Results for &quot;&quot;Language Development Disorders&quot;&quot;[mesh_terms]

Prevalence and risk factors of developmental language delay in a sample of children aged <6 years old in the Aseer region, Saudi Arabia: A community-based study.

Reema Mohammed Abdullah Alshehri, Yara Ahmed Salem Alshehri, Lamia Ahmed M Saddah, Rawan Alqahtani, Reema Saeed Almater, Razan Mubarak Alqahtani, Layan Saeed Alshmrani, Ayed A Shati, Hebatalla Abdelmaksoud Abdelmonsef Ahmed, Hoda Ali Ahmed Shiba, Saleh M Al-Qahtani, Ramy Mohamed Ghazy

Medicine 2025;104(30):e43459

Dynamic electro-clinical features in Guanidinoacetate N-methyltransferase deficiency: A familial case series.

Mariapaola Schifino, Emanuele Bartolini, Stefano Pagano, Camilla Meossi, Rosa Pasquariello, Roberta Battini

Epilepsia open 2025;10(4):1244-1252

Should creatine kinase be checked in all boys presenting with speech delay?

Elaine M Hicks, Claire T Lundy, Gary M Doherty

Archives of disease in childhood 2007;92(7):647-9

Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.

John D Eicher, Jeffrey R Gruen

Autism research : official journal of the International Society for Autism Research 2016;8(2):229-34

Review: Human guanidinoacetate n-methyl transferase (GAMT) deficiency: A treatable inborn error of metabolism.

Furhan Iqbal

Pakistan journal of pharmaceutical sciences 2016;28(6):2207-11

Novel de novo variant in is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published cases.

Filippo Pinto E Vairo, Pavel N Pichurin, Eric W Klee, Duygu Selcen, Raul A Urrutia, Matthew J Ferber, Zhiyv Niu, Charu Kaiwar, Margot A Cousin, Michael T Zimmermann, Sarah S Barnett, Patrick R Blackburn

Cold Spring Harbor molecular case studies 2017;3(3):a001743

Monogenic and chromosomal causes of isolated speech and language impairment.

C P Barnett, B W M van Bon

Journal of medical genetics 2016;52(11):719-29

Epileptic and electroencephalographic manifestations of guanidinoacetate-methyltransferase deficiency.

Ibrahim Abu Gheida, Alhan Shamseddine, Mohamad A Mikati, Pascale E Karam, Abdul G Mikati

Epileptic disorders : international epilepsy journal with videotape 2014;15(4):407-16

Massage therapy improves the development of HIV-exposed infants living in a low socio-economic, peri-urban community of South Africa.

E M Perez, H Carrara, L Bourne, A Berg, S Swanevelder, M K Hendricks

Infant behavior & development 2015;38():135-46

A pilot study to estimate incidence of guanidinoacetate methyltransferase deficiency in newborns by direct sequencing of the GAMT gene.

A Pop, S Mercimek-Mahmutoglu, W Kanhai, U Holwerda, G S Salomons, P C J I Schielen, J G Loeber, D Smith, M Fernandez Ojeda

Gene 2016;575(1):127-31

Cerebral creatine deficiencies: a group of treatable intellectual developmental disorders.

Sylvia Stockler-Ipsiroglu, Clara D M van Karnebeek

Seminars in neurology 2015;34(3):350-6

Delayed diagnosis of Duchenne muscular dystrophy.

R Appleton, K Mohamed, P Nicolaides

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2001;4(5):219-23

Folinic acid improves verbal communication in children with autism and language impairment: a randomized double-blind placebo-controlled trial.

R E Frye, J Slattery, L Delhey, B Furgerson, T Strickland, M Tippett, A Sailey, R Wynne, S Rose, S Melnyk, S Jill James, J M Sequeira, E V Quadros

Molecular psychiatry 2019;23(2):247-256

Neurocognitive function of 10-year-old multiples born less than 28 weeks of gestational age.

Karl C K Kuban, Alan Leviton, Timothy Heeren, T T Michael O'Shea, Robert M Joseph, Michael E Msall, Elizabeth N Allred, J Wells Logan

Journal of perinatology : official journal of the California Perinatal Association 2020;39(2):237-247