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1

Effets paradoxaux du cannabis sur la mémoire

Gilgenkrantz, Hélène

Journal:

médecine/sciences

Year:

2018

Language:

french

File:

PDF, 119 KB

french, 2018

2

Notre cerveau

Gilgenkrantz, HÃ©lÃ¨ne

Journal:

médecine/sciences

Year:

2020

File:

PDF, 663 KB

2020

3

Cholangiocarcinomes intrahépatiques : une entité en cours de démembrement

Coulouarn, C., Cavard, C., Rubbia Brandt, L., Audebourg, A., Dumont, F., Just, P.-A., Jacques, S., Clément, B., Gilgenkrantz, H., Perret, C., Terris, B.

Journal:

Annales de Pathologie

Year:

2012

Language:

french

File:

PDF, 182 KB

french, 2012

4

SPIE Proceedings [SPIE 27th European Mask and Lithography Conference - Dresden, Germany (Tuesday 18 January 2011)] 27th European Mask and Lithography Conference - Augmented reality for wafer prober

Gilgenkrantz, Pascal, Behringer, Uwe F.W.

Year:

2011

Language:

english

File:

PDF, 397 KB

english, 2011

5

La scintigraphie myocardique au thallium 201 à I’effort dans la maladie coronaire

Aliot, E., Laurens, M.H., Thouvenot, P., Fontaine, B., Bruntz, J., Robert, J., Gilgenkrantz, J.M.

Journal:

Year:

1981

Language:

french

File:

PDF, 964 KB

french, 1981

6

Antagonistes du récepteur CB1 des cannabinoïdes et obésité

Gilgenkrantz, Hélène, Lotersztajn, Sophie

Journal:

médecine/sciences

Year:

2018

Language:

french

File:

PDF, 1.64 MB

french, 2018

7

Génomique de l’hémophilie de la reine Victoria

Gilgenkrantz, Simone

Journal:

médecine/sciences

Year:

2010

Language:

french

File:

PDF, 423 KB

french, 2010

8

Démographie japonaise

Gilgenkrantz, Simone

Journal:

médecine/sciences

Year:

2009

File:

PDF, 123 KB

2009

9

Un symbionte de la glossine : Wigglesworthia glossinidia

Gilgenkrantz, Simone

Journal:

médecine/sciences

Year:

2003

File:

PDF, 73 KB

2003

10

Les Japonais et nous

Gilgenkrantz, Simone

Journal:

médecine/sciences

Year:

2010

Language:

french

File:

PDF, 220 KB

french, 2010

11

Prix L’Oréal-Unesco pour les femmes et la science

Gilgenkrantz, Simone

Journal:

médecine/sciences

Year:

2007

Language:

french

File:

PDF, 74 KB

french, 2007

12

Un dialogue prÃ©coce indispensable entre cellules MAIT et microbiote

Gilgenkrantz, HÃ©lÃ¨ne

Journal:

Year:

2020

File:

PDF, 1.17 MB

2020

13

Autosomal recessive lateralization and midline defects: Blastogenesis recessive 1

Debrus, Sophie, Sauer, Ursula, Gilgenkrantz, Simone, Jost, Wolfgang, Jesberger, Hans-Jürgen, Bouvagnet, Patrice

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 181 KB

english, 1997

14

Cardiac functional improvement by a human Bcl-2 transgene in a mouse model of ischemia/reperfusion injury

Valérie Brocheriou, Albert A. Hagège, Abdou Oubenaïssa, Martine Lambert, Vincent O. Mallet, Micheline Duriez, Michel Wassef, Axel Kahn, Philippe Menasché, Hélène Gilgenkrantz

Journal:

The Journal of Gene Medicine

Year:

2000

Language:

english

File:

PDF, 287 KB

english, 2000

15

TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment

Marie Gomot, Nathalie Ronce, Sabine Dessay, Ramzi Zemni, Anne-Dominique Ayrault, Marie-Pierre Moizard, Annie Nivelon, Simone Gilgenkrantz, Julliette Dourlens, Vincent Des Portes, Jamel Chelly, Claude

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 96 KB

english, 2002

16

Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy

Dr. S. Gilgenkrantz, C. Vigneron, M. J. Gregoire, C. Pernot, A. Raspiller, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1982

Language:

english

File:

PDF, 542 KB

english, 1982

17

Monozygotic twins discordant for trisomy 21 or chimeric dizygotic twins?

Simone Gilgenkrantz, Christian Janot, J. G. Rogers, L. Voullaire, H. Gold, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1983

Language:

english

File:

PDF, 88 KB

english, 1983

18

Probable localisation of the Coffin-Lowry locus in Xp22.2-P22.1 by multipoint linkage analysis

A. Hanauer, Y. Alembik, S. Gilgenkrantz, P. Mujica, A. Nivelon-Chevallier, M. E. Pembrey, I. D. Young, J. L. Mandel

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 349 KB

english, 1988

19

New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA Interval

I. Oberlé, A. Vincent, N. Abbadi, F. Rousseau, P. E. Hupkes, M. C. Hors-Cayla, S. Gilgenkrantz, B. A. Oostra, J. L. Mandel

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 1.32 MB

english, 1991

20

No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families

Wayne F. Flintoff, Michel Bahuau, Stanislas Lyonnet, Simone Gilgenkrantz, Didier Lacombe, François Marçon, Jacqueline Levilliers, Jean Kachaner, Arnold Munnich, Martine Le Merrer

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 497 KB

english, 1993

21

X inactivation in Rett syndrome: A preliminary study showing partial preferential inactivation of paternal X with the M27β probe

P. Camus, N. Abbadi, S. Gilgenkrantz

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 161 KB

english, 1994

22

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation

N. Abbadi, C. Philippe, M. Chery, H. Gilgenkrantz, F. Tome, H. Collin, D. Theau, D. Recan, O. Broux, M. Fardeau, J.-C. Kaplan, Pr. S. Gilgenkrantz

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 904 KB

english, 1994

23

Lafora disease is not linked to the Unverricht-Lundborg locus

Pierre Labauge, Corrine Beck, Hélène Bellet, Georges Coquillat, Hervé Vespignani, Olivier Dulac, Simone Gilgenkrantz, Charlotte Dravet, Pierre Genton, Jean-François Pellissier, Michèle Chery, Michel B

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 382 KB

english, 1995

24

Gene transfer to schwann cells after peripheral nerve injury: A delivery system for therapeutic agents

Jesper Sørensen, Georg Haase, Christian Krarup, Helene Gilgenkrantz, Axel Kahn, Dr Henning Schmalbruch

Journal:

Annals of Neurology

Year:

1998

Language:

english

File:

PDF, 2.50 MB

english, 1998

25

Identification of a yeast artificial chromosome (YAC) spanning the synovial sarcoma-specific t(X;18)(p11.2;q11.2) breakpoint

B. De Leeuw, W. Berger, R. J. Sinke, R. F. Suijkerbuijk, S. Gilgenkrantz, M. T. Geraghty, D. Valle, A. P. Monaco, H. Lehrach, H. H. Ropers, A. Geurts Van Kessel

Journal:

Genes, Chromosomes and Cancer

Year:

1993

Language:

english

File:

PDF, 680 KB

english, 1993

26

Mesenchymal stem cells: An alternative source of hepatocytes?

Hélène Gilgenkrantz

Journal:

Year:

2004

Language:

english

File:

PDF, 66 KB

english, 2004

27

Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes

S. Gilgenkrantz, P. Droulle, E. Seboun, M. Casanova, M. Schweitzer, M. Goosens, M. Fellous

Journal:

Prenatal Diagnosis

Year:

1986

Language:

english

File:

PDF, 363 KB

english, 1986

28

Distal trisomy 14q

Genoveva Keyeux, Simone Gilgenkrantz, Gérard Lefranc, Marie-Paule Lefranc

Journal:

Year:

1990

Language:

english

File:

PDF, 1.17 MB

english, 1990

29

Distal trisomy 14q

Simone Gilgenkrantz, Jacqueline Vigneron, Marie-Odile Peter, J. L. Dufier, M. Teboul, Michèle Chery, Genoveva Keyeux, Marie-Paule Lefranc

Journal:

Year:

1990

Language:

english

File:

PDF, 1.02 MB

english, 1990

30

Refined mapping of the human Ets-related gene Elk-1 to Xp11.2–p11.4, distal to the OATL1 region

Martin Janz, Ulrich Lehmann, Danielle Olde Weghuis, Bertie Leeuw, Ad Geurts Kessel, Simone Gilgenkrantz, Robert A. Hipskind, Alfred Nordheim

Journal:

Year:

1994

Language:

english

File:

PDF, 298 KB

english, 1994

31

Hypomagensemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint

Michèle Chery, Valérie Biancalana, Christophe Philippe, Georges Malpuech, Hélène Carla, Simone Gilgenkrantz, Jean-Louis Mandel, André Hanauer

Journal:

Year:

1994

Language:

english

File:

PDF, 656 KB

english, 1994

32

A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1

Nacer Abbas, Giuseppe Novelli, Narcisio Carlo Stella, Onofrio Triolo, Francesco Corrado, Marc Fellous, Michèle Chery, Simone Gilgenkrantz, Bruno Dallapiccola

Journal:

Year:

1990

Language:

english

File:

PDF, 848 KB

english, 1990

33

A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23

Patrizia Amati, Jean-Claude Chomel, Annie Nivelon-Chevalier, Simone Gilgenkrantz, Alain Kitzis, Josseline Kaplan, Dominique Bonneau

Journal:

Year:

1995

Language:

english

File:

PDF, 298 KB

english, 1995

34

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene

J. Bonaventure, C. Philippe, G. Plessis, J. Vigneron, C. Lasselin, P. Maroteaux, S. Gilgenkrantz

Journal:

Year:

1992

Language:

english

File:

PDF, 1.02 MB

english, 1992

35

Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints

R. J. Sinke, B. Leeuw, H. A. P. Janssen, D. Olde Weghuis, R. F. Suijkerbuijk, A. M. Meloni, S. Gilgenkrantz, W. Berger, H. H. Ropers, A. A. Sandberg, A. Geurts Kessel

Journal:

Year:

1993

Language:

english

File:

PDF, 553 KB

english, 1993

36

Interstitial deletion of chromosome 15: two cases

L. de F. Formiga, L. Poenaru, F. Couronne, E. Flori, J. L. Eibel, M. M. Deminatti, J. B. Savary, J. L. Lai, S. Gilgenkrantz, M. Pierson

Journal:

Year:

1988

Language:

english

File:

PDF, 621 KB

english, 1988

37

Correlation between the number of sex chromosomes and the H-Y antigen titer

M. Fraccaro, Antonia Mayerová, U. Wolf, Erika Bühler, J. Gebauer, Simone Gilgenkrantz, J. Lindsten, F. Curto, E. M. Ritzen

Journal:

Year:

1982

Language:

english

File:

PDF, 599 KB

english, 1982

38

Incontinentia pigmenti and X-autosome translocations

John A. Crolla, Simone Gilgenkrantz, Jean Grouchy, Tadashi Kajii, Martin Bobrow

Journal:

Year:

1989

Language:

english

File:

PDF, 473 KB

english, 1989

39

Translocation X sur autosome et replication tardive

S. Gilgenkrantz, G. Mauuary, B. Dutrillaux, G. Masocco

Journal:

Year:

1975

File:

PDF, 1.27 MB

1975

40

Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members

S. Gilgenkrantz, C. Defeche, S. Stehlin, M. J. Gregoire

Journal:

Year:

1981

Language:

english

File:

PDF, 1.01 MB

english, 1981

41

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes

Simone Gilgenkrantz, Marie-Elisabeth Briquel, J. -L. Mandel, Isabelle Oberle

Journal:

Year:

1986

Language:

english

File:

PDF, 521 KB

english, 1986

42

Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

B. Chadefaux, D. Allard, M. O. Rethoré, O. Raoul, M. Poissonnier, S. Gilgenkrantz, C. Cheruy, H. Jérôme

Journal:

Year:

1984

Language:

english

File:

PDF, 273 KB

english, 1984

43

Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci

Genoveva Keyeux, Simone Gilgenkrantz, Gérard Lefranc, Marie-Paule Lefranc

Journal:

Year:

1989

Language:

english

File:

PDF, 562 KB

english, 1989

44

Hypohidrotic ectodermal dysplasia

Simone Gilgenkrantz, Claudine Blanchet-Bardon, V. Nazzaro, Lorena Formiga, Patricia Mujica, Y. Alembik

Journal:

Year:

1989

Language:

english

File:

PDF, 328 KB

english, 1989

45

Duplication 15q22»15qter and its phenotypic expression

M. J. Gregoire, J. Boue, C. Junien, C. Pernot, S. Gilgenkrantz, L. Zergollern

Journal:

Year:

1981

Language:

english

File:

PDF, 1022 KB

english, 1981

46

Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

R. A. Pfeiffer, R. Ott, S. Gilgenkrantz, P. Alexandre

Journal:

Year:

1982

Language:

english

File:

PDF, 507 KB

english, 1982

47

Striking conservation of the brain-specific region of the dystrophin gene

Jean-Philippe Hugnot, Hélène Gilgenkrantz, Marc Jeanpierre, Jamel Chelly, Jean-Claude Kaplan, Axel Kahn

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 550 KB

english, 1993

48

Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker

A. Hanauer, Y. Alembik, B. Arveiler, L. Formiga, S. Gilgenkrantz, J. L. Mandel

Journal:

Year:

1988

Language:

english

File:

PDF, 395 KB

english, 1988

49

Aspect clinique et épidémiologique de quelques cas d'infection

M. Pierson, E. de Lavergne, S. Gilgenkrantz, A. M. Worms

Journal:

Archives of Virology

Year:

1963

File:

PDF, 355 KB

1963

50

Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11

A. Sefiani, D. Sinnett, L. Abel, S. Szpiro-Tapia, S. Heuertz, I. Craig, N. Fraser, T. A. Kruse, M. Frydman, M. O. Peter, J. L. Schmutz, S. Gilgenkrantz, G. Mitchell, J. Frézal, S. Melançon, L. Lavergn

Journal:

Year:

1988

Language:

english

File:

PDF, 488 KB

english, 1988

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