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Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations.
J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1394-8. doi: 10.1136/jnnp.2008.162263.
J Neurol Neurosurg Psychiatry. 2009.
PMID: 19917821
2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene.
Rooryck C, Stef M, Burgelin I, Simon D, Souakri N, Thambo JB, Chateil JF, Lacombe D, Arveiler B.
Rooryck C, et al. Among authors: souakri n.
Eur J Med Genet. 2009 Nov-Dec;52(6):446-9. doi: 10.1016/j.ejmg.2009.08.005. Epub 2009 Sep 3.
Eur J Med Genet. 2009.
PMID: 19733267
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Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum.
Rooryck C, VuPhi Y, Souakri N, Burgelin I, Saura R, Lacombe D, Arveiler B, Taine L.
Rooryck C, et al. Among authors: souakri n.
Eur J Med Genet. 2010 Mar-Apr;53(2):104-7. doi: 10.1016/j.ejmg.2010.01.003. Epub 2010 Feb 2.
Eur J Med Genet. 2010.
PMID: 20132917
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Array-CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum.
Rooryck C, Souakri N, Cailley D, Bouron J, Goizet C, Delrue MA, Marlin S, Lacombe FD, Arveiler B.
Rooryck C, et al. Among authors: souakri n.
Am J Med Genet A. 2010 Aug;152A(8):1984-9. doi: 10.1002/ajmg.a.33491.
Am J Med Genet A. 2010.
PMID: 20635336
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Sexual quality of life is impaired in patients with chronic hepatitis C.
Vergniol J, Duc S, Hou G, Hiriart JB, Foucher J, Chenus F, Fabères C, Chermak F, Lafournière A, Souakri N, de Lédinghen V.
Vergniol J, et al. Among authors: souakri n.
Int J Impot Res. 2016 Mar-Apr;28(2):68-73. doi: 10.1038/ijir.2016.5. Epub 2016 Feb 11.
Int J Impot Res. 2016.
PMID: 26865102
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