Format
Sort by

Send to

Choose Destination

Search results

Items: 2

1.

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients.

Ben-Khemis L, Mekki N, Ben-Mustapha I, Rouault K, Mellouli F, Khemiri M, Bejaoui M, Essaddam L, Ben-Becher S, Boughamoura L, Hassayoun S, Ben-Ali M, Barbouche MR.

Mol Immunol. 2017 Oct;90:57-63. doi: 10.1016/j.molimm.2017.06.248. Epub 2017 Jul 10.

PMID:
28704707
2.

[Radiological case of the month. Chronic septic granulomatous disease revealed by pulmonary aspergillosis in a girl].

Ben Meriem C, Pousse H, Golli M, el Aouini-Rea P, Radhouane M, Bejaoui M, Ganouni A.

Arch Pediatr. 1997 Jul;4(7):683-4. French. No abstract available.

PMID:
9295910

Supplemental Content

Loading ...
Support Center