Evans' syndrome: from diagnosis to treatment

S Audia, N Grienay, M Mounier, M Michel… - Journal of clinical …, 2020 - mdpi.com
Evans' syndrome (ES) is defined as the concomitant or sequential association of warm auto-
immune haemolytic anaemia (AIHA) with immune thrombocytopenia (ITP), and less …

After 95 years, it's time to eRASe JMML

S Meynier, F Rieux-Laucat - Blood Reviews, 2020 - Elsevier
Juvenile myelomonocytic leukaemia (JMML) is a rare clonal disorder of early childhood.
Constitutive activation of the RAS pathway is the initial event in JMML. Around 90% of …

Clinical outcomes after allogeneic hematopoietic stem cell transplantation in children with juvenile myelomonocytic leukemia: a report from the Japan Society for …

N Yoshida, H Sakaguchi, M Yabe, D Hasegawa… - Biology of Blood and …, 2020 - Elsevier
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for juvenile
myelomonocytic leukemia (JMML), but few large studies of HSCT for JMML exist. Using data …

Single-center experience with epigenetic treatment for juvenile myelomonocytic leukemia

A Marcu, A Colita, LE Radu, CG Jercan, AM Bica… - Frontiers in …, 2020 - frontiersin.org
Background: Juvenile myelomonocytic leukemia (JMML) is a rare myelodysplastic/
myeloproliferative neoplasm diagnosed in young children, characterized by somatic or …

Molecular genetics of MDS/MPN overlap syndromes

AM Hunter, E Padron - Best Practice & Research Clinical Haematology, 2020 - Elsevier
The myelodysplastic/myeloproliferative neoplasms (MDS/MPN) are a heterogenous group of
myeloid malignancies hallmarked by clinicopathologic features that overlap with …

PTPN11 mutation with additional somatic alteration indicates unfavorable outcome in juvenile myelomonocytic leukemia: a retrospective clinical study from a single …

Y Miao, B Li, L Ding, H Zhu, C Luo, J Wang… - European Journal of …, 2020 - Springer
Juvenile myelomonocytic leukemia (JMML) is a heterogeneous childhood leukemia. The
management of patients with JMML requires accurate assessment of genetic and clinical …

[HTML][HTML] 骨髓增生异常综合征RAS 基因突变的分子学特征及预后意义

黄慧君, 李冰, 秦铁军, 徐泽锋, 胡耐博… - Chinese Journal of …, 2020 - ncbi.nlm.nih.gov
骨髓增生异常综合征RAS基因突变的分子学特征及预后意义- PMC Back to Top Skip to main
content NIH NLM Logo Access keys NCBI Homepage MyNCBI Homepage Main Content Main …

Detection of 6pLOH in an aplastic anemia patient by in phase HLA genotyping

E Kikkawa, T Shiina, A Shigenari, Y Ozaki, S Suzuki… - HLA, 2020 - Wiley Online Library
Recent studies have reported loss of heterozygosity in the chromosome 6p arms (6pLOH) of
acquired aplastic anemia (AA) patients, and in tumor cells trying to escape the autoimmune …

A case of uveitis in a patient with juvenile myelomonocytic leukemia successfully treated with adalimumab

LC Wiel, S Pastore, A Taddio… - Journal of Pediatric …, 2020 - journals.lww.com
Patients with juvenile myelomonocytic leukemia due to germline CBL mutation (10% to
15%) may have a subacute course occasionally associated with autoimmune disorders …

RAS pathway mutation patterns in patients with juvenile myelomonocytic leukemia: a developing country single-center experience

N Hamdy, H Bokhary, A Elsayed, W Hozayn… - … Myeloma and Leukemia, 2020 - Elsevier
Introduction Juvenile myelomonocytic leukemia (JMML) is a rare clonal myelodysplastic/
myeloproliferative neoplasm of early childhood. Historically, it was difficult to diagnose …