D l'Allemand - JoVE Visualize

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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1993

[Adrenal cortex function in children with bronchial asthma in fluticasone therapy]A Hoffmann-Streb, D L'Allemand, B Niggemann, et al.

The Journal of Pediatrics|March 10, 2001

Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathyB Köhler, V Schumacher, D l'Allemand, et al.

Clinical Genetics|August 1, 1992

Ring Y chromosome: cytogenetic and molecular characterizationR D Wegner, G Scherer, M Pohlschmidt, et al.

Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2004

The use of L-T4 as liquid solution improves the practicability and individualized dosage in newborns and infants with congenital hypothyroidismJ H von Heppe, H Krude, D L'Allemand, et al.

Endocrine Research|November 1, 1996

Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?D l'Allemand, E Keller, W Hoeppner, et al.

The Journal of Clinical Endocrinology and Metabolism|January 3, 2001

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiencyD L'Allemand, V Tardy, A Grüters, et al.

Pflugers Archiv : European Journal of Physiology|May 1, 1988

Aldosterone metabolism in rat renal tissue in vitro. Formation of lipid soluble metabolitesD l'Allemand, H Siebe, D Tsiakiras, et al.

Revue Medicale Suisse|April 12, 2008

[How to treat childhood obesity? Importance of primary prevention]N J Farpour-Lambert, A Nydegger, S Kriemler, et al.

Hormone Research|October 25, 2000

Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapyU Eiholzer, D l'Allemand, I van der Sluis, et al.

Hormone Research in Paediatrics|March 4, 2010

Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiencyS Rosa, M Steigert, M Lang-Muritano, et al.

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Showing results (11-20 of 31) with videos related to

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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1993

[Adrenal cortex function in children with bronchial asthma in fluticasone therapy]A Hoffmann-Streb, D L'Allemand, B Niggemann, et al.

The Journal of Pediatrics|March 10, 2001

Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathyB Köhler, V Schumacher, D l'Allemand, et al.

Clinical Genetics|August 1, 1992

Ring Y chromosome: cytogenetic and molecular characterizationR D Wegner, G Scherer, M Pohlschmidt, et al.

Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2004

The use of L-T4 as liquid solution improves the practicability and individualized dosage in newborns and infants with congenital hypothyroidismJ H von Heppe, H Krude, D L'Allemand, et al.

Endocrine Research|November 1, 1996

Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: does genotyping predict the clinical manifestation?D l'Allemand, E Keller, W Hoeppner, et al.

The Journal of Clinical Endocrinology and Metabolism|January 3, 2001

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiencyD L'Allemand, V Tardy, A Grüters, et al.

Pflugers Archiv : European Journal of Physiology|May 1, 1988

Aldosterone metabolism in rat renal tissue in vitro. Formation of lipid soluble metabolitesD l'Allemand, H Siebe, D Tsiakiras, et al.

Revue Medicale Suisse|April 12, 2008

[How to treat childhood obesity? Importance of primary prevention]N J Farpour-Lambert, A Nydegger, S Kriemler, et al.

Hormone Research|October 25, 2000

Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapyU Eiholzer, D l'Allemand, I van der Sluis, et al.

Hormone Research in Paediatrics|March 4, 2010

Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiencyS Rosa, M Steigert, M Lang-Muritano, et al.

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