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Hakima Lakhdar
Observed institution:
Centre Hospitalier Universitaire Ibn Rochd
OpenAlex ID:
A5111739958
Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome
2001
·
Caroline Lefèvre
, Florence Jobard
, et al.
·
The American Journal of Human Genetics
·
477
Cutaneous tuberculosis in Morocco
2006
·
Kawtar Zouhair
, Nadia Akhdari
, et al.
·
International Journal of Infectious Diseases
·
66
PDF
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome
1998
·
Michel Bahuau
, Claude Houdayer
, et al.
·
American Journal of Medical Genetics
·
52
Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13
2006
·
Fabienne Lesueur
, Bakar Bouadjar
, et al.
·
Journal of Investigative Dermatology
·
46
Pemphigus: analysis of 262 cases
2008
·
Hakima Benchikhi
, Siham Ghafour
, et al.
·
International Journal of Dermatology
·
10
Annular lichen planus involving the esophagus: a rare diagnosis
2004
·
Lamia Belloul
, Nadia Akhdari
, et al.
·
International Journal of Dermatology
·
8
Erythematous Lesions on the Scalp—Quiz Case
2004
·
Nadia Akhdari
, Hayat Dahbi Skalli
, et al.
·
Archives of Dermatology
·
6
Profil épidémiologique du psoriasis au service de dermatologie de Casablanca Étude de 3 021 cas
2009
·
Samira Skali
, Radia Berrada
, et al.
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Works count:
9
Citation count:
665
H-index:
6
I10-index:
5
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