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Farid Ben Chehida

Showing results (11-20 of 36) with videos related to

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Skeletal Radiology|February 8, 2008
A hypoplastic atlas and long odontoid process in a girl manifesting phenotypic features resembling spondyloepimetaphyseal dysplasia joint laxity syndromeAli Al Kaissi, Farid Ben Chehida, Maher Ben Ghachem, et al.
African Journal of Paediatric Surgery : AJPS|August 10, 2016
Lower limbs deformities in patients with McCune-Albright syndrome: Tomography and treatmentAli Al Kaissi, Vladimir Kenis, Farid Ben Chehida, et al.
Scoliosis|October 18, 2006
Atlanto-axial rotatory fixation in a girl with Spondylocarpotarsal synostosis syndromeAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Orphanet Journal of Rare Diseases|January 11, 2007
Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndromeAli Al Kaissi, Franz Grill, Hatem Safi, et al.
Clinical Dysmorphology|June 20, 2002
Hypohidrotic ectodermal dysplasia with tibial aplasiaAli Al Kaissi, Maher Ben Ghachem, Mohamed Nebil Necib, et al.
Orthopaedic Surgery|November 29, 2014
Corrections of lower limb deformities in patients with diastrophic dysplasiaAli Al Kaissi, Vladimir Kenis, Eugeniy Melchenko, et al.
Spine|May 25, 2006
Progressive congenital torticollis in VATER association syndromeAli Al Kaissi, Farid Ben Chehida, Hatem Safi, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|January 25, 2007
Persistent torticollis, facial asymmetry, grooved tongue, and dolicho-odontoid process in connection with atlas malformation complex in three family subjectsAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Clinical Dysmorphology|October 18, 2003
Siblings with glaucoma, mental retardation and short statureAli AlKaissi, Aza Hammou, Maher Ben Ghachem, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial vertebral segmentation defects, Sprengel anomaly, and omovertebral bone with variable expressivityAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Skeletal Radiology|February 8, 2008
A hypoplastic atlas and long odontoid process in a girl manifesting phenotypic features resembling spondyloepimetaphyseal dysplasia joint laxity syndromeAli Al Kaissi, Farid Ben Chehida, Maher Ben Ghachem, et al.
African Journal of Paediatric Surgery : AJPS|August 10, 2016
Lower limbs deformities in patients with McCune-Albright syndrome: Tomography and treatmentAli Al Kaissi, Vladimir Kenis, Farid Ben Chehida, et al.
Scoliosis|October 18, 2006
Atlanto-axial rotatory fixation in a girl with Spondylocarpotarsal synostosis syndromeAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Orphanet Journal of Rare Diseases|January 11, 2007
Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndromeAli Al Kaissi, Franz Grill, Hatem Safi, et al.
Clinical Dysmorphology|June 20, 2002
Hypohidrotic ectodermal dysplasia with tibial aplasiaAli Al Kaissi, Maher Ben Ghachem, Mohamed Nebil Necib, et al.
Orthopaedic Surgery|November 29, 2014
Corrections of lower limb deformities in patients with diastrophic dysplasiaAli Al Kaissi, Vladimir Kenis, Eugeniy Melchenko, et al.
Spine|May 25, 2006
Progressive congenital torticollis in VATER association syndromeAli Al Kaissi, Farid Ben Chehida, Hatem Safi, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|January 25, 2007
Persistent torticollis, facial asymmetry, grooved tongue, and dolicho-odontoid process in connection with atlas malformation complex in three family subjectsAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Clinical Dysmorphology|October 18, 2003
Siblings with glaucoma, mental retardation and short statureAli AlKaissi, Aza Hammou, Maher Ben Ghachem, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial vertebral segmentation defects, Sprengel anomaly, and omovertebral bone with variable expressivityAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Pageof 4