Morlot M - Search Results

Year	Number of Results
1980	2
1990	1
1993	1
1997	2
2000	1
2003	2
2004	1
2005	1
2006	1
2011	1
2012	1
2015	1
2016	1
2017	1
2019	1
2025	0

1

No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome.

Tröger B, Kutsche K, Bolz H, Lüttgen S, Gal A, Almassy Z, Caliebe A, Freisinger P, Hobbiebrunken E, Morlot M, Stefanova M, Streubel B, Wieczorek D, Meinecke P. Tröger B, et al. Among authors: morlot m. Am J Med Genet A. 2003 Aug 15;121A(1):82-4. doi: 10.1002/ajmg.a.20122. Am J Med Genet A. 2003. PMID: 12900909 No abstract available.

2

Effectiveness and Safety of rhIGF-1 Therapy in Children: The European Increlex® Growth Forum Database Experience.

Bang P, Polak M, Woelfle J, Houchard A; EU IGFD Registry Study Group. Bang P, et al. Horm Res Paediatr. 2015;83(5):345-57. doi: 10.1159/000371798. Epub 2015 Mar 21. Horm Res Paediatr. 2015. PMID: 25824333 Free article.

3

Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.

Xie J, Pannain S, Pohlenz J, Weiss RE, Moltz K, Morlot M, Asteria C, Persani L, Beck-Peccoz P, Parma J, Vassart G, Refetoff S. Xie J, et al. Among authors: morlot m. J Clin Endocrinol Metab. 1997 Dec;82(12):3933-40. doi: 10.1210/jcem.82.12.4418. J Clin Endocrinol Metab. 1997. PMID: 9398691

4

Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study.

Köhler B, Kleinemeier E, Lux A, Hiort O, Grüters A, Thyen U; DSD Network Working Group. Köhler B, et al. J Clin Endocrinol Metab. 2012 Feb;97(2):577-88. doi: 10.1210/jc.2011-1441. Epub 2011 Nov 16. J Clin Endocrinol Metab. 2012. PMID: 22090272

5

The A645D mutation in the hinge region of the human androgen receptor (AR) gene modulates AR activity, depending on the context of the polymorphic glutamine and glycine repeats.

Werner R, Holterhus PM, Binder G, Schwarz HP, Morlot M, Struve D, Marschke C, Hiort O. Werner R, et al. Among authors: morlot m. J Clin Endocrinol Metab. 2006 Sep;91(9):3515-20. doi: 10.1210/jc.2006-0372. Epub 2006 Jun 27. J Clin Endocrinol Metab. 2006. PMID: 16804045

6

Clinical, endocrine, and molecular genetic findings in patients with 17beta-hydroxysteroid dehydrogenase deficiency.

Twesten W, Holterhus P, Sippell WG, Morlot M, Schumacher H, Schenk B, Hiort O. Twesten W, et al. Among authors: morlot m. Horm Res. 2000;53(1):26-31. doi: 10.1159/000023509. Horm Res. 2000. PMID: 10965217

7

Testicular growth and spermatogenesis: new goals for pubertal hormone replacement in boys with hypogonadotropic hypogonadism? -a multicentre prospective study of hCG/rFSH treatment outcomes during adolescence.

Rohayem J, Hauffa BP, Zacharin M, Kliesch S, Zitzmann M; “German Adolescent Hypogonadotropic Hypogonadism Study Group”. Rohayem J, et al. Clin Endocrinol (Oxf). 2017 Jan;86(1):75-87. doi: 10.1111/cen.13164. Epub 2016 Sep 7. Clin Endocrinol (Oxf). 2017. PMID: 27467188 Clinical Trial.

8

Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneity.

Riepe FG, Krone N, Morlot M, Ludwig M, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: morlot m. J Clin Endocrinol Metab. 2003 Apr;88(4):1683-6. doi: 10.1210/jc.2002-021556. J Clin Endocrinol Metab. 2003. PMID: 12679457

9

Looking for the hidden mutation: Bannayan-Riley-Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A.

Golas MM, Auber B, Ripperger T, Pabst B, Schmidt G, Morlot M, Diebold U, Steinemann D, Schlegelberger B, Morlot S. Golas MM, et al. Among authors: morlot m. Am J Med Genet A. 2019 Jul;179(7):1383-1389. doi: 10.1002/ajmg.a.61166. Epub 2019 May 6. Am J Med Genet A. 2019. PMID: 31062505

10

Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene.

Riepe FG, Krone N, Morlot M, Peter M, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: morlot m. J Clin Endocrinol Metab. 2004 May;89(5):2150-2. doi: 10.1210/jc.2003-031555. J Clin Endocrinol Metab. 2004. PMID: 15126534

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