C. Vogler

C. Vogler, E. Wood, S. Eliason, 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Increased life span and correction of metabolic defects in murine mucopolysaccharidosis type VII after syngeneic bone marrow transplantation.

W. Sly, B. Gwynn, E. Birkenmeier, 1991, Blood.

A murine model of mucopolysaccharidosis VII. Gross and microscopic findings in beta-glucuronidase-deficient mice.

W. Sly, W. Beamer, E. Birkenmeier, 1990, The American journal of pathology.

Clinical response to persistent, low-level β-glucuronidase expression in the murine model of mucopolysaccharidosis type VII

M. Sands, C. Vogler, B. Levy, 2007, Journal of Inherited Metabolic Disease.

Role of Influenza B virus in hepatic steatosis and mitochondrial abnormalities in a mouse model of reye syndrome

K. Schwarz, C. Sippel, C. Vogler, 1991, Hepatology.

Intrathecal enzyme replacement therapy reduces lysosomal storage in the brain and meninges of the canine model of MPS I.

W. Mobley, M. Mcentee, P. Dickson, 2004, Molecular genetics and metabolism.

Adenovirus-mediated gene transfer and expression of human beta-glucuronidase gene in the liver, spleen, and central nervous system in mucopolysaccharidosis type VII mice.

W. Sly, T. Ohashi, K. Watabe, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Neonatal retroviral vector-mediated hepatic gene therapy reduces bone, joint, and cartilage disease in mucopolysaccharidosis VII mice and dogs.

M. Haskins, M. Sands, K. Ponder, 2004, Molecular genetics and metabolism.

AAV2/5 vector expressing galactocerebrosidase ameliorates CNS disease in the murine model of globoid-cell leukodystrophy more efficiently than AAV2.

Corinne R. Fantz, M. Sands, D. Wenger, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Infused Fc-tagged β-glucuronidase crosses the placenta and produces clearance of storage in utero in mucopolysaccharidosis VII mice

W. Sly, G. Shah, J. Grubb, 2008, Proceedings of the National Academy of Sciences.

Enzyme therapy in mannose receptor-null mucopolysaccharidosis VII mice defines roles for the mannose 6-phosphate and mannose receptors

W. Sly, J. Grubb, S. Tomatsu, 2006, Proceedings of the National Academy of Sciences.

Neonatal intramuscular injection with recombinant adeno-associated virus results in prolonged beta-glucuronidase expression in situ and correction of liver pathology in mucopolysaccharidosis type VII mice.

T. Daly, N. Muzyczka, M. Haskins, 1999, Human gene therapy.

Gene therapy for murine mucopolysaccharidosis type VII

W. Sly, N. Muzyczka, M. Sands, 1997, Neuromuscular Disorders.

Defining the pathway for Tat-mediated delivery of beta-glucuronidase in cultured cells and MPS VII mice.

W. Sly, Q. Mao, B. Davidson, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Glycosylation-independent targeting enhances enzyme delivery to lysosomes and decreases storage in mucopolysaccharidosis type VII mice.

W. Sly, J. Grubb, J. LeBowitz, 2004, Proceedings of the National Academy of Sciences of the United States of America.

In utero fetal liver cell transplantation without toxic irradiation alleviates lysosomal storage in mice with mucopolysaccharidosis type VII.

C. Vogler, B. Levy, J. Barker, 2001, Blood cells, molecules & diseases.

Biochemical evidence for superior correction of neuronal storage by chemically modified enzyme in murine mucopolysaccharidosis VII

W. Sly, J. Grubb, C. Vogler, 2012, Proceedings of the National Academy of Sciences.

Biodistribution, Kinetics, and Efficacy of Highly Phosphorylated and Non-phosphorylated β-Glucuronidase in the Murine Model of Mucopolysaccharidosis VII*

W. Sly, J. Grubb, M. Sands, 2001, The Journal of Biological Chemistry.

Case Report: Sclerosing Cholangitis, Inflammatory Bowel Disease, and Glomerulonephritis (A Case Report of a Rare Triad)

B. Neuschwander‐Tetri, J. Roche, C. Janney, 1997, Digestive Diseases and Sciences.

Microangiopathic glomerulopathy in children with sickle cell anemia.

B. Cole, C. Vogler, P. Lane, 1996, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.

Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates.

W. Sly, M. Sands, B. Gwynn, 1993, Laboratory investigation; a journal of technical methods and pathology.

Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

M. Sands, J. Wolfe, B. Gwynn, 1992, Nature.

Central nervous system-directed AAV2/5-mediated gene therapy synergizes with bone marrow transplantation in the murine model of globoid-cell leukodystrophy.

M. Sands, C. Vogler, B. Levy, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Amniotic Infection Syndrome: Nosology and Reproducibility of Placental Reaction Patterns

R. Redline, D. Heller, C. Vogler, 2003, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Chemically modified β-glucuronidase crosses blood–brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII

W. Sly, J. Grubb, C. Vogler, 2008, Proceedings of the National Academy of Sciences.

Murine Mucopolysaccharidosis VII: Impact of Therapies on the Phenotype, Clinical Course, and Pathology in a Model of a Lysosomal Storage Disease

W. Sly, M. Sands, C. Vogler, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Replacing the Enzyme α-l-Iduronidase at Birth Ameliorates Symptoms in the Brain and Periphery of Dogs with Mucopolysaccharidosis Type I

R. D. Whitley, C. Vite, E. Riedesel, 2010, Science Translational Medicine.

Genetic ablation of acid ceramidase in Krabbe disease confirms the psychosine hypothesis and identifies a new therapeutic target

J. Medin, D. Wozniak, Yedda Li, 2019, Proceedings of the National Academy of Sciences.

Murine mucopolysaccharidosis type VII: long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation.

W. Sly, M. Sands, B. Gwynn, 1997, The Journal of clinical investigation.

Numerous transcriptional alterations in liver persist after short-term enzyme-replacement therapy in a murine model of mucopolysaccharidosis type VII.

W. Sly, C. Semenkovich, M. Sands, 2004, The Biochemical journal.

Transgene produces massive overexpression of human β-glucuronidase in mice, lysosomal storage of enzyme, and strain-dependent tumors

W. Sly, X. Zhou, C. Vogler, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of a Mouse with /O-Glucuronidase Deficiency

M. Davisson, K. Lyford, R. Ganschow, 1989 .

Murine mucopolysaccharidosis type VII: The impact of therapies on the clinical course and pathology in a murine model of lysosomal storage disease

W. Sly, M. Sands, C. Vogler, 1998, Journal of Inherited Metabolic Disease.

Enzyme replacement therapy for murine mucopolysaccharidosis type VII.

W. Sly, J. Grubb, M. Sands, 1994, The Journal of clinical investigation.

Enzyme Replacement with Recombinant β-Glucuronidase in the Newborn Mucopolysaccharidosis Type VII Mouse

W. Sly, M. Sands, E. Birkenmeier, 1993, Pediatric Research.

Toxoplasmic polymyositis revisited: case report and review of literature

G. Hayat, C. Vogler, M. Cuturic, 1997, Neuromuscular Disorders.

Clinical and pathologic findings in two new allelic murine models of polycystic kidney disease.

E. Birkenmeier, C. Vogler, C. Thorpe, 1999, Journal of the American Society of Nephrology : JASN.

Renal Pathology in the Pediatric Transplant Patient

C. Belsha, C. Vogler, P. Walker, 2007, Advances in anatomic pathology.

Expression of proliferating cell nuclear antigen in Spitz nevus.

G. Nahass, N. Penneys, C. Vogler, 1995, Journal of the American Academy of Dermatology.

Bone marrow transplantation in type IIa glycogen storage disease.

R. Harris, C. Vogler, G. Hug, 1986, Birth defects original article series.

Renal and extrarenal rhabdoid tumors in children: a clinicopathologic study of 14 patients.

W. Gooch, F. Gonzalez-crussi, D. Demello, 1986, Seminars in diagnostic pathology.

Staging and treatment of Wilms' tumors.

C. Sotelo-Avila, C. Vogler, G. Gale, 1986, Mayo Clinic proceedings.

Attenuation of murine lysosomal storage disease by allogeneic neonatal bone marrow transplantation using costimulatory blockade and donor lymphocyte infusion without myeloablation.

M. Lessard, J. Proctor, B. Soper, 2006, Clinical immunology.

Erratum: Intracranial injection of recombinant adeno-associated virus improves cognitive function in a murine model of mucopolysaccharidosis type VII (Molecular Therapy (2001) vol. 3 (3) (351-358))

T. Daly, S. Walkley, M. Sands, 2001 .

AAV Vector Integration Sites in Mouse Hepatocellular Carcinoma

Daniel G. Miller, Elizabeth M. Brunt, D. Russell, 2007, Science.

Observed incidence of tumorigenesis in long-term rodent studies of rAAV vectors

T. Flotte, T. Daly, N. Muzyczka, 2001, Gene Therapy.

Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.

M. Davisson, K. Lyford, R. Ganschow, 1989, The Journal of clinical investigation.

Focal mucinosis of the upper aerodigestive tract in children.

D. Gnepp, C. Sotelo-Avila, C. Vogler, 1990, Human pathology.

Early versus late treatment of spinal cord compression with long-term intrathecal enzyme replacement therapy in canine mucopolysaccharidosis type I.

C. Vite, M. Mcentee, M. Haskins, 2010, Molecular genetics and metabolism.

Syngeneic bone marrow transplantation reduces the hearing loss associated with murine mucopolysaccharidosis type VII.

W. Sly, M. Sands, L. Erway, 1995, Blood.

Intravitreal Gene Therapy Reduces Lysosomal Storage in Specific Areas of the CNS in Mucopolysaccharidosis VII Mice

M. Sands, S. Bassnett, J. Ogilvie, 2003, The Journal of Neuroscience.

Prevention of systemic clinical disease in MPS VII mice following AAV-mediated neonatal gene transfer

M. Sands, C. Vogler, T. Daly, 2001, Gene Therapy.

Retinal function is improved in a murine model of a lysosomal storage disease following bone marrow transplantation.

M. Sands, C. Vogler, N. Galvin, 2000, Experimental eye research.

Enzyme Replacement with Recombinant β-Glucuronidase in Murine Mucopolysaccharidosis Type VII: Impact of Therapy during the First Six Weeks of Life on Subsequent Lysosomal Storage, Growth, and Survival

W. Sly, M. Sands, E. Birkenmeier, 1996, Pediatric Research.

Enzyme replacement therapy for murine mucopolysaccharidosis type VII leads to improvements in behavior and auditory function.

W. Sly, M. Sands, L. Erway, 1998, The Journal of clinical investigation.

Brain-directed gene therapy for lysosomal storage disease: Going well beyond the blood– brain barrier

W. Sly, C. Vogler, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Enzyme Replacement in Murine Mucopolysaccharidosis Type VII: Neuronal and Glial Response to β-Glucuronidase Requires Early Initiation of Enzyme Replacement Therapy

W. Sly, J. Baty, M. Sands, 1999, Pediatric Research.

Lentiviral‐Transduced Human Mesenchymal Stem Cells Persistently Express Therapeutic Levels of Enzyme in a Xenotransplantation Model of Human Disease

J. Nolta, M. Sands, T. Meyerrose, 2008, Stem cells.

Ewing sarcoma in a phalanx of an infant's finger. A case report.

D. Hanel, F. Schajowicz, D. Strege, 1989, The Journal of bone and joint surgery. American volume.

Neonatal cystic testicular gonadoblastoma. Sonographic and pathologic findings.

G. Steinhardt, C. Vogler, A. Luisiri, 1991, Journal of ultrasound in medicine.

The inflammatory response in pediatric biliary disease: macrophage phenotype and distribution.

E. S. Fox, P. Dillon, K. Minnick, 1996, Journal of pediatric surgery.

Correction of murine mucopolysaccharidosis VII by a human beta-glucuronidase transgene.

W. Sly, B. Gwynn, E. Birkenmeier, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Electron microscopy in the diagnosis of lysosomal storage diseases.

J. Williams, H. Rosenberg, I. Butler, 1987, American journal of medical genetics. Supplement.

Intramuscular hematopoiesis in hypotonic infants with type 1 muscle fiber dysmaturation.

S. Iannaccone, K. Bove, C. Vogler, 1986, Archives of pathology & laboratory medicine.

Adeno-associated virus 2-mediated gene therapy decreases autofluorescent storage material and increases brain mass in a murine model of infantile neuronal ceroid lipofuscinosis

J. Cooper, M. Sands, E. Bible, 2004, Neurobiology of Disease.

Hypertrophic cardiomyopathy in a newborn infant.

C. Vogler, S. Chen, J. Hoffmann, 1999, The Journal of pediatrics.

Electron microscopy in the diagnosis of pediatric disease.

J. J. Buchino, C. Vogler, C. Daugherty, 1989, Pediatric clinics of North America.

Paucifascicular congenital sensory neuropathy in identical twins.

S. Iannaccone, K. Bove, C. Vogler, 1986, American journal of diseases of children.

Oxidative stress as a therapeutic target in globoid cell leukodystrophy

M. Sands, C. Vogler, Adarsh S. Reddy, 2012, Experimental Neurology.

Bone Marrow Transplantation Augments the Effect of Brain- and Spinal Cord-Directed Adeno-Associated Virus 2/5 Gene Therapy by Altering Inflammation in the Murine Model of Globoid-Cell Leukodystrophy

Joong Hee Kim, Sheng-Kwei Song, R. Klein, 2011, The Journal of Neuroscience.

A Murine Model of Infantile Neuronal Ceroid Lipofuscinosis—Ultrastructural Evaluation of Storage in the Central Nervous System and Viscera

M. Sands, A. Kovács, C. Vogler, 2008, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22).

J. Batanian, J. Bridge, C. Vogler, 2002, Cancer genetics and cytogenetics.

Neuropathology of murine mucopolysaccharidosis type VII

W. Sly, E. Birkenmeier, C. Vogler, 1996, Acta Neuropathologica.

Human CD34+ hematopoietic progenitor cell-directed lentiviral-mediated gene therapy in a xenotransplantation model of lysosomal storage disease.

M. Sands, S. Devine, C. Vogler, 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

Placental Pathology for the Surgical Pathologist

C. Sotelo‐Avila, C. Vogler, J. Petterchak, 2000, Advances in anatomic pathology.

Type 1 fiber size disproportion: morphometric data from 37 children with myopathic, neuropathic, or idiopathic hypotonia.

S. Iannaccone, K. Bove, J. J. Buchino, 2009, Pediatric pathology.

Morphology of skeletal muscle in children. An assessment of normal growth and differentiation.

K. Bove, C. Vogler, 1985, Archives of pathology & laboratory medicine.

A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency

W. Ferguson, C. Vogler, A. Knutsen, 2008, Pediatric blood & cancer.

Pericardial cysts in children: surgical or conservative approach?

B. Noyes, C. Vogler, T. Weber, 2003, Journal of pediatric surgery.

Aluminum-containing emboli in infants treated with extracorporeal membrane oxygenation.

J. Schreifels, D. Lagunoff, C. Sotelo-Avila, 1988, The New England journal of medicine.

Laryngeal fibromatosis in the neonate.

L. Close, H. Rosenberg, C. Vogler, 1981, Archives of otolaryngology.

Glomerular basement membrane and lamina densa in infants and children: an ultrastructural evaluation.

S. Homan, A. J. Mcadams, C. Vogler, 1987, Pediatric pathology.

Pathology of the ear in murine mucopolysaccharidosis type VII. Morphologic correlates of hearing loss.

W. Sly, E. Birkenmeier, C. Vogler, 1994, Laboratory investigation; a journal of technical methods and pathology.

A Novel Model of Murine Mucopolysaccharidosis Type VII due to an Intracisternal A Particle Element Transposition into the β-Glucuronidase Gene: Clinical and Pathologic Findings

W. Sly, M. Sands, E. Birkenmeier, 2001, Pediatric Research.

Early Onset of Lysosomal Storage Disease in a Murine Model of Mucopolysaccharidosis Type VII: Undegraded Substrate Accumulates in Many Tissues in the Fetus and Very Young MPS VII Mouse

B. Soper, C. Vogler, B. Levy, 2005, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Enzyme Replacement Therapy Improves Reproductive Performance in Mucopolysaccharidosis Type VII Mice But Does Not Prevent Postnatal Losses

W. Sly, J. Grubb, B. Soper, 1999, Pediatric Research.

Mucopolysaccharidosis VII: postmortem biochemical and pathological findings in a young adult with beta-glucuronidase deficiency.

W. Sly, M. Whyte, J. W. Kyle, 1994, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Recombinant NAGLU-IGF2 prevents physical and neurological disease and improves survival in Sanfilippo B syndrome

Jodi D. Smith, T. Chou, J. Cooper, 2021, bioRxiv.

Intrathecal enzyme replacement therapy: successful treatment of brain disease via the cerebrospinal fluid.

M. Mcentee, P. Dickson, C. Vogler, 2007, Molecular genetics and metabolism.

Nonablative neonatal marrow transplantation attenuates functional and physical defects of beta-glucuronidase deficiency.

W. Sly, M. Lessard, W. Beamer, 2001, Blood.

Donor cell replacement in mice transplanted in utero is limited by immune-independent mechanisms.

M. Lessard, B. Soper, A. Schuldt, 2003, Blood cells, molecules & diseases.

Missense models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of murine mucopolysaccharidosis type VII produced by targeted mutagenesis

W. Sly, J. Grubb, K. Orii, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Murine model (Galns(tm(C76S)slu)) of MPS IVA with missense mutation at the active site cysteine conserved among sulfatase proteins.

W. Sly, S. Tomatsu, T. Orii, 2007, Molecular genetics and metabolism.

Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns-/-) produced by targeted disruption of the gene defective in Morquio A disease.

W. Sly, J. Grubb, K. Orii, 2003, Human molecular genetics.

Mouse model of N -acetylgalactosamine-6-sulfate sulfatase deﬁciency ( Galns (cid:1) / (cid:1) ) produced by targeted disruption of the gene defective in Morquio A disease

W. Sly, J. Nakayama, K. Orii, 2003 .

The Final Frontier – Crossing the Blood-brain Barrier

W. Sly, C. Vogler, 2013, EMBO molecular medicine.

Synchronous quadruple primary neoplasms: glioblastoma, neuroendocrine tumor, schwannoma and sessile serrated adenoma in a patient with history of prostate cancer.

N. Phillips, S. Alkaade, J. Batanian, 2015, Anticancer research.

Gene therapy for lysosomal storage disease: A no-brainer?

W. Sly, C. Vogler, 1997, Nature Medicine.

Glomerular membranopathy in adolescents with insulin-dependent diabetes.

A. J. Mcadams, C. Vogler, P. Mcenery, 1986, Human pathology.

Remission of Congenital Nephrotic Syndrome from Diffuse Mesangial Sclerosis with IVIG Therapy

C. Vogler, A. Knutsen, A. Beck, 2008 .

A clinical-pathological study of nonsurvivors of newborn ECMO.

C. Vogler, T. Tracy, T. Weber, 1993, Journal of pediatric surgery.

Clinicopathologic conference: neurologic dysfunction in a premature infant.

G. Fenton, C. Vogler, A. Manepalli, 2002, The Journal of pediatrics.

Transplanted ER-MP12hi20-58med/hi myeloid progenitors produce resident macrophages from marrow that are therapeutic for lysosomal storage disease.

M. Lessard, B. Soper, A. Schuldt, 2004, Blood cells, molecules & diseases.

Influence of maternal obesity and metabolic and vascular mediators in twin-twin transfusion syndrome.

B. Plunkett, Chi Wang, S. Crawford, 2019, Reproductive biology.

Viral infections of the fetus and the neonate.

H. Rosenberg, C. Vogler, S. Kohl, 1981, Monographs in pathology.

Solitary osteochondroma occurring on the transverse process of the lumbar spine. A case report.

A. Crawford, P. Esposito, C. Vogler, 1985, Spine.

Production of MPS VII mouse (Gus(tm(hE540A x mE536A)Sly)) doubly tolerant to human and mouse beta-glucuronidase.

W. Sly, J. Grubb, K. Orii, 2003, Human molecular genetics.

Central nervous system pathology progresses independently of KC and CXCR 2 in globoid-cell leukodystrophy

R. Klein, M. Sands, Jigisha R. Patel, 2019 .

Central Nervous System Pathology Progresses Independently of KC and CXCR2 in Globoid-Cell Leukodystrophy

R. Klein, M. Sands, Jigisha R. Patel, 2013, PloS one.

Enhanced Efficacy and Increased Long-Term Toxicity of CNS-Directed, AAV-Based Combination Therapy for Krabbe disease.

Christopher A. Miller, T. Ley, D. Ory, 2020, Molecular therapy : the journal of the American Society of Gene Therapy.

Cytomegalovirus infection and fetal death in a twin. A case report.

H. Rosenberg, C. Vogler, S. Kohl, 1986, The Journal of reproductive medicine.

Biodistribution and efficacy of donor T lymphocytes in a murine model of lysosomal storage disease.

M. Sands, P. Young, C. Vogler, 2003, Molecular therapy : the journal of the American Society of Gene Therapy.

Valproate use associated with persistent hyperammonemia and mitochondrial injury in a child with Down's syndrome.

B. Bacon, C. Vogler, R. Kane, 1992, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Mediastinal Granular Cell Tumor in a 16-Year-Old Boy: A Surgical and Pathologic Perspective

Y. Puckett, C. Vogler, J. Greenspon, 2016, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Muscle maturation delay in infantile myotonic dystrophy.

S. Iannaccone, K. Bove, C. Vogler, 1986, Archives of pathology & laboratory medicine.

Intracranial injection of recombinant adeno-associated virus improves cognitive function in a murine model of mucopolysaccharidosis type VII.

T. Daly, S. Walkley, M. Sands, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Morphology of liver repair following cholestatic liver injury: resolution of ductal hyperplasia, matrix deposition and regression of myofibroblasts.

S. Carr, B. Bacon, R. Britton, 2000, Liver.

Nonablative neonatal marrow transplantation attenuates functional and physical defects of beta-glucuronidase deficiency.

W. Sly, M. Lessard, W. Beamer, 2001, Blood.