Nancy Galvin

UCLouvain Saint-Louis Brussels — Belgium

Medicine · Health Sciences

26h-index2.5kcitations42works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Lysosomal Storage Disorders Research(20), Trypanosoma species research and implications(10), Cellular transport and secretion(9), Protease and Inhibitor Mechanisms(5), Glycogen Storage Diseases and Myoclonus(5)

Publications42 total

Detection of elemental mercury in abdominal wall soft tissue
Journal of Medical Toxicology·2009· 8 citedOpen Access
A Murine Model of Infantile Neuronal Ceroid Lipofuscinosis—Ultrastructural Evaluation of Storage in the Central Nervous System and Viscera
Pediatric and Developmental Pathology·2008· 33 citedOpen Access
Chemically modified β-glucuronidase crosses blood–brain barrier and clears neuronal storage in murine mucopolysaccharidosis VII
Proceedings of the National Academy of Sciences·2008· 115 citedOpen Access
Enzyme therapy in mannose receptor-null mucopolysaccharidosis VII mice defines roles for the mannose 6-phosphate and mannose receptors
Proceedings of the National Academy of Sciences·2006· 53 citedOpen Access
Attenuation of murine lysosomal storage disease by allogeneic neonatal bone marrow transplantation using costimulatory blockade and donor lymphocyte infusion without myeloablation
Clinical Immunology·2006· 5 cited
A murine model of infantile neuronal ceroid lipofuscinosis - Ultrastructural evaluation of storage in the central nervous system and viscera
Pediatric and Developmental Pathology·2006· 1 cited
Overcoming the blood-brain barrier with high-dose enzyme replacement therapy in murine mucopolysaccharidosis VII
Proceedings of the National Academy of Sciences·2005· 170 citedOpen Access
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
Pediatric and Developmental Pathology·2005· 28 cited
Electrocardiographic and other cardiac anomalies in β-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation
Proceedings of the National Academy of Sciences·2004· 12 citedOpen Access
Intravitreal Gene Therapy Reduces Lysosomal Storage in Specific Areas of the CNS in Mucopolysaccharidosis VII Mice
Journal of Neuroscience·2003· 79 citedOpen Access
Transgene produces massive overexpression of human β-glucuronidase in mice, lysosomal storage of enzyme, and strain-dependent tumors
Proceedings of the National Academy of Sciences·2003· 43 citedOpen Access
Murine Mucopolysaccharidosis VII: Impact of Therapies on the Phenotype, Clinical Course, and Pathology in a Model of a Lysosomal Storage Disease
Pediatric and Developmental Pathology·2001· 38 cited
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
Pediatric Research·2001· 24 citedOpen Access
Retinal Function is Improved in a Murine Model of a Lysosomal Storage Disease Following Bone Marrow Transplantation
Experimental Eye Research·2000· 46 cited
SPONTANEOUS RUPTURE OF THE LIVER UPON REVASCULARIZATION DURING TRANSPLANTATION
Transplantation·2000· 15 cited
Repetitive Self-Limited Acute Pancreatitis Induces Pancreatic Fibrogenesis in the Mouse
Digestive Diseases and Sciences·2000· 110 cited
Non-amyloid fibrils in heavy chain deposition disease
Kidney International·1999· 10 cited
Enzyme Replacement in Murine Mucopolysaccharidosis Type VII: Neuronal and Glial Response to β-Glucuronidase Requires Early Initiation of Enzyme Replacement Therapy
Pediatric Research·1999· 100 citedOpen Access
Murine mucopolysaccharidosis type VII: The impact of therapies on the clinical course and pathology in a murine model of lysosomal storage disease
Journal of Inherited Metabolic Disease·1998· 42 cited
Early fetal development of lung vasculature.
American Journal of Respiratory Cell and Molecular Biology·1997· 289 cited
page 1 of 3Next →

Frequent Co-authors

Carole Vogler(20), Beth Levy(17), William S. Sly(12), Mark S. Sands(11), William A. Frazier(8), E H Birkenmeier(7), Jane E. Barker(7), Vishva M. Dixit(5), Jeffrey H. Grubb(4), Yun Tan(3), Barry C. Holwerda(3), Karen O’Rourke(3), Mark D. Lessard(3), John W. Kyle(2), Thomas Baranski(2), Samuel A. Santoro(2), Constance Thorpe(2), Beth L. Meyers-Hutchins(2), Megan A. Griffey(2), Brian W. Soper(2)