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1

The Theories of Henri Wallon: From Act to Thought

Netchine-Grynberg, Gaby

Journal:

Human Development

Year:

1991

File:

PDF, 3.28 MB

1991

2

Ovarian-sparing surgery for ovarian teratoma in children

M. Chabaud-Williamson, I. Netchine, S. Fasola, M. Larroquet, M. Lenoir, C. Patte, J.L. Bénifla, A. Coulomb-L'herminé, C. Grapin, G. Audry, F. Auber

Journal:

Pediatric Blood & Cancer

Year:

2011

Language:

english

File:

PDF, 191 KB

english, 2011

3

Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes

Salah Azzi, Virginie Steunou, Alexandra Rousseau, Sylvie Rossignol, Nathalie Thibaud, Fabienne Danton, Marilyne Le Jule, Christine Gicquel, Yves Le Bouc, Irène Netchine

Journal:

Year:

2011

Language:

english

File:

PDF, 349 KB

english, 2011

4

New insights into the pathogenesis of beckwith–wiedemann and silver–russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects

Julie Demars, Sylvie Rossignol, Irène Netchine, Kai Syin Lee, Mansur Shmela, Laurence Faivre, Jacques Weill, Sylvie Odent, Salah Azzi, Patrick Callier, Josette Lucas, Christèle Dubourg, Joris Andrieux

Journal:

Year:

2011

Language:

english

File:

PDF, 651 KB

english, 2011

5

IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development

Irène Netchine, Salah Azzi, Yves Le Bouc, Martin O. Savage

Journal:

Best Practice & Research Clinical Endocrinology & Metabolism

Year:

2011

Language:

english

File:

PDF, 588 KB

english, 2011

6

O08 Prévalence et prise en charge des troubles digestifs et nutritionnels chez les enfants ayant un syndrome de Silver-Russell

Marsaud, C., Rossignol, S., Vu-Hong, T-A., Tounian, P., Girardet, J-P., Netchine, I., Dubern, B.

Journal:

Cahiers de Nutrition et de Diététique

Year:

2011

Language:

french

File:

PDF, 81 KB

french, 2011

7

11p15 ICR1 partial deletions associated with IGF2/H19 DMR hypomethylation and Silver-Russell Syndrome

Habib, Walid Abi, Brioude, Frederic, Azzi, Salah, Salem, Jennifer, Neves, Cristina Das, Personnier, Claire, Chantot-Bastaraud, Sandra, Keren, Boris, Bouc, Yves Le, Harbison, Madeleine, Netchine, Irene

Journal:

Year:

2016

Language:

english

File:

PDF, 1.11 MB

english, 2016

8

[Advances in Psychology] Theoretical and Applied Aspects of Eye Movement Research, Selected/Edited Proceedings of The Second European Conference on Eye Movements Volume 22 || Cephalic and Ocular Components of Gaze Displacement During Oral and Silent Reading In Children and Adults

Netchine, Serge

Year:

1984

Language:

english

File:

PDF, 457 KB

english, 1984

9

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

Eggermann, Thomas, Elbracht, Miriam, Kurth, Ingo, Juul, Anders, Johannsen, Trine Holm, Netchine, IrÃ¨ne, Mastorakos, George, Johannsson, Gudmundur, Musholt, Thomas J., Zenker, Martin, Prawitt, Dirk, P

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 741 KB

2020

10

Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptor

Michael P. Wajnrajch, Joseph M. Gertner, Alisa S. Sokoloff, Irina Ten, Madeleine D. Harbison, Irène Netchine, Hiralal G. Maheshwari, David B. Goldstein, Serge Amselem, Gerhard Baumann, Rudolph L. Leib

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 135 KB

english, 2003

11

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary

Marie-Laure Sobrier, Irène Netchine, Claudine Heinrichs, Nathalie Thibaud, Marie-Pierre Vié-Luton, Guy Van Vliet, Serge Amselem

Journal:

Year:

2005

Language:

english

File:

PDF, 878 KB

english, 2005

12

Plural psychological developmental models: An ordinal generalization of the Guttman scale

B. Monjardet, G. Netchine-Grynberg

Journal:

Journal of Mathematical Psychology

Year:

1988

Language:

english

File:

PDF, 1.17 MB

english, 1988

13

Beckwith–Wiedemann syndrome in association with posterior hypoplasia of the cerebellar vermis

C. Bui, O. Picone, A. E. Mas, J. M. Levaillant, O. Ami, I. Netchine, R. Frydman, M. V. Senat

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 91 KB

english, 2009

14

Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene

Lorenzo Iughetti, Marie-Laure Sobrier, Barbara Predieri, Irene Netchine, Cesare Carani, Sergio Bernasconi, Fiorella Balli, Serge Amselem

Journal:

Clinical Endocrinology

Year:

2008

Language:

english

File:

PDF, 122 KB

english, 2008

15

10.1038/76041

Amselem, Serge, Netchine, Irène, Sobrier, Marie-Laure, Krude, Heiko, Schnabel, Dirk, Maghnie, Mohamed, Marcos, Elisabeth, Duriez, Bénédicte, Cacheux, Valère, Moers, Arpard v., Goossens, Michel, Grüter

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 611 KB

english, 2000

16

Spatial semiotics and general rules in the construction of graphic structures by young children

Gaby Netchine-Grynberg, Serge Netchine, Laurence Pannier

Journal:

European Journal of Psychology of Education

Year:

1993

Language:

english

File:

PDF, 1.48 MB

english, 1993

17

Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development

M.-L. Sobrier, T. Attié-Bitach, I. Netchine, F. Encha-Razavi, M. Vekemans, S. Amselem

Journal:

Gene Expression Patterns

Year:

2004

Language:

english

File:

PDF, 488 KB

english, 2004

18

Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases

Azzi, Salah, Rossignol, Sylvie, Bouc, Yves Le, Netchine, Irène

Journal:

Year:

2010

Language:

english

File:

PDF, 1.39 MB

english, 2010

19

Acute lymphocytic leukaemia in a child with Beckwith–Wiedemann syndrome harbouring a CDKN1C mutation

C. Abadie, F. Bernard, I. Netchine, D. Sanlaville, A. Roque, S. Rossignol, I. Coupier

Journal:

European Journal of Medical Genetics

Year:

2010

Language:

english

File:

PDF, 148 KB

english, 2010

20

Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency

Philippe Duquesnoy, Anne Roy, Florence Dastot, Isis Ghali, Cécile Teinturier, Irène Netchine, Valère Cacheux, Mona Hafez, Nermine Salah, Jean-Louis Chaussain, Michel Goossens, Pierre Bougnères, Serge

Journal:

Year:

1998

Language:

english

File:

PDF, 162 KB

english, 1998

21

Pathologie moléculaire du récepteur du GHRH

I. Netchine, P. Talon, S. Amselem

Journal:

Archives de Pédiatrie

Year:

2000

File:

PDF, 230 KB

2000

22

Pathologie moléculaire des facteurs de transcription impliqués dans le développement de l'antéhypophyse

I. Netchine, M.L. Sobrier, S. Amselem

Journal:

Archives de Pédiatrie

Year:

2000

File:

PDF, 299 KB

2000

23

Les déficits idiopathiques en hormone de croissance : du phénotype au génotype

I Netchine, ML Sobrier, P Duquesnoy, B Duriez, S Amselem, M Goossens, R Brauner

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 235 KB

1996

24

O08 Prévalence et prise en charge des troubles digestifs et nutritionnels chez les enfants ayant un syndrome de Silver-Russell

C. Marsaud, S. Rossignol, T-A. Vu-Hong, P. Tounian, J-P. Girardet, I. Netchine, B. Dubern

Journal:

Nutrition Clinique et Métabolisme

Year:

2011

Language:

french

File:

PDF, 80 KB

french, 2011

25

P-17 Heterogeneous clinical presentation in patients with yet-unreported type 1 IGF receptor molecular defects

S. Azzi, N. Thibaud, J-M. Ricort, P-F. Souchon, F. Danton, S. Rossignol, L. Perin, V. Steunou, M. Jesuran, M. Jule, G. Pinto, R. Coutant, Y. Le Bouc, I. Netchine

Journal:

Growth Hormone & IGF Research

Year:

2008

Language:

english

File:

PDF, 51 KB

english, 2008

26

OR11,2 A central role of insulin-like growth factor-II in embryonic growth and the development of brain and pancreas in zebrafish

I. Netchine, H. Mizuno, J. Song, H. Huang, S. Lin, P. Cohen

Journal:

Growth Hormone & IGF Research

Year:

2008

Language:

english

File:

PDF, 49 KB

english, 2008

27

P-83 Study of two IGF-1R gene expression variants

V. Steunou, S. Azzi, S. Rossignol, I. Netchine, Y. Le Bouc

Journal:

Growth Hormone & IGF Research

Year:

2008

Language:

english

File:

PDF, 47 KB

english, 2008

28

P-18 Russell-Silver Syndrome: clinical scoring system and molecular investigations on a large series of patients

I. Netchine, S. Rossignol, S. Azzi, F. Danton, V. Steunou, N. Thibaud, M. Le Jule, C. Gicquel, S. Cabrol, Y. Le Bouc

Journal:

Growth Hormone & IGF Research

Year:

2008

Language:

english

File:

PDF, 51 KB

english, 2008

29

Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4

Kalotina Machinis, Jacques Pantel, Irène Netchine, Juliane Léger, Olivier J.A. Camand, Marie-Laure Sobrier, Florence Dastot-Le Moal, Philippe Duquesnoy, Marc Abitbol, Paul Czernichow, Serge Amselem

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 700 KB

english, 2001

30

Epigenetics in Silver-Russell syndrome

Sylvie Rossignol, Irène Netchine, Yves Le Bouc, Christine Gicquel

Journal:

Best Practice & Research Clinical Endocrinology & Metabolism

Year:

2008

Language:

english

File:

PDF, 258 KB

english, 2008

31

CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome

Brioude, F., Oliver-Petit, I., Blaise, A., Praz, F., Rossignol, S., Jule, M. L., Thibaud, N., Faussat, A.-M., Tauber, M., Bouc, Y. L., Netchine, I.

Journal:

Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 2.85 MB

english, 2013

32

Epigenetics, genomic imprinting and assisted reproductive technology

Le Bouc, Y., Rossignol, S., Azzi, S., Steunou, V., Netchine, I., Gicquel, C.

Journal:

Annales d'Endocrinologie

Year:

2010

Language:

french

File:

PDF, 126 KB

french, 2010

33

SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

Keren, Boris, Chantot-Bastaraud, Sandra, Brioude, Frédéric, Mach, Corinne, Fonteneau, Eric, Azzi, Salah, Depienne, Christel, Brice, Alexis, Netchine, Irène, Le Bouc, Yves, Siffroi, Jean-Pierre, Rossig

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 658 KB

english, 2013

34

PO4-9: Complex tissue-specific epigenotypes in Russell Silver syndrome with 11p15 ICR1 hypomethylation: major consequences for the diagnosis

Azzi, S., Blaise, A., Steunou, V., Thibaud, N., Le Bouc, Y., Netchine, I.

Journal:

Growth Hormone & IGF Research

Year:

2014

Language:

english

File:

PDF, 457 KB

english, 2014

35

Genetic variants within the second intron of the KCNQ1 gene affect CTCF binding and confer a risk of Beckwith-Wiedemann syndrome upon maternal transmission

Demars, J., Shmela, M. E., Khan, A. W., Lee, K. S., Azzi, S., Dehais, P., Netchine, I., Rossignol, S., Le Bouc, Y., El-Osta, A., Gicquel, C.

Journal:

Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 3.66 MB

english, 2014

36

Retard sévère de croissance, déficit psychomoteur, dysmorphie faciale – un cas de duplication de novo 15q21.2–q24.1

Braha, E., Rusu, C., Chantot-Bastaraud, S., Netchine, I., Manolachie, A., Crumpei, I., Fadur, A., Armasu, I., Vulpoi, C.

Journal:

Annales d'Endocrinologie

Year:

2014

Language:

french

File:

PDF, 381 KB

french, 2014

37

11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

Netchine, Irène, Rossignol, Sylvie, Dufourg, Marie-Noëlle, Azzi, Salah, Rousseau, Alexandra, Perin, Laurence, Houang, Muriel, Steunou, Virginie, Esteva, Blandine, Thibaud, Nathalie, Raux Demay, Marie-

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2007

Language:

english

File:

PDF, 271 KB

english, 2007

38

Panhypopituitarisme congénital par mutation LHX4 : à propos d’un cas

Valentin, C., Legendre, M., Netchine, I., Brioude, F.

Journal:

Annales d'Endocrinologie

Year:

2014

Language:

french

File:

PDF, 214 KB

french, 2014

39

Extensive Phenotypic Analysis of a Family with Growth Hormone (GH) Deficiency Caused by a Mutation in the GH-Releasing Hormone Receptor Gene 1

Netchine, Irène, Talon, Philippe, Dastot, Florence, Vitaux, Françoise, Goossens, Michel, Amselem, Serge

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1998

Language:

english

File:

PDF, 423 KB

english, 1998

40

Degree of methylation of ZAC1 ( PLAGL1 ) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort

Azzi, Salah, Sas, Theo CJ, Koudou, Yves, Le Bouc, Yves, Souberbielle, Jean-Claude, Dargent-Molina, Patricia, Netchine, Irène, Charles, Marie-Aline

Journal:

Year:

2014

Language:

english

File:

PDF, 708 KB

english, 2014

41

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

Fritez, Nabila, Sobrier, Marie-Laure, Iraqi, Hinde, Vié-Luton, Marie-Pierre, Netchine, Irène, El Annas, Abdessamad, Pantel, Jacques, Collot, Nathalie, Rose, Sophie, Piterboth, William, Legendre, Marie

Journal:

Clinical Endocrinology

Year:

2015

Language:

english

File:

PDF, 448 KB

english, 2015

42

P310: Étude du comportement alimentaire des enfants ayant un syndrome de Silver-Russell

Aroulandom, J., Kao-Tchangai, S., Peretti, N., Tounian, P., Netchine, I., Niklaus, S., Dubern, B.

Journal:

Nutrition Clinique et Métabolisme

Year:

2014

Language:

french

File:

PDF, 44 KB

french, 2014

43

Germline correction of an epimutation related to Silver-Russell syndrome

Bruno, C., Carmignac, V., Netchine, I., Choux, C., Duffourd, Y., Faivre, L., Thauvin-Robinet, C., Le Bouc, Y., Sagot, P., Bourc'his, D., Fauque, P.

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 285 KB

english, 2015

44

Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders

Demars, J., Shmela, M. E., Rossignol, S., Okabe, J., Netchine, I., Azzi, S., Cabrol, S., Le Caignec, C., David, A., Le Bouc, Y., El-Osta, A., Gicquel, C.

Journal:

Human Molecular Genetics

Year:

2010

Language:

english

File:

PDF, 592 KB

english, 2010

45

Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical care

Eggermann, Thomas, Netchine, Irène, Temple, I, Tümer, Zeynep, Monk, David, Mackay, Deborah, Grønskov, Karin, Riccio, Andrea, Linglart, Agnès, Maher, Eamonn R

Journal:

Clinical Epigenetics

Year:

2015

Language:

english

File:

PDF, 1.03 MB

english, 2015

46

Beckwith–Wiedemann and Russell–Silver Syndromes

Azzi, Salah, Abi Habib, Walid, Netchine, Irene

Journal:

Current Opinion in Endocrinology Diabetes and Obesity

Year:

2014

Language:

english

File:

PDF, 540 KB

english, 2014

47

Case Report of GNAS Epigenetic Defect Revealed by a Congenital Hypothyroidism

Romanet, P., Osei, L., Netchine, I., Pertuit, M., Enjalbert, A., Reynaud, R., Barlier, A.

Journal:

Year:

2015

Language:

english

File:

PDF, 925 KB

english, 2015

48

Olfactory Anomalies in CHARGE Syndrome: Imaging Findings of a Potential Major Diagnostic Criterion

Blustajn, J., Kirsch, C.F.E., Panigrahy, A., Netchine, I.

Journal:

American Journal of Neuroradiology

Year:

2008

Language:

english

File:

PDF, 132 KB

english, 2008

49

Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development

Netchine, Irène, Azzi, Salah, Houang, Muriel, Seurin, Danielle, Perin, Laurence, Ricort, Jean-Marc, Daubas, Claudine, Legay, Christine, Mester, Jan, Herich, Robert, Godeau, François, Le Bouc, Yves

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 433 KB

english, 2009

50

Prevalence and management of gastrointestinal manifestations in Silver–Russell syndrome

Marsaud, Céline, Rossignol, Sylvie, Tounian, Patrick, Netchine, Irène, Dubern, Béatrice

Journal:

Archives of Disease in Childhood

Year:

2015

Language:

english

File:

PDF, 1.05 MB

english, 2015