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Expert Reviews in Molecular Medicine, ISSN 1462-3994, 01/2008, Volume 10, Issue 1, pp. 1 - 18
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S25 - S26
Journal Article
Human Performance, ISSN 0895-9285, 08/2017, Volume 30, Issue 4, pp. 212 - 230
Because organizational citizenship behavior (OCB) performance contributes to overall performance ratings and failure to perform expected behaviors detracts... 
MECHANICAL TURK | WOMEN SCALE | PROSOCIAL BEHAVIOR | DARK SIDES | STEREOTYPES | WORK-FAMILY CONFLICT | GOOD SOLDIER | PSYCHOLOGY, APPLIED | CONSEQUENCES | COMPONENTS | SEX-DIFFERENCES | Human factors research | Gender differences | Ideology
Journal Article
Journal of Applied Social Psychology, ISSN 0021-9029, 12/2016, Volume 46, Issue 12, pp. 701 - 717
Despite a vast body of literature evidencing the negative effects of workplace sexual harassment it remains unclear whether sexual harassment experienced by... 
MEDIATING ROLE | RESPONSES | PSYCHOLOGY, SOCIAL | ACADEMIC CONTEXT | ORGANIZATIONAL JUSTICE | CONSEQUENCES | WORKPLACE AGGRESSION | POWER | OUTCOMES | UNIVERSITY-STUDENTS | PERCEPTIONS | Analysis | Job satisfaction
Journal Article
Pediatrics, ISSN 0031-4005, 02/2016, Volume 137, Issue Supplement 3, pp. 212 - 212A
Journal Article
Expert Opinion on Pharmacotherapy, ISSN 1465-6566, 02/2008, Volume 9, Issue 2, pp. 311 - 317
Journal Article
Pediatrics, ISSN 0031-4005, 01/2009, Volume 123, Issue 1, pp. 19 - 29
Journal Article
Expert Reviews in Molecular Medicine, ISSN 1462-3994, 07/2009, Volume 11
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2016, Volume 117, Issue 2, pp. 217 - 217
Morquio A Syndrome (mucopolysaccharidosis IVA [MPS IVA]) is an inherited, autosomal recessive lysosomal storage disorder that occurs in ~ 1 in 200,000 to... 
Enzyme Replacement Therapy | Humans | Chondroitinsulfatases - therapeutic use | Clinical Protocols | Quality of Life | Mucopolysaccharidosis IV - genetics | Mucopolysaccharidosis IV - drug therapy | Precision Medicine | Physiological aspects | Keratin | Enzymes | Sulfates | Analysis
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S28 - S29
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2019, Volume 179, Issue 12, pp. 2425 - 2432
Mucopolysaccharidosis Type I (MPS I), caused by deficiency of α‐L‐iduronidase results in progressive, multisystemic disease with a broad phenotypic spectrum... 
mucopolysaccharidosis | natural history | disease‐specific growth curves | lysosomal storage disorders | Phenotypes | Mucopolysaccharidosis | Growth curves | Health risk assessment | Age | Growth patterns
Journal Article
Expert Review of Endocrinology & Metabolism, ISSN 1744-6651, 11/2011, Volume 6, Issue 6, pp. 755 - 768
A decade has passed since the initial report that parenteral use of recombinant human α-L-iduronidase results in amelioration of symptoms in patients with... 
glycosaminoglycans | Hurler syndrome | enzyme replacement therapy | human recombinant protein | lysosomal storage disease | iduronidase | mucopolysaccharidosis | Scheie syndrome | Hurler-Scheie syndrome | Enzymes | Development and progression | Mucopolysaccharidosis | Glycosaminoglycans | Hormone therapy
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