper, Steven J Thomas, Susan L Bellis

Publikováno v: PLoS ONE, Vol 10, Iss 3, p e0122359 (2015)

Electrospun scaffolds serve as promising substrates for tissue repair due to their nanofibrous architecture and amenability to tailoring of chemical composition. In this study, the regenerative potential of a microporous electrospun scaffold pre-seed

Externí odkaz: https://doaj.org/article/062518178acb4348b2123e357cd3fdbd

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Akademický článek

Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase

Autor: Coleman Turgeon, Kari Casas, Ryan Flanagan, Amy White, Dawn Peck, Gisele Bentz Pino, April Studinski Jones, Dimitar Gavrilov, Devin Oglesbee, Matthew J. Schultz, Silvia Tortorelli, Dietrich Matern, Patricia L. Hall

Publikováno v: Molecular Genetics and Metabolism Reports, Vol 40, Iss , Pp 101110- (2024)

Treatment of phenylketonuria (PKU) has evolved since the initial introduction of a phenylalanine (Phe) restricted diet. The most recent option for adults affected with PKU is treatment with an alternate enzyme, phenylalanine ammonia lyase (PAL), that

Externí odkaz: https://doaj.org/article/3186e1c501f647c78e2451cc78f87724

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Akademický článek

PIGO‐CDG: A case study with a new genotype, expansion of the phenotype, literature review, and nosological considerations

Autor: Rodrigo Tzovenos Starosta, Nino Kerashvili, Cassandra Pruitt, Matthew J. Schultz, Suzanne W. Boyer, Eva Morava, Maria Laura Duque Lasio, Dorothy K. Grange

Publikováno v: JIMD Reports, Vol 64, Iss 6, Pp 424-433 (2023)

Abstract The phosphatidylinositol glycan anchor biosynthesis class O protein (PIGO) enzyme is an important step in the biosynthesis of glycosylphosphatidylinositol (GPI), which is essential for the membrane anchoring of several proteins. Bi‐allelic

Externí odkaz: https://doaj.org/article/510be21bafd74ecaa71d96b94efdc25c

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Akademický článek

Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2

Autor: Patrick R. Blackburn, Matthew J. Schultz, Carrie A. Lahner, Dong Li, Elizabeth Bhoj, Laura J. Fisher, Deborah L. Renaud, Amy Kenney, Niema Ibrahim, Mais Hashem, Mohammed Zain Seidahmed, Linda Hasadsri, Samantha A. Schrier Vergano, Fowzan S. Alkuraya, Brendan C. Lanpher

Publikováno v: Annals of Clinical and Translational Neurology, Vol 7, Iss 6, Pp 1013-1028 (2020)

Abstract Objective We describe the clinical characteristics and genetic etiology of several new cases within the ACO2‐related disease spectrum. Mitochondrial aconitase (ACO2) is a nuclear‐encoded tricarboxylic acid cycle enzyme. Homozygous pathog

Externí odkaz: https://doaj.org/article/a04c331bd519443b858efb712f9f4d19

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