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Journal of Inherited Metabolic Disease
|
January 27, 2005
Filter paper cards contaminated with EMLA cream produce artefacts on acylcarnitine analysis
T Kuster, T Torresani, P Kleinert, et al.
Diabetologia
|
June 1, 1989
Preclinical and manifest diabetes mellitus in young patients with Friedreich's ataxia: no evidence of immune process behind the islet cell destruction
E J Schoenle, E J Boltshauser, S Baekkeskov, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 20, 1999
Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia
J Fitness, N Dixit, D Webster, et al.
Diabetologia
|
September 1, 1991
Recombinant human insulin-like growth factor I (rhIGF I) reduces hyperglycaemia in patients with extreme insulin resistance
E J Schoenle, P D Zenobi, T Torresani, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
January 27, 1999
The relationship of serum-eosinophil cationic protein and eosinophil count to disease activity in children with bronchial asthma
A Prehn, R A Seger, J Faber, et al.
European Journal of Pediatrics
|
June 13, 1998
Treatment with human growth hormone in patients with Prader-Labhart-Willi syndrome reduces body fat and increases muscle mass and physical performance
U Eiholzer, R Gisin, C Weinmann, et al.
Molecular Genetics and Metabolism
|
May 22, 2012
Positive effect of a simplified diet on blood phenylalanine control in different phenylketonuria variants, characterized by newborn BH4 loading test and PAH analysis
M Zimmermann, P Jacobs, R Fingerhut, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2007
First ISNS Reference Preparation for Neonatal Screening for thyrotropin, phenylalanine and 17alpha-hydroxyprogesterone in blood spots
L H Elvers, J G Loeber, J-L Dhondt, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1993
Urinary growth hormone in growth-impaired children with chronic inflammatory bowel disease
C P Braegger, T Torresani, S H Murch, et al.
Acta Endocrinologica. Supplementum
|
January 1, 1986
Sixty children with congenital hypothyroidism detected by neonatal thyroid: mental development at 1, 4, and 7 years: a longitudinal study
R Illig, R H Largo, M Weber, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 68) with videos related to
Sort By:
Page
of 7
Journal of Inherited Metabolic Disease
|
January 27, 2005
Filter paper cards contaminated with EMLA cream produce artefacts on acylcarnitine analysis
T Kuster, T Torresani, P Kleinert, et al.
Diabetologia
|
June 1, 1989
Preclinical and manifest diabetes mellitus in young patients with Friedreich's ataxia: no evidence of immune process behind the islet cell destruction
E J Schoenle, E J Boltshauser, S Baekkeskov, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 20, 1999
Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia
J Fitness, N Dixit, D Webster, et al.
Diabetologia
|
September 1, 1991
Recombinant human insulin-like growth factor I (rhIGF I) reduces hyperglycaemia in patients with extreme insulin resistance
E J Schoenle, P D Zenobi, T Torresani, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
January 27, 1999
The relationship of serum-eosinophil cationic protein and eosinophil count to disease activity in children with bronchial asthma
A Prehn, R A Seger, J Faber, et al.
European Journal of Pediatrics
|
June 13, 1998
Treatment with human growth hormone in patients with Prader-Labhart-Willi syndrome reduces body fat and increases muscle mass and physical performance
U Eiholzer, R Gisin, C Weinmann, et al.
Molecular Genetics and Metabolism
|
May 22, 2012
Positive effect of a simplified diet on blood phenylalanine control in different phenylketonuria variants, characterized by newborn BH4 loading test and PAH analysis
M Zimmermann, P Jacobs, R Fingerhut, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2007
First ISNS Reference Preparation for Neonatal Screening for thyrotropin, phenylalanine and 17alpha-hydroxyprogesterone in blood spots
L H Elvers, J G Loeber, J-L Dhondt, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1993
Urinary growth hormone in growth-impaired children with chronic inflammatory bowel disease
C P Braegger, T Torresani, S H Murch, et al.
Acta Endocrinologica. Supplementum
|
January 1, 1986
Sixty children with congenital hypothyroidism detected by neonatal thyroid: mental development at 1, 4, and 7 years: a longitudinal study
R Illig, R H Largo, M Weber, et al.
Page
of 7