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T Meissner

Showing results (21-30 of 48) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|September 1, 2001
Hyperinsulinism in syndromal disordersT Meissner, W Rabl, K Mohnike, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 20, 2010
[Infantile hemangioma. Successful treatment with propranolol]J Baetz, S Eigelshoven, J Marquard, et al.
Pediatric Diabetes|June 4, 2014
Impact of regular physical activity on blood glucose control and cardiovascular risk factors in adolescents with type 2 diabetes mellitus--a multicenter study of 578 patients from 225 centresA Herbst, T Kapellen, E Schober, et al.
Klinische Padiatrie|November 27, 2010
Detection of a mutation in the thyroid hormone receptor beta gene as a cause of pathological laboratory test results in an euthyreotic toddlerG Kameda, G Kameda, S Knauer-Fischer, et al.
Klinische Padiatrie|March 18, 2014
Granulocyte colony stimulating factor for treatment of neutropenia-associated infection in Pearson syndromeF Baertling, T Meissner, A Troeger, et al.
Archives of Disease in Childhood|February 24, 2001
Exercise induced hypoglycaemic hyperinsulinismT Meissner, T Otonkoski, R Feneberg, et al.
Diabetes Research and Clinical Practice|July 19, 2022
Prevalence trends of type 1 and type 2 diabetes in children and adolescents in North Rhine-Westphalia, the most populous federal state in Germany, 2002-2020C Baechle, A Stahl-Pehe, N Prinz, et al.
Human Genetics|February 24, 2001
Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndromeR Santer, M Kinner, M Passarge, et al.
European Journal of Endocrinology|January 13, 2011
Genetic and clinical characteristics of patients with HNF1A gene variations from the German-Austrian DPV databaseW L Awa, A Thon, K Raile, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 2001
Hyperinsulinism in syndromal disordersT Meissner, W Rabl, K Mohnike, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 20, 2010
[Infantile hemangioma. Successful treatment with propranolol]J Baetz, S Eigelshoven, J Marquard, et al.
Pediatric Diabetes|June 4, 2014
Impact of regular physical activity on blood glucose control and cardiovascular risk factors in adolescents with type 2 diabetes mellitus--a multicenter study of 578 patients from 225 centresA Herbst, T Kapellen, E Schober, et al.
Klinische Padiatrie|November 27, 2010
Detection of a mutation in the thyroid hormone receptor beta gene as a cause of pathological laboratory test results in an euthyreotic toddlerG Kameda, G Kameda, S Knauer-Fischer, et al.
Klinische Padiatrie|March 18, 2014
Granulocyte colony stimulating factor for treatment of neutropenia-associated infection in Pearson syndromeF Baertling, T Meissner, A Troeger, et al.
Archives of Disease in Childhood|February 24, 2001
Exercise induced hypoglycaemic hyperinsulinismT Meissner, T Otonkoski, R Feneberg, et al.
Diabetes Research and Clinical Practice|July 19, 2022
Prevalence trends of type 1 and type 2 diabetes in children and adolescents in North Rhine-Westphalia, the most populous federal state in Germany, 2002-2020C Baechle, A Stahl-Pehe, N Prinz, et al.
Human Genetics|February 24, 2001
Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndromeR Santer, M Kinner, M Passarge, et al.
European Journal of Endocrinology|January 13, 2011
Genetic and clinical characteristics of patients with HNF1A gene variations from the German-Austrian DPV databaseW L Awa, A Thon, K Raile, et al.
Pageof 5