Hauffa BP - Search Results

1

Venous sampling can be crucial in identifying the testicular origin of idiopathic male luteinising hormone-independent sexual precocity.

Richter-Unruh A, Jorch N, Wessels HT, Weber EA, Hauffa BP. Richter-Unruh A, et al. Among authors: hauffa bp. Eur J Pediatr. 2002 Dec;161(12):668-71. doi: 10.1007/s00431-002-1094-6. Epub 2002 Nov 6. Eur J Pediatr. 2002. PMID: 12447668

2

Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment.

Richter-Unruh A, Knauer-Fischer S, Kaspers S, Albrecht B, Gillessen-Kaesbach G, Hauffa BP. Richter-Unruh A, et al. Among authors: hauffa bp. Eur J Pediatr. 2004 Apr;163(4-5):251-6. doi: 10.1007/s00431-004-1406-0. Epub 2004 Feb 18. Eur J Pediatr. 2004. PMID: 14986122

3

Male LH-independent sexual precocity in a 3.5-year-old boy caused by a somatic activating mutation of the LH receptor in a Leydig cell tumor.

Richter-Unruh A, Wessels HT, Menken U, Bergmann M, Schmittmann-Ohters K, Schaper J, Tappeser S, Hauffa BP. Richter-Unruh A, et al. Among authors: hauffa bp. J Clin Endocrinol Metab. 2002 Mar;87(3):1052-6. doi: 10.1210/jcem.87.3.8294. J Clin Endocrinol Metab. 2002. PMID: 11889161

4

Increase of serum leptin after short-term pulsatile GnRH administration in children with delayed puberty.

Grasemann C, Wessels HT, Knauer-Fischer S, Richter-Unruh A, Hauffa BP. Grasemann C, et al. Among authors: hauffa bp. Eur J Endocrinol. 2004 May;150(5):691-8. doi: 10.1530/eje.0.1500691. Eur J Endocrinol. 2004. PMID: 15132726 Clinical Trial.

5

Semen quality and testicular adrenal rest tumour development in 46,XY congenital adrenal hyperplasia: the importance of optimal hormonal replacement.

Rohayem J, Bäumer LM, Zitzmann M, Fricke-Otto S, Mohnike K, Gohlke B, Reschke F, Jourdan C, Müller HL, Dunstheimer D, Weigel J, Jorch N, Müller-Rossberg E, Lankes E, Gätjen I, Richter-Unruh A, Hauffa BP, Kliesch S, Krumbholz A, Brämswig J. Rohayem J, et al. Among authors: hauffa bp. Eur J Endocrinol. 2021 Apr;184(4):487-501. doi: 10.1530/EJE-20-1154. Eur J Endocrinol. 2021. PMID: 33524003

6

Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domain.

Richter-Unruh A, Verhoef-Post M, Malak S, Homoki J, Hauffa BP, Themmen AP. Richter-Unruh A, et al. Among authors: hauffa bp. J Clin Endocrinol Metab. 2004 Oct;89(10):5161-7. doi: 10.1210/jc.2004-0298. J Clin Endocrinol Metab. 2004. PMID: 15472221

7

Congenital primary hypothyroidism in a turkish family caused by a homozygous nonsense mutation (R609X) in the thyrotropin receptor gene.

Richter-Unruh A, Hauffa BP, Pfarr N, Pohlenz J. Richter-Unruh A, et al. Among authors: hauffa bp. Thyroid. 2004 Nov;14(11):971-4. doi: 10.1089/thy.2004.14.971. Thyroid. 2004. PMID: 15671778

8

Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndrome.

Schmittmann-Ohters K, Huebner A, Richter-Unruh A, Hauffa BP. Schmittmann-Ohters K, et al. Among authors: hauffa bp. Horm Res. 2001;56(1-2):67-72. doi: 10.1159/000048093. Horm Res. 2001. PMID: 11815731

9

Mosaic trisomy 15 in a short girl with hemihypotrophy and mental retardation.

Knauer-Fischer SA, Richter-Unruh A, Albrecht B, Gillessen-Kaesbach G, Hauffa BP. Knauer-Fischer SA, et al. Among authors: hauffa bp. Clin Dysmorphol. 2004 Jul;13(3):183-186. doi: 10.1097/01.mcd.0000134478.87995.4b. Clin Dysmorphol. 2004. PMID: 15194957

10

Microarray analysis reveals differential gene expression patterns and regulation of single target genes contributing to the opposing phenotype of TrkA- and TrkB-expressing neuroblastomas.

Schulte JH, Schramm A, Klein-Hitpass L, Klenk M, Wessels H, Hauffa BP, Eils J, Eils R, Brodeur GM, Schweigerer L, Havers W, Eggert A. Schulte JH, et al. Among authors: hauffa bp. Oncogene. 2005 Jan 6;24(1):165-77. doi: 10.1038/sj.onc.1208000. Oncogene. 2005. PMID: 15637590

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