Search Results - "BARGE, D"

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    Reduced Stress-Sensitivity or Increased Reward Experience: The Psychological Mechanism of Response to Antidepressant Medication by WICHERS, M. C, BARGE-SCHAAPVELD, D. Q. C. M, NICOLSON, N. A, PEETERS, F, DE VRIES, M, MENGELERS, R, VAN OS, J

    Published in Neuropsychopharmacology (New York, N.Y.) (01-03-2009)
    “…Depression has often been associated with increased negative affect reactivity to stress (Stress-Sensitivity) and reduced capacity to experience pleasure or…”
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    Journal Article
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    Low thermal budget for Si and SiGe surface preparation for FD-SOI technology by Labrot, M., Cheynis, F., Barge, D., Müller, P., Juhel, M.

    Published in Applied surface science (15-05-2016)
    “…Epitaxy of Si or SiGe on Si substrates needs perfectly cleaned substrates. When bulk substrates can be cleaned at high temperature, FD-SOI substrates must be…”
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    Journal Article
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    Improvement of etching and cleaning methods for integration of raised source and drain in FD-SOI technologies by Labrot, M., Cheynis, F., Barge, D., Maury, P., Juhel, M., Lagrasta, S., Müller, P.

    Published in Microelectronic engineering (05-08-2017)
    “…The Fully-Depleted Silicon-on-Insulator (FD-SOI) technology for advanced CMOS devices is based on SOI substrates formed by an ultra-thin Si or SiGe film on a…”
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    Journal Article
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    Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome? by van der Werf - ’t Lam, A.S., van Haeringen, A., Rinnen, T., Robles de Medina, R.M., Wilde, A.A.M., Hennekam, R.C., Barge - Schaapveld, D.Q.C.M.

    Published in European journal of medical genetics (01-01-2022)
    “…Andersen-Tawil syndrome (ATS) and Noonan syndrome (NS) are both autosomal dominantly inherited disorders that share anomalies in the same body systems, i.e…”
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    Journal Article
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    Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome by Gennery, A.R, Slatter, M.A, Rice, J, Hoefsloot, L.H, Barge, D, McLean-Tooke, A, Montgomery, T, Goodship, J.A, Burt, A.D, Flood, T.J, Abinun, M, Cant, A.J, Johnson, D

    Published in Clinical and experimental immunology (01-07-2008)
    “…More than 11 genetic causes of severe combined immunodeficiency (SCID) have been identified, affecting development and/or function of T lymphocytes, and…”
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    Journal Article
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    Flow Cytometric Analysis of TCR Vβ Repertoire in Patients with 22q11.2 Deletion Syndrome by McLean‐Tooke, A., Barge, D., Spickett, G. P., Gennery, A. R.

    Published in Scandinavian journal of immunology (01-06-2011)
    “…In 22q11.2 deletion patients, the normal decrease in T lymphocyte counts after 1–2 years is blunted such that relatively T lymphocyte numbers increase over…”
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    Journal Article
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    Intrasinus Catheter-Directed Heparin Infusion in the Treatment of Dural Venous Sinus Thrombosis by La Barge, D.V., III, Bishop, F.S, Stevens, E.A, Eskandari, R, Schmidt, R.H, Skalabrin, E.J, Ng, P.P

    Published in American journal of neuroradiology : AJNR (01-10-2009)
    “…In this small series, local intrasinus catheter-directed heparin infusion with or without balloon thrombectomy was safe in the treatment of dural venous sinus…”
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    Journal Article
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    Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome by Gennery, A R, Barge, D, O'Sullivan, J J, Flood, T J, Abinun, M, Cant, A J

    Published in Archives of disease in childhood (01-06-2002)
    “…Background: Although severe T cell immunodeficiency in DiGeorge anomaly is rare, previous studies of humoral function in these patients have found no antibody…”
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    Journal Article
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    Sphenoidal Electrode Placement Using Biplane Fluoroscopy and Rotational Flat Panel CT Imaging by La Barge, D.V., III, Ng, P.P, Stevens, E.A

    Published in American journal of neuroradiology : AJNR (01-10-2009)
    “…Assessment of otherwise occult seizure foci arising from the anterior mesial temporal region occasionally necessitates placement of sphenoidal electrodes…”
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    Journal Article
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    Lymphocyte subsets in term and significantly preterm UK infants in the first year of life analysed by single platform flow cytometry by Berrington, J. E., Barge, D., Fenton, A. C., Cant, A. J., Spickett, G. P.

    Published in Clinical and experimental immunology (01-05-2005)
    “…Summary This observational study describes the ranges observed for lymphocyte subsets for significantly preterm infants (<32 weeks) in the first year of life,…”
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    Journal Article
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    Single centre experience of umbilical cord stem cell transplantation for primary immunodeficiency by BHATTACHARYA, A, SLATTER, M. A, CHAPMAN, C. E, BARGE, D, JACKSON, A, FLOOD, T. J, ABINUN, M, CANT, A. J, GENNERY, A. R

    Published in Bone marrow transplantation (Basingstoke) (01-08-2005)
    “…Primary immunodeficiencies (PID) are an important cause of childhood mortality. Haematopoietic stem cell transplantation (HSCT) is the best treatment for many…”
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    14nm FDSOI upgraded device performance for ultra-low voltage operation by Weber, O., Josse, E., Mazurier, J., Degors, N., Chhun, S., Maury, P., Lagrasta, S., Barge, D., Manceau, J.-P, Haond, M.

    “…A performance upgrade of our 14nm FDSOI technology is reported in this paper. Compared to our previous 14nm FDSOI assessment, a -17% delay at the same leakage…”
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    Conference Proceeding Journal Article
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    T cell receptor Vβ repertoire of T lymphocytes and T regulatory cells by flow cytometric analysis in healthy children by McLean-Tooke, A, Barge, D, Spickett, G.P, Gennery, A.R

    Published in Clinical and experimental immunology (01-01-2008)
    “…Evaluation of the T cell receptor (TCR) Vβ repertoire by flow cytometric analysis has been used for studying the T cell compartments for diseases in which T…”
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    Journal Article
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    The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia by Gennery, A.R., Slatter, M.A., Bhattacharya, A., Barge, D., Haigh, S., O'Driscoll, M., Coleman, R., Abinun, M., Flood, T.J., Cant, A.J., Jeggo, P.A.

    Published in Clinical immunology (Orlando, Fla.) (01-11-2004)
    “…Fanconi anemia (FA), an autosomal recessive chromosomal instability syndrome, is characterized clinically by developmental abnormalities, growth retardation,…”
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    Journal Article
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    Nanowell Field-Effect Transistors for Highly Sensitive Molecular Detection by Liu, L., Santermans, S., Barge, D., Delport, J., Chaudhuri, A. Ray, Willems, K., Ha, S., Severi, S., Van Dorpe, P., Martens, K.

    “…We report a novel, highly sensitive bio-molecular sensor device, a nanowell FET. Its unique structure contains a 25 nm size nanowell in the center of a 35-40…”
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    Conference Proceeding