Safa Saker
Overview
Explore the profile of Safa Saker including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
162
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0
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Recent Articles
1.
Giovannelli I, Bayatti N, Brown A, Wang D, Mickunas M, Camu W, et al.
Brain Commun
. 2021 Aug;
3(3):fcab141.
PMID: 34409288
Amyotrophic lateral sclerosis is a fatal neurodegenerative disease causing upper and lower motor neuron loss and currently no effective disease-modifying treatment is available. A pathological feature of this disease is...
2.
Camu W, Mickunas M, Veyrune J, Payan C, Garlanda C, Locati M, et al.
EBioMedicine
. 2020 Jul;
59:102844.
PMID: 32651161
Background: Low-dose interleukin-2 (ld-IL-2) enhances regulatory T-cell (Treg) function in auto-inflammatory conditions. Neuroinflammation being a pathogenic feature of amyotrophic lateral sclerosis (ALS), we evaluated the pharmacodynamics and safety of ld-IL-2...
3.
Clermont D, Santoni S, Saker S, Gomard M, Gardais E, Bizet C
Biopreserv Biobank
. 2014 Jun;
12(3):176-83.
PMID: 24955733
A new procedure for room-temperature storage of DNA was evaluated whereby DNA samples from human tissue, bacteria, and plants were stored under an anoxic and anhydrous atmosphere in small glass...
4.
Megarbane H, Florence J, Sass J, Schwonbeck S, Foglio M, de Cid R, et al.
J Invest Dermatol
. 2009 Feb;
129(7):1650-5.
PMID: 19194475
Cutis laxa (CL) is a heterogeneous group of connective tissue disorders characterized by loose, sagging skin and variable involvement of other organs. Autosomal-dominant forms are relatively mild, and may be...
5.
Claus S, Fischer J, Megarbane H, Megarbane A, Jobard F, Debret R, et al.
J Invest Dermatol
. 2008 Jan;
128(6):1442-50.
PMID: 18185537
Cutis laxa (CL) is a rare genodermatosis, which is clinically and genetically heterogeneous. It is characterized by redundant, loose, sagging, and inelastic skin. In a consanguineous family from Lebanon with...
6.
Lesueur F, Bouadjar B, Lefevre C, Jobard F, Audebert S, Lakhdar H, et al.
J Invest Dermatol
. 2006 Dec;
127(4):829-34.
PMID: 17139268
We report clinical and molecular findings in 20 patients from 11 families with autosomal recessive congenital ichthyosis (ARCI) linked to chromosome 17p13, and attributed to mutations in the ALOX gene...
7.
Beauchamp-Nicoud A, Da Costa L, Proust A, Rince P, Saker S, Tchernia G
J Pediatr Hematol Oncol
. 2004 Dec;
26(12):847-8.
PMID: 15591911
Diamond-Blackfan anemia (DBA) is a rare etiology for congenital anemia, but this diagnosis should be considered when aregenerative hypoplastic anemia occurs in infancy. A term infant girl received a red...
8.
Lefevre C, Bouadjar B, Karaduman A, Jobard F, Saker S, Ozguc M, et al.
Hum Mol Genet
. 2004 Aug;
13(20):2473-82.
PMID: 15317751
We report the genomic localization by homozygosity mapping and the identification of a gene for a new form of non-syndromic autosomal recessive congenital ichthyosis. The phenotype usually presents as non-bullous...
9.
de Lonlay P, Mugnier C, Sanlaville D, Chantrel-Groussard K, Benit P, Lebon S, et al.
Hum Mol Genet
. 2002 Dec;
11(26):3273-81.
PMID: 12471054
The mapping and identification of respiratory chain deficiency genes is particularly tedious owing to the large number of genes encoding catalytic subunits and involved in respiratory chain (RC) assembly and...