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M Lakomek

Showing results (51-60 of 72) with videos related to

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European Journal of Pediatrics|August 1, 1997
Glucose phosphate isomerase deficiency: biochemical and molecular genetic studies on the enzyme variants of two patients with severe haemolytic anaemiaP Huppke, D Wünsch, A Pekrun, et al.
European Journal of Pediatrics|November 19, 1997
Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretionC Roth, A Pekrun, M Bartz, et al.
Pediatric Research|May 17, 2000
Cranial irradiation of female rats causes dose-dependent and age-dependent activation or inhibition of pubertal developmentC Roth, H Schmidberger, O Schaper, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
Autoimmune thyreoiditis in childhood--epidemiology, clinical and laboratory findings in 61 patientsC Roth, M Scortea, P Stubbe, et al.
Enzyme & Protein|January 1, 1994
Erythrocyte pyruvate kinase deficiency. The influence of physiologically important metabolites on the function of normal and defective enzymesM Lakomek, H Winkler, A Pekrun, et al.
European Journal of Haematology|August 1, 1992
Erythrocyte pyruvate kinase deficiency: relations of residual enzyme activity, altered regulation of defective enzymes and concentrations of high-energy phosphates with the severity of clinical manifestationM Lakomek, B Neubauer, A von der Lühe, et al.
Clinical Genetics|April 1, 1995
Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosisA Pekrun, B A Neubauer, S W Eber, et al.
Blut|March 1, 1984
Erythrocyte pyruvate kinase deficiency: characterization of a new variant (PK "Aarau")M Lakomek, H Winkler, M Scharnetzky, et al.
Deutsche Medizinische Wochenschrift (1946)|April 18, 2001
[The iodine supply of newborns. Comparison of iodine absorption and iodine excretion of mother and child]C Roth, J Meller, S Bobrzik, et al.
Human Genetics|December 18, 1998
Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiencyW Kugler, K Breme, P Laspe, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
European Journal of Pediatrics|August 1, 1997
Glucose phosphate isomerase deficiency: biochemical and molecular genetic studies on the enzyme variants of two patients with severe haemolytic anaemiaP Huppke, D Wünsch, A Pekrun, et al.
European Journal of Pediatrics|November 19, 1997
Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretionC Roth, A Pekrun, M Bartz, et al.
Pediatric Research|May 17, 2000
Cranial irradiation of female rats causes dose-dependent and age-dependent activation or inhibition of pubertal developmentC Roth, H Schmidberger, O Schaper, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
Autoimmune thyreoiditis in childhood--epidemiology, clinical and laboratory findings in 61 patientsC Roth, M Scortea, P Stubbe, et al.
Enzyme & Protein|January 1, 1994
Erythrocyte pyruvate kinase deficiency. The influence of physiologically important metabolites on the function of normal and defective enzymesM Lakomek, H Winkler, A Pekrun, et al.
European Journal of Haematology|August 1, 1992
Erythrocyte pyruvate kinase deficiency: relations of residual enzyme activity, altered regulation of defective enzymes and concentrations of high-energy phosphates with the severity of clinical manifestationM Lakomek, B Neubauer, A von der Lühe, et al.
Clinical Genetics|April 1, 1995
Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosisA Pekrun, B A Neubauer, S W Eber, et al.
Blut|March 1, 1984
Erythrocyte pyruvate kinase deficiency: characterization of a new variant (PK "Aarau")M Lakomek, H Winkler, M Scharnetzky, et al.
Deutsche Medizinische Wochenschrift (1946)|April 18, 2001
[The iodine supply of newborns. Comparison of iodine absorption and iodine excretion of mother and child]C Roth, J Meller, S Bobrzik, et al.
Human Genetics|December 18, 1998
Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiencyW Kugler, K Breme, P Laspe, et al.
Pageof 8