Some chronic obstructive pulmonary disease will originate in neonatal intensive care units. by Bentham, JR, Shaw, N

Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT)n polymorphism. by Parkinson, D, Shaw, N, Himsworth, R, Thakker, R

Product data models / by 248054 Shaw, N. K., Bloor, Susan, De Pennington, A.

Permanent neonatal diabetes in an Asian infant. by Porter, JR, Shaw, N, Barrett, T, Hattersley, A, Ellard, S, Gloyn, A

Different subtypes of pseudohypoparathyroidism in the same family with an unusual psychiatric presentation of the index case. by Pollard, A, Prendergast, M, al-Hammouri, F, Rayner, P, Shaw, N

Observation of the iron-sulfur cluster in Escherichia coli biotin synthase by nanoflow electrospray mass spectrometry. by Hernández, H, Hewitson, K, Roach, P, Shaw, N, Baldwin, J, Robinson, C

X-linked hypophosphataemia: burden of disease using United Kingdom primary care data by Javaid, M, Delmestri, A, Shaw, N, Prieto-Alhambra, D, Cooper, C, Pinedo Villanueva, R

Prevalence and mortality of individuals with X-linked hypophosphataemia: a United Kingdom real world data analysis by Hawley, S, Shaw, N, Delmestri, A, Prieto Alhambra, D, Cooper, C, Pinedo Villanueva, R, Javaid, M

Bone mineral density at diagnosis and following successful treatment of pediatric Cushing's disease. by Scommegna, S, Greening, J, Storr, H, Davies, K, Shaw, N, Monson, J, Grossman, AB, Savage, M

Asian MODY: are we missing an important diagnosis? by Porter, JR, Rangasami, J, Ellard, S, Gloyn, A, Shields, B, Edwards, J, Anderson, J, Shaw, N, Hattersley, A, Frayling, T, Plunkett, M, Barrett, T

Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia. by Storr, H, Mitchell, H, Swords, F, Main, K, Hindmarsh, P, Betts, P, Shaw, N, Johnston, D, Clark, A, Reznek, R, Grossman, AB, Savage, M

CYP3A4 mutation causes vitamin D-dependent rickets type 3 by Roizen, J, Li, D, O'Lear, L, Javaid, M, Shaw, N, Ebeling, P, Nguyen, H, Rodda, C, Thummel, K, Thacher, T, Hakonarson, H, Levine, M

Mutational analysis of PHEX gene in X-linked hypophosphatemia. by Dixon, P, Christie, P, Wooding, C, Trump, D, Grieff, M, Holm, I, Gertner, J, Schmidtke, J, Shah, B, Shaw, N, Smith, C, Tau, C, Schlessinger, D, Whyte, M, Thakker, R

Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hyp... by Bowl, MR, Mirczuk, S, Grigorieva, I, Piret, SE, Cranston, T, Southam, L, Allgrove, J, Bahl, S, Brain, C, Loughlin, J, Mughal, Z, Ryan, F, Shaw, N, Thakker, Y, Tiosano, D, Nesbit, M, Thakker, R

GATA3 haplo-insufficiency causes human HDR syndrome. by Van Esch, H, Groenen, P, Nesbit, M, Schuffenhauer, S, Lichtner, P, Vanderlinden, G, Harding, B, Beetz, R, Bilous, R, Holdaway, I, Shaw, N, Fryns, J, Van de Ven, W, Thakker, R, Devriendt, K

Near-atomic structure of Japanese encephalitis virus reveals critical determinants of virulence and stability. by Wang, X, Li, S, Zhu, L, Nian, Q, Yuan, S, Gao, Q, Hu, Z, Ye, Q, Li, X, Xie, D, Shaw, N, Wang, J, Walter, T, Huiskonen, J, Fry, E, Qin, C, Stuart, D, Rao, Z

Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium by Javaid, M, Boyce, A, Appelman-Dijkstra, N, Ong, J, Defabianis, P, Offiah, A, Arunde, P, Shaw, N, Pos, V, Underhil, A, Portero, D, Heral, L, Heegaard, A, Masi, L, Monsell, F, Stanton, R, Dijkstra, P, Brandi, M, Chapurlat, R, Hamdy, N, Collins, M

OPERATION OF THE CDF SILICON VERTEX DETECTOR WITH COLLIDING BEAMS AT FERMILAB by Bedeschi, F, Bolognesi, V, Dellagnello, S, Galeotti, S, Grieco, G, Mariotti, M, Menzione, A, Punzi, G, Raffaelli, F, Ristori, L, Tartarelli, F, Turini, N, Wenzel, H, Zetti, F, Bailey, M, Garfinkel, A, Kruse, M, Shaw, N, Carithers, W, Ely, R, Haber, C, Holland, S, Kleinfelder, S, Merrick, T, Schneider, O

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcrip... by Ali, A, Christie, P, Grigorieva, I, Harding, B, Van Esch, H, Ahmed, S, Bitner-Glindzicz, M, Blind, E, Bloch, C, Christin, P, Clayton, P, Gecz, J, Gilbert-Dussardier, B, Guillen-Navarro, E, Hackett, A, Halac, I, Hendy, G, Lalloo, F, Mache, C, Mughal, Z, Ong, A, Rinat, C, Shaw, N, Smithson, S, Tolmie, J

CONSTRUCTION OF THE CDF SILICON VERTEX DETECTOR by Skarha, J, Barnett, B, Boswell, C, Snider, F, Spies, A, Tseng, J, Vejcik, S, Carter, H, Flaugher, B, Gonzales, B, Hrycyk, M, Nelson, C, Segler, S, Shaw, T, Tkaczyk, S, Turner, K, Wesson, T, Carithers, W, Ely, R, Haber, C, Holland, S, Kleinfelder, S, Merrick, T, Schneider, O, Wester, W, Wong, M, Amidei, D, Derwent, P, Gold, M, Matthews, J, Bacchetta, N, Bisello, D, Busetto, G, Castro, A, Loreti, M, Pescara, L, Bedeschi, F, Bolognesi, V, Dellagnello, S, Galeotti, S, Mariotti, M, Menzione, A, Punzi, G, Raffaelli, F, Ristori, L, Tartarelli, F, Turini, N, Wenzel, H, Zetti, F, Bailey, M, Garfinkel, A, Shaw, N, Tipton, P, Watts, G, IEEE