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Prenatal diagnosis of Pfeiffer syndrome type II.
Blaumeiser B, Loquet P, Wuyts W, Nöthen MM. Blaumeiser B, et al. Among authors: nothen mm. Prenat Diagn. 2004 Aug;24(8):644-6. doi: 10.1002/pd.960. Prenat Diagn. 2004. PMID: 15305355
Familial aggregation of alopecia areata.
Blaumeiser B, van der Goot I, Fimmers R, Hanneken S, Ritzmann S, Seymons K, Betz RC, Ruzicka T, Wienker TF, De Weert J, Lambert J, Kruse R, Nöthen MM. Blaumeiser B, et al. Among authors: nothen mm. J Am Acad Dermatol. 2006 Apr;54(4):627-32. doi: 10.1016/j.jaad.2005.12.007. Epub 2006 Jan 23. J Am Acad Dermatol. 2006. PMID: 16546583
High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA).
Storm K, Moens E, Vits L, De Vlieger H, Delaere G, D'Hollander M, Wuyts W, Biervliet M, Van Schil L, Desager K, Nöthen MM. Storm K, et al. Among authors: nothen mm. J Cyst Fibros. 2007 Nov 30;6(6):371-5. doi: 10.1016/j.jcf.2006.10.013. Epub 2007 May 3. J Cyst Fibros. 2007. PMID: 17481968 Free article.
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
Betz RC, Pforr J, Flaquer A, Redler S, Hanneken S, Eigelshoven S, Kortüm AK, Tüting T, Lambert J, De Weert J, Hillmer AM, Schmael C, Wienker TF, Kruse R, Lutz G, Blaumeiser B, Nöthen MM. Betz RC, et al. Among authors: nothen mm. J Invest Dermatol. 2007 Nov;127(11):2539-43. doi: 10.1038/sj.jid.5700915. Epub 2007 Jun 21. J Invest Dermatol. 2007. PMID: 17581619 Free article.
1,052 results