H Kentrup|J Altmüller|R Pfäffle|G Heimann - JoVE Visualize

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European Journal of Endocrinology|October 20, 1999

Neonatal diabetes mellitus with hypergalactosemiaH Kentrup, J Altmüller, R Pfäffle, et al.

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

[Glucose homeostasis in cystic fibrosis. Oral glucose tolerance test in comparison with formula administration]H Skopnik, H Kentrup, G Kusenbach, et al.

Klinische Padiatrie|May 17, 2000

[Minibrain/DYRK1A gene: candidate gene for mental retardation in Down's syndrome?]H Kentrup, H G Joost, G Heimann, et al.

Biology of the Neonate|February 5, 2000

Effect of cisapride on acid gastro-oesophageal reflux during treatment with caffeineH Kentrup, H J Baisch, G Kusenbach, et al.

Hormone Research|September 6, 2000

Idiopathic growth hormone deficiency: a vanishing diagnosis?R Pfäffle, O Blankenstein, S Wüller, et al.

Klinische Padiatrie|January 1, 1996

[Antacids for postoperative prevention of stress ulcer in infants: a dose finding study]H Kentrup, H Skopnik, L Wolter, et al.

Zeitschrift Fur Geburtshilfe Und Neonatologie|December 19, 1998

[Lipoma of the corpus callosum in a newborn infant: misinterpretation of cranial ultrasound by coincidence with thrombocytopenia]K J Abou Lebdi, H Kentrup, J Reul, et al.

International Journal of Clinical Pharmacology and Therapeutics|February 1, 1994

Midazolam and ketamine as premedication in colonoscopies: a pharmacodynamic studyH Kentrup, H Skopnik, D Menke, et al.

Hormone Research|February 16, 2002

A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminusO Blankenstein, R Mühlenberg, C Kim, et al.

European Journal of Pediatrics|December 10, 1997

Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: a case reportR W Holl, R Pfäffle, C Kim, et al.

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Pageof 15

European Journal of Endocrinology|October 20, 1999

Neonatal diabetes mellitus with hypergalactosemiaH Kentrup, J Altmüller, R Pfäffle, et al.

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

[Glucose homeostasis in cystic fibrosis. Oral glucose tolerance test in comparison with formula administration]H Skopnik, H Kentrup, G Kusenbach, et al.

Klinische Padiatrie|May 17, 2000

[Minibrain/DYRK1A gene: candidate gene for mental retardation in Down's syndrome?]H Kentrup, H G Joost, G Heimann, et al.

Biology of the Neonate|February 5, 2000

Effect of cisapride on acid gastro-oesophageal reflux during treatment with caffeineH Kentrup, H J Baisch, G Kusenbach, et al.

Hormone Research|September 6, 2000

Idiopathic growth hormone deficiency: a vanishing diagnosis?R Pfäffle, O Blankenstein, S Wüller, et al.

Klinische Padiatrie|January 1, 1996

[Antacids for postoperative prevention of stress ulcer in infants: a dose finding study]H Kentrup, H Skopnik, L Wolter, et al.

Zeitschrift Fur Geburtshilfe Und Neonatologie|December 19, 1998

[Lipoma of the corpus callosum in a newborn infant: misinterpretation of cranial ultrasound by coincidence with thrombocytopenia]K J Abou Lebdi, H Kentrup, J Reul, et al.

International Journal of Clinical Pharmacology and Therapeutics|February 1, 1994

Midazolam and ketamine as premedication in colonoscopies: a pharmacodynamic studyH Kentrup, H Skopnik, D Menke, et al.

Hormone Research|February 16, 2002

A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminusO Blankenstein, R Mühlenberg, C Kim, et al.

European Journal of Pediatrics|December 10, 1997

Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: a case reportR W Holl, R Pfäffle, C Kim, et al.

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