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Items: 7

1.

A Randomized Controlled Trial of an Intensive Nutrition Intervention Versus Standard Nutrition Care to Avoid Excess Weight Gain After Kidney Transplantation: The INTENT Trial.

Henggeler CK, Plank LD, Ryan KJ, Gilchrist EL, Casas JM, Lloyd LE, Mash LE, McLellan SL, Robb JM, Collins MG.

J Ren Nutr. 2018 Sep;28(5):340-351. doi: 10.1053/j.jrn.2018.03.001. Epub 2018 May 2.

2.

Clinical sequencing: From raw data to diagnosis with lifetime value.

Caspar SM, Dubacher N, Kopps AM, Meienberg J, Henggeler C, Matyas G.

Clin Genet. 2018 Mar;93(3):508-519. doi: 10.1111/cge.13190. Review.

3.

Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency.

Meienberg J, Rohrbach M, Neuenschwander S, Spanaus K, Giunta C, Alonso S, Arnold E, Henggeler C, Regenass S, Patrignani A, Azzarello-Burri S, Steiner B, Nygren AO, Carrel T, Steinmann B, Mátyás G.

Eur J Hum Genet. 2010 Dec;18(12):1315-21. doi: 10.1038/ejhg.2010.105. Epub 2010 Jul 21.

4.

A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.

Jamsheer A, Henggeler C, Wierzba J, Loeys B, De Paepe A, Stheneur Ch, Badziag N, Matuszewska K, Matyas G, Latos-Bielenska A.

J Appl Genet. 2009;50(4):405-10. Review.

PMID:
19875893
5.

Molecular characterization of the key switch F provides a basis for understanding the rapid divergence of the sex-determining pathway in the housefly.

Hediger M, Henggeler C, Meier N, Perez R, Saccone G, Bopp D.

Genetics. 2010 Jan;184(1):155-70. doi: 10.1534/genetics.109.109249. Epub 2009 Oct 19.

6.

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome.

Mátyás G, Alonso S, Patrignani A, Marti M, Arnold E, Magyar I, Henggeler C, Carrel T, Steinmann B, Berger W.

Hum Genet. 2007 Aug;122(1):23-32. Epub 2007 May 10.

7.

[Three endemics of transient lung infiltrates with blood eosinophilia (Loeffler's syndrome)].

HENGGELER C.

Schweiz Med Wochenschr. 1959 Apr 11;89:402-4. German. No abstract available.

PMID:
14401027

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