Zobrazeno 101 - 110
of 2 031
pro vyhledávání: '"Mendlewicz J"'
K L Kahlbaum published in 1874 the first recorded description of catatonia. Akinetic catatonia is now defined as a neuropsychiatric syndrome principally characterised by akinesia, mutism, stupor, and catalepsy.1 Even if some advances have been made i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cd1c6c129a5f4242695d11f10de9b4
https://europepmc.org/articles/PMC1738544/
https://europepmc.org/articles/PMC1738544/
Autor:
Mandelli, L., Serretti, A., Souery, D., Mendlewicz, J., Kasper, S., Montgomery, S., Zohar, J.
Publikováno v:
In European Neuropsychopharmacology October 2016 26 Supplement 2:S468-S468
Autor:
Bartova, L., Dold, M., Kautzky, A., Rabl, U., Souery, D., Mendlewicz, J., Porcelli, S., Serretti, A., Zohar, J., Montgomery, S., Kasper, S.
Publikováno v:
In European Neuropsychopharmacology October 2016 26 Supplement 2:S417-S418
Publikováno v:
Europe PubMed Central
The Department of Psychiatry was first opened in April 1978. It is one of the largest sector of the hospital and contains 90 beds including a sleep laboratory and an adolescent unit. The clinical activities are broad and multidisciplinary, including
The co-segregation in one pedigree of bipolar affective disorder with Darier’s disease whose gene is on chromosome 12q23-q24.1, and findings from linkage and association studies with the neighbouring gene of phospholipase A2 (PLA2) indicate that PL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::1b61240e5eb4c5ccb7291ddfbf65147d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084749
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084749
Autor:
Goossens, D., van Gestel, S., Claes, Stephan, De Rijk, Peter, Souery, D., Massat, I., Van den Bossche, Dirk, Backhovens, H., Mendlewicz, J., Van Broeckhoven, Christine, Del-Favero, Jurgen
Publikováno v:
Molecular psychiatry
Autor:
Segurado, R., Detera-Wadleigh, S.D., Levinson, D.F., Lewis, C.M., Gill, M., Nurnberger, J.I., Craddock, N., DePaulo, J.R., Baron, M., Gershon, E.S., Ekholm, J., Cichon, S., Turecki, G., Claes, S., Kelsoe, J.R., Schofield, P.R., Badenhop, R.F., Morissette, J., Coon, H., Blackwood, D., McInnes, L.A., Foroud, T., Edenberg, H.J., Reich, T., Rice, J.P., Goate, A., McInnis, M.G., McMahon, F.J., Badner, J.A., Goldin, L.R., Bennett, P., Willour, V.L., Zandi, P.P., Liu, J., Gilliam, C., Juo, S.H., Berrettini, W.H., Yoshikawa, T., Peltonen, L., Lonnqvist, J., Nothen, M.M., Schumacher, J., Windemuth, C., Rietschel, M., Propping, P., Maier, W., Alda, M., Grof, P., Rouleau, G.A., Del-Favero, J., Van Broeckhoven, C., Mendlewicz, J., Adolfsson, R., Spence, M.A., Luebbert, H., Adams, L.J., Donald, J.A., Mitchell, P.B., Barden, N., Shink, E., Byerley, W., Muir, W., Visscher, P.M., Macgregor, S., Gurling, H., Kalsi, G., McQuillin, A., Escamilla, M.A., Reus, V.I., Leon, P., Freimer, N.B., Ewald, H., Kruse, T.A., Mors, O., Radhakrishna, U., Blouin, J.L., Antonarakis, S.E., Akarsu, N.
Publikováno v:
Segurado, R, Detera-Wadleigh, S D, Levinson, D F, Lewis, C M, Gill, M, Nurnberger, J I, Craddock, N, DePaulo, J R, Baron, M, Gershon, E S, Ekholm, J, Cichon, S, Turecki, G, Claes, S, Kelsoe, J R, Schofield, P R, Badenhop, R F, Morissette, J, Coon, H, Blackwood, D, McInnes, L A, Foroud, T, Edenberg, H J, Reich, T, Rice, J P, Goate, A, McInnis, M G, McMahon, F J, Badner, J A, Goldin, L R, Bennett, P, Willour, V L, Zandi, P P, Liu, J, Gilliam, C, Juo, S H, Berrettini, W H, Yoshikawa, T, Peltonen, L, Lonnqvist, J, Nothen, M M, Schumacher, J, Windemuth, C, Rietschel, M, Propping, P, Maier, W, Alda, M, Grof, P, Rouleau, G A, Del-Favero, J, Van Broeckhoven, C, Mendlewicz, J, Adolfsson, R, Spence, M A, Luebbert, H, Adams, L J, Donald, J A, Mitchell, P B, Barden, N, Shink, E, Byerley, W, Muir, W, Visscher, P M, Macgregor, S, Gurling, H, Kalsi, G, McQuillin, A, Escamilla, M A, Reus, V I, Leon, P, Freimer, N B, Ewald, H, Kruse, T A, Mors, O, Radhakrishna, U, Blouin, J L, Antonarakis, S E & Akarsu, N 2003, ' Genome scan meta-analysis of schizophrenia and bipolar disorder, part III : Bipolar disorder ', American Journal of Human Genetics, vol. 73(1), pp. 49-62 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::77fdc3543bbec047f034e986725ffcda
https://portal.findresearcher.sdu.dk/da/publications/1ee73b00-6fd1-11db-81a9-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/1ee73b00-6fd1-11db-81a9-000ea68e967b
We report here a case-control association study with T102C polymorphism in the serotonin 2A receptor gene (HTR2A) in patients affected by unipolar affective disorder (UPAD) and in controls. A total of 284 subjects were genotyped (142 UPAD and 142 con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e49056a6de13d78c3200ecb9450e6bb7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084421
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084421
Autor:
Del-Favero, J., Gestel, S.V., Borglum, A.D., Muir, W. , Ewald, H., Mors, O., Ivezić, Slađana, Oruč, Lilijana, Adolfsson, R., Blackwood, D., Kruse, T., Mendlewicz, J., Schalling, M., Van Broeckhoven, C.
Several groups have reported association between large CAG/CTG repeats in the genome and BP disorder using the Repeat Expansion Detection (RED) method. Molecular interpretation studies demonstrated that around 90% of the large CAG/CTG repeats detecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::0af9e9fba06b92a0582e24a137d03bd4
https://www.bib.irb.hr/238734
https://www.bib.irb.hr/238734