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Quoted phrase not found in phrase index: "Erythrocytosis, familial, 7"
Page 1
High-oxygen-affinity hemoglobinopathy-associated erythrocytosis: Clinical outcomes and impact of therapy in 41 cases.
Gangat N, Oliveira JL, Hoyer JD, Patnaik MM, Pardanani A, Tefferi A. Gangat N, et al. Am J Hematol. 2021 Dec 1;96(12):1647-1654. doi: 10.1002/ajh.26375. Epub 2021 Oct 19. Am J Hematol. 2021. PMID: 34633117 Free article.
We describe presenting features, treatment strategies, and follow-up events involving 41 patients (median age 39 years, range 1-81; 54% males) with high oxygen affinity (HOA) hemoglobinopathy-associated erythrocytosis, seen at our institution (1973-2020). Thirty-four (83%) …
We describe presenting features, treatment strategies, and follow-up events involving 41 patients (median age 39 years, range 1-81; 54% male …
Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study.
Yesilaltay A, Degirmenci H, Bilgen T, Sirin DY, Bayir D, Degirmenci P, Tekinalp A, Alpsoy S, Okuturlar Y, Turgut B. Yesilaltay A, et al. Medicine (Baltimore). 2022 Aug 12;101(32):e29881. doi: 10.1097/MD.0000000000029881. Medicine (Baltimore). 2022. PMID: 35960118 Free PMC article.
BACKGROUND: We have aimed at exposing left ventricular diastolic functions and the presence of known genetic mutations for familial erythrocytosis, in patients who exhibit idiopathic erythrocytosis. METHODS: Sixty-four patients with idiopathic erythrocytos …
BACKGROUND: We have aimed at exposing left ventricular diastolic functions and the presence of known genetic mutations for familial …
Monochorionic diamniotic twins: What do I tell the prospective parents?
Lewi L. Lewi L. Prenat Diagn. 2020 Jun;40(7):766-775. doi: 10.1002/pd.5705. Epub 2020 Apr 27. Prenat Diagn. 2020. PMID: 32279339 Review.
In about 15%, an imbalance in blood exchange occurs, such as twin-twin transfusion syndrome and twin anemia polycythemia sequence. In this review, we summarize the latest evidence on the management of monochorionic diamniotic twin pregnancies and their specific complicatio …
In about 15%, an imbalance in blood exchange occurs, such as twin-twin transfusion syndrome and twin anemia polycythemia sequence. In …
Prevalence and risk factors for dementia in the Tibetan region: A population-based cross-sectional study.
Mima D, Wang LP, Zhai Y, De Q, Ba S, Da G, Wang BY, Zhao JB, Tang Y. Mima D, et al. J Affect Disord. 2023 Aug 1;334:159-165. doi: 10.1016/j.jad.2023.04.075. Epub 2023 Apr 23. J Affect Disord. 2023. PMID: 37094660
Permanent residents of the region were invited to participate, and the response rate was 90.7 %. METHODS: The participants underwent neuropsychological testing and clinical assessments, from which physical measurements (e.g., body mass index, blood pressure), demographic i …
Permanent residents of the region were invited to participate, and the response rate was 90.7 %. METHODS: The participants underwent …
Familial risk of small intestinal carcinoid and adenocarcinoma.
Kharazmi E, Pukkala E, Sundquist K, Hemminki K. Kharazmi E, et al. Clin Gastroenterol Hepatol. 2013 Aug;11(8):944-9. doi: 10.1016/j.cgh.2013.02.025. Epub 2013 Mar 15. Clin Gastroenterol Hepatol. 2013. PMID: 23500615
The familial risk of concordant histologic subtypes increased for siblings diagnosed with adenocarcinoma, but only 2 familial cases were identified. ...Family members of patients with SIC of the carcinoid subtype had an increased risk for kidney cancer and …
The familial risk of concordant histologic subtypes increased for siblings diagnosed with adenocarcinoma, but only 2 familial …
Hepatic vein thrombosis (Budd Chiari syndrome): possible association with the use of oral contraceptives.
Maddrey WC. Maddrey WC. Semin Liver Dis. 1987 Feb;7(1):32-9. doi: 10.1055/s-2008-1040561. Semin Liver Dis. 1987. PMID: 3296214 Review.
Hepatic vein thrombosis may develop without an apparent underlying cause or as a complication of an illness known to be associated with vascular thromboses such as polycythemia rubra vera or paroxysmal nocturnal hemoglobinuria. In relation to the large numbers of women tak …
Hepatic vein thrombosis may develop without an apparent underlying cause or as a complication of an illness known to be associated with vasc …
Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutation.
Cakmak HM, Kartal O, Kocaaga A, Bildirici Y. Cakmak HM, et al. Pediatr Neonatol. 2022 Nov;63(6):613-617. doi: 10.1016/j.pedneo.2022.06.006. Epub 2022 Aug 6. Pediatr Neonatol. 2022. PMID: 36002380 Free article.
Others (n = 35) had persistent and idiopathic polycythemia. Here, we compared the idiopathic and secondary cases. We found that the ratio of family history of polycythemia (n = 4 (9.5%) vs 0%, respectively) was higher in the second group (p = 0.009). In addit …
Others (n = 35) had persistent and idiopathic polycythemia. Here, we compared the idiopathic and secondary cases. We found that the r …
Effects of Placental Transfusion on Late Preterm Infants Admitted to a Mother-Baby Unit.
Chiruvolu A, George R, Stanzo KC, Kindla CM, Desai S. Chiruvolu A, et al. Am J Perinatol. 2022 Dec;39(16):1812-1819. doi: 10.1055/s-0041-1726387. Epub 2021 Mar 15. Am J Perinatol. 2022. PMID: 33723833
However, there are concerns of adverse effects of increased blood volume such as polycythemia and hyperbilirubinemia. The purpose of this study is to examine the short-term effects of placental transfusion on late preterm infants born between 35(0/7) and 36(6/7 …
However, there are concerns of adverse effects of increased blood volume such as polycythemia and hyperbilirubinemia. The purpose of …
Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies.
Hamadou WS, Bourdon V, Gaildrat P, Besbes S, Fabre A, Youssef YB, Regaieg H, Laatiri MA, Eisinger F, Mari V, Gesta P, Dreyfus H, Bonadona V, Dugast C, Zattara H, Faivre L, Jemni SY, Noguchi T, Khélif A, Sobol H, Soua Z. Hamadou WS, et al. Ann Hematol. 2016 Jun;95(7):1043-50. doi: 10.1007/s00277-016-2678-y. Epub 2016 Apr 23. Ann Hematol. 2016. PMID: 27106701
Familial aggregation of hematological malignancies has been reported highlighting inherited genetic predisposition. ...The aim of this study is to determine whether JAK2, CBL, RUNX1, and NPM1 germline genes mutations are involved in familial hematological malignanci …
Familial aggregation of hematological malignancies has been reported highlighting inherited genetic predisposition. ...The aim of thi …
Germline variants in DNA repair genes, including BRCA1/2, may cause familial myeloproliferative neoplasms.
Elbracht M, Meyer R, Kricheldorf K, Gezer D, Eggermann T, Betz B, Kurth I, Teichmann LL, Brümmendorf TH, Germing U, Isfort S, Koschmieder S. Elbracht M, et al. Blood Adv. 2021 Sep 14;5(17):3373-3376. doi: 10.1182/bloodadvances.2021004811. Blood Adv. 2021. PMID: 34477817 Free PMC article.
In 4 families, we detected rare germline variants in known tumor predisposition genes of the DNA repair pathway, including the highly penetrant BRCA1 and BRCA2 genes. ...Two patients with essential thrombocythemia or polycythemia vera experienced progression to acut …
In 4 families, we detected rare germline variants in known tumor predisposition genes of the DNA repair pathway, including the highly …
31 results