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R Pfäffle

Showing results (1-10 of 26) with videos related to

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Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Pituitary transcription factors in the aetiology of combined pituitary hormone deficiencyR Pfäffle, J Klammt
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
IGF1R mutations as cause of SGAJ Klammt, W Kiess, R Pfäffle
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 30, 1999
Seminoma in a 31-year-old patient on long-term growth hormone therapyR Ochsenkühn, R Pfäffle, E Nieschlag
Acta Paediatrica (Oslo, Norway : 1992)|April 29, 1998
The hypothalamic-pituitary-adrenal axis in preterm infants weighing < or = 1250 g: association with perinatal data and chronic lung diseaseU Merz, R Pfäffle, T Peschgens, et al.
Klinische Padiatrie|May 12, 2006
Decreased factor XIII activity during severe Henoch-Schoenlein purpura -- does it play a role?F Prenzel, R Pfäffle, F Thiele, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|March 10, 1998
[Function of the hypothalamo-hypophyseal-adrenal axis to corticotropin-releasing hormone test in premature infants with bronchopulmonary dysplasia]U Merz, R Pfäffle, T Peschgens, et al.
European Journal of Endocrinology|October 20, 1999
Neonatal diabetes mellitus with hypergalactosemiaH Kentrup, J Altmüller, R Pfäffle, et al.
Clinical Endocrinology|May 3, 2000
Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 geneH Frisch, C Kim, G Häusler, et al.
Hormone Research|September 6, 2000
Idiopathic growth hormone deficiency: a vanishing diagnosis?R Pfäffle, O Blankenstein, S Wüller, et al.
Pituitary|June 19, 2003
Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 geneC Lamesch, S Neumann, R Pfäffle, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Pituitary transcription factors in the aetiology of combined pituitary hormone deficiencyR Pfäffle, J Klammt
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
IGF1R mutations as cause of SGAJ Klammt, W Kiess, R Pfäffle
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 30, 1999
Seminoma in a 31-year-old patient on long-term growth hormone therapyR Ochsenkühn, R Pfäffle, E Nieschlag
Acta Paediatrica (Oslo, Norway : 1992)|April 29, 1998
The hypothalamic-pituitary-adrenal axis in preterm infants weighing < or = 1250 g: association with perinatal data and chronic lung diseaseU Merz, R Pfäffle, T Peschgens, et al.
Klinische Padiatrie|May 12, 2006
Decreased factor XIII activity during severe Henoch-Schoenlein purpura -- does it play a role?F Prenzel, R Pfäffle, F Thiele, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|March 10, 1998
[Function of the hypothalamo-hypophyseal-adrenal axis to corticotropin-releasing hormone test in premature infants with bronchopulmonary dysplasia]U Merz, R Pfäffle, T Peschgens, et al.
European Journal of Endocrinology|October 20, 1999
Neonatal diabetes mellitus with hypergalactosemiaH Kentrup, J Altmüller, R Pfäffle, et al.
Clinical Endocrinology|May 3, 2000
Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 geneH Frisch, C Kim, G Häusler, et al.
Hormone Research|September 6, 2000
Idiopathic growth hormone deficiency: a vanishing diagnosis?R Pfäffle, O Blankenstein, S Wüller, et al.
Pituitary|June 19, 2003
Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 geneC Lamesch, S Neumann, R Pfäffle, et al.
Pageof 3