I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Mansour‐Hendili, Lamisse
66
results:
Search for persons
X
Format
Online (66)
Mediatypes
Articles (Online) (18)
OpenAccess-fulltext (48)
Languages
english (54)
french (3)
Sorted by: Relevance
Sorted by: Year
?
1
Intragenic deletions in SPTB are associated with hereditary..:
Evrard, Ophélie
;
Billes, Alexis
;
Badens, Catherine
...
British Journal of Haematology. , 2024
Link:
https://doi.org/10.1111/..
?
2
Late‐onset refractory hemolytic anemia in siblings treated ..:
Nguyen, Alexandre
;
Deshayes, Samuel
;
Nowoczyn, Marie
...
JIMD Reports. 65 (2024) 3 - p. 163-170 , 2024
Link:
https://doi.org/10.1002/..
?
3
Connecting the dots: Xanthoma, haemolytic anaemia, stomatoc..:
Rieu, Jean‐Baptiste
;
Jamme, Thibaut
;
Astudillo, Léonardo
...
eJHaem. 4 (2023) 4 - p. 1166-1167 , 2023
Link:
https://doi.org/10.1002/..
?
4
Use of minigene assays as a useful tool to confirm the path..:
Lunati‐Rozie, Ariane
;
Janin, Alexandre
;
Faubert, Emmanuelle
...
British Journal of Haematology. 201 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1111/..
?
5
Acquired spherocytosis due to somatic ANK1 mutations as a m..:
Mansour‐Hendili, Lamisse
;
Flamarion, Edouard
;
Michel, Marc
...
American Journal of Hematology. 97 (2022) 8 - p. , 2022
Link:
https://doi.org/10.1002/..
?
6
VPS4A mutation in syndromic congenital hemolytic anemia wit..:
Lunati, Ariane
;
Petit, Arnaud
;
Lapillonne, Hélène
...
American Journal of Hematology. 96 (2021) 4 - p. , 2021
Link:
https://doi.org/10.1002/..
?
7
Multiple thrombosis in a patient with Gardos channelopathy ..:
Mansour‐Hendili, Lamisse
;
Egée, Stéphane
;
Monedero‐Alonso, David
...
American Journal of Hematology. 96 (2021) 9 - p. , 2021
Link:
https://doi.org/10.1002/..
?
8
Inherited or acquired modifiers of iron status may dramatic..:
Orvain, Corentin
;
Da Costa, Lydie
;
Van Wijk, Richard
...
European Journal of Haematology. 101 (2018) 4 - p. 566-569 , 2018
Link:
https://doi.org/10.1111/..
?
9
Recurrent "outsider" intronic variation in the SLC5A6 gene ..:
Mansour-Hendili, Lamisse
;
Gitiaux, Cyril
;
Harion, Madeleine
...
Frontiers in Genetics. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
10
Characterization of genetic variants in the EGLN1/PHD2 gene..:
Delamare, Marine
;
Le Roy, Amandine
;
Pacault, Mathilde
...
Haematologica. 108 (2023) 11 - p. 3068-3085 , 2023
Link:
https://doi.org/10.3324/..
?
11
Comprehensive in silico and functional studies for classifi..:
Karaghiannis, Valéna
;
Maric, Darko
;
Garrec, Céline
...
Haematologica. 108 (2023) 6 - p. 1652-1666 , 2023
Link:
https://doi.org/10.3324/..
?
12
Rapid Gardos Hereditary Xerocytosis Diagnosis in 8 Families..:
Picard, Véronique
;
Guitton, Corinne
;
Mansour-Hendili, Lamisse
...
Frontiers in Physiology. 11 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
13
Les anémies hémolytiques constitutionnelles de causes multi..:
Mansour-Hendili, Lamisse
;
Egee, Stéphane
;
Tarfi, Sihem
...
Transfusion Clinique et Biologique. 28 (2021) 4 - p. S45 , 2021
Link:
https://doi.org/10.1016/..
?
14
Exome sequencing for diagnosis of congenital hemolytic anem..:
Mansour-Hendili, Lamisse
;
Aissat, Abdelrazak
;
Badaoui, Bouchra
...
Orphanet Journal of Rare Diseases. 15 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
15
GermlineSFTPA1mutation in familial idiopathic interstitial ..:
Nathan, Nadia
;
Giraud, Violaine
;
Picard, Clément
...
Human Molecular Genetics. 25 (2016) 8 - p. 1457-1467 , 2016
Link:
https://doi.org/10.1093/..
1-15