Found: 20
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Association Between Trace Element Status and Depression in HTLV-1-Infected Patients: a Retrospective Cohort Study.
- Published in:
- Biological Trace Element Research, 2019, v. 191, n. 1, p. 75, doi. 10.1007/s12011-018-1613-6
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- Publication type:
- Article
Misdiagnosed Aicardi Goutières Syndrome Patient: A Case Report.
- Published in:
- Reviews in Clinical Medicine, 2021, v. 8, n. 4, p. 166
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- Publication type:
- Article
The effect of nanomicelle curcumin, sorafenib, and combination of the two on the cyclin D1 gene expression of the hepatocellular carcinoma cell line (HUH7).
- Published in:
- Iranian Journal of Basic Medical Sciences, 2019, v. 22, n. 10, p. 1198
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- Publication type:
- Article
A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.
- Published in:
- Public Health Genomics, 2017, v. 20, n. 3, p. 188, doi. 10.1159/000477560
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- Publication type:
- Article
A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.
- Published in:
- Public Health Genomics, 2017, v. 20, n. 2, p. 188, doi. 10.1159/000477560
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- Publication type:
- Article
Hereditary thrombophilia genetic variants in recurrent pregnancy loss.
- Published in:
- 2019
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- Publication type:
- journal article
Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.
- Published in:
- 2021
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- Publication type:
- journal article
Expanding the clinical phenotype of IARS2-related mitochondrial disease.
- Published in:
- BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0709-3
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- Publication type:
- Article
Curcumin in tissue engineering: A traditional remedy for modern medicine.
- Published in:
- Biofactors, 2019, v. 45, n. 2, p. 135, doi. 10.1002/biof.1474
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- Publication type:
- Article
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report.
- Published in:
- BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0539-y
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- Publication type:
- Article
Limb-Girdle Muscular Dystrophy Type 2B (LGMD2B) caused by Pathogenic Splice and Missense Variants of DYSF Gene among Iranians with Muscular Dystrophy.
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- Advanced Biomedical Research, 2023, v. 12, n. 6, p. 1, doi. 10.4103/abr.abr_131_22
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- Publication type:
- Article
A Novel Splice Site Variant in the LDLRAP1 Gene Causes Familial Hypercholesterolemia.
- Published in:
- 2021
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- Publication type:
- journal article
Association Between the Post-Mortem and Poisoning Concentration of Tramadol and Its Main Metabolite and Genotype of CYP2D6.
- Published in:
- Pharmaceutical Chemistry Journal, 2023, v. 57, n. 3, p. 327, doi. 10.1007/s11094-023-02886-1
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- Publication type:
- Article
Circulating exosomal miRNAs in cardiovascular disease pathogenesis: New emerging hopes.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 12, p. 21796, doi. 10.1002/jcp.28942
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- Publication type:
- Article
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 11, p. 1919, doi. 10.1093/hmg/ddz032
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- Publication type:
- Article
Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.
- Published in:
- Journal of Research in Medical Sciences, 2017, v. 22, p. 1, doi. 10.4103/jrms.JRMS_976_16
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- Publication type:
- Article
Congenital heart defects among Down syndrome patients: a clinical profiling.
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- Journal of Public Health (09431853), 2016, v. 24, n. 1, p. 57, doi. 10.1007/s10389-015-0696-1
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- Publication type:
- Article
ECEL1 novel mutation in arthrogryposis type 5D: A molecular dynamic simulation study.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 6, p. 1, doi. 10.1002/mgg3.2153
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- Publication type:
- Article
Identification of a Novel ASAH1 Gene Mutation in Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy.
- Published in:
- Iranian Journal of Child Neurology, 2024, v. 18, n. 3, p. 131, doi. 10.22037/ijcn.v18i3.44081
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- Article
Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis.
- Published in:
- Iranian Journal of Child Neurology, 2019, v. 13, n. 2, p. 155
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- Publication type:
- Article