Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Merav Burg"'
Autor:
Miri Keren, Omri Weisman, Merav Burg-Malki, Ronny Geva, Gil Diesendruck, Ruth Feldman, Doron Gothelf
Publikováno v:
Journal of Intellectual Disability Research. 61:1083-1093
Background Numerous studies have assessed the socio-cognitive profile in Williams syndrome (WS) and, independently, in 22q11.2 deletion syndrome (22q11.2DS). Yet, a cross-syndrome comparison of these abilities between individuals with these two syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4978ccb3595968f1612d7f5d853d18aa
https://doi.org/10.1111/jir.12424
https://doi.org/10.1111/jir.12424
Autor:
Doron Gothelf, Ronny Geva, Gil Diesendruck, Ruth Feldman, Merav Burg-Malki, Miri Keren, Omri Weisman
Publikováno v:
Journal of autism and developmental disorders. 45(8)
Mother-child interactions in 22q11.2 Deletion syndrome (22q11.2DS) and Williams syndrome (WS) were coded for maternal sensitivity/intrusiveness, child's expression of affect, levels of engagement, and dyadic reciprocity. WS children were found to exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a8d526506acd8cedc35a20581b4b47c
https://pubmed.ncbi.nlm.nih.gov/25791124
https://pubmed.ncbi.nlm.nih.gov/25791124
Autor:
Gadi Presburger, Doron Gothelf, Abrahahm Weizman, Alan Apter, Merav Burg, Ariela Nahmani, Yehuda Finkelstein, Leonard C. Blieden, Michael Berant, Darya Levy, Amos Frisch
Publikováno v:
Scopus-Elsevier
Velocardiofacial syndrome (VCFS) is a relatively common developmental neuropsychiatric syndrome caused by a 22q11 microdeletion. There is an extensive variability in the phenotypic expression of this disease. The most common psychiatric disorder in V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec99ece9b8ba86d88e34f6fa30a2cc02
https://doi.org/10.1002/ajmg.b.20144
https://doi.org/10.1002/ajmg.b.20144
Autor:
Alan Apter, Inbar Dotan, Merav Burg, Abraham Weizman, Gadi Presburger, Dov Inbar, Ayelet Brand-Gothelf, Reut Gruber, Amos Frisch, Doron Gothelf, Tamar Steinberg
Publikováno v:
The Journal of Clinical Psychiatry. 64:1163-1169
Background Velocardiofacial syndrome (VCFS) is a common microdeletion syndrome associated with psychiatric morbidity and developmental disabilities. Although attention-deficit/hyperactivity disorder (ADHD) is the most common psychiatric problem assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e6baa78e857f806961709c0d0ec619a
https://doi.org/10.4088/jcp.v64n1004
https://doi.org/10.4088/jcp.v64n1004
Autor:
Merav Burg-Malki, Doron Gothelf, Omri Weisman, Ronny Geva, Gil Diesendruck, Ruth Feldman, Miri Keren
Publikováno v:
European Neuropsychopharmacology. 27:S605
Background Numerous studies have assessed the socio-cognitive profile in Williams syndrome (WS) and, independently, in 22q11.2 deletion syndrome (22q11.2DS). Yet, a cross-syndrome comparison of these abilities between individuals with these two syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deeebb284813e16c114c20df0c4794ac
https://doi.org/10.1016/s0924-977x(17)31151-3
https://doi.org/10.1016/s0924-977x(17)31151-3
Autor:
Abraham Weizman, Doron Gothelf, Tamar Steinberg, Miri Carmel, Alan Apter, Michael Korostishevsky, Amos Frisch, Elena Michaelovsky, Dov Inbar, Merav Burg
Publikováno v:
The international journal of neuropsychopharmacology. 11(3)
The 22q11.2 deletion syndrome (22q11.2DS) is the most common hemizygous deletion syndrome in humans. In addition to a wide range of physical abnormalities 22q11.2DS subjects show high prevalence of several psychiatric disorders. In our previous study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edae70aaf2ef4996b578b430012f8a9d
https://pubmed.ncbi.nlm.nih.gov/17949513
https://pubmed.ncbi.nlm.nih.gov/17949513
Autor:
Muhammad Mahajnah, Gil Zalsman, Abraham Weizman, Ayala Aviram-Goldring, Tami Steinberg, D. Gothelf, Amos Frisch, Merav Burg, Shmuel Fennig
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 114(11)
Velocardiofacial syndrome (VCFS) is characterized by both physical manifestations and neuropsychiatric disabilities. About 6–28% of cases are familial. The aim of the present study was to compare the clinical characteristics of subjects with famili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ef0f289771179a5b0a5fe8f65ae982b
https://pubmed.ncbi.nlm.nih.gov/17557124
https://pubmed.ncbi.nlm.nih.gov/17557124
Autor:
Josepha Yeshaya, Moshe Frydman, Alan Apter, Ada H. Zohar, Elena Michaelovsky, Abraham Weizman, Gadi Presburger, Michael Korostishevsky, Ayala Aviram-Goldring, Mordechai Shohat, Amos Frisch, Doron Gothelf, Merav Burg
Publikováno v:
The international journal of neuropsychopharmacology. 10(3)
Velocardiofacial syndrome (VCFS) is caused by a microdeletion in chromosome 22 and is a risk factor for the development of schizophrenia and other psychiatric disorders. The catechol- O -methyltransferase ( COMT ), residing in the 22q11.2 microdeleti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e58dadf35f5b32f32f60b8789a1c3de
https://pubmed.ncbi.nlm.nih.gov/16734939
https://pubmed.ncbi.nlm.nih.gov/16734939
Autor:
Moshe Frydman, Josepha Yeshaya, Alan Apter, Ada H. Zohar, Ariela Nahmani, Mordechai Shohat, Merav Burg, Abraham Weizman, Tamar Steinberg, Dov Inbar, Gadi Presburger, Yehuda Finkelstein, Ayala Aviram-Goldring, Doron Gothelf, Amos Frisch
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)
The study of neurogenetic microdeletion syndromes provides an insight into the developmental psychopathology of psychiatric disorders. The aim of the study was to evaluate the prevalence of psychiatric disorders, especially obsessive-compulsive disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51e92f7fd4665a138238c187b6c371b2
https://pubmed.ncbi.nlm.nih.gov/15048657
https://pubmed.ncbi.nlm.nih.gov/15048657
Autor:
Doron Gothelf, Elena Michaelovsky, Amos Frisch, Ada H. Zohar, Gadi Presburger, Merav Burg, Ayala Aviram-Goldring, Moshe Frydman, Josepha Yeshaya, Mordechai Shohat, Michael Korostishevsky, Alan Apter, Abraham Weizman
Publikováno v:
International Journal of Neuropsychopharmacology; Jun2007, Vol. 10 Issue 3, p301-308, 8p