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Quoted phrase not found in phrase index: "Adult Extramedullary Hematopoiesis"
Page 1
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. ...Several differen …
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 in pyogenic granuloma.
Waraasawapati S, Koonmee S, Kusama H, Kudo M. Waraasawapati S, et al. Pathol Int. 2013 Oct;63(10):492-5. doi: 10.1111/pin.12096. Epub 2013 Oct 18. Pathol Int. 2013. PMID: 24147429 Review.
Extramedullary hematopoiesis (EMH) suggests the presence of hematopoietic stem cells (HSC) outside bone marrow. ...
Extramedullary hematopoiesis (EMH) suggests the presence of hematopoietic stem cells (HSC) outside bone marrow. ...
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 …
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 …
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 …
Choosing between stem cell therapy and drugs in myelofibrosis.
Kröger N, Mesa RA. Kröger N, et al. Leukemia. 2008 Mar;22(3):474-86. doi: 10.1038/sj.leu.2405080. Epub 2008 Jan 10. Leukemia. 2008. PMID: 18185525 Review.
Optimal clinical management of patients with primary myelofibrosis and post-essential thrombocythemia/polycythemia vera myelofibrosis is a challenge, given the typically advanced age of presentation and variability of the disease course and prognosis. Current medica …
Optimal clinical management of patients with primary myelofibrosis and post-essential thrombocythemia/polycythemia vera myelofibrosis is a c …
Case Report of Clinical Vignette: Osteopetrosis.
Moore JB, Hoang TD, Shwayhat AF. Moore JB, et al. Mil Med. 2017 Mar;182(3):e1886-e1888. doi: 10.7205/MILMED-D-16-00234. Mil Med. 2017. PMID: 28290981
In severe cases, usually inherited in an autosomal recessive pattern, the medullary cavity important in the production of normal blood cell progenitors is replaced by defective endochondral bone, leading to pancytopenia and consequential extramedullary hematopoiesis
In severe cases, usually inherited in an autosomal recessive pattern, the medullary cavity important in the production of normal blood cell …
Allogeneic haematopoietic cell transplantation for myelofibrosis: a real-life perspective.
Savani M, Dulery R, Bazarbachi AH, Mohty R, Brissot E, Malard F, Bazarbachi A, Nagler A, Mohty M. Savani M, et al. Br J Haematol. 2021 Nov;195(4):495-506. doi: 10.1111/bjh.17469. Epub 2021 Apr 21. Br J Haematol. 2021. PMID: 33881169 Review.
Allogeneic haematopoietic stem cell transplantation (HSCT) offers an important curative treatment option for primary MF and post-essential thrombocythaemia/polycythaemia vera MF or secondary MF. With a disease course that varies from indolent to highly progressive, we are …
Allogeneic haematopoietic stem cell transplantation (HSCT) offers an important curative treatment option for primary MF and post-essential t …
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 …
165 results