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Ben Rekaya, M.
~ 100
results:
Search for persons
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Format
Online
Mediatypes
Articles (Online)
Bookchapter (Online)
OpenAccess-fulltext
Languages
english (91)
french (7)
Sorted by: Relevance
Sorted by: Year
?
1
Clinical, genealogical and molecular investigation of the x..:
Jerbi, M.
;
Ben Rekaya, M.
;
Naouali, C.
...
British Journal of Dermatology. 174 (2015) 2 - p. 439-443 , 2015
Link:
https://doi.org/10.1111/..
?
2
Le mélanome cutané en Tunisie : un cancer sous-estimé:
Naouali, C.
;
Marnissi, B.
;
Jones, M.
...
Annales de Dermatologie et de Vénéréologie. 141 (2014) 6-7 - p. S84-S85 , 2014
Link:
https://doi.org/10.1016/..
?
3
Développement d'un test de diagnostic moléculaire simple po..:
Ben Rekaya, M.
;
Laroussi, N.
;
Messaoud, O.
...
Annales de Dermatologie et de Vénéréologie. 141 (2014) 6-7 - p. S86 , 2014
Link:
https://doi.org/10.1016/..
?
4
Association xéroderma pigmentosum et anomalies thyroïdienne..:
Jones, M.
;
Nakouri, I.
;
Zghal, M.
...
Annales de Dermatologie et de Vénéréologie. 141 (2014) 12 - p. S378 , 2014
Link:
https://doi.org/10.1016/..
?
5
Severe phenotypes in two Tunisian families with novel XPA m..:
Messaoud, O.
;
Ben Rekaya, M.
;
Ouragini, H.
...
Archives of Dermatological Research. 304 (2011) 2 - p. 171-176 , 2011
Link:
https://doi.org/10.1007/..
?
6
Identification of a primarily neurological phenotypic expre..:
Messaoud, O.
;
Ben Rekaya, M.
;
Kefi, R.
...
British Journal of Dermatology. 162 (2010) 4 - p. 883-886 , 2010
Link:
https://doi.org/10.1111/..
?
7
High frequency of the V548A fs X572 XPC mutation in Tunisia..:
Ben Rekaya, M
;
Messaoud, O
;
Talmoudi, F
...
Journal of Human Genetics. 54 (2009) 7 - p. 426-429 , 2009
Link:
https://doi.org/10.1038/..
?
8
The Experience of a Tunisian Referral Centre in Prenatal Di..:
Messaoud, O.
;
Rekaya, M. Ben
;
Jerbi, M.
...
Public Health Genomics. 16 (2013) 5 - p. 251-254 , 2013
Link:
https://www.jstor.org/st..
?
9
Maladies dermatologiques en Algérie:
Tiar, A.
;
Romdhane, L.
;
Messaoud, O.
...
Annales de Dermatologie et de Vénéréologie. 140 (2013) 12 - p. S652 , 2013
Link:
https://doi.org/10.1016/..
?
10
Constitutional mismatch repair deficiency syndrome with aty..:
Akrout, Firas
;
Achour, Ahlem
;
Tops, Carli M. J.
...
Frontiers in Oncology. 13 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
11
Table_1_Constitutional mismatch repair deficiency syndrome ..:
Firas Akrout
;
Ahlem Achour
;
Carli M. J. Tops
...
doi:10.3389/fonc.2023.1195814.s001. , 2023
Link:
https://doi.org/10.3389/..
?
12
Constitutional mismatch repair deficiency syndrome with aty..:
Firas Akrout
;
Ahlem Achour
;
Carli M. J. Tops
...
https://www.frontiersin.org/articles/10.3389/fonc.2023.1195814/full. , 2023
Link:
https://doi.org/10.3389/..
?
13
Évaluation de l'état nutritionnel des allogreffés de moelle..:
Mben Khaled, M.
;
Rekaya, S.
;
Ouederni, M.
...
Annales d'Endocrinologie. 77 (2016) 4 - p. 484 , 2016
Link:
https://doi.org/10.1016/..
?
14
Le retard statural et déficits immunitaires primitifs : fré..:
Ben Khaled, M.
;
Ouederni, M.
;
Ben Fradj, I.
...
Annales d'Endocrinologie. 77 (2016) 4 - p. 318 , 2016
Link:
https://doi.org/10.1016/..
?
15
L'hypoparathyroïdie complication rare de l'hémochromatose s..:
Ben Khaled, M.
;
Rhouma, K.
;
Ouederni, M.
...
Annales d'Endocrinologie. 77 (2016) 4 - p. 368 , 2016
Link:
https://doi.org/10.1016/..
1-15