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5. Glanzmann thrombasthenia in a neonate. Zenciroglu A; Bas AY; Demirel N; Yarali N Indian Pediatr; 2007 Jan; 44(1):40-2. PubMed ID: 17277431 [TBL] [Abstract][Full Text] [Related]
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7. Two homozygous missense mutations in ITGB3 gene as a cause of Glanzmann Thrombasthenia in four consanguineous Pakistani pedigrees. Ali T; Gul S; Amar A; Shakoor M; Farhan S; Mohsin S; Khaliq S Int J Lab Hematol; 2020 Oct; 42(5):628-635. PubMed ID: 32558238 [TBL] [Abstract][Full Text] [Related]
8. Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations. Sandrock-Lang K; Oldenburg J; Wiegering V; Halimeh S; Santoso S; Kurnik K; Fischer L; Tsakiris DA; Sigl-Kraetzig M; Brand B; Bührlen M; Kraetzer K; Deeg N; Hund M; Busse E; Kahle A; Zieger B Thromb Haemost; 2015 Apr; 113(4):782-91. PubMed ID: 25373348 [TBL] [Abstract][Full Text] [Related]
9. A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of Bury L; Zetterberg E; Leinøe EB; Falcinelli E; Marturano A; Manni G; Nurden AT; Gresele P Haematologica; 2018 Jun; 103(6):e259-e263. PubMed ID: 29439184 [No Abstract] [Full Text] [Related]
10. Identification of one novel pathogenic Lu Z; Nikuze L; Zhong Z; Li F; Zhang F; Liang K; Wei M; Wei H Platelets; 2020; 31(3):355-359. PubMed ID: 31088191 [TBL] [Abstract][Full Text] [Related]
11. Should studies on Glanzmann thrombasthenia not be telling us more about cardiovascular disease and other major illnesses? Nurden AT Blood Rev; 2017 Sep; 31(5):287-299. PubMed ID: 28395882 [TBL] [Abstract][Full Text] [Related]
12. Management of Abdominoperineal Excision of the Rectum in a Patient with Glanzmann Thrombasthenia. Buckley F; Norris A; Kerr R Acta Haematol; 2018; 139(4):243-246. PubMed ID: 29945125 [No Abstract] [Full Text] [Related]
13. In silico analysis of structural modifications in and around the integrin αIIb genu caused by ITGA2B variants in human platelets with emphasis on Glanzmann thrombasthenia. Pillois X; Peters P; Segers K; Nurden AT Mol Genet Genomic Med; 2018 Mar; 6(2):249-260. PubMed ID: 29385657 [TBL] [Abstract][Full Text] [Related]
14. Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families. Sandrock K; Halimeh S; Wiegering V; Kappert G; Sauer K; Deeg N; Busse E; Zieger B Klin Padiatr; 2012 Apr; 224(3):174-8. PubMed ID: 22513797 [TBL] [Abstract][Full Text] [Related]
15. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia. Tokgoz H; Torun Ozkan D; Caliskan U; Akar N Platelets; 2015; 26(8):779-82. PubMed ID: 25734216 [TBL] [Abstract][Full Text] [Related]
16. Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations. Gultekin ND; Yilmaz FH; Tokgoz H; Tarakci N; Caliskan U Indian Pediatr; 2019 Feb; 56(2):143-144. PubMed ID: 30819996 [TBL] [Abstract][Full Text] [Related]
17. Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations? Nurden AT; Fiore M; Nurden P; Heilig R; Pillois X Platelets; 2011; 22(7):547-51. PubMed ID: 21557682 [TBL] [Abstract][Full Text] [Related]