Supernumerary Nostril in a 15-Year-Old Girl by Ann Christie P. Lluisma

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Stock editing: creating guidelines for University of the Arts London by Cannon, C, Christie, P

The relationship between the income and behavioural biases by Renu Isidore R, Christie P

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Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1). by Turner, J, Christie, P, Pearce, S, Turnpenny, P, Thakker, R

APOL1 Kidney Risk Variants and Long-Term Kidney Function in Healthy Middle-Aged Black Individuals: The Atherosclerosis Risk in Communities (ARIC) Study by Mona D. Doshi, Lihua Li, Abhijit S. Naik, Christie P. Thomas

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A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challenges. by Burren, C, Curley, A, Christie, P, Rodda, C, Thakker, R

Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease. by Devuyst, O, Christie, P, Courtoy, P, Beauwens, R, Thakker, R

X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene. by Christie, P, Harding, B, Nesbit, M, Whyte, M, Thakker, R

A novel AVPR2 mutation in a kindred with nephrogenic diabetes insipidus by Lemos, M, Rodrigues, D, Gomes, L, Christie, P, Thakker, R, Carvalheiro, M

X-linked hypophosphataemic rickets due to pseudo-exons of the PHEX gene. by Christie, P, Harding, B, Nesbit, M, Eddy, M, Whyte, M, Thakker, R

Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship. by Wu, F, Roche, P, Christie, P, Loh, N, Reed, A, Esnouf, R, Thakker, R

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene. by Hannan, F, Nesbit, M, Christie, P, Fratter, C, Dudley, N, Sadler, G, Thakker, R

Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia. by Dixon, P, Wooding, C, Christie, P, Grieff, M, Schlessinger, D, Whyte, M, Thakker, R

Secretion of soluble vascular endothelial growth factor receptor 1 (sVEGFR1/sFlt1) requires Arf1, Arf6, and Rab11 GTPases. by Jae-Joon Jung, Ajit Tiwari, Shivangi M Inamdar, Christie P Thomas, Apollina Goel, Amit Choudhury

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A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis. by Lemos, M, Kotanko, P, Christie, P, Harding, B, Javor, T, Smith, C, Eastell, R, Thakker, R

Immunotherapy with Antibodies in Multiple Myeloma: Monoclonals, Bispecifics, and Immunoconjugates by Christie P. M. Verkleij, Wassilis S. C. Bruins, Sonja Zweegman, Niels W. C. J. van de Donk

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Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome. by Looij, v, Meijers-Heijboer, H, Beetz, R, Thakker, R, Christie, P, Feenstra, L, van Zanten, BG

A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and sever... by Hannan, F, Nesbit, M, Christie, P, Lissens, W, Van der Schueren, B, Bex, M, Bouillon, R, Thakker, R

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences:... by Hannan, F, Nesbit, M, Turner, J, Stacey, J, Cianferotti, L, Christie, P, Conigrave, A, Whyte, M, Thakker, R

Mutational analysis in X-linked Spondyloepiphyseal Dysplasia Tarda (SEDT). by Christie, P, Curley, A, Nesbit, M, Chapman, C, Genet, S, Harper, P, Keeling, S, Wilkie, A, Winter, R, Thakker, R