Items where Author is "Bahreini, A."

Article

(2022) Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia. ANNALS OF NEUROLOGY. pp. 304-321. ISSN 0364-5134 1531-8249 J9 - ANN NEUROL

(2022) Investigation of the expression of P-element-induced wimpy testis-interacting RNAs in human acute myeloid leukemia. META GENE. ISSN 2214-5400 J9 - META GENE

(2022) The Role of Tissue Inhibitor of Metalloproteinase-1 and 2 in Echinococcus granulosus senso lato-Induced Human Hepatic Fibrosis. ACTA PARASITOLOGICA. pp. 851-857. ISSN 1230-2821 1896-1851 J9 - ACTA PARASITOL

(2022) A recurrent homozygous missense DPM3 variant leads to muscle and brain disease. Clin Genet. ISSN 0009-9163

(2021) Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy. EPILEPSY RESEARCH. ISSN 0920-1211 1872-6844 J9 - EPILEPSY RES

(2021) A novel carcinogenic PI3K alpha mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domain. Life Sciences. ISSN 0024-3205

(2018) Recurrent hyperactive ESR1 fusion proteins in endocrine therapy-resistant breast cancer. Annals of Oncology. pp. 872-880. ISSN 0923-7534

(2017) Associating liver partition and portal vein ligation for staged hepatectomy: A surgical technique for liver resections. Journal of Research in Medical Sciences. ISSN 1735-1995

(2017) Is Education Enough for Improving Organ Donation or Something Even More Important is Missing? Transplantation. S20-S20. ISSN 0041-1337