Neuroimaging findings in infantile Pompe patients treated with enzyme replacement therapy.

Autor: McIntosh PT; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA., Hobson-Webb LD; Department of Neurology, Neuromuscular Division, Duke University, Durham, NC, USA., Kazi ZB; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA., Prater SN; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA., Banugaria SG; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA., Austin S; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA., Wang R; Department of Metabolic Disorders, Children's Hospital of Orange County, Orange, CA, USA., Enterline DS; Department of Radiology, Division of Neuroradiology, Duke University, Durham, NC, USA., Frush DP; Department of Radiology, Division of Pediatric Radiology, Duke University, Durham, NC, USA., Kishnani PS; Department of Pediatrics, Division of Medical Genetics, Duke University, Durham, NC, USA. Electronic address: Priya.kishnani@duke.edu.

Publikováno v: Molecular genetics and metabolism [Mol Genet Metab] 2018 Feb; Vol. 123 (2), pp. 85-91. Date of Electronic Publication: 2017 Oct 13.

CRIM-negative infantile Pompe disease: characterization of immune responses in patients treated with ERT monotherapy.

Autor: Berrier KL; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Kazi ZB; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Prater SN; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Bali DS; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Goldstein J; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Stefanescu MC; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA., Rehder CW; Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA., Botha EG; Department of Human Genetics, Emory University, Atlanta, Georgia, USA., Ellaway C; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, Australia., Bhattacharya K; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, Australia., Tylki-Szymanska A; Department of Pediatrics, Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland., Karabul N; Center for Pediatric and Adolescent Medicine, University Medical Center, Mainz, Germany., Rosenberg AS, Kishnani PS; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina, USA.

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2015 Nov; Vol. 17 (11), pp. 912-8. Date of Electronic Publication: 2015 Mar 05.

Non-depleting anti-CD4 monoclonal antibody induces immune tolerance to ERT in a murine model of Pompe disease.

Autor: Sun B; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA., Banugaria SG; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA., Prater SN; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA., Patel TT; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA., Fredrickson K; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA., Ringler DJ; Tolerx, Inc., Cambridge, MA, USA., de Fougerolles A; Tolerx, Inc., Cambridge, MA, USA., Rosenberg AS; Division of Therapeutic Proteins, U.S. Food and Drug Administration, Silver Spring, MD, USA., Waldmann H; Sir William Dunn School of Pathology, Oxford University, Oxford, UK., Kishnani PS; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.

Publikováno v: Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2014 Oct 12; Vol. 1, pp. 446-450. Date of Electronic Publication: 2014 Oct 12 (Print Publication: 2014).

Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERT.

Autor: Banugaria SG; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, United States of America., Prater SN, Patel TT, Dearmey SM, Milleson C, Sheets KB, Bali DS, Rehder CW, Raiman JA, Wang RA, Labarthe F, Charrow J, Harmatz P, Chakraborty P, Rosenberg AS, Kishnani PS

Publikováno v: PloS one [PLoS One] 2013 Jun 25; Vol. 8 (6), pp. e67052. Date of Electronic Publication: 2013 Jun 25 (Print Publication: 2013).

Structures of the compact helical core domains of feline calicivirus and murine norovirus VPg proteins.

Autor: Leen EN; Division of Cell and Molecular Biology, Department of Life Sciences, Imperial College London, London, United Kingdom., Kwok KY, Birtley JR, Simpson PJ, Subba-Reddy CV, Chaudhry Y, Sosnovtsev SV, Green KY, Prater SN, Tong M, Young JC, Chung LM, Marchant J, Roberts LO, Kao CC, Matthews S, Goodfellow IG, Curry S

Publikováno v: Journal of virology [J Virol] 2013 May; Vol. 87 (10), pp. 5318-30. Date of Electronic Publication: 2013 Mar 13.