Hypereosinophilic Syndrome research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Hypereosinophilic Syndrome treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
Designed by medical professionals, for medical professionals, with doctorAsyou you can visualize research in a unique evidence dashboard. You can also export, save and sort results.
Sign up for free for full access.
All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 22 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
Sort by
Date
Institutional score
Impact
Patients
List order
Sort
Categories
Studies
23044 Unclassified
14444 Case Reports
9360 Research
8993 Reviews
3888 Early Trials
3681 Other Trials
3433 Advanced Trials
137 Meta-Analysis
Guidelines
66 Guidelines
56 Cochrane
35 Consensuses
Congresses
5835 Abstracts
Research
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Khajuria Rajiv K, Munschauer Mathias, Ulirsch Jacob C, Fiorini Claudia, Ludwig Leif S ...
Cell Vol 173(1)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 22 Mar 2018
Research
Partial V(D)J recombination activity leads to Omenn syndrome.
Villa A, Santagata S, Bozzi F, Giliani S, Frattini A ...
Cell Vol 93(5)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 29 May 1998
Research
Crosstalk between sentinel and helper macrophages permits neutrophil migration into infected uroepithelium.
Schiwon Marzena, Weisheit Christina, Franken Lars, Gutweiler Sebastian, Dixit Akanksha ...
Cell Vol 156(3)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 30 Jan 2014
Research
Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice.
Ueki Yasuyoshi, Lin Chin-Yu, Senoo Makoto, Ebihara Takeshi, Agata Naoki ...
Cell Vol 128(1)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 12 Jan 2007
Research
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
Ho M, Chelly J, Carter N, Danek A, Crocker P ...
Cell Vol 77(6)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 17 Jun 1994
Research
Physiogenomic resources for rat models of heart, lung and blood disorders.
Malek Renae L, Wang Hong-ying, Kwitek Anne E, Greene Andrew S, Bhagabati Nirmal ...
Nature genetics Vol 38(2)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Feb 2006
Research
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Iotchkova Valentina, Huang Jie, Morris John A, Jain Deepti, Barbieri Caterina ...
Nature genetics Vol 48(11)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Nov 2016
Research
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
Guernsey Duane L, Jiang Haiyan, Campagna Dean R, Evans Susan C, Ferguson Meghan ...
Nature genetics Vol 41(6)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Jun 2009
Research
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.
Noetzli Leila, Lo Richard W, Lee-Sherick Alisa B, Callaghan Michael, Noris Patrizia ...
Nature genetics Vol 47(5)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 May 2015
Research
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Kamatani Yoichiro, Matsuda Koichi, Okada Yukinori, Kubo Michiaki, Hosono Naoya ...
Nature genetics Vol 42(3)
ReadAdd to library
Add to library
Select a folder
Create a new folder +
Cancel
Date 01 Mar 2010
View
per page
Page
1
2
3
4
5
6
7
8
9
10
Last
