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1982 1
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Page 1
Acne and rosacea: What's new for treatment?
Dursun R, Daye M, Durmaz K. Dursun R, et al. Dermatol Ther. 2019 Sep;32(5):e13020. doi: 10.1111/dth.13020. Epub 2019 Jul 22. Dermatol Ther. 2019. PMID: 31294907 Review.
G6PC3 Deficiency.
Banka S. Banka S. 2015 Apr 16. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2015 Apr 16. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 25879134 Free Books & Documents. Review.
Severe G6PC3 deficiency (classic G6PC3 deficiency plus involvement of non-myeloid hematopoietic cell lines, additional extra-hematologic features, and pulmonary hypertension; known as Dursun syndrome). Neutropenia usually presents with recurrent bacterial infections in the …
Severe G6PC3 deficiency (classic G6PC3 deficiency plus involvement of non-myeloid hematopoietic cell lines, additional extra-hematologic fea …
Arthroscopic shoulder suspensioplasty in painful hemiplegic shoulder subluxation-a case series.
Bozon O, Casamenti V, Coroian F, Laffont I, Coulet B. Bozon O, et al. JSES Int. 2023 Nov 29;8(1):80-84. doi: 10.1016/j.jseint.2023.11.001. eCollection 2024 Jan. JSES Int. 2023. PMID: 38312297 Free PMC article.
The assessment, at a minimum of 1 year, included a clinical evaluation (pectoralis major spasticity, pain, range of motion, satisfaction) and a radiographic evaluation (Dursun classification, height of subacromial space). RESULTS: Five patients with a mean age of 51 years …
The assessment, at a minimum of 1 year, included a clinical evaluation (pectoralis major spasticity, pain, range of motion, satisfaction) an …
Mutations in the G6PC3 gene cause Dursun syndrome.
Banka S, Newman WG, Ozgül RK, Dursun A. Banka S, et al. Am J Med Genet A. 2010 Oct;152A(10):2609-11. doi: 10.1002/ajmg.a.33615. Am J Med Genet A. 2010. PMID: 20799326
Dursun syndrome is a triad of familial primary pulmonary hypertension, leucopenia, and atrial septal defect. ...Identification of the genetic basis of Dursun syndrome expands the pre-existing knowledge about the phenotypic effects of mutations in G6PC3. ...
Dursun syndrome is a triad of familial primary pulmonary hypertension, leucopenia, and atrial septal defect. ...Identification of the …
2,504 results