Browsing by Author Alcausin, Melanie

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)Citation
2013Intravenous Pamidronate Treatment in Children with Moderate-to-Severe Osteogenesis Imperfecta Started under Three Years of AgeAlcausin, Melanie; Munns, Craig; Sillence, David; Ault, Jenny E.; Bridge, Corinne; Briody, Julie N.; Engelbert, R.H.H.; McQuade, Mary; Pacey, V; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthIntravenous Pamidronate Treatment in Children with Moderate-to-Severe Osteogenesis Imperfecta Started under Three Years of Age, Hormone Research in Paediatrics, vol.79, 6, 2013,pp 333-340
2010The natural history and osteodystrophy of mucolipidosis types II and IIIMunns, Craig; Sillence, David; Alcausin, Melanie; Ault, Jenny E.; Briody, Julie N.; Cathey, Sara; David-Vizcarra, Grace; Edwards, Matthew J.; Fietz, M.; Fletcher, Janice; McGill, Jim; Savarirayan, Ravi; Wilson, Meredith J.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthThe natural history and osteodystrophy of mucolipidosis types II and III, Journal of Paediatrics and Child Health, vol.46, 6, 2010,pp 316-322
2011TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new familiesAlcausin, Melanie; Sillence, David; Aftimos, Salim; Andreucci, Elena; Haan, Eric; Hunter, Warwick; Kannu, Peter; Kerr, Bronwyn; Lamande, Shireen R.; McGillivray, G; McKinlay Gardner, R J; Patricelli, Maria; Savarirayan, Ravi; Thompson, Elizabeth M.; Zacharin, Margaret R.; Zankl, Andreas; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthTRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families, Orphanet Journal of Rare Diseases, vol.6, 1, 2011,pp Article number 37-1-Article number 37-8