Plauchu H - Search Results

1

Acute mitral regurgitation caused by papillary muscle rupture in the immediate postpartum period revealing Ehlers-Danlos syndrome type IV.

Sève P, Dubreuil O, Farhat F, Plauchu H, Touboul P, Broussolle C. Sève P, et al. Among authors: plauchu h. J Thorac Cardiovasc Surg. 2005 Mar;129(3):680-1. doi: 10.1016/j.jtcvs.2004.07.041. J Thorac Cardiovasc Surg. 2005. PMID: 15746759 Free article. No abstract available.

2

[Hemophilia. Diagnosis, genetics, complications].

Négrier C, Vinciguerra C, Pinson S, Plauchu H. Négrier C, et al. Among authors: plauchu h. Rev Prat. 1998 Mar 15;48(6):657-9. Rev Prat. 1998. PMID: 9781139 Review. French. No abstract available.

3

Pheochromocytoma as the first manifestation of von Hippel-Lindau disease.

Richard S, Beigelman C, Duclos JM, Fendler JP, Plauchu H, Plouin PF, Resche F, Schlumberger M, Vermesse B, Proye C. Richard S, et al. Among authors: plauchu h. Surgery. 1994 Dec;116(6):1076-81. Surgery. 1994. PMID: 7985090

4

Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome 15q12-q15 and refinement to a 4.4 Mb region.

Michon L, Morlé L, Bozon M, Duret L, Zech JC, Godet J, Plauchu H, Edery P. Michon L, et al. Among authors: plauchu h. Eur J Hum Genet. 2004 Jul;12(7):574-8. doi: 10.1038/sj.ejhg.5201197. Eur J Hum Genet. 2004. PMID: 15083168

5

[Duchenne muscular dystrophy. Fragile X syndrome. Epidemiology, genetics, diagnosis].

Pinson S, Plauchu H. Pinson S, et al. Among authors: plauchu h. Rev Prat. 1998 Mar 1;48(5):565-9. Rev Prat. 1998. PMID: 9781124 French. No abstract available.

6

Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.

Pinson S, Yaouanq J, Jouanolle AM, Turlin B, Plauchu H. Pinson S, et al. Among authors: plauchu h. J Med Genet. 1998 Nov;35(11):954-6. doi: 10.1136/jmg.35.11.954. J Med Genet. 1998. PMID: 9832046 Free PMC article.

7

[Single-factor heredity. Construction and interpretation of a genealogical tree. Principles of genetic counseling].

Plauchu H. Plauchu H. Rev Prat. 1994 Dec 1;44(19):2627-35. Rev Prat. 1994. PMID: 7855533 French. No abstract available.

8

[Genetic counseling and consanguinity].

Plauchu H, de Martinville B. Plauchu H, et al. Rev Prat. 1976 Feb 1;26(7):465-72, 477-8, 483-6. Rev Prat. 1976. PMID: 1265397 French. No abstract available.

9

A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.

Huber C, Delezoide AL, Guimiot F, Baumann C, Malan V, Le Merrer M, Da Silva DB, Bonneau D, Chatelain P, Chu C, Clark R, Cox H, Edery P, Edouard T, Fano V, Gibson K, Gillessen-Kaesbach G, Giovannucci-Uzielli ML, Graul-Neumann LM, van Hagen JM, van Hest L, Horovitz D, Melki J, Partsch CJ, Plauchu H, Rajab A, Rossi M, Sillence D, Steichen-Gersdorf E, Stewart H, Unger S, Zenker M, Munnich A, Cormier-Daire V. Huber C, et al. Among authors: plauchu h. Eur J Hum Genet. 2009 Mar;17(3):395-400. doi: 10.1038/ejhg.2008.200. Epub 2008 Oct 29. Eur J Hum Genet. 2009. PMID: 19225462 Free PMC article.

10

Marfan Sartan: a randomized, double-blind, placebo-controlled trial.

Milleron O, Arnoult F, Ropers J, Aegerter P, Detaint D, Delorme G, Attias D, Tubach F, Dupuis-Girod S, Plauchu H, Barthelet M, Sassolas F, Pangaud N, Naudion S, Thomas-Chabaneix J, Dulac Y, Edouard T, Wolf JE, Faivre L, Odent S, Basquin A, Habib G, Collignon P, Boileau C, Jondeau G. Milleron O, et al. Among authors: plauchu h. Eur Heart J. 2015 Aug 21;36(32):2160-6. doi: 10.1093/eurheartj/ehv151. Epub 2015 May 2. Eur Heart J. 2015. PMID: 25935877 Clinical Trial.

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