Search details
1.
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.
Brain
; 146(8): 3273-3288, 2023 08 01.
Article
in English
| MEDLINE | ID: mdl-36757831
2.
Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.
Genet Med
; 25(1): 90-102, 2023 01.
Article
in English
| MEDLINE | ID: mdl-36318270
3.
Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency.
Hum Mutat
; 43(3): 403-419, 2022 03.
Article
in English
| MEDLINE | ID: mdl-34989426
4.
Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative condition.
Genet Med
; 23(3): 524-533, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33188300
5.
Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies.
Genet Med
; 23(11): 2138-2149, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34244665
6.
Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.
Brain
; 144(10): e85, 2021 11 29.
Article
in English
| MEDLINE | ID: mdl-34373908
7.
Examining the psychometric characteristics of the metacognition questionnaire in teaching: a cross-sectional study.
Ann Med Surg (Lond)
; 86(3): 1352-1358, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38463116
8.
Reducing symptoms of attention deficit/hyperactivity disorder (ADHD) in elementary students: the effectiveness of neurofeedback.
Ann Med Surg (Lond)
; 86(5): 2651-2656, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38694339
9.
Brown-Vialetto-Van Laere syndrome.
Iran J Child Neurol
; 18(2): 141-146, 2024.
Article
in English
| MEDLINE | ID: mdl-38617395
10.
Improving mental health infrastructure across the Middle East.
Asian J Psychiatr
; 93: 103908, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38237532
11.
Transient blindness due to mild reversible encephalopathy in a 7-year-old boy.
Clin Case Rep
; 12(2): e8493, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38380378
12.
Increasing the tolerance of mothers with children with autism: the effectiveness of cognitive therapy based on mindfulness - experimental research.
Ann Med Surg (Lond)
; 86(1): 207-211, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-38222757
13.
Discovery of common molecular signatures and drug repurposing for COVID-19/Asthma comorbidity: ACE2 and multi-partite networks.
Cell Cycle
; 23(4): 405-434, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38640424
14.
An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders.
bioRxiv
; 2024 Jan 09.
Article
in English
| MEDLINE | ID: mdl-38260472
15.
Therapeutical impacts of transcranial direct current stimulation on drug-resistant epilepsy in pediatric patients: A double-blind parallel-group randomized clinical trial.
Epilepsy Res
; 190: 107074, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36657251
16.
Oral manifestations of COVID-19 and its management in pediatric patients: A systematic review and practical guideline.
Clin Exp Dent Res
; 9(5): 922-934, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37602892
17.
A case report of Posterior reversible encephalopathy syndrome with spinal cord involvement (PRES-SCI) as an atypical presentation of PRES in children: A case report and review of the literature.
Iran J Child Neurol
; 16(2): 149-154, 2022.
Article
in English
| MEDLINE | ID: mdl-35497107
18.
Recurrent Painful Ophthalmoplegic Neuropathy with Unilateral Oculomotor and Trochlear Nerve Palsy in an 8-year-old Girl.
J Binocul Vis Ocul Motil
; 72(4): 199-204, 2022.
Article
in English
| MEDLINE | ID: mdl-35867412
19.
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
Orphanet J Rare Dis
; 17(1): 286, 2022 07 19.
Article
in English
| MEDLINE | ID: mdl-35854306
20.
A Novel Approach to Minimally Invasive Management of Sigmoid Volvulus.
Acta Med Iran
; 54(10): 640-643, 2016 Oct.
Article
in English
| MEDLINE | ID: mdl-27888591
Results
1 -
20
de 20
1
Next >
>>