|
|
|
|
| LEADER |
01000caa a22002652c 4500 |
| 001 |
NLM240199367 |
| 003 |
DE-627 |
| 005 |
20250217070441.0 |
| 007 |
cr uuu---uuuuu |
| 008 |
231224s2014 xx |||||o 00| ||eng c |
| 024 |
7 |
|
|a 10.1016/j.clim.2014.07.001
|2 doi
|
| 028 |
5 |
2 |
|a pubmed25n0800.xml
|
| 035 |
|
|
|a (DE-627)NLM240199367
|
| 035 |
|
|
|a (NLM)25038527
|
| 035 |
|
|
|a (PII)S1521-6616(14)00168-5
|
| 040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
| 041 |
|
|
|a eng
|
| 100 |
1 |
|
|a Torres, Leuridan Cavalcante
|e verfasserin
|4 aut
|
| 245 |
1 |
0 |
|a NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
|
| 264 |
|
1 |
|c 2014
|
| 336 |
|
|
|a Text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
| 338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
| 500 |
|
|
|a Date Completed 04.11.2014
|
| 500 |
|
|
|a Date Revised 13.09.2014
|
| 500 |
|
|
|a published: Print-Electronic
|
| 500 |
|
|
|a Citation Status MEDLINE
|
| 520 |
|
|
|a Copyright © 2014 Elsevier Inc. All rights reserved.
|
| 520 |
|
|
|a The mucopolysaccharidoses (MPSs) are a group of rare, inherited lysosomal storage disorders that are clinically characterized by abnormalities in multiple organ systems and reduced life expectancy. Whereas the lysosome is essential to the functioning of the immune system, some authors suggest that the MPS patients have abnormalities in the immune system similar to the patients with primary immunodeficiency. In this study, we evaluated 8 male MPS type II patients of the same family with novel mutation in the IDS gene. We found in this MPS family a quantitative deficiency of NK and B cells with normal values of IgG, IgM and IgA serum antibodies and normal response to polysaccharide antigens. Interestingly, abnormalities found in these patients were not observed in other MPS patients, suggesting that the type of mutation found in the IDS gene can be implicated in the immunodeficiency
|
| 650 |
|
4 |
|a Journal Article
|
| 650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
| 650 |
|
4 |
|a Autoimmunity
|
| 650 |
|
4 |
|a B cells
|
| 650 |
|
4 |
|a Immunodeficiency
|
| 650 |
|
4 |
|a Mucopolysaccharidoses
|
| 650 |
|
4 |
|a NK cells
|
| 650 |
|
7 |
|a Immunoglobulins
|2 NLM
|
| 650 |
|
7 |
|a Iduronate Sulfatase
|2 NLM
|
| 650 |
|
7 |
|a EC 3.1.6.13
|2 NLM
|
| 700 |
1 |
|
|a Soares, Diogo Cordeiro de Queiroz
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Kulikowski, Leslie Domenici
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Franco, Jose Francisco
|e verfasserin
|4 aut
|
| 700 |
1 |
|
|a Kim, Chong Ae
|e verfasserin
|4 aut
|
| 773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 154(2014), 2 vom: 23. Okt., Seite 100-4
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnas
|
| 773 |
1 |
8 |
|g volume:154
|g year:2014
|g number:2
|g day:23
|g month:10
|g pages:100-4
|
| 856 |
4 |
0 |
|u http://dx.doi.org/10.1016/j.clim.2014.07.001
|3 Volltext
|
| 912 |
|
|
|a GBV_USEFLAG_A
|
| 912 |
|
|
|a SYSFLAG_A
|
| 912 |
|
|
|a GBV_NLM
|
| 912 |
|
|
|a GBV_ILN_11
|
| 912 |
|
|
|a GBV_ILN_24
|
| 912 |
|
|
|a GBV_ILN_350
|
| 951 |
|
|
|a AR
|
| 952 |
|
|
|d 154
|j 2014
|e 2
|b 23
|c 10
|h 100-4
|