AAAAAA

   
Results: 1-25 |
Results: 25
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations
Authors: Witsch-Raumgartner, M Ciara, E Loffler, J Menzel, HJ Seedorf, U Burn, J Gillessen-Kaesbach, G Hoffmann, GF Fitzy, BU Mundy, H Clayton, P Kelley, RI Krajewska-Walasek, M Utermann, G
Citation: M. Witsch-raumgartner et al., Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations, EUR J HUM G, 9(1), 2001, pp. 45-50
Improvement of symptoms in infant colic following reduction of lactose load with lactase
Authors: Kanabar, D Randhawa, M Clayton, P
Citation: D. Kanabar et al., Improvement of symptoms in infant colic following reduction of lactose load with lactase, J HUM NU DI, 14(5), 2001, pp. 359-363
Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society (Reprinted from J Clin Endocrinol Metab, vol 85, pg 3990-3993,2000)
Authors: Attie, KM Bengtsson, BA Blethen, SL Blum, W Cameron, F Carel, JC Carlsson, L Chipman, JJ Christiansen, JS Clayton, P Clemmons, DR Cohen, P Drop, S Fujieda, K Ghigo, E Hintz, RL Ho, K Ilondo, MM Jasper, H Jesussek, B Kappelgaard, AM Laron, Z Lippe, BM Malozowski, S Mullis, PE de Muinck-Keizer-Schrama, S Nishi, Y Parks, JS Phelps, C Ranke, M Robinson, I Rosenfeld, RG Rose, S Saenger, P Saggese, G Savage, M Shalet, S Sizonenko, PC Strasburger, C Tachibana, K Tanaka, T Thorner, MO Wikland, KA Zadik, Z
Citation: Km. Attie et al., Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society (Reprinted from J Clin Endocrinol Metab, vol 85, pg 3990-3993,2000), J PED END M, 14(4), 2001, pp. 377-382
Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation
Authors: Mills, P Mills, K Clayton, P Johnson, A Whitehouse, D Winchester, B
Citation: P. Mills et al., Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation, BIOCHEM J, 359, 2001, pp. 249-254
Instrumental psychosis (Svejkosis)
Authors: Clayton, P
Citation: P. Clayton, Instrumental psychosis (Svejkosis), J ROY S MED, 94(3), 2001, pp. 156-156
Diversity of congenital disorders of glycosylation
Authors: Leonard, J Grunewald, S Clayton, P
Citation: J. Leonard et al., Diversity of congenital disorders of glycosylation, LANCET, 357(9266), 2001, pp. 1382-1383
Science and poetry
Authors: Clayton, P
Citation: P. Clayton, Science and poetry, NATURE, 409(6823), 2001, pp. 979-980
Neonatal presentation of coenzyme Q(10) deficiency
Authors: Rahman, S Hargreaves, I Clayton, P Heales, S
Citation: S. Rahman et al., Neonatal presentation of coenzyme Q(10) deficiency, J PEDIAT, 139(3), 2001, pp. 456-458
Australian academic use of the Internet: implications for university administrators
Authors: Applebee, A Clayton, P Pascoe, C Bruce, H
Citation: A. Applebee et al., Australian academic use of the Internet: implications for university administrators, INTERNET R, 10(2), 2000, pp. 141-149
Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG
Authors: Aebi, M Helenius, A Schenk, B Barone, R Fiumara, A Berger, EG Hennet, T Imbach, T Stutz, A Bjursell, C Uller, A Wahlstrom, JG Briones, P Cardo, E Clayton, P Winchester, B Cormier-Daire, V de Lonlay, P Cuer, M Dupre, T Seta, N de Koning, T Dorland, L de Loos, F Kupers, L Fabritz, L Hasilik, M Marquardt, T Niehues, R Freeze, H Grunewald, S Heykants, L Jaeken, J Matthijs, G Schollen, E Keir, G Kjaergaard, S Schwartz, M Skovby, F Klein, A Roussel, P Korner, C Lubke, T Thiel, C von Figura, K Koscielak, J Krasnewich, D Lehle, L Peters, V Raab, M Saether, O Schachter, H Van Schaftingen, E Verbert, A Vilaseca, A Wevers, R Yamashita, K
Citation: M. Aebi et al., Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG, GLYCOBIOLOG, 10(6), 2000, pp. III-V
High-speed five-axis milling of hardened tool steel
Authors: Becze, CE Clayton, P Chen, L El-Wardany, TI Elbestawi, MA
Citation: Ce. Becze et al., High-speed five-axis milling of hardened tool steel, INT J MACH, 40(6), 2000, pp. 869-885
Neuroscience, the person, and God: An emergentist account
Authors: Clayton, P
Citation: P. Clayton, Neuroscience, the person, and God: An emergentist account, ZYGON, 35(3), 2000, pp. 613-652
On the value of the panentheistic analogy: A response to Willem Drees
Authors: Clayton, P
Citation: P. Clayton, On the value of the panentheistic analogy: A response to Willem Drees, ZYGON, 35(3), 2000, pp. 699-704
Genotypes and phenotypes of patients in the UK with carbohydrate-deficientglycoprotein syndrome type 1
Authors: Imtiaz, F Worthington, V Champion, M Beesley, C Charlwood, J Clayton, P Keir, G Mian, N Winchester, B
Citation: F. Imtiaz et al., Genotypes and phenotypes of patients in the UK with carbohydrate-deficientglycoprotein syndrome type 1, J INH MET D, 23(2), 2000, pp. 162-174
Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society
Authors: Israel, E Attie, KM Bengtsson, BA Blethen, SL Blum, W Cameron, F Carel, JC Carlsson, L Chipman, JJ Christiansen, JS Clayton, P Clemmons, DR Cohen, P Drop, S Fujieda, K Ghigo, E Hintz, RL Ho, K Ilondo, MM Jasper, H Jesussek, B Kappelgaard, AM Laron, Z Lippe, BM Malozowski, S Mullis, PE de Munick-Keizer-Schrama, S Nishi, Y Parks, JS Phelps, C Ranke, M Robinson, I Rosenfeld, RG Rose, S Saenger, P Saggese, G Savage, M Shalet, S Sizonenko, PC Strasburger, C Tachibana, K Tanaka, T Thorner, MO Wikland, KA Zadik, Z
Citation: E. Israel et al., Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH Research Society, J CLIN END, 85(11), 2000, pp. 3990-3993
Practice guideline for the treatment of patients with major depressive disorder (revision)
Authors: Karasu, TB Gelenberg, A Wang, P Merriam, A McIntyre, JS Charles, SC Zarin, DA Altshuler, K Tasman, A Cook, I Twemlow, S Cross, CD Woods, S Egger, H Yager, J Moench, LA Bittker, T Peele, R Clayton, P Stabinsky, S Das, A Johnston, R Flynn, L Nininger, J Goin, M Urbaitis, J Goldstein, M D'Agostino, A Gray, SH Berg, J Meltzer, H Lurie, L Norquist, G Walker, RD Davis, LS Thaler, RM Marcus, PB
Citation: Tb. Karasu et al., Practice guideline for the treatment of patients with major depressive disorder (revision), AM J PSYCHI, 157(4), 2000, pp. 1-45
Practice guideline for the treatment of patients with eating disorders (revision)
Authors: Bell, C Bulik, C Clayton, P Crow, S Davis, DM DeMaso, DR Dogin, J Fairburn, CG Fink, AH Fisher, M Forman, S Garner, DM Golden, NH Hagan, J Kaplan, AS Katzman, DK Katzman, MA Keddy, D Kottke, TE Kreipe, R Lonegran, E Motto, JA Mickley, D Rubel, JB Schienholtz, M Schyve, PM Sloan, R Sokol, M Sparrow, J Strober, M Stunkard, A Suchinsky, RT Swanson, J Treasure, J Westermeyer, J Wilfley, D Wonderlich, S
Citation: C. Bell et al., Practice guideline for the treatment of patients with eating disorders (revision), AM J PSYCHI, 157(1), 2000, pp. 1
Mutational spectrum in the Delta 7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome
Authors: Witsch-Baumgartner, M Fitzky, BU Ogorelkova, M Kraft, HG Moebius, FF Glossmann, H Seedorf, U Gillessen-Kaesbach, G Hoffmann, GF Clayton, P Kelley, RI Utermann, G
Citation: M. Witsch-baumgartner et al., Mutational spectrum in the Delta 7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome, AM J HU GEN, 66(2), 2000, pp. 402-412
Signal transduction defects in growth hormone insensitivity - Discussion
Authors: Ross, R Clayton, P Norman, M Rotwein, P Rosenfeld, R
Citation: R. Ross et al., Signal transduction defects in growth hormone insensitivity - Discussion, ACT PAEDIAT, 88, 1999, pp. 179-179
Serum levels of insulin-like growth factor binding proteins in Ecuadorean children with growth hormone insensitivity - Discussion
Authors: Savage, M Rosenfeld, R Underwood, L Chatelain, P Guevara-Aguirre, J Clayton, P
Citation: M. Savage et al., Serum levels of insulin-like growth factor binding proteins in Ecuadorean children with growth hormone insensitivity - Discussion, ACT PAEDIAT, 88, 1999, pp. 192-192
Shaping the field of theology and science: A critique of Nancey Murphy
Authors: Clayton, P
Citation: P. Clayton, Shaping the field of theology and science: A critique of Nancey Murphy, ZYGON, 34(4), 1999, pp. 609-618
The ultimate hypothesis
Authors: Clayton, P
Citation: P. Clayton, The ultimate hypothesis, FORBES, 1999, pp. 241-242
A case of reversible blindness in maple syrup urine disease
Authors: Backhouse, O Leitch, RJ Thompson, D Kriss, A Charris, D Clayton, P Russell-Eggitt, I
Citation: O. Backhouse et al., A case of reversible blindness in maple syrup urine disease, BR J OPHTH, 83(2), 1999, pp. 250-251
Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation
Authors: Keir, G Winchester, BG Clayton, P
Citation: G. Keir et al., Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation, ANN CLIN BI, 36, 1999, pp. 20-36
Androgens and fetal growth
Authors: de Zegher, F Francois, I Boehmer, ALM Saggese, G Muller, J Hiort, O Sultan, C Clayton, P Brauner, R Cacciari, E Ibanez, L Van Vliet, G Tiulpakov, A Saka, N Ritzen, M Sippell, WG
Citation: F. De Zegher et al., Androgens and fetal growth, HORMONE RES, 50(4), 1998, pp. 243-244
Risultati: 1-25 |