Search Results - "Joosse, M."

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    High‐rate volatile fatty acid (VFA) production by a granular sludge process at low pH by Tamis, J., Joosse, B.M., Loosdrecht, M.C.M.van, Kleerebezem, R.

    Published in Biotechnology and bioengineering (01-11-2015)
    “…ABSTRACT Volatile fatty acids (VFA) are proposed platform molecules for the production of basic chemicals and polymers from organic waste streams. In this…”
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    Phenotypic variation in hereditary frontotemporal dementia with tau mutations by Van Swieten, J. C., Stevens, M., Rosso, S. M., Rizzu, P., Joosse, M., De Koning, I., Kamphorst, W., Ravid, R., Spillantini, M. G., Niermeijer, M. F., Heutink, P.

    Published in Annals of neurology (01-10-1999)
    “…Several mutations in the tau gene have been found in families with hereditary frontotemporal dementia and parkinsonism linked to chromosome 17q21‐22 (FTDP‐17)…”
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    Quantitative perimetry under binocular viewing conditions in microstrabismus by Joosse, M.V., Simonsz, H.J., Van Minderhout, H.M., De Jong, P.T.V.M., Noordzij, B., Mulder, P.G.H.

    Published in Vision research (Oxford) (01-10-1997)
    “…In order to elucidate the type, size and depth of suppression scotomata in microstrabismus and small angle convergent strabismus, we performed binocular static…”
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    A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease by BERTOLI AVELLA, A. M, MARCHECO TERUEL, B, LLIBRE RODRIGUEZ, J. J, GOMEZ VIERA, N, BORRAJERO MARTINEZ, I, SEVERIJNEN, E. A, JOOSSE, M, VAN DUIJN, C. M, HEREDERO BAUTE, L, HEUTINK, P

    Published in Neurogenetics (01-10-2002)
    “…We studied a Cuban family with presenile dementia (autosomal dominant) consisting of 281 members within six generations, the proband descended from a Spanish…”
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    P063 Expression of the coinhibitory receptor TIGIT on memory CD4+ T cells is induced by TCR ligation and retinoic acid co-stimulation and is elicited during microbial colonization of the intestine by Barendregt, D, Joosse, M E, van Berkel, L A, van Schoonhoven, A, Samsom, J N

    Published in Journal of Crohn's and colitis (21-01-2022)
    “…Abstract Background The coinhibitory receptor T cell immunoglobulin and ITIM domain (TIGIT) is widely expressed by immune cells, including CD4+ T cells…”
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    Quantitative visual fields under binocular viewing conditions in primary and consecutive divergent strabismus by JOOSSE, M. V, SIMONSZ, H. J, VAN MINDERHOUT, E. M, MULDER, P. G. H, DE JONG, P. T. V. M

    “…Although there have been a number of studies on the size of the suppression scotoma in divergent strabismus, there have been no reports on the full extent…”
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    P045 TIGIT expression differentiates regulatory from inflammatory Th1 gut-homing effector CD4+ T cells in inflammatory bowel disease patients by Heredia, M, Costes, L M M, Tindemans, I, Aardoom, M A, Klomberg, R C W, Kemos, P, Joosse, M E, van Haaften, D H, Tuk, B, Ruemmele, F, Croft, N M, Escher, J C, de Ridder, L, Samsom, J N

    Published in Journal of Crohn's and colitis (21-01-2022)
    “…Abstract Background Crohn’s disease (CD) and ulcerative colitis (UC) are characterized by intestinal infiltration of pathogenic effector CD4+ T cells. The…”
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    Deletion of exon 18 is a frequent mutation in glycogen storage disease type II by Van der Kraan, M, Kroos, M A, Joosse, M, Bijvoet, A G, Verbeet, M P, Kleijer, W J, Reuser, A J

    “…An abnormal 2.3 kb SacI fragment of the human lysosomal alpha-glucosidase gene (GAA) was identified in patients with glycogen storage disease type II. The…”
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    P012 Low frequencies of circulating inhibitory TIGIT+CD38+ effector T cells identify an immunologically distinct subgroup of pediatric patients with severe Crohn’s disease by Heredia, M, Costes, L, Tindemans, I, Aardoom, M, Klomberg, R, Kemos, P, Joosse, M, van Haaften, D, Tuk, B, Ruemmele, F, Croft, N, Escher, J, de Ridder, L, Samsom, J

    Published in Journal of Crohn's and colitis (27-05-2021)
    “…Abstract Background Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is a T cell driven intestinal inflammation…”
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    A novel acid α‐glucosidase mutation identified in a Pakistani family with glycogen storage disease type II by Kroos, M. A., Waitfield, A. E., Joosse, M., Winchester, B., Reuser, A. J. J., MacDermot, K. D.

    Published in Journal of inherited metabolic disease (01-08-1997)
    “…A novel mutation, C118t, in exon 2 of the acid α‐glucosidase gene has been found in an infant with glycogen storage disease type II. This mutation is predicted…”
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    P819 Whole-exome sequencing in early-onset primary sclerosing cholangitis: first results of the WHELP study by Haisma, S-M, Weersma, R, Joosse, M, de Koning, B, de Meij, T, Koot, B, Wolters, V, Norbruis, O, Daly, M, Stevens, C, Xavier, R, Rivas, M, Barbieri, R, Jansen, D, Festen, N, Verkade, H, Visschedijk, M, van Diemen, C

    Published in Journal of Crohn's and colitis (25-01-2019)
    “…Abstract Background Primary sclerosing cholangitis (PSC) is a severe liver disease leading to fibrotic destruction of the bile ducts and ultimately to the need…”
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    The optimal stimulus to elicit suppression in small-angle convergent strabismus by Joosse, M.V., Simonsz, H.J., Spekreijse, H., Mulder, P.G.H., van Minderhout, H.M.

    Published in Strabismus (2000)
    “…PURPOSE: To determine the optimal stimulus duration as well as the most appropriate luminance profile to elicit suppression in small-angle convergent…”
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    Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder by Verkerk, Annemieke J.M.H., Mathews, Carol A., Joosse, Marijke, Eussen, Bert H.J., Heutink, Peter, Oostra, Ben A.

    Published in Genomics (San Diego, Calif.) (01-07-2003)
    “…Gilles de la Tourette syndrome (GTS) is a sporadic or inherited complex neuropsychiatric disorder characterized by involuntary motor and vocal tics. There is…”
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