Faculty of Medicine
Faculty of Medicine
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[FG] Szinnai Gabor

Publications

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Awchi, Mo et al. (2024) ‘Metabolic trajectories of diabetic ketoacidosis onset described by breath analysis’, Frontiers in Endocrinology, 15. Available at: https://doi.org/10.3389/fendo.2024.1360989.

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Bachmann, Freya et al. (2024) ‘Computing optimal drug dosing regarding efficacy and safety: the enhanced OptiDose method in NONMEM’, Journal of Pharmacokinetics and Pharmacodynamics, 51, pp. 919–934. Available at: https://doi.org/10.1007/s10928-024-09940-9.

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Burckhardt, Marie-Anne, Addala, Ananta and de Bock, Martin (2024) ‘Editorial: Equity in type 1 diabetes technology and beyond: where are we in 2022?’, Frontiers in Endocrinology, 15. Available at: https://doi.org/10.3389/fendo.2024.1400240.

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Schulte, Janine et al. (2024) ‘Exploring the potential of genetic analysis in historical blood spots for patients with iodine-deficient goiter and thyroid carcinomas in Switzerland and Germany (1929–1989)’, BMC Medical Genomics, 17(1). Available at: https://doi.org/10.1186/s12920-024-01947-y.

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Bachmann, Freya et al. (2023) ‘Computing optimal drug dosing with OptiDose: implementation in NONMEM’, Journal of Pharmacokinetics and Pharmacodynamics, 50, pp. 173–188. Available at: https://doi.org/10.1007/s10928-022-09840-w.

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Deichmann, Julia et al. (2023) ‘New model of glucose-insulin regulation characterizes effects of physical activity and facilitates personalized treatment evaluation in children and adults with type 1 diabetes’, PLoS Computational Biology, 19. Available at: https://doi.org/10.1371/journal.pcbi.1010289.

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Leadley, Connor et al. (2023) ‘Following in Banting’s footsteps or straying from the path? Observations from contemporary diabetes innovation’, Frontiers in Endocrinology, 14. Available at: https://doi.org/10.3389/fendo.2023.1270517.

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Marx, Alexander et al. (2023) ‘Blood glucose forecasting from temporal and static information in children with T1D’, Frontiers in Pediatrics, 11. Available at: https://doi.org/10.3389/fped.2023.1296904.

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Otto, Marije E. et al. (2023) ‘Semimechanistic modeling of copeptin and aldosterone kinetics and dynamics in response to rehydration treatment for diabetic ketoacidosis in children’, CPT: Pharmacometrics and Systems Pharmacology, 12(2), pp. 207–220. Available at: https://doi.org/10.1002/psp4.12891.

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Steffens, Britta et al. (2023) ‘Clinically practical pharmacometrics computer model to evaluate and personalize pharmacotherapy in pediatric rare diseases: application to Graves” disease’, Frontiers in Medicine, 10. Available at: https://doi.org/10.3389/fmed.2023.1099470.

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Nahum U et al. (2022) ‘Machine learning-based algorithm as an innovative approach for the differentiation between diabetes insipidus and primary polydipsia in clinical practice.’, European journal of endocrinology, 187(6), pp. 777–786. Available at: https://doi.org/10.1530/eje-22-0368.

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Claude F, Ubertini G and Szinnai G (2022) ‘Endocrine Disorders in Children with Brain Tumors: At Diagnosis, after Surgery, Radiotherapy and Chemotherapy.’, Children (Basel, Switzerland), 9(11). Available at: https://doi.org/10.3390/children9111617.

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Deichmann, J. et al. (2022) New model of glucose-insulin regulation characterizes effects of physical activity and facilitates personalized treatment evaluation in children and adults with type 1 diabetes. Cold Spring Harbor Laboratory. Available at: https://doi.org/10.1101/2022.06.10.495592.

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Bösch F et al. (2022) ‘Caregiver burden, and parents” perception of disease severity determine health-related quality of life in paediatric patients with intoxication-type inborn errors of metabolism.’, Molecular genetics and metabolism reports, 31, p. 100876. Available at: https://doi.org/10.1016/j.ymgmr.2022.100876.

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Atila C et al. (2022) ‘Glucagon-stimulated copeptin measurements in the differential diagnosis of diabetes insipidus: a double-blind, randomized, placebo-controlled study.’, European journal of endocrinology, 187(1), pp. 65–74. Available at: https://doi.org/10.1530/eje-22-0033.

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Marg W. et al. (2022) ‘Treatment of diabetes mellitus in childhood and adolescence, today and tomorrow: a view of Germany in comparison to Belgium, Austria and Switzerland Versorgung von Diabetes mellitus im Kindes- und Jugendalter, heute und morgen: ein Blick auf Deutschland im Vergleich zu Belgien, Österreich und der Schweiz’, Monatsschrift fur Kinderheilkunde, 170(5), pp. 412–421. Available at: https://doi.org/10.1007/s00112-019-00836-4.

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Cordon NM et al. (2022) ‘The relationship between meal carbohydrate quantity and the insulin to carbohydrate ratio required to maintain glycaemia is non-linear in young people with type 1 diabetes: A randomized crossover trial.’, Diabetic medicine : a journal of the British Diabetic Association, 39(2), p. e14675. Available at: https://doi.org/10.1111/dme.14675.

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Bachmann, Freya et al. (2022) ‘A SENSITIVITY ANALYSIS OF THE OPTIMAL DRUG DOSING ALGORITHM OPTIDOSE’, Pure and Applied Functional Analysis, 7, pp. 1127–1140.

Baumann, Philipp et al. (2022) ‘The kinetic profiles of copeptin and mid regional proadrenomedullin (MR-proADM) in pediatric lower respiratory tract infections’, PLoS ONE, 17. Available at: https://doi.org/10.1371/journal.pone.0264305.

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Ebrahimi, Fahim et al. (2022) ‘Lifetime risk and health-care burden of diabetic ketoacidosis: A population-based study’, Frontiers in Endocrinology, 13. Available at: https://doi.org/10.3389/fendo.2022.940990.

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Glocker V et al. (2022) ‘Fear of hypoglycemia and quality of life in young people with type 1 diabetes and their parents in the era of sensor glucose monitoring.’, Frontiers in endocrinology, 13, p. 958671. Available at: https://doi.org/10.3389/fendo.2022.958671.

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Hauser, Stephanie Isabelle et al. (2022) ‘Trends and outcomes of children, adolescents, and adults hospitalized with inherited metabolic disorders: A population-based cohort study’, JIMD Reports, 63, pp. 581–592. Available at: https://doi.org/10.1002/jmd2.12320.

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Burckhardt MA et al. (2021) ‘Impact of Hybrid Closed Loop Therapy on Hypoglycemia Awareness in Individuals with Type 1 Diabetes and Impaired Hypoglycemia Awareness.’, Diabetes technology & therapeutics, 23(7), pp. 482–490. Available at: https://doi.org/10.1089/dia.2020.0593.

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Lenherr N. et al. (2021) ‘Co-therapy with S-adenosylmethionine and nicotinamide riboside improves t-cell survival and function in Arts Syndrome (PRPS1 deficiency).’, 26. Available at: https://doi.org/10.1016/j.ymgmr.2021.100709.

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van Trotsenburg P et al. (2021) ‘Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.’, Thyroid : official journal of the American Thyroid Association, 31(3), pp. 387–419. Available at: https://doi.org/10.1089/thy.2020.0333.

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Bachmann F et al. (2021) ‘OptiDose: Computing the Individualized Optimal Drug Dosing Regimen Using Optimal Control.’, Journal of optimization theory and applications, 189(1), pp. 46–65. Available at: https://doi.org/10.1007/s10957-021-01819-w.

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Bachmann, Sara et al. (2021) ‘Autonomic cardiac regulation during spontaneous nocturnal hypoglycemia in children with type 1 diabetes’, Pediatric Diabetes, 22(7), pp. 1023–1030. Available at: https://doi.org/10.1111/pedi.13262.

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Deichmann J et al. (2021) ‘Simulation-Based Evaluation of Treatment Adjustment to Exercise in Type 1 Diabetes.’, Frontiers in endocrinology, 12, p. 723812. Available at: https://doi.org/10.3389/fendo.2021.723812.

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Diesch-Furlanetto T. et al. (2021) ‘Pregnancy and pregnancy outcomes after hematopoietic stem cell transplantation in childhood: A cross-sectional survey of the EBMT Pediatric Diseases Working Party’, Human Reproduction, 36(11), pp. 2871–2882. Available at: https://doi.org/10.1093/humrep/deab199.

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Burckhardt MA et al. (2020) ‘Copeptin Kinetics and Its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children.’, The Journal of clinical endocrinology and metabolism, 105(11). Available at: https://doi.org/10.1210/clinem/dgaa568.

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Carré A et al. (2020) ‘Ex vivo model for elucidating the functional and structural differentiation of the embryonic mouse thyroid.’, Molecular and cellular endocrinology, 510, p. 110834. Available at: https://doi.org/10.1016/j.mce.2020.110834.

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Stoupa A et al. (2020) ‘High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis.’, Frontiers in endocrinology, 11, p. 545339. Available at: https://doi.org/10.3389/fendo.2020.545339.

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Sasivari Z et al. (2019) Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case report. 11, pp. 1299–1303. Available at: https://doi.org/10.1515/jpem-2019-0051.

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Burckhardt MA et al. (2019) ‘Use of remote monitoring with continuous glucose monitoring in young children with Type 1 diabetes: the parents” perspective.’, Diabetic medicine : a journal of the British Diabetic Association, 36(11), pp. 1453–1459. Available at: https://doi.org/10.1111/dme.14061.

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Burckhardt MA et al. (2019) ‘Improvement in Psychosocial Outcomes in Children with Type 1 Diabetes and Their Parents Following Subsidy for Continuous Glucose Monitoring.’, Diabetes technology & therapeutics, 21(10), pp. 575–580. Available at: https://doi.org/10.1089/dia.2019.0149.

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Szinnai, G. (2019) ‘Thyroid’, Yearbook of Paediatric Endocrinology [Preprint]. Available at: https://doi.org/10.1530/ey.16.3.

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Bachmann, Sara et al. (2019) ‘What hypoglycemia does to the heart: Impact of nocturnal hypoglycemia on cardiac repolarization in diabetic children’. KARGER, 91.

Burckhardt, Marie-Anne et al. (2019) ‘Copeptin kinetics and its relationship to osmolality during rehydration for diabetic ketoacidosis in children: an observational study’. KARGER, 91.

Dufort G. et al. (2019) ‘Correction to: Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism (Thyroid (2019) 29:7 (1018-1022) DOI: 10.1089/thy.2018.0461)’, Thyroid, 29(9), p. 1347. Available at: https://doi.org/10.1089/thy.2018.0461.correx.

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Winzeler B et al. (2019) ‘Arginine-stimulated copeptin measurements in the differential diagnosis of diabetes insipidus: a prospective diagnostic study.’, Lancet (London, England), 394(10198), pp. 587–595. Available at: https://doi.org/10.1016/s0140-6736(19)31255-3.

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Malone SA et al. (2019) ‘Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism.’, eLife. 10.07.2019, 8. Available at: https://doi.org/10.7554/elife.47198.

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Dufort G et al. (2019) ‘Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.’, Thyroid : official journal of the American Thyroid Association, 29(7), pp. 1018–1022. Available at: https://doi.org/10.1089/thy.2018.0461.

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Jackson, C. B. et al. (2019) ‘Mutations in MRPS14 cause intellectual disability, neonatal lactic acidosis, cachexia and hypertrophic cardiomyopathy with distinct dysmorphic features’. NATURE PUBLISHING GROUP, 27.

Koch, G. et al. (2019) ‘O29 Pharmacometric modelling of free thyroxine dynamics after initiation of antithyroid drug treatment in children with Graves’ disease: a tool for personalized drug dosing in children’, Archives of Disease in Childhood, 104(6), p. e13.1–e13. Available at: https://doi.org/10.1136/archdischild-2019-esdppp.29.

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Jackson CB et al. (2019) ‘A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement’, Human Molecular Genetics, 28(4), pp. 639–649. Available at: https://doi.org/10.1093/hmg/ddy374.

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Burckhardt MA et al. (2019) ‘Use of Continuous Glucose Monitoring Trends to Facilitate Exercise in Children with Type 1 Diabetes.’, Diabetes technology & therapeutics, 21(1), pp. 51–55. Available at: https://doi.org/10.1089/dia.2018.0292.

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Bossong O et al. (2018) ‘Severe Disruption of Water and Electrolyte Balance After Appendectomy: A Case Report.’, A&A practice, 11(11), pp. 299–303. Available at: https://doi.org/10.1213/xaa.0000000000000812.

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Burckhardt MA et al. (2018) ‘The Use of Continuous Glucose Monitoring With Remote Monitoring Improves Psychosocial Measures in Parents of Children With Type 1 Diabetes: A Randomized Crossover Trial.’, Diabetes care, 41(12), pp. 2641–2643. Available at: https://doi.org/10.2337/dc18-0938.

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Burckhardt MA et al. (2018) ‘Real-world outcomes of insulin pump compared to injection therapy in a population-based sample of children with type 1 diabetes.’, Pediatric diabetes, 19(8), pp. 1459–1466. Available at: https://doi.org/10.1111/pedi.12754.

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Fuchs A. et al. (2018) ‘Cytokine kinetic profiles in children with acute lower respiratory tract infection: a post hoc descriptive analysis from a randomized control trial’, Clinical Microbiology and Infection, 24(12), p. 1341.e1–1341.e7. Available at: https://doi.org/10.1016/j.cmi.2018.03.016.

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Stoupa A et al. (2018) ‘TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology.’, EMBO molecular medicine, 10(12). Available at: https://doi.org/10.15252/emmm.201809569.

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Diesch, T. et al. (2018) ‘Pregnancy Rates and Pregnancy Outcomes after Hematopoietic Stem Cell Transplantation in Childhood: a Cross-Sectional Survey of the EBMT Pediatric WP’, Blood, 132(Supplement 1), pp. 3418–3418. Available at: https://doi.org/10.1182/blood-2018-99-110437.

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Tacke, Uta et al. (2018) ‘THE PEDIATRIC BRAIN AND SPINE TUMOR CENTER AT THE UNIVERSITY CHILDREN’S HOSPITAL IN BASEL, SWITZERLAND’. OXFORD UNIV PRESS INC, 20.

Cassatella D et al. (2018) ‘Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures’, European Journal of Endocrinology, 178(4), pp. 377–388. Available at: https://doi.org/10.1530/eje-17-0568.

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Carre, Aurore et al. (2018) ‘Beta1-Tubulin Gene (TUBB1) Mutations Cause Thyroid Dysgenesis Associated to Abnormal Platelet Morphology and Hyper-Aggregation’. KARGER, 90.

Dufort, Gabrielle et al. (2018) ‘DUOX2 Deficiency in Quebec: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism’. KARGER, 90.

Stoupa, A and Szinnai, G (2018) ‘Yearbook in Paediatric Endocrinology, Chapter Thyroid’.

Szinnai G (2018) ‘Jod - das Spurenelement als Schlüssel für normale Entwicklung und Wachstum’, Paediatrica, 29(4), pp. 19–21.

Baumann P et al. (2017) ‘Procalcitonin for Diagnostics and Treatment Decisions in Pediatric Lower Respiratory Tract Infections.’, Frontiers in pediatrics. 28.08.2017, 5, p. 183. Available at: https://doi.org/10.3389/fped.2017.00183.

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Gotta V et al. (2017) ‘Drivers of antibiotic prescribing in children and adolescents with febrile lower respiratory tract infections.’, PloS one. 28.09.2017, 12(9), p. e0185197. Available at: https://doi.org/10.1371/journal.pone.0185197.

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Mack I et al. (2017) ‘Symptomatic Congenital Cytomegalovirus Infection in Children of Seropositive Women.’, 5. Available at: https://doi.org/10.3389/fped.2017.00134.

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Stoupa, Athanasia et al. (2017) ‘THE PARIS-IMAGINE ‘HYPOTHYSEQ NGS PANEL’ IS NOW FUNCTIONAL AND BRINGS VALUABLE INFORMATION ON THE GENETICS IN A LARGE COHORT OF CHILDREN WITH CONGENITAL HYPOTHYROIDISM’. KARGER, 88.

Lenherr, N et al. (2017) ‘Phenylketonuria and Hirschsprung Disease—A Report of an Unusual Neonatal Presentation. ’, Int J Neonatal Screen . (published online August 30th 2017) doi:10.3390/ijns3030024, 3.

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Polak, M et al. (2017) ‘Pediatric Endocrinology and Inborn Errors of Metabolism; Disorders of the Thyroid Gland’, in Sarafoglou K, Hoffmann GF, Roth KS (ed.) Pediatric Endocrinology and Inborn Errors of Metabolism. 2nd edn. New York: McGrawHill Eductaion (Pediatric Endocrinology and Inborn Errors of Metabolism), pp. 481–512.

Stoupa, A, Gawade, S and Szinnai, G (2017) ‘Yearbook in Paediatric Endocrinology 2017, Chapter: Thyroid’, in K. Ong/Z.Hochberg (ed.) Yearbook in Paediatric Endocrinology 2017. london: haymarket (Yearbook in Paediatric Endocrinology 2017), pp. 34–49.

Gawade S et al. (2016) ‘Cell Growth Dynamics in Embryonic and Adult Mouse Thyroid Revealed by a Novel Approach to Detect Thyroid Gland Subpopulations.’, Thyroid : official journal of the American Thyroid Association. 09.03.2016, 26(4), pp. 591–9. Available at: https://doi.org/10.1089/thy.2015.0523.

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Diesch, Tamara et al. (2016) ‘Fertility preservation in pediatric and adolescent cancer patients in Switzerland: A qualitative cross-sectional survey’, Cancer Epidemiology, 44, pp. 141–146. Available at: https://doi.org/10.1016/j.canep.2016.08.013.

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Gawade,S, Stoupa,A and Szinnai,G (2016) ‘Yearbook in Paediatric Endocrinology, ChapterThyroid’, in K.Ong/Z.Hochberg (ed.) Yearbook of Paediatric Endocrinology. London: Haymarket (Yearbook of Paediatric Endocrinology), pp. 34–48.

Oliveira Cerqueira, Taise Lima et al. (2015) ‘Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion’, JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM. WOS.SCI, 28, pp. 777–784. Available at: https://doi.org/10.1515/jpem-2014-0194.

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Walther K. et al. (2015) ‘Implementation of pertussis immunization in health-care personnel’, Vaccine, 33(17), pp. 2009–2014. Available at: https://doi.org/10.1016/j.vaccine.2015.03.013.

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Burckhardt MA et al. (2015) ‘Tumor-associated FGF-23-induced hypophosphatemic rickets in children: a case report and review of the literature.’, Pediatric nephrology (Berlin, Germany), 30(1), pp. 179–82. Available at: https://doi.org/10.1007/s00467-014-2979-0.

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Polak, Michel and Szinnai, Gabor (2015) ‘Paediatric Thyroid Disorders: New Insights’. KARGER, 83. Available at: https://doi.org/10.1159/000375280.

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Burckhardt MA* et al. (2015) ‘Ovarian and uterine development and hormonal feedback mechanism in a 46 XX Patient with CYP19A1 Deficiency under low dose Estrogen Replacement.’, Gynecologocal Endocrinology, 5(31 ), pp. 349–54.

Burckhardt MA et al. (2015) ‘Human 3β-hydroxysteroid dehydrogenase deficiency seems to affect fertility but may not harbor a tumor risk: lesson from an experiment of nature. ’, European Journal of Endocrinology. Epub 2015 Aug 19, 5(173), p. K1–K12. .

Szinnai,G et al. (2015) ‘Yearbook of Paediatric Endocrinology, Chapter Thyroid’, in K.Ong/Z.Hochberg (ed.) Yearbook of Paediatric Endocrinology 2015. (Yearbook of Paediatric Endocrinology 2015), pp. 27–39.

Fenske WK et al. (2014) ‘A copeptin-based classification of the osmoregulatory defects in the syndrome of inappropriate antidiuresis.’, Journal of the American Society of Nephrology : JASN. 10.04.2014, 25(10), pp. 2376–83. Available at: https://doi.org/10.1681/asn.2013080895.

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Ramos HE et al. (2014) ‘Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.’, European journal of endocrinology, 171(4), pp. 499–507. Available at: https://doi.org/10.1530/eje-13-1006.

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Burckhardt MA et al. (2014) ‘Sexual disparity of copeptin in healthy newborn infants.’, The Journal of clinical endocrinology and metabolism, 99(9), pp. E1750–3. Available at: https://doi.org/10.1210/jc.2014-2244.

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Szinnai G (2014) ‘Genetics of normal and abnormal thyroid development in humans.’, Best practice & research. Clinical endocrinology & metabolism, 28(2), pp. 133–50. Available at: https://doi.org/10.1016/j.beem.2013.08.005.

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Onigata K and Szinnai G (2014) ‘Resistance to thyroid hormone.’, Endocrine development, 26, pp. 118–29. Available at: https://doi.org/10.1159/000363159.

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Polak, M. and Szinnai, G. (2014) ‘Thyroid Disorders’. Elsevier. Available at: https://doi.org/10.1016/b978-0-12-801238-3.05556-2.

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Szinnai G (2014) ‘Clinical genetics of congenital hypothyroidism.’, Endocrine development, 26, pp. 60–78. Available at: https://doi.org/10.1159/000363156.

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Szinnai G. (2014) ‘Preface’, 26, p. VII.

Szinnai G et al. (2014) ‘Clinical case seminar in pediatric thyroid disease.’, Endocrine development. 29.08.2014, 26, pp. 214–44. Available at: https://doi.org/10.1159/000363166.

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Wellmann,Sven et al. (2014) ‘Cardiovascular biomarkers in preeclampsia at triage.’, Fetal diagnosis and therapy. 17.05.2014, 36(3), pp. 202–7. Available at: https://doi.org/10.1159/000361016.

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Szinnai,G (2014) Endocrine Development. (252).

Szinnai,G et al. (2014) ‘Thyroid’, pp. 27–44.

Polak M. and Szinnai G. (2013) ‘Thyroid disorders’. Elsevier Ltd, pp. 1–24. Available at: https://doi.org/10.1016/b978-0-12-383834-6.00088-4.

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Burckhardt MA and Zumsteg U (2013) ‘[Growth hormone in children and adolescents: facts and fiction].’, Praxis, 102(13), pp. 777–84. Available at: https://doi.org/10.1024/1661-8157/a001338.

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Fenske, W. et al. (2013) ‘Copeptin for subtype differentiation of abnormal vasopressin release in SIADH: reclassification and characterization of a novel subtype’, Endocrine Abstracts [Preprint]. Available at: https://doi.org/10.1530/endoabs.32.p702.

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Baer, G. et al. (2013) ‘Procalcitonin guidance to reduce antibiotic treatment of lower respiratory tract infection in children and adolescents (ProPAED): a randomized controlled trial’, PLoS ONE, 8(8), p. e68419. Available at: https://doi.org/10.1371/journal.pone.0068419.

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Carré, A. et al. (2013) ‘Thyroid’. Basel: S. KARGER AG, pp. 31–44. Available at: https://doi.org/10.1159/000353830.

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Wuttke, A. et al. (2013) ‘Copeptin as a marker for arginine-vasopressin/antidiuretic hormone secretion in the diagnosis of paraneoplastic syndrome of inappropriate ADH secretion’, Endocrine, 44(3), pp. 744–749. Available at: https://doi.org/10.1007/s12020-013-9919-9.

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Burckhardt MA et al. (2013) ‘Meropenem associated severe neutropenia in an infant with brain abscess.’, Journal of Pediatric Infectious Diseases, ( 8), p. 49–52.

Polak,M and Szinnai,G (2013) ‘Emery and Rimoin’s Principles and Practice of Medical Genetics, Thyroid disorders’, in Rimoin DL, Connor JM, Pyeritz RE, Korf BR (ed.) Emery and Rimoin’s Principles and Practice of Medical Genetics. Oxford: Churchill Livingstone Elsevier (Emery and Rimoin’s Principles and Practice of Medical Genetics), pp. 1–24.

Soggia A et al. (2012) ‘Activation of the transcription factor carbohydrate-responsive element-binding protein by glucose leads to increased pancreatic beta cell differentiation in rats.’, Diabetologia. 05.07.2012, 55(10), pp. 2713–2722. Available at: https://doi.org/10.1007/s00125-012-2623-0.

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Admaty D et al. (2012) ‘Plasma midregional proadrenomedullin in newborn infants: impact of prematurity and perinatal infection.’, Pediatric research, 72(1), pp. 70–6. Available at: https://doi.org/10.1038/pr.2012.38.

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Szinnai G. (2012) Paediatric thyroidology. S. Karger AG. Available at: https://doi.org/10.1159/isbn.978-3-318-02721-1.

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Benzing J et al. (2012) ‘Plasma pro-endothelin-1 and respiratory distress in newborn infants.’, The Journal of pediatrics. 20.11.2011, 160(3), pp. 517–9. Available at: https://doi.org/10.1016/j.jpeds.2011.10.011.

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Filges I et al. (2012) ‘Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4.’, Pediatrics. 09.01.2012, 129(2), pp. e529–34. Available at: https://doi.org/10.1542/peds.2010-3849.

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