Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Baraa A. Hijaz"'
Autor:
Hassan Abdulrahman, Stephanie Bousleiman, Mustafe Mumin, Ibrahim Caqli, Baraa A. Hijaz, Bizu Gelaye, Gregory Fricchione, Zeina Chemali
Publikováno v:
South African Journal of Psychiatry, Vol 29, Iss 0, Pp e1-e7 (2023)
Background: In Somaliland, an estimated one person in every two households suffers from psychiatric disorders. Despite this, access to mental health care is limited because of shortages in facilities, human resources, funding and stigma. Aim: To pre
Externí odkaz:
https://doaj.org/article/f31e30e8e4774c20873217da9f02921f
Autor:
Charlotte F. Brzozowski, Baraa A. Hijaz, Vijay Singh, Nolwazi Z. Gcwensa, Kaela Kelly, Edward S. Boyden, Andrew B. West, Deblina Sarkar, Laura A. Volpicelli-Daley
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-18 (2021)
Abstract Pathologic inclusions composed of α-synuclein called Lewy pathology are hallmarks of Parkinson’s Disease (PD). Dominant inherited mutations in leucine rich repeat kinase 2 (LRRK2) are the most common genetic cause of PD. Lewy pathology is
Externí odkaz:
https://doaj.org/article/529d6d304c07412f8ead36c5d416d3e5
Publikováno v:
Molecular Neurodegeneration, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract The two main pathological hallmarks of Parkinson’s disease are loss of dopamine neurons in the substantia nigra pars compacta and proteinaceous amyloid fibrils composed mostly of α-synuclein, called Lewy pathology. Levodopa to enhance dop
Externí odkaz:
https://doaj.org/article/c9e2a9e6e56b4175831d03f33dd2da49
Autor:
Thais P Salazar Mather, Benjamin Gallo Marin, Giancarlo Medina Perez, Briana Christophers, Marcelo L Paiva, Rocío Oliva, Baraa A Hijaz, Andrea M Prado, Mateo C Jarquín, Katelyn Moretti, Catalina González Marqués, Alejandro Murillo, Elizabeth Tobin-Tyler
Publikováno v:
The Lancet Global Health, Vol 8, Iss 6, Pp e773- (2020)
Externí odkaz:
https://doaj.org/article/a302e5bd4f8042f294c235740f89c397
Autor:
Nolwazi Z. Gcwensa, Edward S. Boyden, Laura A. Volpicelli-Daley, Vijay Singh, Deblina Sarkar, Kaela Kelly, Andrew B. West, Baraa A. Hijaz, Charlotte F. Brzozowski
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-18 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Pathologic inclusions composed of α-synuclein called Lewy pathology are hallmarks of Parkinson’s Disease (PD). Dominant inherited mutations in leucine rich repeat kinase 2 (LRRK2) are the most common genetic cause of PD. Lewy pathology is found in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88f83c404955d9677941eb3b5389dec1
https://doi.org/10.1101/2021.10.04.463043
https://doi.org/10.1101/2021.10.04.463043
Autor:
Ricardo V. Lloyd, Baraa A. Hijaz, Renata Jaskula-Sztul, Alexander W. Chang, Samuel Jang, Danilea M. Carmona Matos, Herbert Chen
Publikováno v:
Surgery. 165:64-68
Background Certain human carcinomas have demonstrated a distinct expression of somatostatin receptors. Data on somatostatin receptor expression in follicular thyroid cancer and anaplastic thyroid cancer has been limited and conflicting. This study se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89e91c5304236deee3517b774c70b489
https://doi.org/10.1016/j.surg.2018.05.077
https://doi.org/10.1016/j.surg.2018.05.077
Autor:
Briana Christophers, Elizabeth Tobin-Tyler, Andrea Prado, Rocío Oliva, Giancarlo Medina Perez, Marcelo Paiva, Catalina González Marqués, Benjamin Gallo Marin, Mateo C Jarquín, Alejandro Murillo, Baraa A. Hijaz, Thais P Salazar Mather, Katelyn Moretti
Publikováno v:
The Lancet Global Health
The Lancet. Global Health
The Lancet Global Health, Vol 8, Iss 6, Pp e773-(2020)
The Lancet. Global Health
The Lancet Global Health, Vol 8, Iss 6, Pp e773-(2020)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::363d690ca1b13d07db933bb577d5827f
Autor:
Ashley N, Turner, Reagan S, Andersen, Ivy E, Bookout, Lauren N, Brashear, James C, Davis, David M, Gahan, John P, Gotham, Baraa A, Hijaz, Ashish S, Kaushik, Jordan B, Mcgill, Victoria L, Miller, Zachariah P, Moseley, Cerissa L, Nowell, Riddhi K, Patel, Mia C, Rodgers, Yazen A, Shihab, Austin P, Walker, Sarah R, Glover, Samantha D, Foster, Anil K, Challa
Publikováno v:
Journal of genetics. 97(5)
Nodal-related protein (ndr2) is amember of the transforming growth factor type β superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene encoding no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bf5e2a2369f51902d41d48e350d19ee
https://pubmed.ncbi.nlm.nih.gov/30555080
https://pubmed.ncbi.nlm.nih.gov/30555080
Autor:
Anil K. Challa, Baraa A. Hijaz, John P. Gotham, Yazen A. Shihab, Riddhi K. Patel, David M. Gahan, Jordan B. Mcgill, Ivy E. Bookout, Mia C. Rodgers, Samantha D. Foster, Cerissa L. Nowell, Ashley N. Turner, Victoria L. Miller, Austin P. Walker, James C. Davis, Sarah R. Glover, Ashish S Kaushik, Zachariah P. Moseley, Lauren N. Brashear, Reagan S Andersen
Nodal-related protein (ndr2) is a member of the transforming growth factor type $$\upbeta $$ superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2ba3f6663bd83c0bf48a6fdf1c4b74
https://doi.org/10.1101/277715
https://doi.org/10.1101/277715