Found: 17
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Regional and national burden of leukemia and its attributable burden to risk factors in 21 countries and territories of North Africa and Middle East, 1990–2019: results from the GBD study 2019.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2023, v. 149, n. 8, p. 4149, doi. 10.1007/s00432-022-04293-7
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- Article
Neuroblastoma‐targeted nanoparticles and novel nanotechnology‐based treatment methods.
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- Journal of Cellular Physiology, 2021, v. 236, n. 3, p. 1751, doi. 10.1002/jcp.29979
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- Article
microRNA‐related single‐nucleotide polymorphisms and breast cancer.
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- Journal of Cellular Physiology, 2021, v. 236, n. 3, p. 1593, doi. 10.1002/jcp.29966
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- Article
DNAH11 and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the Literature.
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- Case Reports in Medicine, 2023, p. 1, doi. 10.1155/2023/8436715
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- Publication type:
- Article
The Efficacy of Celecoxib during Chemoradiation in Locally Advanced Head and Neck Carcinoma; A Phase 2 Randomized Placebo Control Clinical Trial.
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- International Journal of Cancer Management, 2021, v. 14, n. 5, p. 1, doi. 10.5812/ijcm.103653
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- Article
Coronary slow flow phenomenon and microalbuminuria: Is there any relationship?
- Published in:
- Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi, 2019, v. 47, n. 8, p. 657, doi. 10.5543/tkda.2019.82258
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- Article
A novel VPS13B mutation in Cohen syndrome: a case report and review of literature.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01075-1
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- Publication type:
- Article
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers.
- Published in:
- 2023
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- Publication type:
- Case Study
Whole‐exome sequencing to identify undiagnosed primary immunodeficiency disorders in children with community‐acquired sepsis, admitted in the pediatric intensive care unit.
- Published in:
- Pediatric Allergy & Immunology, 2023, v. 34, n. 12, p. 1, doi. 10.1111/pai.14066
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- Article
A novel homozygous RAG1 mutation is associated with severe combined immunodeficiency and neurological presentations.
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- Allergologia & Immunopathologia, 2021, v. 49, n. 4, p. 91, doi. 10.15586/aei.v49i4.194
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- Publication type:
- Article
Novel BTK mutation in X-linked agammaglobulinemia: Report of a 17-year-old male.
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- Allergologia & Immunopathologia, 2021, v. 49, n. 2, p. 80, doi. 10.15586/aei.v49i2.62
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- Publication type:
- Article
Novel CYBA mutation in a family with BCGitis.
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- Acta Microbiologica et Immunologica Hungarica, 2020, v. 67, n. 1, p. 56, doi. 10.1556/030.66.2019.043
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- Article
The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects.
- Published in:
- 2022
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- Publication type:
- journal article
Cancer Immunotherapy: The Way to Nobel Prize in Medicine.
- Published in:
- Acta Medica Iranica, 2018, v. 56, n. 10, p. 623
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- Publication type:
- Article
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patient.
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- Allergy, Asthma & Clinical Immunology, 2023, v. 19, n. 1, p. 1, doi. 10.1186/s13223-023-00804-4
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- Publication type:
- Article
The significant coronary tortuosity and atherosclerotic coronary artery disease; What is the relation?
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- Journal of Cardiovascular & Thoracic Research, 2018, v. 10, n. 4, p. 209, doi. 10.15171/jcvtr.2018.36
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- Publication type:
- Article
The burden of childhood and adolescent cancers in North Africa and the Middle East (NAME) region: findings from the Global Burden of Disease study 2019.
- Published in:
- BMC Pediatrics, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12887-023-03931-4
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- Publication type:
- Article