طبيب اليستار كالدر

Shelmerdine, SC., Brittain, H., Arthurs, OJ., Calder, AD. 2016. Achondroplasia: Really rhizomelic? Am J Med Genet A. 170(8) pp. 2039-2043.

Tooley, M., Lynch, D., Bernier, F., Parboosingh, J., Bhoj, E., Zackai, E., Calder, A., Itasaki, N., Wakeling, E., Scott, R., Lees, M., Clayton-Smith, J., Blyth, M., Morton, J., Shears, D., Kini, U., Homfray, T., Clarke, A., Barnicoat, A., Wallis, C., Hewitson, R., Offiah, A., Saunders, M., Langton-Hewer, S., Hilliard, T., Davis, P., Smithson, S. 2016. Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings. Am J Med Genet A. 170(5) pp. 1115-1126. 

Calder, AD. 2015.  Radiology of Osteogenesis Imperfecta, Rickets and Other Bony Fragility States. Endocr Dev. 28 pp.56-71.

Merrick, B., Calder, A., Wakeling, E. 2015. Dysspondyloenchondromatosis (DSC) associated with COL2A1 mutation: Clinical and radiological overlap with spondyloepimetaphyseal dysplasia-Strudwick type (SEMD-S). Am J Med Genet A. 167(12) pp. 3103 – 3107.

Watson, SG., Calder, AD., Offiah, AC., Negus, S. 2015. A review of imaging protocols for suspected skeletal dysplasia and a proposal for standardisation. Pediatr Radiol. 45(12) pp. 1733 – 1737.

Calder, AD., Offiah, AC. 2015. Foetal radiography for suspected skeletal dysplasia: technique, normal appearances, diagnostic approach. Pediatr Radiol. 45(4) pp. 536 – 548.

Calder, AD., Bush, A., Brody, AS., Owens, CM. 2014. Scoring of chest CT in children with cystic fibrosis: state of the art. Pediatr Radiol. 44(12) pp. 1496 – 1506.

Goodwin, SJ., Randle, E., Iguchi, A., Brown, K., Hoskote, A., Calder, AD. 2014. Chest computed tomography in children undergoing extra-corporeal membrane oxygenation: a 9-year single-centre experience. Pediatr Radiol. 44(6) pp. 750 – 760.

Parry, DA., Logan, CV., Stegmann, AP., Abdelhamed, ZA., Calder, A,. Khan, S., Bonthron, DT., Clowes, V., Sheridan, E., Ghali, N., Chudley, AE., Dobbie, A., Stumpel, CT., Johnson, CA. 2013. SAMS, a syndrome of short stature, auditory-canal atresia, mandibular hypoplasia,and skeletal abnormalities is a unique neurocristopathy caused by mutations in Goosecoid. Am J Hum Genet. 93(6) pp.1135 – 1142.

Sousa, SB., Jenkins, D., Chanudet, E., Tasseva, G., Ishida, M., Anderson, G., Docker, J., Ryten, M., Sa, J., Saraiva, JM., Barnicoat, A., Scott, R., Calder, A., Wattanasirichaigoon, D., Chrzanowska, K., Simandlová, M., Van Maldergem, L., Stanier, P., Beales, PL., Vance, JE., Moore, GE. 2014. Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome. Nat Genet. 46(1).