Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Timothy Gofine"'
Autor:
Brianna Barsanti-Innes, Jessica Suddaby, Hanna Faghfoury, Joyce So, Timothy Gofine, Venuja Sriretnakumar
Publikováno v:
Can J Psychiatry
Objective:There is a paucity of literature on genetic diagnosis in psychiatric populations, particularly the vulnerable population of patients with concomitant neurodevelopmental disorder (NDD). In this cross-sectional study, we investigated the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aec1b74c005255477cade2f0a4060b15
https://doi.org/10.1177/0706743720931234
https://doi.org/10.1177/0706743720931234
Autor:
Beverly Guttman, Laurene Sellers, Lezlee Lindzon, Peter Szatmari, Timothy Gofine, Rosie Smith, Tracy Nejm, Anne S. Bassett, Mary Secco, Bernard Lawless, O. Carter Snead, Mary Pat McAndrews, Ayman Hassan, Peter Camfield, Danielle M. Andrade, Marie Slegr, Lisa Graves, Maya Guttman-Slater, Berge A. Minassian, Lysa Boissé Lomax, Rima Nabbout, Michelle Shapiro, Dolly Menna-Dack, Eyal Cohen, Megan Henze, Esther Bui, Jon Greenaway, Janice Mulligan, Anastasia Vogt, Sharon Whiting, Guida Quaglia Clozza, Miriam Kaufman, Felippe Borlot, Leeping Tao, Eduard Bercovici, Hannah Lee
Publikováno v:
Epilepsia. 58(9)
The transition from a pediatric to adult health care system is challenging for many youths with epilepsy and their families. Recently, the Ministry of Health and Long-Term Care of the Province of Ontario, Canada, created a transition working group (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50fa5d823d6f5bdf250f7ea2131e3bfb
https://pubmed.ncbi.nlm.nih.gov/28681381
https://pubmed.ncbi.nlm.nih.gov/28681381
Publikováno v:
European journal of medical genetics. 58(11)
Background Interstitial deletions at chromosome 8q22.2-q22.3 have been rarely reported in the literature. To date, six patients have been described in the literature with deletions varying in size from 1.36 Mb to 6.44 Mb. These patients range in age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da054228f3370135a1266562d112fa1e
https://pubmed.ncbi.nlm.nih.gov/26455667
https://pubmed.ncbi.nlm.nih.gov/26455667
Autor:
So, Joyce, Sriretnakumar, Venuja, Suddaby, Jessica, Barsanti-Innes, Brianna, Faghfoury, Hanna, Gofine, Timothy
Publikováno v:
Canadian Journal of Psychiatry; Dec2020, Vol. 65 Issue 12, p865-873, 9p
Autor:
Andrade, Danielle M., Bassett, Anne S., Bercovici, Eduard, Borlot, Felippe, Bui, Esther, Camfield, Peter, Clozza, Guida Quaglia, Cohen, Eyal, Gofine, Timothy, Graves, Lisa, Greenaway, Jon, Guttman, Beverly, Guttman‐Slater, Maya, Hassan, Ayman, Henze, Megan, Kaufman, Miriam, Lawless, Bernard, Lee, Hannah, Lindzon, Lezlee, Lomax, Lysa Boissé
Publikováno v:
Epilepsia (Series 4); Sep2017, Vol. 58 Issue 9, p1502-1517, 16p
Autor:
So, Joyce, Venuja Sriretnakumar, Suddaby, Jessica, Barsanti-Innes, Brianna, Faghfoury, Hanna, Gofine, Timothy
Supplemental Material, Supplementary_Tables for High Rates of Genetic Diagnosis in Psychiatric Patients with and without Neurodevelopmental Disorders: Toward Improved Genetic Diagnosis in Psychiatric Populations by Joyce So, Venuja Sriretnakumar, Jes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acb104ae88038b3506d4e898833489a8
