Krude H - Search Results

1

Mutations in TITF-1 are associated with benign hereditary chorea.

Breedveld GJ, van Dongen JW, Danesino C, Guala A, Percy AK, Dure LS, Harper P, Lazarou LP, van der Linde H, Joosse M, Grüters A, MacDonald ME, de Vries BB, Arts WF, Oostra BA, Krude H, Heutink P. Breedveld GJ, et al. Among authors: krude h. Hum Mol Genet. 2002 Apr 15;11(8):971-9. doi: 10.1093/hmg/11.8.971. Hum Mol Genet. 2002. PMID: 11971878

2

Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review.

Wilpert NM, Tonduti D, Vaia Y, Krude H, Sarret C, Schuelke M. Wilpert NM, et al. Among authors: krude h. Neuropsychiatr Dis Treat. 2023 Oct 20;19:2195-2216. doi: 10.2147/NDT.S379703. eCollection 2023. Neuropsychiatr Dis Treat. 2023. PMID: 37881807 Free PMC article.

3

Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.

Biebermann H, Schöneberg T, Krude H, Schultz G, Gudermann T, Grüters A. Biebermann H, et al. Among authors: krude h. J Clin Endocrinol Metab. 1997 Oct;82(10):3471-80. doi: 10.1210/jcem.82.10.4286. J Clin Endocrinol Metab. 1997. PMID: 9329388

4

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.

Macchia PE, Lapi P, Krude H, Pirro MT, Missero C, Chiovato L, Souabni A, Baserga M, Tassi V, Pinchera A, Fenzi G, Grüters A, Busslinger M, Di Lauro R. Macchia PE, et al. Among authors: krude h. Nat Genet. 1998 May;19(1):83-6. doi: 10.1038/ng0598-83. Nat Genet. 1998. PMID: 9590296

5

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.

Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A. Krude H, et al. Nat Genet. 1998 Jun;19(2):155-7. doi: 10.1038/509. Nat Genet. 1998. PMID: 9620771

6

Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.

Krude H, Grüters A. Krude H, et al. Trends Endocrinol Metab. 2000 Jan-Feb;11(1):15-22. doi: 10.1016/s1043-2760(99)00213-1. Trends Endocrinol Metab. 2000. PMID: 10652501 Review.

7

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.

Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Grüters A, Amselem S. Netchine I, et al. Among authors: krude h. Nat Genet. 2000 Jun;25(2):182-6. doi: 10.1038/76041. Nat Genet. 2000. PMID: 10835633

8

Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.

Biebermann H, Schöneberg T, Krude H, Gudermann T, Grüters A. Biebermann H, et al. Among authors: krude h. Langenbecks Arch Surg. 2000 Oct;385(6):390-2. doi: 10.1007/s004230000145. Langenbecks Arch Surg. 2000. PMID: 11127522

9

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.

Krude H, Schütz B, Biebermann H, von Moers A, Schnabel D, Neitzel H, Tönnies H, Weise D, Lafferty A, Schwarz S, DeFelice M, von Deimling A, van Landeghem F, DiLauro R, Grüters A. Krude H, et al. J Clin Invest. 2002 Feb;109(4):475-80. doi: 10.1172/JCI14341. J Clin Invest. 2002. PMID: 11854319 Free PMC article.

10

[Gene, fast food and no motion. Causes of childhood obesity].

Grüters A, Wiegand S, Krude H. Grüters A, et al. Among authors: krude h. MMW Fortschr Med. 2002 Feb 28;144(9):34-6. MMW Fortschr Med. 2002. PMID: 11921649 German.

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