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Quoted phrase not found in phrase index: "Adult Extramedullary Hematopoiesis"
Page 1
Adrenal myelolipoma: a comprehensive review.
Decmann Á, Perge P, Tóth M, Igaz P. Decmann Á, et al. Endocrine. 2018 Jan;59(1):7-15. doi: 10.1007/s12020-017-1473-4. Epub 2017 Nov 21. Endocrine. 2018. PMID: 29164520 Review.
INTRODUCTION: Adrenal myelolipoma is an invariably benign neoplasm of the adrenal gland that is the second most common primary adrenal incidentaloma following adrenocortical adenomas. It is composed of elements of adipose tissue and extramedullary hematopoiesis. Hyp …
INTRODUCTION: Adrenal myelolipoma is an invariably benign neoplasm of the adrenal gland that is the second most common primary adrenal incid …
Thalassemia intermedia: revisited.
Taher A, Isma'eel H, Cappellini MD. Taher A, et al. Blood Cells Mol Dis. 2006 Jul-Aug;37(1):12-20. doi: 10.1016/j.bcmd.2006.04.005. Epub 2006 Jun 5. Blood Cells Mol Dis. 2006. PMID: 16737833 Review.
A number of clinical complications commonly associated with thalassemia intermedia are rarely seen in thalassemia major, including extramedullary hematopoiesis, leg ulcers, gallstones and thrombophilia. ...Here, we review the major clinical complications in thalasse …
A number of clinical complications commonly associated with thalassemia intermedia are rarely seen in thalassemia major, including extram …
Liver Regeneration by Hematopoietic Stem Cells: Have We Reached the End of the Road?
Siapati EK, Roubelakis MG, Vassilopoulos G. Siapati EK, et al. Cells. 2022 Jul 27;11(15):2312. doi: 10.3390/cells11152312. Cells. 2022. PMID: 35954155 Free PMC article. Review.
Ample evidence indicates that the fetal liver supports the maturation and expansion of HSCs during development but also later on in life. Moreover, the fact that the adult liver remains one of the few sites for extramedullary hematopoiesis-albeit pathological …
Ample evidence indicates that the fetal liver supports the maturation and expansion of HSCs during development but also later on in life. Mo …
Prognostication in MF: from CBC to cytogenetics to molecular markers.
Zhou A, Oh ST. Zhou A, et al. Best Pract Res Clin Haematol. 2014 Jun;27(2):155-64. doi: 10.1016/j.beha.2014.07.008. Epub 2014 Jul 18. Best Pract Res Clin Haematol. 2014. PMID: 25189726 Review.
Myelofibrosis (MF) is a clonal stem cell disorder characterized by ineffective erythropoiesis and extramedullary hematopoiesis leading to progressive bone marrow failure, severe anemia, constitutional symptoms, hepatosplenomegaly, and thrombosis. ...Cytogenetic abno …
Myelofibrosis (MF) is a clonal stem cell disorder characterized by ineffective erythropoiesis and extramedullary hematopoiesis …
Erythropoiesis and Iron Homeostasis in Non-Transfusion-Dependent Thalassemia Patients with Extramedullary Hematopoiesis.
Huang Y, Liu R, Wei X, Liu J, Pan L, Yang G, Lai Y. Huang Y, et al. Biomed Res Int. 2019 Jan 30;2019:4504302. doi: 10.1155/2019/4504302. eCollection 2019. Biomed Res Int. 2019. PMID: 30834265 Free PMC article.
BACKGROUND: Extramedullary hematopoiesis (EMH) is common in non-transfusion-dependent thalassemia (NTDT) patients. ...CONCLUSIONS: GDF15, EPO, and GDF15 to EPO and GDF15 to sTfR ratios are potential biomarkers for the early prediction of NTDT in patients who …
BACKGROUND: Extramedullary hematopoiesis (EMH) is common in non-transfusion-dependent thalassemia (NTDT) patients. ...CONCLUSI …
Extramedullary Hematopoiesis: Cytomorphologic, Histologic, and Radiologic Findings in Sixteen Cases.
Sheikh U, Rodic N, Maleki Z. Sheikh U, et al. Acta Cytol. 2015;59(2):144-8. doi: 10.1159/000376602. Epub 2015 Apr 3. Acta Cytol. 2015. PMID: 25871506
BACKGROUND: We report a case series of extramedullary hematopoiesis (EMH) diagnosed from the fine needle aspiration (FNA) procedure. ...
BACKGROUND: We report a case series of extramedullary hematopoiesis (EMH) diagnosed from the fine needle aspiration (FNA) proc …
Otorhinolaryngological manifestations of sickle cell disease.
Abou-Elhamd KE. Abou-Elhamd KE. Int J Pediatr Otorhinolaryngol. 2012 Jan;76(1):1-4. doi: 10.1016/j.ijporl.2011.10.004. Epub 2011 Oct 22. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22018730 Review.
Prevalence rate for sensorineural hearing loss in older children and adult patients is reporting a range of 11-41%. Priapism of the turbinates is a cause of nasal obstruction in sickle cell anaemia which needs partial turbinectomy. Extramedullary haematopoiesis …
Prevalence rate for sensorineural hearing loss in older children and adult patients is reporting a range of 11-41%. Priapism of the t …
Sickle cell diseases: What can nuclear medicine offer?
Niccoli Asabella A, Altini C, Nappi AG, Lavelli V, Ferrari C, Marzullo A, Loiodice A, Rubini G. Niccoli Asabella A, et al. Hell J Nucl Med. 2019 Jan-Apr;22(1):2-3. doi: 10.1967/s002449910950. Epub 2019 Mar 7. Hell J Nucl Med. 2019. PMID: 30843001 Free article.
Magnetic resonance cholangiopancreatography (MRCP) is a noninvasive technique without radiation chosen to image cholangiopathy and may be followed by the execution of endoscopic retrograde cholangiopancreatography (ERCP) in case of gallstone disease. Otherwise it can be helpful i …
Magnetic resonance cholangiopancreatography (MRCP) is a noninvasive technique without radiation chosen to image cholangiopathy and may be fo …
The Pyruvate Kinase Deficiency Global Longitudinal (Peak) Registry: rationale and study design.
Grace RF, van Beers EJ, Vives Corrons JL, Glader B, Glenthøj A, Kanno H, Kuo KHM, Lander C, Layton DM, Pospíŝilová D, Viprakasit V, Li J, Yan Y, Boscoe AN, Bowden C, Bianchi P. Grace RF, et al. BMJ Open. 2023 Mar 23;13(3):e063605. doi: 10.1136/bmjopen-2022-063605. BMJ Open. 2023. PMID: 36958777 Free PMC article.
INTRODUCTION: Pyruvate kinase (PK) deficiency is a rare, under-recognised, hereditary condition that leads to chronic haemolytic anaemia and potentially serious secondary complications, such as iron overload, cholecystitis, pulmonary hypertension and extramedullary haem …
INTRODUCTION: Pyruvate kinase (PK) deficiency is a rare, under-recognised, hereditary condition that leads to chronic haemolytic anaemia and …
Hemangioblastomas and neurogenic polyglobulia.
Gläsker S, Krüger MT, Klingler JH, Wlodarski M, Klompen J, Schatlo B, Hippchen B, Neumann HP, Van Velthoven V. Gläsker S, et al. Neurosurgery. 2013 Jun;72(6):930-5; discussion 935. doi: 10.1227/NEU.0b013e31828ba793. Neurosurgery. 2013. PMID: 23407287
BACKGROUND: Neurogenic polyglobulia occurs with central nervous system hemangioblastomas. Among the suggested mechanisms are extramedullary hematopoiesis in the tumor tissue and germline mutations of the von Hippel-Lindau (VHL) tumor suppressor gene. ...Removal of t …
BACKGROUND: Neurogenic polyglobulia occurs with central nervous system hemangioblastomas. Among the suggested mechanisms are extramedulla …
128 results