Publications by authors named "Nabil Nassib"

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Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities.
Ali Al Kaissi, Sergey Ryabykh, Nabil Nassib, Sami Bouchoucha, Lamia Benjemaa

Diagnostics (Basel)· September 2022

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Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome.
Dorra Najjar, Asma Chikhaoui, Sinda Zarrouk, Saifeddine Azouz, Wafa Kamoun, Nabil Nassib

Genes (Basel)· September 2022

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Torticollis in Connection with Spine Phenotype.
Ali Al Kaissi, Nabil Nassib, Sami Bouchoucha, Mohammad Shboul, Franz Grill

Diagnostics (Basel)· July 2022

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Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports.
Ali Al Kaissi, Mirya Kuranova, Nadezhda Pleskach, Vladimir Kenis, Nabil M Nassib

Medicine (Baltimore)· December 2017

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How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports.
Ali Al Kaissi, Christian Windpassinger, Farid Ben Chehida, Maher Ben Ghachem, Nabil M Nassib

Medicine (Baltimore)· September 2017

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Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen-Goldberg syndrome: a report on a family over 4 generations: Case report.
Ali Al Kaissi, Zahra Marrakchi, Nabil M Nassib, Jochen Hofstaetter, Franz Grill

Medicine (Baltimore)· March 2017

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Progressive congenital torticollis in VATER association syndrome.
Ali Al Kaissi, Farid Ben Chehida, Hatem Safi, Nabil Nassib, Maher Ben Ghachem

Spine (Phila Pa 1976)· May 2006

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Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia.
Ali Al Kaissi, Farid Ben Chehida, Nabil Nassib, Hatem Safi, Mrad Djnziri

Afr Health Sci· September 2005

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