Grueters A - Search Results

1

Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis.

Thorwarth A, Mueller I, Biebermann H, Ropers HH, Grueters A, Krude H, Ullmann R. Thorwarth A, et al. Among authors: grueters a. J Clin Endocrinol Metab. 2010 Jul;95(7):3446-52. doi: 10.1210/jc.2009-2195. Epub 2010 Apr 28. J Clin Endocrinol Metab. 2010. PMID: 20427504

2

Two puzzling cases of thyroid dysgenesis.

Kuehnen P, Grueters A, Krude H. Kuehnen P, et al. Among authors: grueters a. Horm Res. 2009 Jan;71 Suppl 1:93-7. doi: 10.1159/000178047. Epub 2009 Jan 21. Horm Res. 2009. PMID: 19153515

3

Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8.

Biebermann H, Ambrugger P, Tarnow P, von Moers A, Schweizer U, Grueters A. Biebermann H, et al. Among authors: grueters a. Eur J Endocrinol. 2005 Sep;153(3):359-66. doi: 10.1530/eje.1.01980. Eur J Endocrinol. 2005. PMID: 16131597

4

The use of FDG-PET and CT for the staging of adrenocortical carcinoma in children.

Kreissig R, Amthauer H, Krude H, Steinmueller P, Stroszczynski C, Hosten N, Grueters A, Felix R. Kreissig R, et al. Among authors: grueters a. Pediatr Radiol. 2000 May;30(5):306. doi: 10.1007/s002470050745. Pediatr Radiol. 2000. PMID: 10836591 No abstract available.

5

An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity.

Kuehnen P, Mischke M, Wiegand S, Sers C, Horsthemke B, Lau S, Keil T, Lee YA, Grueters A, Krude H. Kuehnen P, et al. Among authors: grueters a. PLoS Genet. 2012;8(3):e1002543. doi: 10.1371/journal.pgen.1002543. Epub 2012 Mar 15. PLoS Genet. 2012. PMID: 22438814 Free PMC article.

6

Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.

Rajab A, Kelberman D, de Castro SC, Biebermann H, Shaikh H, Pearce K, Hall CM, Shaikh G, Gerrelli D, Grueters A, Krude H, Dattani MT. Rajab A, et al. Among authors: grueters a. Hum Mol Genet. 2008 Jul 15;17(14):2150-9. doi: 10.1093/hmg/ddn114. Epub 2008 Apr 10. Hum Mol Genet. 2008. PMID: 18407919

7

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation.

Friesema EC, Grueters A, Biebermann H, Krude H, von Moers A, Reeser M, Barrett TG, Mancilla EE, Svensson J, Kester MH, Kuiper GG, Balkassmi S, Uitterlinden AG, Koehrle J, Rodien P, Halestrap AP, Visser TJ. Friesema EC, et al. Among authors: grueters a. Lancet. 2004 Oct 16-22;364(9443):1435-7. doi: 10.1016/S0140-6736(04)17226-7. Lancet. 2004. PMID: 15488219

8

Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism.

Alatzoglou KS, Kelberman D, Cowell CT, Palmer R, Arnhold IJ, Melo ME, Schnabel D, Grueters A, Dattani MT. Alatzoglou KS, et al. Among authors: grueters a. J Clin Endocrinol Metab. 2011 Apr;96(4):E685-90. doi: 10.1210/jc.2010-1239. Epub 2011 Feb 2. J Clin Endocrinol Metab. 2011. PMID: 21289259

9

Molecular analysis of the PDS gene in Pendred syndrome.

Coyle B, Reardon W, Herbrick JA, Tsui LC, Gausden E, Lee J, Coffey R, Grueters A, Grossman4 A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC. Coyle B, et al. Among authors: grueters a. Hum Mol Genet. 1998 Jul;7(7):1105-12. doi: 10.1093/hmg/7.7.1105. Hum Mol Genet. 1998. PMID: 9618167

10

First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature.

Trimborn M, Grueters A, Neitzel H, Tönnies H. Trimborn M, et al. Among authors: grueters a. Cytogenet Genome Res. 2005;108(4):278-82. doi: 10.1159/000081524. Cytogenet Genome Res. 2005. PMID: 15627745 Review.

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