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Results: 1-18 |
Results: 18
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59 Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
Authors: Fluck, CE Deladoey, J Nayak, S Zeller, O Kopp, P Mullis, PE
Citation: Ce. Fluck et al., Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59 Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II), EUR J ENDOC, 145(4), 2001, pp. 439-444
Effect of growth hormone treatment on hypoglycemia in a patient with both hepatic glycogen synthase and isolated growth hormone deficiencies
Authors: Blumel, P Mullis, PE
Citation: P. Blumel et Pe. Mullis, Effect of growth hormone treatment on hypoglycemia in a patient with both hepatic glycogen synthase and isolated growth hormone deficiencies, J PED END M, 14(8), 2001, pp. 1151-1155
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
New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism
Authors: Vuissoz, JM Deladoey, J Buyukgebiz, A Cemeroglu, P Gex, G Gallati, S Mullis, PE
Citation: Jm. Vuissoz et al., New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism, J CLIN END, 86(9), 2001, pp. 4468-4471
Autosomal dominant GH deficiency due to an Arg(183)His GH-1 gene mutation:Clinical and molecular evidence of impaired regulated GH secretion
Authors: Deladoey, J Stocker, P Mullis, PE
Citation: J. Deladoey et al., Autosomal dominant GH deficiency due to an Arg(183)His GH-1 gene mutation:Clinical and molecular evidence of impaired regulated GH secretion, J CLIN END, 86(8), 2001, pp. 3941-3947
Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade
Authors: Schoenle, EJ Lang-Muritano, M Gschwend, S Laimbacher, J Mullis, PE Torresani, T Biason-Lauber, A Molinari, L
Citation: Ej. Schoenle et al., Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade, DIABETOLOG, 44(3), 2001, pp. 286-289
Doping in sport - Preface
Authors: Mullis, PE
Citation: Pe. Mullis, Doping in sport - Preface, BEST PRAC R, 14(1), 2000, pp. IX-IX
Growth hormone regulates growth hormone receptor gene transcription in primary human thyroid cells
Authors: Mullis, PE O'Donovan, N Eble, A Marti, U Diem, P Burgi, U Peter, HJ
Citation: Pe. Mullis et al., Growth hormone regulates growth hormone receptor gene transcription in primary human thyroid cells, MOL C ENDOC, 166(2), 2000, pp. 111-119
Transcription factors in pituitary gland development and their clinical impact on phenotype
Authors: Mullis, PE
Citation: Pe. Mullis, Transcription factors in pituitary gland development and their clinical impact on phenotype, HORMONE RES, 54(3), 2000, pp. 107-119
Effect of growth hormone and oxandrolone treatment on glucose metabolism in Turner syndrome - A longitudinal study
Authors: Joss, EE Zurbrugg, RP Tonz, O Mullis, PE
Citation: Ee. Joss et al., Effect of growth hormone and oxandrolone treatment on glucose metabolism in Turner syndrome - A longitudinal study, HORMONE RES, 53(1), 2000, pp. 1-8
Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line
Authors: Nuoffer, JM Fluck, C Deladoey, J Eble, A Dattani, MT Mullis, PE
Citation: Jm. Nuoffer et al., Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line, J ENDOCR, 165(2), 2000, pp. 313-320
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
Regulation of human growth hormone receptor gene transcription by triiodothyronine (T-3)
Authors: Mullis, PE Eble, A Marti, U Burgi, U Postel-Vinay, MC
Citation: Pe. Mullis et al., Regulation of human growth hormone receptor gene transcription by triiodothyronine (T-3), MOL C ENDOC, 147(1-2), 1999, pp. 17-25
Metabolic control in Bernese children and adolescents with diabetes mellitus type I
Authors: Fluck, CE Kuhlmann, BV Mullis, PE
Citation: Ce. Fluck et al., Metabolic control in Bernese children and adolescents with diabetes mellitus type I, SCHW MED WO, 129(44), 1999, pp. 1650-1655
What is the value of determining growth hormone-releasing factor (GNRH) inacromegaly?
Authors: Muller, B de Marco, D Burgi, U Mullis, PE
Citation: B. Muller et al., What is the value of determining growth hormone-releasing factor (GNRH) inacromegaly?, SCHW MED WO, 129(33), 1999, pp. 1152-1157
"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency
Authors: Deladoey, J Fluck, C Buyukgebiz, A Kuhlmann, BV Eble, A Hindmarsh, PC Wu, W Mullis, PE
Citation: J. Deladoey et al., "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency, J CLIN END, 84(5), 1999, pp. 1645-1650
Aromatase deficiency caused by a novel P450(arom) gene mutation: Impact ofabsent estrogen production on serum gonadotropin concentration in a boy
Authors: Deladoey, J Fluck, C Bex, M Yoshimura, N Harada, N Mullis, PE
Citation: J. Deladoey et al., Aromatase deficiency caused by a novel P450(arom) gene mutation: Impact ofabsent estrogen production on serum gonadotropin concentration in a boy, J CLIN END, 84(11), 1999, pp. 4050-4054
Insulin increases serum leptin concentrations in children and adolescents with newly diagnosed Type I diabetes mellitus with and without ketoacidosis
Authors: Fluck, CE Kuhlmann, BV Mullis, PE
Citation: Ce. Fluck et al., Insulin increases serum leptin concentrations in children and adolescents with newly diagnosed Type I diabetes mellitus with and without ketoacidosis, DIABETOLOG, 42(9), 1999, pp. 1067-1070
Risultati: 1-18 |