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A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing.
- Published in:
- Turkish Journal of Hematology, 2019, v. 36, n. 1, p. 29, doi. 10.4274/tjh.galenos.2018.2018.0325
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- Article
Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
- Published in:
- Rheumatology, 2023, v. 62, n. 9, p. 3188, doi. 10.1093/rheumatology/kead044
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- Article
Çocuk romatolojisinde genetiğin yeri.
- Published in:
- Türk Pediatri Arşivi, 2017, v. 52, n. 3, p. 113, doi. 10.5152/TurkPediatriArs.2017.4953
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- Article
Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2.
- Published in:
- Turkish Journal of Pediatrics, 2019, v. 61, n. 3, p. 413, doi. 10.24953/turkjped.2019.03.014
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- Publication type:
- Article
Whole exome sequencing for candidate gene search in patients with Clippers syndrome.
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- 2018
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- Abstract
Identification of multiple sclerosis-related pathways by integration of genomic and proteomic data.
- Published in:
- 2018
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- Publication type:
- Abstract
C3 glomerulopathy in NLRP12-related autoinflammatory disorder: case-based review.
- Published in:
- 2018
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- Publication type:
- Case Study
Familial Mediterranean fever in childhood: a single-center experience.
- Published in:
- Rheumatology International, 2018, v. 38, n. 1, p. 67, doi. 10.1007/s00296-017-3796-0
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- Publication type:
- Article
CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0122045
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- Publication type:
- Article
Chemerin rs17173608 Gene Polymorphism is not Associated with Type 2 Diabetes Mellitus: a Cross-sectional Study.
- Published in:
- Folia Medica, 2019, v. 61, n. 1, p. 69, doi. 10.2478/folmed-2018-0045
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- Article