Relevant bibliographies by topics / Syndrome du nid vide

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  1. Journal articles
  2. Dissertations / Theses
  3. Books

Academic literature on the topic 'Syndrome du nid vide'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Syndrome du nid vide"

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Schaeffer, Jacqueline. "Les séparations intra-psychiques du milieu de la vie et le syndrome du nid vide." Cahiers de psychologie clinique 31, no. 2 (2008): 89. http://dx.doi.org/10.3917/cpc.031.0089.

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D’Amore, Salvatore. "Alcool et Nid Vide." Cahiers critiques de thérapie familiale et de pratiques de réseaux 42, no. 1 (2009): 231. http://dx.doi.org/10.3917/ctf.042.0231.

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3

Coste, A., P. Dessi, and E. Serrano. "Syndrome du nez vide." Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale 129, no. 2 (2012): 116–21. http://dx.doi.org/10.1016/j.aforl.2012.02.009.

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4

Geijer, Justin R., Heidi I. Stanish, Christopher C. Draheim, and Donald R. Dengel. "Bone Mineral Density in Adults With Down Syndrome, Intellectual Disability, and Nondisabled Adults." American Journal on Intellectual and Developmental Disabilities 119, no. 2 (2014): 107–14. http://dx.doi.org/10.1352/1944-7558-119.2.107.

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Abstract Individuals with intellectual disability (ID) or Down syndrome (DS) may be at greater risk of osteoporosis. The purpose of this study was to compare bone mineral density (BMD) of DS, ID, and non–intellectually disabled (NID) populations. In each group, 33 participants between the ages of 28 and 60 years were compared. BMD was measured with dual-energy x-ray absorptiometry (DXA) scans. BMD (p < .0001) between all groups was significantly different. Participants with DS had significantly lower BMD compared to NID participants. Individuals with ID had significantly lower BMD compared to NID subjects. Participants with DS had the lowest BMD of all groups. DS subjects display a greater risk for osteoporosis than ID subjects or control populations.
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5

Kruusvee, Valdeko, Matthew J. Lyst, Ceitidh Taylor, Žygimantė Tarnauskaitė, Adrian P. Bird, and Atlanta G. Cook. "Structure of the MeCP2–TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders." Proceedings of the National Academy of Sciences 114, no. 16 (2017): E3243—E3250. http://dx.doi.org/10.1073/pnas.1700731114.

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Rett syndrome (RTT) is an X-linked neurological disorder caused by mutations in the methyl-CpG–binding protein 2 (MeCP2) gene. The majority of RTT missense mutations disrupt the interaction of the MeCP2 with DNA or the nuclear receptor corepressor (NCoR)/silencing mediator of retinoic acid and thyroid receptors (SMRT) corepressor complex. Here, we show that the “NCoR/SMRT interaction domain” (NID) of MeCP2 directly contacts transducin beta-like 1 (TBL1) and TBL1 related (TBLR1), two paralogs that are core components of NCoR/SMRT. We determine the cocrystal structure of the MeCP2 NID in complex with the WD40 domain of TBLR1 and confirm by in vitro and ex vivo assays that mutation of interacting residues of TBLR1 and TBL1 disrupts binding to MeCP2. Strikingly, the four MeCP2-NID residues mutated in RTT are those residues that make the most extensive contacts with TBLR1. Moreover, missense mutations in the gene for TBLR1 that are associated with intellectual disability also prevent MeCP2 binding. Our study therefore reveals the molecular basis of an interaction that is crucial for optimal brain function.
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6

Lahlou, A., F. Aziouaz, N. Boufaida, H. El Ouahabi, and F. Ajdi. "Le syndrome de selle turcique vide." Annales d'Endocrinologie 76, no. 4 (2015): 391. http://dx.doi.org/10.1016/j.ando.2015.07.286.

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7

Lahmamssi, F. Z., L. Elazizi, H. Salhi, and H. El Ouahabi. "Le syndrome de selle turcique vide." Annales d'Endocrinologie 82, no. 5 (2021): 362. http://dx.doi.org/10.1016/j.ando.2021.08.303.

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8

Rod, A., L. Chiche, V. Rouleau, et al. "P2-103 - Tumeur hépatique en nid et syndrome de Cushing." Annales d'Endocrinologie 67, no. 5 (2006): 510. http://dx.doi.org/10.1016/s0003-4266(06)72934-1.

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9

Haddad, S., M. Mahfoudhi, M. Eleuch, S. Turki, and T. Ben Abdallah. "Syndrome de selle turcique vide : une présentation atypique." Annales d'Endocrinologie 79, no. 4 (2018): 352. http://dx.doi.org/10.1016/j.ando.2018.06.487.

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10

Volken, Henri. "Le syndrome du précipice. La peur du vide symbolique." Revue européenne des sciences sociales, no. XXXVIII-119 (December 1, 2000): 23–33. http://dx.doi.org/10.4000/ress.670.

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Dissertations / Theses on the topic "Syndrome du nid vide"

1

RONGIER, CATHERINE. "Frequence et pathogenie des selles turciques vides de l'adulte : a propos de 25 observations." Clermont-Ferrand 1, 1988. http://www.theses.fr/1988CLF13010.

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2

DUFLOT, ELISABETH. "La selle turcique vide chez la personne agee : a propos de 2 observations personnelles." Lille 2, 1988. http://www.theses.fr/1988LIL2M140.

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3

Dupont, Nathalie. "Le syndrome de la selle turcique vide primitive : analyse de 40 observations a la martinique." Lyon 1, 1993. http://www.theses.fr/1993LYO1M318.

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4

Villain, Max. "Neuropathies optiques et syndrome de la selle turcique vide primitive : éléments diagnostiques et thérapeutiques, à propos de six observations." Montpellier 1, 1992. http://www.theses.fr/1992MON11068.

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Books on the topic "Syndrome du nid vide"

1

Mais pourquoi tu veux déjà quitter ta mère?, ou, Le syndrome du nid vide. Ramsay, 2003.

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Journal articles
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