Plauchu, H.: search on Z-Library

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1

Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France

Gaëtan Lesca, Henri Plauchu, Florence Coulet, Sylvain Lefebvre, Ghislaine Plessis, Sylvie Odent, Sophie Rivière, Bruno Leheup, Cyril Goizet, Marie-France Carette, Jean-François Cordier, Stéphane Pinso

Journal:

Year:

2004

Language:

english

File:

PDF, 391 KB

english, 2004

2

Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients

Gaëtan Lesca, Nelly Burnichon, Grégory Raux, Mario Tosi, Stéphane Pinson, Marie-Jeanne Marion, Emmanuel Babin, Brigitte Gilbert-Dussardier, Sophie Rivière, Cyril Goizet, Laurence Faivre, Henri Plauchu

Journal:

Year:

2006

Language:

english

File:

PDF, 304 KB

english, 2006

3

Echocardiographic screening discloses increased values of pulmonary artery systolic pressure in 9 of 68 unselected patients affected with hereditary hemorrhagic telangiectasia

Olivieri, Carla, Lanzarini, Lucav, Pagella, Fabio, Semino, Lucia, Corno, Sabrina, Valacca, Cristina, Plauchu, Henry, Lesca, Gaetan, Barthelet, Martine, Buscarini, Elisabetta, Danesino, Cesare

Journal:

Genetics in Medicine

Year:

2006

Language:

english

File:

PDF, 364 KB

english, 2006

4

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)

Shovlin, Claire L., Guttmacher, Alan E., Buscarini, Elisabetta, Faughnan, Marie E., Hyland, Robert H., Westermann, Cornelius J.J., Kjeldsen, Anette D., Plauchu, Henri

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 66 KB

english, 2000

5

Histoire economique: La France de l'entre-deux-guerres || Rebuts ou ressources? La socio-économie du déchetby Gérard Bertolini

Review by: Vincent Plauchu

Journal:

Revue économique

Year:

1980

File:

PDF, 195 KB

1980

6

Piège diagnostique et difficultés du conseil génétique dans une famille de patients porteurs de maladies neuromusculaires

G Lesca, E Ollagnon-Roman, J Lachanat, A Dusser, P Edery, M Jeanpierre, H Plauchu

Journal:

Archives de Pédiatrie

Year:

2001

Language:

french

File:

PDF, 39 KB

french, 2001

7

COMPARATIVE STUDY OF ASYMMETRY ORIGIN OF GALAXIES IN DIFFERENT ENVIRONMENTS. II. NEAR-INFRARED OBSERVATIONS

Plauchu-Frayn, I., Coziol, R.

Journal:

The Astronomical Journal

Year:

2010

Language:

english

File:

PDF, 286 KB

english, 2010

8

Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O-Arab (β121[GH4]Glu→Lys) in a Moroccan man

Faouzi Baklouti, Alain Francina, Evelyne Dorléac, Véronique Baudin-Chich, Germaine Gombaud-Saintonge, Henri Plauchu, Henri Wajcman, Jean Delaunay, Jacqueline Godet

Journal:

American Journal of Hematology

Year:

1988

Language:

english

File:

PDF, 373 KB

english, 1988

9

Probing evolutionary mechanisms in galaxy clusters: neutral atomic hydrogen in Abell 1367

T. C. Scott, H. Bravo-Alfaro, E. Brinks, C. A. Caretta, L. Cortese, A. Boselli, M. J. Hardcastle, J. H. Croston, I. Plauchu

Journal:

Monthly Notices of the Royal Astronomical Society

Year:

2010

Language:

english

File:

PDF, 28.92 MB

english, 2010

10

Grossesse et syndrome d’Ehlers-Danlos vasculaire : prise en charge et complications

Dubruc, E., Dupuis-Girod, S., Khau Van Kien, P., Denis-Belicard, E., Chirossel, C., Fokstuen, S., Touraine, R., Plauchu, H.

Journal:

Journal de Gynécologie Obstétrique et Biologie de la Reproduction

Year:

2013

File:

PDF, 221 KB

2013

11

Macular dystrophy of malattia leventinese. A 25 year follow up

ZECH, J.-C., ZAOUCHE, S., MOURIER, F., PLAUCHU, H., GRANGE, J.-D., TREPSAT, C.

Journal:

British Journal of Ophthalmology

Year:

1999

Language:

english

File:

PDF, 484 KB

english, 1999

12

Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?

T Martin-Denavit, S Duthel, S Giraud, S Olschwang, JC Saurin, H Plauchu

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 1.78 MB

english, 2001

13

COMPARATIVE STUDY OF ASYMMETRY ORIGIN OF GALAXIES IN DIFFERENT ENVIRONMENTS. I. OPTICAL OBSERVATIONS

Plauchu-Frayn, I., Coziol, R.

Journal:

The Astronomical Journal

Year:

2010

Language:

english

File:

PDF, 236 KB

english, 2010

14

Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: Comparison with HLA typing in 17 pregnancies at risk for CAH

Maguelone G. Forest, Hervé Bétuel, Philippe Couillin, André Boué, Michel David, Daniel Floret, René Francois, Pierre Guibaud, Henri Plauchu, Raphaël Rappaport

Journal:

Prenatal Diagnosis

Year:

1981

Language:

english

File:

PDF, 636 KB

english, 1981

15

Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations

Elisabetta Buscarini, Henry Plauchu, Guadalupe Garcia Tsao, Robert I. White Jr., Carlo Sabbà, Franklin Miller, Jean Cristophe Saurin, Jean Pierre Pelage, Gaetan Lesca, Marie Jeanne Marion, Annalisa Pe

Journal:

Liver International

Year:

2006

Language:

english

File:

PDF, 111 KB

english, 2006

16

Maladie de Rendu Osler : nouveau facteur de risque de thrombose ?

S. Riviere, D. Pelenc, S. Dupuis-Girod, B. Lorcerie, P. Kaminsky, A. Le Quellec, H. Plauchu

Journal:

La Revue de Médecine Interne

Year:

2009

Language:

french

File:

PDF, 67 KB

french, 2009

17

A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15

L. Morlé, M. Bozon, J.-C. Zech, N. Alloisio, A. Raas-Rothschild, C. Philippe, J.-C. Lambert, J. Godet, H. Plauchu, P. Edery

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 652 KB

english, 2000

18

Hemorrhagic Hereditary Telangiectasia (Rendu-Osler Disease) and Infectious Diseases: An Underestimated Association

Girod, S. D., Giraud, S., Decullier, E., Lesca, G., Cottin, V., Faure, F., Merrot, O., Saurin, J.-C., Cordier, J.-F., Plauchu, H.

Journal:

Clinical Infectious Diseases

Year:

2007

Language:

english

File:

PDF, 81 KB

english, 2007

19

Vieillards et familles: intégration ou rejet. L'exemple de Chezery-Forens (1856-1872)

Alain Bideau, Guy Brunet, Henri Plauchu and J. M. Robert

Journal:

Year:

1987

File:

PDF, 859 KB

1987

20

Toriello-Carey syndrome

Till, M., Bourgeois, J., Plauchu, H.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 81 KB

english, 1997

21

Bronchiectasis in two pediatric patients with Rothmund–Thomson syndrome

PHILIPPE REIX, JOCELYNE DERELLE, HELENE LEVREY-HADDEN, HENRI PLAUCHU, GABRIEL BELLON

Journal:

Pediatrics International

Year:

2007

Language:

english

File:

PDF, 107 KB

english, 2007

22

Troubleshooting expert systems for industrial maintenance: pre-development guidelines

Michel Bouche, Vincent Plauchu, Didier Retour

Journal:

Year:

1990

Language:

english

File:

PDF, 795 KB

english, 1990

23

Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement

Olivier Boillot, Francesco Bianco, Jean-Paul Viale, Francois Mion, Isabelle Mechet, Danielle Gille, Jacques Delaye, Pierre Paliard, Henri Plauchu

Journal:

Gastroenterology

Year:

1999

Language:

english

File:

PDF, 135 KB

english, 1999

24

Oral anticoagulant treatment – Evaluating the knowledge of patients admitted in physical medicine and rehabilitation units

A. Janoly-Duménil, C. Bourne, K. Loiseau, J. Luauté, P.-O. Sancho, S. Ciancia, F. Caillet, D. Boisson, C. Rioufol, M.M. Plauchu, G. Rode, S. Jacquin-Courtois

Journal:

Annals of Physical and Rehabilitation Medicine

Year:

2011

File:

PDF, 243 KB

2011

25

Traitement des escarres aux différents stades de cicatrisation. Intérêts et justifications de recommandations thérapeutiques écrites pour les personnels médical et paramédical

D. Plantier, B. Rousson, A. Pechard, M.M. Plauchu, N. Matray, M.C. Maria, M.C. Lavorel, H. Breniaux, E. Felber, M. Eyssette

Journal:

Annales de Réadaptation et de Médecine Physique

Year:

1999

File:

PDF, 138 KB

1999

26

SFP-P116 – Génétique – Les syndromes marfanoïdes : quel pronostic vasculaire et orthopédique ?

A. Putoux, A. Topa, S. Douchin, S. Dupuis-Girod, D. Gamondes, P. Khau Van Kien, C. Boileau, P.S. Jouk, P. Edery, H. Plauchu

Journal:

Archives de Pédiatrie

Year:

2008

Language:

french

File:

PDF, 108 KB

french, 2008

27

Systèmes fonciers et développement économiqueby Robert Badouin

Review by: Vincent Plauchu

Journal:

Revue économique

Year:

1981

File:

PDF, 214 KB

1981

28

What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?

Coron, F., Rousseau, T., Jondeau, G., Gautier, E., Binquet, C., Gouya, L., Cusin, V., Odent, S., Dulac, Y., Plauchu, H., Collignon, P., Delrue, M.-A., Leheup, B., Joly, L., Huet, F., Thevenon, J., Mac

Journal:

Prenatal Diagnosis

Year:

2012

Language:

english

File:

PDF, 228 KB

english, 2012

29

3C 57 as an atypical radio-loud quasar: implications for the radio-loud/radio-quiet dichotomy

Sulentic, J. W., Martinez-Carballo, M. A., Marziani, P., del Olmo, A., Stirpe, G. M., Zamfir, S., Plauchu-Frayn, I.

Journal:

Monthly Notices of the Royal Astronomical Society

Year:

2015

Language:

english

File:

PDF, 721 KB

english, 2015

30

Ectodermal abnormalities associated with methimazole intrauterine exposure

T. Martin-Denavit, P. Edery, H. Plauchu, J. Attia-Sobol, D. Raudrant, J.M. Aurand, L. Thomas

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 254 KB

english, 2000

31

Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24

Lucie Verot, Nicole Alloisio, Laurette Morlé, Muriel Bozon, Renaud Touraine, Henri Plauchu, Patrick Edery

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 122 KB

english, 2003

32

Determination of·fouling factors for shell-and-tube type heat exchangers exposed to los azufres geothermal fluids

Jose L. Hernandez-Galan, L. Alberto Plauchu

Journal:

Year:

1989

Language:

english

File:

PDF, 506 KB

english, 1989

33

Les manifestations précoces de la maladie de Tangier

A Lachaux, A Sassolas, R Bouvier, C Le Gall, I Loras, F Regnier, H Plauchu, P Froelich, M Hermier

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 331 KB

1995

34

A gene for hereditary multiple exostoses maps to chromosome 19p

Le Merrer, Marline, Legeai-Mallet, Laurence, Jeannin, Patricia Margaritte, Horsthemke, Bernhard, Schlnzel, Albert, Plauchu, Henri, Toutaln, Annick, Achard, Frédéric, Munnich, Arnold, Maroteaux, Pierre

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 403 KB

english, 1994

35

Echographie avec produit de contraste dans les atteintes hepatiques de la maladie de rendu osler

Marion, D., Cuinet, M., Biaise, B., Deshayes, E., Valette, P.J., Plauchu, H., Dupuis Girod, S.

Journal:

Journal de Radiologie

Year:

2009

Language:

french

File:

PDF, 208 KB

french, 2009

36

Démographie historique et génétique des populations : la concentration géographique d'une maladie héréditaire rare

Bideau, Alain, Plauchu, Henri, Jacquard, Albert

Journal:

Annales Histoire Sciences Sociales

Year:

1979

Language:

french

File:

PDF, 1.47 MB

french, 1979

37

Hereditary hemorrhagic telangiectasia: from molecular biology to patient care

S. DUPUIS-GIROD, S. BAILLY, H. PLAUCHU

Journal:

Journal of Thrombosis and Haemostasis

Year:

2010

Language:

english

File:

PDF, 471 KB

english, 2010

38

Bone Morphogenetic Protein-9 Is a Circulating Vascular Quiescence Factor

David, L., Mallet, C., Keramidas, M., Lamande, N., Gasc, J.-M., Dupuis-Girod, S., Plauchu, H., Feige, J.-J., Bailly, S.

Journal:

Circulation Research

Year:

2008

Language:

english

File:

PDF, 1.84 MB

english, 2008

39

Doppler Ultrasonographic Grading of Hepatic Vascular Malformations in Hereditary Hemorrhagic Telangiectasia - Results of Extensive Screening

Buscarini, E, Danesino, C, Olivieri, C, Lupinacci, G, De Grazia, F, Reduzzi, L, Blotta, P, Gazzaniga, P, Pagella, F, Grosso, M, Pongiglione, G, Buscarini, L, Plauchu, H, Zambelli, A

Journal:

Ultraschall in der Medizin / European Journal of Ultrasound

Year:

2004

Language:

english

File:

PDF, 425 KB

english, 2004

40

Lissencephaly type III, stippled epiphyses and loose, thick skin: A new recessively inherited syndrome

Jocelyne Attia-Sobol, Férechté Encha-Razavi, Marc Hermier, Danielle Vitrey, Alain Verloes, Henri Plauchu

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 330 KB

english, 2001

41

Orofaciodigital syndrome with cerebral dysgenesis

Gaetan Lesca, Catherine Fallet-Bianco, Henri Plauchu, Danielle Vitrey, Alain Verloes, Jocelyne Attia-Sobol

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 430 KB

english, 2006

42

Evaluation of previously nonscreened hereditary hemorrhagic telangiectasia patients shows frequent liver involvement and early cardiac consequences

Rodica Gincul, Gaetan Lesca, Bénédicte Gelas-Dore, Nathalie Rollin, Martine Barthelet, Sophie Dupuis-Girod, Franck Pilleul, Sophie Giraud, Henri Plauchu, Jean-Christophe Saurin

Journal:

Year:

2008

Language:

english

File:

PDF, 151 KB

english, 2008

43

Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assay

H. Plauchu, C. Junien, I. Maire, R. Said, R. Gozlan, J. M. Lalouel

Journal:

Year:

1982

Language:

english

File:

PDF, 448 KB

english, 1982

44

A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12

Bonnet, Damien, Pelet, Anna, Legeai-Mallet, Laurence, Sidi, Daniel, Mathieu, Michèle, Parent, Philippe, Plauchu, Henri, Serville, Françoise, Schinzel, Albert, Weissenbach, Jean

Journal:

Nature Genetics

Year:

1994

File:

PDF, 399 KB

1994

45

Perforations coliques spontanées révélatrices d'un syndrome d'Ehlers-Danlos de type IV

C Henry, S Geiss, E Wodey, A Pennerath, M.T Zabot, S Peyrol, H Plauchu

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 271 KB

1995

46

Retard mental lié l'X avec aspect marfanoïde (syndrome de Lujan-Fryns) associé à une diminution de l'expression de la fibrilline dans deux families

O. Boespflug-Tanguy, M.T. Zabot, S. Peyrol, O. Talon, D. Bonneau, A. Tanguy, H. Plauchu

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 133 KB

1995

47

Syndrome d'ehlers-danlos vasculaire. diagnostic 17 ans après les premières manifestations digestives

T. Zenone, C. Grange, P. Pelissier, M.T. Zabot, H. Plauchu, D. Vital Durand, R. Levrat

Journal:

La Revue de Médecine Interne

Year:

1999

File:

PDF, 245 KB

1999

48

RENAL ARTERIOVENOUS MALFORMATION REQUIRING SURGERY IN RENDU-OSLER-WEBER DISEASE (HEREDITARY HEMORRHAGIC TELANGIECTASIA)

ZIANI, MOHAMED, VALIGNAT, CHRISTOPHE, LOPEZ, JEAN-GABRIEL, RUFFION, ALAIN, PLAUCHU, HENRI, PERRIN, PAUL

Journal:

The Journal of Urology

Year:

2000

Language:

english

File:

PDF, 188 KB

english, 2000

49

Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Follow-up and Pathophysiologic Considerations

Cottin, Vincent, Plauchu, Henri, Dupuis-Girod, Sophie, Cordier, Jean-François

Journal:

Journal of Vascular and Interventional Radiology

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

50

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q

Vincent, P., Plauchu, H., Hazan, J., Faure, S., Weissenbach, J., Godet, J.

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 423 KB

english, 1995

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