scholarly journals Durable remission with ruxolitinib in a chronic neutrophilic leukemia patient harboring a truncation and membrane proximal CSF3R compound mutation

Author(s):  
Anna Hinze ◽  
Jenny Rinke ◽  
Andreas Hochhaus ◽  
Thomas Ernst
Haematologica ◽  
2017 ◽  
Vol 102 (5) ◽  
pp. e207-e209 ◽  
Author(s):  
Zohra Nooruddin ◽  
Nicholas Miltgen ◽  
Qi Wei ◽  
Jeffrey Schowinsky ◽  
Zengang Pan ◽  
...  

Hematology ◽  
2019 ◽  
Vol 24 (1) ◽  
pp. 455-458 ◽  
Author(s):  
Qi-Guo Zhang ◽  
Jing Wang ◽  
Wen-Yu Gong ◽  
Qi-Chuan Jin

2020 ◽  
Vol 13 (12) ◽  
pp. e236202
Author(s):  
Omkaar Jaikaran ◽  
Derek Lim ◽  
Brian Binetti ◽  
Vadim Meytes

Portomesenteric thrombosis is an important but rarely reported complication following bariatric surgery. It has been suggested that the incidence of portal vein thrombosis is directly related to many risk factors inherent in the bariatric population as well as factors related to local and systemic effects of laparoscopic surgery. Possible aetiologies vary from systemic inherited hypercoagulable states to a direct inflammatory reaction of portosystemic vessels. Here we present a case report of a 47-year-old obese women who underwent a robotic sleeve gastrectomy with subsequent development of a main portal vein, complete right intrahepatic portal vein and splenic vein thrombosis ultimately found to have a compound mutation of the methylenetetrahydrofolate reductase C677T and A1298C alleles.


2010 ◽  
Vol 76 (3) ◽  
pp. 250-251 ◽  
Author(s):  
L.-X. Yan ◽  
F.-M. Zhu ◽  
W. Wang ◽  
W. Zhang ◽  
H.-J. Lv

Author(s):  
Margarete Voigt ◽  
Konrad Sinn ◽  
Amer Malouhi ◽  
Thomas Gecks ◽  
Jan Zinke ◽  
...  

Blood ◽  
1989 ◽  
Vol 73 (3) ◽  
pp. 814-817 ◽  
Author(s):  
B Opalka ◽  
U Wandl ◽  
O Kloke ◽  
C Oberle ◽  
J Koppe ◽  
...  

Abstract The BCR gene on chromosome 22 has received increasing attention because of its involvement in the Philadelphia (Ph′) translocation. For most restriction enzymes, this locus has been found to be nonpolymorphic. Two alleles have only been found when Taql-digested DNA is hybridized to a 5′ bcr-specific probe. We describe another two-allele polymorphism detected by the same probe in PvuII-digested DNA. The polymorphism is characterized by an additional PvuII site in the bcr region: this causes the appearance of an additional band of about 2.3 kb or 2.5 kb besides a 4.8-kb fragment in hybridizations with the 5′ bcr or a 3′ bcr probe. The incidence of the second allele is very low. It has only been found in some patients with hematopoietic malignancies and in a group of volunteers having a leukemia patient in their families.


1992 ◽  
Vol 41 (1) ◽  
pp. 50-56 ◽  
Author(s):  
Tetsuya Ohtsuki ◽  
Hiroaki Mizukami ◽  
Fumihiko Kimura ◽  
Mayumi Ohnishi ◽  
Naokazu Nagata ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document