Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Yoav Kohn"'
Autor:
Asael Lubotzky, Ilana Pelov, Ronen Teplitz, Daniel Neiman, Adama Smadja, Hai Zemmour, Sheina Piyanzin, Bracha-Lea Ochana, Kirsty L Spalding, Benjamin Glaser, Ruth Shemer, Yuval Dor, Yoav Kohn
Publikováno v:
eLife, Vol 11 (2022)
Schizophrenia is a common, severe, and debilitating psychiatric disorder. Despite extensive research there is as yet no biological marker that can aid in its diagnosis and course prediction. This precludes early detection and intervention. Imaging st
Externí odkaz:
https://doaj.org/article/99c557cbe6234e8c8dd6f08840d16183
Autor:
Yoav Kohn, Amir Shmueli
Publikováno v:
Israel Journal of Health Policy Research, Vol 9, Iss 1, Pp 1-7 (2020)
Abstract Background In 2015, mental health services were added to the Israeli National Health Insurance package of services. As such, these services are financed by the budget which is allocated to the Health Plans according to a risk adjustment sche
Externí odkaz:
https://doaj.org/article/994dfa1d65994fb1b391ea7dec5740e9
Publikováno v:
Israel Journal of Health Policy Research, Vol 8, Iss 1, Pp 1-3 (2019)
Abstract Recently, Miodownik et al. reported in this journal the results of a study on seclusion and mechanical restraint of psychiatric patients in Israel (Isr J Health Policy Res 8:9, 2019). The study was a retrospective examination over a year of
Externí odkaz:
https://doaj.org/article/7e256759a5b644a7a3d3a4e7e4a26af4
Autor:
Anna Alkelai, Lior Greenbaum, Sara Lupoli, Yoav Kohn, Kyra Sarner-Kanyas, Edna Ben-Asher, Doron Lancet, Fabio Macciardi, Bernard Lerer
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29228 (2012)
Many reports in different populations have demonstrated linkage of the 10q24-q26 region to schizophrenia, thus encouraging further analysis of this locus for detection of specific schizophrenia genes. Our group previously reported linkage of the 10q2
Externí odkaz:
https://doaj.org/article/8ae2aa725ab54667b0d6e4323167704c
Autor:
Anna Alkelai, Lior Greenbaum, Shahar Shohat, Gundula Povysil, Ayan Malakar, Zhong Ren, Joshua E. Motelow, Tanya Schechter, Benjamin Draiman, Eti Chitrit-Raveh, Daniel Hughes, Vaidehi Jobanputra, Sagiv Shifman, David B. Goldstein, Yoav Kohn
Publikováno v:
Schizophrenia Research. 252:138-145
Autor:
Sagit Israeli, Ilya Kagan, Sarit Yerushalmi, Sophi Gelman, Inbal Yarkoni, Larisa Levitan, Daniel Argo, Yoav Kohn
Publikováno v:
Journal of child and adolescent psychiatric nursing : official publication of the Association of Child and Adolescent Psychiatric Nurses, Inc.
Autor:
Tomer Levy, Miriam Peskin, Yoav Kohn, Sapir Sheinhorn, Gila Schoen, Abraham Weizman, Pavel Golubchik
Publikováno v:
Clinical child psychology and psychiatry. 27(4)
Background: Attention-deficit/hyperactivity disorder (ADHD) is associated with increased risk for conduct problems (CP), as well as with callous-unemotional traits (CUt) and lower accuracy in face emotional recognition (FER). It is unclear, however,
Autor:
Ilana Pelov, Asael Lubotzky, Ronen Teplitz, Daniel Neiman, Adama Smadja, Hai Zemmour, Sheina Piyanzin, Bracha-Lea Ochana, Kirsty L Spalding, Benjamin Glaser, Ruth Shemer, Yuval Dor, Yoav Kohn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95227507a15d80a6825acd329889bc16
https://doi.org/10.7554/elife.76391.sa2
https://doi.org/10.7554/elife.76391.sa2
Publikováno v:
Sexes. 1:32-38
The prevalence of children and adolescents who identify themselves as transgender is significant. Transgender youth are at a high risk for mental health problems, sometimes requiring hospitalization in a psychiatric ward. This situation is specifical
Autor:
Yoav Kohn, Neha Dagaonkar, Shlomit Rienstein, David Goldstein, Shahar Shohat, Eti Chitrit-Raveh, Erin L. Heinzen, Vimla S. Aggarwal, Sagiv Shifman, Anna Alkelai, Tanya Schechter, Daniel Hughes, Benjamin Draiman, Lior Greenbaum
Publikováno v:
Journal of Human Genetics. 66:339-343
Childhood-onset schizophrenia (COS) is a rare form of schizophrenia with an onset before 13 years of age. There is rising evidence that genetic factors play a major role in COS etiology, yet, only a few single gene mutations have been discovered. Her