Detalhe da pesquisa
1.
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia.
BMC Med Genet
; 20(1): 119, 2019 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31272422
2.
Impact of the International Nosocomial Infection Control Consortium (INICC)'s multidimensional approach on rates of ventilator-associated pneumonia in intensive care units in 22 hospitals of 14 cities of the Kingdom of Saudi Arabia.
J Infect Public Health
; 11(5): 677-684, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29945849
3.
Prospective multicentre study in intensive care units in five cities from the Kingdom of Saudi Arabia: Impact of the International Nosocomial Infection Control Consortium (INICC) multidimensional approach on rates of central line-associated bloodstream infection.
J Infect Prev
; 18(1): 25-34, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28989500
4.
Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families.
Int J Dermatol
; 55(6): 673-9, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27061915
5.
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T.
Gene
; 536(1): 217-20, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24315819
6.
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.
Eur J Med Genet
; 56(1): 43-5, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23085305