Janner, Marco

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2016

Saner, Christoph; Simonetti, Giacomo; Wühl, Elke; Mullis, Primus-Eugen; Janner, Marco (2016). Circadian and ultradian cardiovascular rhythmicity in obese children. European journal of pediatrics, 175(8), pp. 1031-1038. Springer 10.1007/s00431-016-2736-4

2015

Miletta, Maria Consolata; Eblé, Andrée; Janner, Marco; Parween, Shaheena; Pandey, Amit Vikram; Flück, Christa Emma; Mullis, Primus-Eugen (2015). IGHD II: A Novel GH-1 Gene Mutation (GH-L76P) Severely Affects GH Folding, Stability, and Secretion. Journal of clinical endocrinology and metabolism, 100(12), E1575-E1583. Endocrine Society 10.1210/jc.2015-3265

Mansour-Hendili, Lamisse; Blanchard, Anne; Le Pottier, Nelly; Roncelin, Isabelle; Lourdel, Stéphane; Treard, Cyrielle; González, Wendy; Vergara-Jaque, Ariela; Morin, Gilles; Colin, Estelle; Holder-Espinasse, Muriel; Bacchetta, Justine; Baudouin, Véronique; Benoit, Stéphane; Bérard, Etienne; Bourdat-Michel, Guylhène; Bouchireb, Karim; Burtey, Stéphane; Cailliez, Mathilde; Cardon, Gérard; ... (2015). Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1. Human mutation, 36(8), pp. 743-752. Wiley-Blackwell 10.1002/humu.22804

Saner, Christoph; Simonetti, Giacomo; Wühl, Elke; Mullis, Primus-Eugen; Janner, Marco (2015). Increased ambulatory arterial stiffness index in obese children. Atherosclerosis, 238(2), pp. 185-189. Elsevier 10.1016/j.atherosclerosis.2014.12.009

Burckhardt, Marie-Anne; Obmann, Verena Carola; Wolf, Rainer Walter; Janner, Marco; Flück, Christa E; Mullis, Primus-Eugen (2015). Ovarian and uterine development and hormonal feedback mechanism in a 46 XX patient with CYP19A1 deficiency under low dose estrogen replacement. Gynecological endocrinology, 31(5), pp. 349-354. Informa Healthcare 10.3109/09513590.2014.995619

2014

Del Pozo, Emilio; Janner, Marco; Mackenzie, Andrew R; Arampatzis, Spyridon; Dixon, Arnold K; Perrelet, Romain; Ruch, Walter; Lippuner, Kurt; Zapf, Juergen; Lamberts, Steven W; Mullis, Primus-Eugen (2014). Radiometrical, hormonal and biological correlates of skeletal growth in the female rat from birth to senescence. Growth hormone & IGF research, 24(2-3), pp. 83-88. Elsevier 10.1016/j.ghir.2014.03.003

2013

Bonafé, Luisa; Giunta, Cecillia; Hasler, Carol; Janner, Marco; Kränzlin, Marius; Link, Bianca; Meier, Christian; Leonard, E. Ramseier; Rohrbach, Marianne; Unger, Sheila (2013). Osteogenesis imperfecta: Klinik, Diagnose und Management vom Kindes- bis ins Erwachsenenalter. Swiss Medical Forum, 13(46), pp. 925-931. EMH Swiss Medical Publishers

Bieri, Andreas; Oser-Meier, Monika; Janner, Marco; Cripe-Mamie, Chantal; Pipczynski-Suter, Kathrin; Mullis, Primus-Eugen; Flück, Christa E. (2013). Children's and adolescent's self - assessment of metabolic control versus professional judgment: a cross-sectional retrospective and prospective cohort study. International journal of pediatric endocrinology, 2013(1), p. 21. BioMed Central 10.1186/1687-9856-2013-21

2012

L'allemand, Dagmar; Neuhaus, Thomas; Janner, Marco; Braegger, Christian; Laimbacher, Josef (2012). Empfehlungen des Bundesamtes für Gesundheit zur Vitamin-D-Versorgung in der Schweiz — was bedeuten sie für den Pädiater? Paediatrica, 23(4), pp. 22-24. Schweizerische Gesellschaft für Pädiatrie

Camats, N.; Pandey, A. V.; Fernández-Cancio, M.; Andaluz, P.; Janner, M.; Torán, N.; Moreno, F.; Bereket, A.; Akcay, T.; García-García, E.; Muñoz, M. T.; Gracia, R.; Nistal, M.; Castaño, L.; Mullis, P. E.; Carrascosa, A.; Audí, L.; Flück, C. E. (2012). Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals. Journal of clinical endocrinology and metabolism, 97(7), E1294-306. Chevy Chase, Md.: Endocrine Society 10.1210/jc.2011-3169

Janner, Marco; Flück, Christa E.; Mullis, Primus E. (2012). Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency. Hormone research in paediatrics, 78(4), pp. 261-268. Basel: Karger 10.1159/000341585

2010

Molinari-Büchi, B.; Barth, J.; Janner, M.; Frey, P. (2010). Overweight and obesity in children: known facts and new trends. Revue médicale suisse, 6(249), pp. 1022-1025. Genève: Médecine & Hygiène

Molinari-Büchi, Beatrice; Barth, Jürgen; Janner, Marco; Frey, Peter (2010). Surcharge pondérale et obésité chez l'enfant: les acquis et les nouvelles tendances. Revue médicale suisse, 6(249), pp. 1022-1025. Genève: Médecine & Hygiène

Janner, Marco; Ballinari, Pietro; Mullis, Primus E.; Flueck, Christa E. (2010). High prevalence of vitamin D deficiency in children and adolescents with type 1 diabetes. Swiss medical weekly, 140, w13091. Muttenz: EMH Schweizerischer Ärzteverlag 10.4414/smw.2010.13091

2009

del Pozo, E.; Zapf, J.; Mackenzie, A. R.; Janner, M.; Perrelet, R.; Lippuner, K.; Mullis, P. (2009). Experimental arthritis: effect on growth parameters and total skeletal calcium. Growth hormone & IGF research, 19(5), pp. 442-446. Oxford: Elsevier 10.1016/j.ghir.2009.01.003

2008

Janner, Marco (2008). Adipositasprävention in der Karibik. Paediatrica, 19(4), pp. 56-57. Schweizerische Gesellschaft für Pädiatrie SGP

Räz, Barbara; Janner, Marco; Petkovic, Vibor; Lochmatter, Didier; Eblé, Andrée; Dattani, Mehul T.; Hindmarsh, Peter C.; Flück, Christa E.; Mullis, Primus E. (2008). Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiency. Journal of clinical endocrinology and metabolism, 93(3), pp. 974-980. Chevy Chase, Md.: Endocrine Society 10.1210/jc.2007-1382

2007

Janner, M.; Mullis, P. E. (2007). Impaired calcium homeostasis, clinical impact. Therapeutische Umschau, 64(5), pp. 271-275. Bern: Huber

2006

Janner, Marco; Pandey, Amit V.; Mullis, Primus E.; Flück, Christa E. (2006). Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 protein. European journal of endocrinology, 155(1), pp. 143-151. Bristol: BioScientifica Ltd. 10.1530/eje.1.02172

Janner, M.; Mullis, P. E.; Flück, C. E. (2006). Is the metabolic syndrome a new childhood disease? Praxis - schweizerische Rundschau für Medizin, 95(13), pp. 493-500. Bern: Huber

1994

Janner, M.; Knill, S. E.; Diem, P.; Zuppinger, K. A.; Mullis, P. E. (1994). Persistent microalbuminuria in adolescents with type I (insulin-dependent) diabetes mellitus is associated to early rather than late puberty. Results of a prospective longitudinal study. European journal of pediatrics, 153(6), pp. 403-408. Berlin: Springer 10.1007/s004310050162

1991

Mühlbauer, R. C.; Bauss, F.; Schenk, R.; Janner, M.; Bosies, E.; Strein, K.; Fleisch, H. (1991). BM 21.0955, a potent new bisphosphonate to inhibit bone resorption. Journal of bone and mineral research, 6(9), pp. 1003-1011. Wiley-Blackwell

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