Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome.
Authors | Anne Rensing-Ehl, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, Myriam Ricarda Lorenz, Benedicte Neven, Ilka Fuchs, Ulrich Salzer, Carsten Speckmann, Anne Strauss, Eberhard Maaβ, Benedicte Collet, Anselm Enders, Remi Favier, Marie Christine Alessi, Frederic Rieux-Laucat, Barbara Zieger, Klaus Schwarz, Stephan Ehl |
Journal | Blood
(Blood)
Vol. 126
Issue 16
Pg. 1967-9
(Oct 15 2015)
ISSN: 1528-0020 [Electronic] United States |
PMID | 26472737
(Publication Type: Case Reports, Clinical Trial, Letter, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Blood Proteins
- FAS protein, human
- FASLG protein, human
- Fas Ligand Protein
- NBEAL2 protein, human
- Nerve Tissue Proteins
- PLXNB1 protein, human
- Receptors, Cell Surface
- fas Receptor
|
Topics |
- Autoimmune Lymphoproliferative Syndrome
(diagnosis, genetics, metabolism, pathology)
- Blood Proteins
(genetics, metabolism)
- Child, Preschool
- Fas Ligand Protein
(genetics, metabolism)
- Female
- Gray Platelet Syndrome
(diagnosis, genetics, metabolism, pathology)
- Humans
- Infant
- Male
- Nerve Tissue Proteins
(genetics, metabolism)
- Receptors, Cell Surface
(genetics, metabolism)
- fas Receptor
(genetics, metabolism)
|
|
Join CureHunter, for free Research Interface BASIC access!
Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease.
Find out why thousands of doctors, pharma researchers and patient activists
around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!
|