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Quoted phrase not found in phrase index: "Hereditary Myelodysplastic Syndrome"
Page 1
Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes.
Sahoo SS, Kozyra EJ, Wlodarski MW. Sahoo SS, et al. Best Pract Res Clin Haematol. 2020 Sep;33(3):101197. doi: 10.1016/j.beha.2020.101197. Epub 2020 Jul 29. Best Pract Res Clin Haematol. 2020. PMID: 33038986 Free PMC article. Review.
The main focus lies in delineation of phenotypes, genetics and management of GATA2 deficiency and the novel SAMD9/SAMD9L-related disorders. Combined, GATA2 and SAMD9/SAMD9L (SAMD9/9L) syndromes are recognized as most frequent causes of primary paediatric myelodysplastic …
The main focus lies in delineation of phenotypes, genetics and management of GATA2 deficiency and the novel SAMD9/SAMD9L-related disorders. …
GATA2 deficiency and MDS/AML: Experimental strategies for disease modelling and future therapeutic prospects.
Kotmayer L, Romero-Moya D, Marin-Bejar O, Kozyra E, Català A, Bigas A, Wlodarski MW, Bödör C, Giorgetti A. Kotmayer L, et al. Br J Haematol. 2022 Nov;199(4):482-495. doi: 10.1111/bjh.18330. Epub 2022 Jun 26. Br J Haematol. 2022. PMID: 35753998 Free PMC article. Review.
This is emphasized by the establishment of a novel WHO disease category in 2016 called "myeloid neoplasms with germline predisposition". A major syndrome within this group is GATA2 deficiency, a heterogeneous immunodeficiency syndrome with a very high lifetime risk …
This is emphasized by the establishment of a novel WHO disease category in 2016 called "myeloid neoplasms with germline predisposition". A m …
Hematological Malignancies in Adults With a Family Predisposition.
Bochtler T, Haag GM, Schott S, Kloor M, Krämer A, Müller-Tidow C. Bochtler T, et al. Dtsch Arztebl Int. 2018 Dec 14;115(50):848-854. doi: 10.3238/arztebl.2018.0848. Dtsch Arztebl Int. 2018. PMID: 30722840 Free PMC article. Review.
BACKGROUND: Some hematological malignancies arise in persons with a hereditary predisposition. The hereditary nature of these diseases often goes unrecognized, particularly when symptoms begin in adulthood. ...RESULTS: Many rare germline mutations have been identifi …
BACKGROUND: Some hematological malignancies arise in persons with a hereditary predisposition. The hereditary nature of these …
Anemia as the Main Manifestation of Myelodysplastic Syndromes.
Santini V. Santini V. Semin Hematol. 2015 Oct;52(4):348-56. doi: 10.1053/j.seminhematol.2015.06.002. Epub 2015 Jun 30. Semin Hematol. 2015. PMID: 26404446 Review.
Myelodysplastic syndromes (MDS) are a constellation of different diseases sharing anemia in the great majority of cases, and this cytopenia defines these pathologies and their most dramatic clinical manifestations. ...MDS with del5q constitute a unique model of anem …
Myelodysplastic syndromes (MDS) are a constellation of different diseases sharing anemia in the great majority of cases, and t …
Acquired platelet function defects.
Bick RL. Bick RL. Hematol Oncol Clin North Am. 1992 Dec;6(6):1203-28. Hematol Oncol Clin North Am. 1992. PMID: 1452509 Review.
Platelet dysfunctions, especially acquired forms, are common causes of hemorrhage, especially when associated with trauma or surgery. Although the hereditary platelet function defects are generally quite rare, hereditary storage-pool disease is common enough to be s …
Platelet dysfunctions, especially acquired forms, are common causes of hemorrhage, especially when associated with trauma or surgery. Althou …
Carcinogenic potential of antitumor therapies - is the risk predictable?
Nenova I, Grudeva-Popova J. Nenova I, et al. J BUON. 2017 Nov-Dec;22(6):1378-1384. J BUON. 2017. PMID: 29332326 Free article. Review.
Hematological malignancies, especially t MDS (therapy-related myelodysplastic syndrome) and t AML (therapy-related acute myeloid leukemia), are causally associated with cytotoxic chemotherapy, while secondary solid tumors are related to radiotherapy. ...For example, …
Hematological malignancies, especially t MDS (therapy-related myelodysplastic syndrome) and t AML (therapy-related acute myelo …
Refractory anemia in the elderly.
Gardner FH. Gardner FH. Adv Intern Med. 1987;32:155-75. Adv Intern Med. 1987. PMID: 3548248 Review.
In the absence of tumor, elderly patients have an increasing frequency of refractory anemias that can be called preleukemia or myelodysplastic syndrome. Morphological observations have emphasized the importance of abnormal megakaryocytes and platelets in all …
In the absence of tumor, elderly patients have an increasing frequency of refractory anemias that can be called preleukemia or myelodyspl …
Role of hepcidin in physiology and pathophysiology. Emerging experimental and clinical evidence.
Wojciechowska M, Wisniewski OW, Kolodziejski P, Krauss H. Wojciechowska M, et al. J Physiol Pharmacol. 2021 Feb;72(1). doi: 10.26402/jpp.2021.1.03. Epub 2021 Jun 3. J Physiol Pharmacol. 2021. PMID: 34099582 Free article. Review.
There is a wide range of iron disorders, which arise from iron deficiency or overload. In addition, disturbances in iron metabolism are observed in the course of numerous chronic diseases. Since iron is an essential constituent of hemoglobin, different types of anemia are …
There is a wide range of iron disorders, which arise from iron deficiency or overload. In addition, disturbances in iron metabolism are o …
Orbital/ocular inflammatory involvement in VEXAS syndrome: Data from the international AIDA network VEXAS registry.
Vitale A, Caggiano V, Martin-Nares E, Frassi M, Dagna L, Hissaria P, Sfriso P, Hernández-Rodríguez J, Ruiz-Irastorza G, Monti S, Tufan A, Piga M, Giardini HAM, Lopalco G, Viapiana O, De Paulis A, Triggianese P, Vitetta R, de-la-Torre A, Fonollosa A, Caroni F, Sota J, Conticini E, Sbalchiero J, Renieri A, Casamassima G, Wiesik-Szewczyk E, Yildirim D, Hinojosa-Azaola A, Crisafulli F, Franceschini F, Campochiaro C, Tomelleri A, Callisto A, Beecher M, Bindoli S, Baggio C, Gómez-Caverzaschi V, Pelegrín L, Soto-Peleteiro A, Milanesi A, Vasi I, Cauli A, Antonelli IPB, Iannone F, Bixio R, Casa FD, Mormile I, Gurnari C, Fiorenza A, Mejia-Salgado G, Kawakami-Campos PA, Ragab G, Ciccia F, Ruscitti P, Bocchia M, Balistreri A, Tosi GM, Frediani B, Cantarini L, Fabiani C. Vitale A, et al. Semin Arthritis Rheum. 2024 Jun;66:152430. doi: 10.1016/j.semarthrit.2024.152430. Epub 2024 Mar 18. Semin Arthritis Rheum. 2024. PMID: 38554594 Free article.
A significant association was observed between relapsing polychondritis and orbital/ocular involvement in VEXAS syndrome (Relative Risk: 2.37, 95 % C.I. 1.03-5.46, p = 0.048). ...This makes ophthalmologists a key figure in the diagnostic process of VEXAS syndrome …
A significant association was observed between relapsing polychondritis and orbital/ocular involvement in VEXAS syndrome (Rela …
Clinical and immunological features in ACKR1/DARC-associated neutropenia.
Palmblad J, Sohlberg E, Nilsson CC, Lindqvist H, Deneberg S, Ratcliffe P, Meinke S, Mörtberg A, Klimkowska M, Höglund P. Palmblad J, et al. Blood Adv. 2024 Feb 13;8(3):571-580. doi: 10.1182/bloodadvances.2023010400. Blood Adv. 2024. PMID: 38039514 Free PMC article.
ANCs often normalized during inflammation, even mild. Individuals with ADAN (of 327 observed person-years) showed no cases of myelodysplastic syndrome (MDS), which is frequently encountered in SCNP. ...Collectively, more severe neutropenia in ADAN than previo …
ANCs often normalized during inflammation, even mild. Individuals with ADAN (of 327 observed person-years) showed no cases of myel …
41 results