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1
Material Type:
Vídeo
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Toutes les nuits Todas as noites

Eugene Green; Alain Bellon; Anny Romand; Claude Bonnefoy; Olivier Trémolet; Raphael O'Byrne; Emmanuelle Baude; Charlotte Teillar D'Eyry; Frédéric de Ravignan; Olivier Laurent; Adeline Caron; Brigitte Laurendeau; Pierre Bouillon; Cristina Baraldi; Alexis Loret; Adrien Michaux; Christelle Prot; Anna Bielecka; Claude Merlin; Xavier Denamur; Laurène Cheilan

França Ellabel Productions produção 2001

Localização: ECA - Escola de Comunicações e Artes    (DVD3411 )(Acessar)

2
One NF1 Mutation may Conceal Another
Material Type:
Artigo
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One NF1 Mutation may Conceal Another

Pacot, Laurence ; Burin des Roziers, Cyril ; Laurendeau, Ingrid ; Briand-Suleau, Audrey ; Coustier, Audrey ; Mayard, Théodora ; Tlemsani, Camille ; Faivre, Laurence ; Thomas, Quentin ; Rodriguez, Diana ; Blesson, Sophie ; Dollfus, Hélène ; Muller, Yvon-Gauthier ; Parfait, Béatrice ; Vidaud, Michel ; Gilbert-Dussardier, Brigitte ; Yardin, Catherine ; Dauriat, Benjamin ; Derancourt, Christian ; Vidaud, Dominique ; Pasmant, Eric

Genes, 2019-08, Vol.10 (9), p.633 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
Severe Phenotype in Patients with Large Deletions of NF1
Material Type:
Artigo
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Severe Phenotype in Patients with Large Deletions of NF1

Pacot, Laurence ; Vidaud, Dominique ; Sabbagh, Audrey ; Laurendeau, Ingrid ; Briand-Suleau, Audrey ; Coustier, Audrey ; Maillard, Théodora ; Barbance, Cécile ; Morice-Picard, Fanny ; Sigaudy, Sabine ; Glazunova, Olga ; Damaj, Lena ; Layet, Valérie ; Quelin, Chloé ; Gilbert-Dussardier, Brigitte ; Audic, Frédérique ; Dollfus, Hélène ; Guerrot, Anne-Marie ; Lespinasse, James ; Julia, Sophie ; Vantyghem, Marie-Christine ; Drouard, Magali ; Lackmy, Marilyn ; Leheup, Bruno ; Alembik, Yves ; Lemaire, Alexia ; Nitschké, Patrick ; Petit, Florence ; Dieux Coeslier, Anne ; Mutez, Eugénie ; Taieb, Alain ; Fradin, Mélanie ; Capri, Yline ; Nasser, Hala ; Ruaud, Lyse ; Dauriat, Benjamin ; Bourthoumieu, Sylvie ; Geneviève, David ; Audebert-Bellanger, Séverine ; Nizon, Mathilde ; Stoeva, Radka ; Hickman, Geoffroy ; Nicolas, Gaël ; Mazereeuw-Hautier, Juliette ; Jannic, Arnaud ; Ferkal, Salah ; Parfait, Béatrice ; Vidaud, Michel ; Wolkenstein, Pierre ; Pasmant, Eric

Cancers, 2021-06, Vol.13 (12), p.2963 [Periódico revisado por pares]

Basel: MDPI AG

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4
Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities
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Artigo
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Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities

Gilbert-Dussardier, Brigitte ; Briand-Suleau, Audrey ; Laurendeau, Ingrid ; Bilan, Frédéric ; Cavé, Hélène ; Verloes, Alain ; Vidaud, Michel ; Vidaud, Dominique ; Pasmant, Eric

Orphanet journal of rare diseases, 2016-07, Vol.11 (1), p.101-101, Article 101 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)
Material Type:
Artigo
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Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)

BAHUAU, MICHEL ; LAURENDEAU, INGRID ; PELET, ANNA ; ASSOULINE, BRIGITTE ; LAMIREAU, THIERRY ; TAINE, LAURENCE ; LE BAIL, BRIGITTE ; VERGNES, PIERRE ; GALLET, SERGE ; VIDAUD, MICHEL ; LYONNET, STANISLAS ; LACOMBE, DIDIER ; VIDAUD, DOMINIQUE

Journal of medical genetics, 2000-02, Vol.37 (2), p.146-150 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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6
Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia typeB (INDB)
Material Type:
Artigo
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Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia typeB (INDB)

BAHUAU, MICHEL ; LAURENDEAU, INGRID ; PELET, ANNA ; ASSOULINE, BRIGITTE ; LAMIREAU, THIERRY ; TAINE, LAURENCE ; LE BAIL, BRIGITTE ; VERGNES, PIERRE ; GALLET, SERGE ; VIDAUD, MICHEL ; LYONNET, STANISLAS ; LACOMBE, DIDIER ; VIDAUD, DOMINIQUE

Journal of medical genetics, 2000-02, Vol.37 (2), p.146 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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7
Additional file 1: Table S1. of Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities
Material Type:
Dataset
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Additional file 1: Table S1. of Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities

Gilbert-Dussardier, Brigitte ; Briand-Suleau, Audrey ; Laurendeau, Ingrid ; Bilan, Frédéric ; Cavé, Hélène ; Verloes, Alain ; Vidaud, Michel ; Vidaud, Dominique ; Pasmant, Eric

Figshare 2016

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8
La linguistique insatisfaite
Material Type:
Artigo
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La linguistique insatisfaite

Elimam, Abdou ; Lafont, Robert ; Laurendeau, Paul ; Nussbaum, Luci ; Puig i Moreno, Gentil ; Schlieben-Lange, Brigitte ; Schwartz, Yves

Cahiers de praxématique, 1990

Presses universitaires de la Méditerranée

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Deste Autor:

  1. Green, E
  2. Caron, A
  3. Laurendeau, B
  4. Laurent, O
  5. Ravignan, F

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