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R W Pfäffle

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|September 1, 1992
New genetic findings in old syndromesJ S Parks, R W Pfäffle, M R Brown
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Combined pituitary hormone deficiency: role of Pit-1 and Prop-1R W Pfäffle, O Blankenstein, S Wüller, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritanceB M Doeker, R W Pfäffle, J Pohlenz, et al.
The Journal of Pediatric Endocrinology|July 1, 1993
Pit-1 and pituitary functionR W Pfäffle, J S Parks, M R Brown, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Tandem mass spectrometric determination of succinylacetone in dried blood spots enables presymptomatic detection in a case of hepatorenal tyrosinaemiaJ F W Weigel, N Janzen, R W Pfäffle, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
GH and TSH deficiencyR W Pfäffle, R Martinez, C Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutationF G Riepe, C J Partsch, O Blankenstein, et al.
Hormone Research|January 1, 1993
Genetics of growth hormone gene expressionJ S Parks, H Abdul-Latif, E Kinoshita, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|March 27, 2013
[Does childhood obesity affect sexual development?]I V Wagner, E Sergeyev, K Dittrich, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2013
Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiencyG M C Flemming, J Klammt, G Ambler, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Acta Paediatrica (Oslo, Norway : 1992). Supplement|September 1, 1992
New genetic findings in old syndromesJ S Parks, R W Pfäffle, M R Brown
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
Combined pituitary hormone deficiency: role of Pit-1 and Prop-1R W Pfäffle, O Blankenstein, S Wüller, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritanceB M Doeker, R W Pfäffle, J Pohlenz, et al.
The Journal of Pediatric Endocrinology|July 1, 1993
Pit-1 and pituitary functionR W Pfäffle, J S Parks, M R Brown, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Tandem mass spectrometric determination of succinylacetone in dried blood spots enables presymptomatic detection in a case of hepatorenal tyrosinaemiaJ F W Weigel, N Janzen, R W Pfäffle, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
GH and TSH deficiencyR W Pfäffle, R Martinez, C Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutationF G Riepe, C J Partsch, O Blankenstein, et al.
Hormone Research|January 1, 1993
Genetics of growth hormone gene expressionJ S Parks, H Abdul-Latif, E Kinoshita, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|March 27, 2013
[Does childhood obesity affect sexual development?]I V Wagner, E Sergeyev, K Dittrich, et al.
The Journal of Clinical Endocrinology and Metabolism|February 15, 2013
Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiencyG M C Flemming, J Klammt, G Ambler, et al.
Pageof 2